| geneid | 23112 |
|---|---|
| ensemblid | ENSG00000100354.21 |
| hgncid | 29190 |
| symbol | TNRC6B |
| name | trinucleotide repeat containing adaptor 6B |
| refseq_nuc | NM_001162501.2 |
| refseq_prot | NP_001155973.1 |
| ensembl_nuc | ENST00000454349.7 |
| ensembl_prot | ENSP00000401946.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 40177925 |
| end | 40335808 |
| strand | + |
| ver | v1.2 |
| region | chr22:40177925-40335808 |
| region5000 | chr22:40172925-40340808 |
| regionname0 | TNRC6B_chr22_40177925_40335808 |
| regionname5000 | TNRC6B_chr22_40172925_40340808 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1833 | 246 | 37 | 38 | 130 | 11 | 28 | 98 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002 | 0/0 | 1832 | 44 | 21 | 13 | 2 | 1 | 7 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0003 | 0/0 | 1833 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0004 | 0/0 | 1833 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0005 | 0/0 | 1833 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0006 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0007 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0008 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0009 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0010 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0011 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0012 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0013 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0014 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5502 | 238 | 36 | 37 | 126 | 9 | 28 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0002 | 0/0 | 5499 | 44 | 21 | 13 | 2 | 1 | 7 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0003 | 0/0 | 5502 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0004 | 0/0 | 5502 | 3 | 2 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0005 | 0/0 | 5502 | 2 | 0 | 0 | 0 | 2 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0006 | 0/0 | 5502 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0007 | 0/0 | 5502 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0008 | 0/0 | 5502 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0009 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0010 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0011 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0012 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0013 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0014 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0015 | 0/0 | 5502 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0016 | 0/0 | 5502 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0017 | 0/0 | 5502 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0018 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0019 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| c0020 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| 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 | 12784 | 32 | 0 | 4 | 27 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0002 | 0/0 | 12785 | 26 | 0 | 4 | 16 | 2 | 4 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0003 | 0/0 | 12785 | 9 | 0 | 2 | 5 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0004 | 0/0 | 12785 | 9 | 0 | 1 | 6 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0005 | 0/0 | 12786 | 8 | 0 | 0 | 8 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0006 | 0/0 | 12784 | 7 | 7 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0007 | 0/0 | 12784 | 6 | 0 | 3 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0008 | 0/0 | 12786 | 6 | 0 | 3 | 2 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0009 | 0/0 | 12781 | 6 | 1 | 3 | 0 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0010 | 0/0 | 12785 | 5 | 0 | 1 | 4 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0011 | 0/0 | 12785 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0012 | 0/0 | 12786 | 5 | 2 | 0 | 1 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0013 | 0/0 | 12786 | 4 | 0 | 1 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0014 | 0/0 | 12783 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0015 | 0/0 | 12783 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0016 | 0/0 | 12786 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0017 | 0/0 | 12785 | 3 | 0 | 1 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0018 | 0/0 | 12786 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0019 | 0/0 | 12786 | 3 | 1 | 1 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0020 | 0/0 | 12785 | 3 | 0 | 0 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0021 | 0/0 | 12784 | 3 | 1 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0022 | 0/0 | 12785 | 3 | 0 | 0 | 0 | 0 | 3 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0023 | 0/1 | 12784 | 2 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0024 | 0/0 | 12784 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0025 | 0/0 | 12785 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0026 | 1/0 | 12779 | 2 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0027 | 0/0 | 12786 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0028 | 0/0 | 12784 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0029 | 0/0 | 12785 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0030 | 0/0 | 12785 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0031 | 0/0 | 12785 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0032 | 0/0 | 12781 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0033 | 0/0 | 12784 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0034 | 0/0 | 12784 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0035 | 0/0 | 12782 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0036 | 0/0 | 12785 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0037 | 0/0 | 12783 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0038 | 0/0 | 12786 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0039 | 0/0 | 12782 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0040 | 0/0 | 12785 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0041 | 0/0 | 12782 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0042 | 0/0 | 12782 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0043 | 0/0 | 12783 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0044 | 0/0 | 12783 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0045 | 0/0 | 12785 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0046 | 0/0 | 12781 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0047 | 0/0 | 12781 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0048 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0049 | 0/0 | 12781 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0050 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0051 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0052 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0053 | 0/0 | 12782 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0054 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0055 | 0/0 | 12785 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0056 | 0/0 | 12785 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0057 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0058 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0059 | 0/0 | 12777 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0060 | 0/0 | 12778 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0061 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0062 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0063 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0064 | 0/0 | 12783 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0065 | 0/0 | 12783 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0066 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0067 | 0/0 | 12783 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0068 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0069 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0070 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0071 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0072 | 0/0 | 12786 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0073 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0074 | 0/0 | 12785 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0075 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0076 | 0/0 | 12781 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0077 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0078 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0079 | 0/0 | 12785 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0080 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0081 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0082 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0083 | 0/0 | 12781 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0084 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0085 | 0/0 | 12787 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0086 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0087 | 0/0 | 12775 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0088 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0089 | 0/0 | 12785 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0090 | 0/0 | 12784 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0091 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0092 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0093 | 0/0 | 12785 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0094 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0095 | 0/0 | 12781 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0096 | 0/0 | 12783 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0097 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0098 | 0/0 | 12780 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0099 | 0/0 | 12781 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0100 | 0/0 | 12780 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0101 | 0/0 | 12782 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0102 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0103 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0104 | 0/0 | 12781 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0105 | 0/0 | 12782 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0106 | 0/0 | 12781 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0107 | 0/0 | 12783 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0108 | 0/0 | 12785 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0109 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0110 | 0/0 | 12781 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0111 | 0/0 | 12784 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0112 | 0/0 | 12785 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0113 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0114 | 0/0 | 12785 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0115 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0116 | 0/0 | 12782 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0117 | 0/0 | 12784 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0118 | 0/0 | 12783 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0119 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0120 | 0/0 | 12787 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0121 | 0/0 | 12786 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0122 | 0/0 | 12785 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0123 | 0/0 | 12786 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0124 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0125 | 0/0 | 12787 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0126 | 0/0 | 12780 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0127 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0128 | 0/0 | 12784 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0129 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0130 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0131 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0132 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0133 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0134 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0135 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0136 | 0/0 | 12783 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0137 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0138 | 0/0 | 12783 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0139 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0140 | 0/0 | 12787 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0141 | 0/0 | 12786 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0142 | 0/0 | 12786 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0143 | 0/0 | 12787 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0144 | 0/0 | 12783 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0145 | 0/0 | 12785 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0146 | 0/0 | 12782 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0147 | 0/0 | 12782 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0148 | 0/0 | 12784 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0149 | 0/0 | 12784 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0150 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0151 | 0/0 | 12782 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0152 | 0/0 | 12785 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0153 | 0/0 | 12784 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0154 | 0/0 | 12782 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0155 | 0/0 | 12786 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0156 | 0/0 | 12787 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| t0157 | 0/0 | 12783 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0303 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5502 | 238 | 36 | 37 | 126 | 9 | 28 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0005 | 0/0 | 5502 | 2 | 0 | 0 | 0 | 2 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0008 | 0/0 | 5502 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0013 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0015 | 0/0 | 5502 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0017 | 0/0 | 5502 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0020 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002 | 0/0 | 5499 | 44 | 21 | 13 | 2 | 1 | 7 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0003c0003 | 0/0 | 5502 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0004c0004 | 0/0 | 5502 | 3 | 2 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0005c0007 | 0/0 | 5502 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0006c0006 | 0/0 | 5502 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0007c0018 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0008c0016 | 0/0 | 5502 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0009c0014 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0010c0012 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0011c0011 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0012c0010 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0013c0019 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0014c0009 | 0/0 | 5502 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 18285 | 29 | 0 | 4 | 24 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0002 | 0/0 | 18286 | 24 | 0 | 4 | 14 | 2 | 4 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0003 | 0/0 | 18286 | 9 | 0 | 2 | 5 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0004 | 0/0 | 18286 | 7 | 0 | 1 | 5 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0005 | 0/0 | 18287 | 6 | 0 | 0 | 6 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0006 | 0/0 | 18285 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0007 | 0/0 | 18285 | 6 | 0 | 3 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0008 | 0/0 | 18287 | 6 | 0 | 3 | 2 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0010 | 0/0 | 18286 | 5 | 0 | 1 | 4 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0011 | 0/0 | 18286 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0012 | 0/0 | 18287 | 5 | 2 | 0 | 1 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0013 | 0/0 | 18287 | 4 | 0 | 1 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0014 | 0/0 | 18284 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0015 | 0/0 | 18284 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0016 | 0/0 | 18287 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0017 | 0/0 | 18286 | 3 | 0 | 1 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0018 | 0/0 | 18287 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0019 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0020 | 0/0 | 18286 | 3 | 0 | 0 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0021 | 0/0 | 18285 | 3 | 1 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0022 | 0/0 | 18286 | 3 | 0 | 0 | 0 | 0 | 3 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0023 | 0/1 | 18285 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0024 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0025 | 0/0 | 18286 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0026 | 1/0 | 18280 | 2 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0027 | 0/0 | 18287 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0028 | 0/0 | 18285 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0029 | 0/0 | 18286 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0030 | 0/0 | 18286 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0031 | 0/0 | 18286 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0033 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0034 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0035 | 0/0 | 18283 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0037 | 0/0 | 18284 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0038 | 0/0 | 18287 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0039 | 0/0 | 18283 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0040 | 0/0 | 18286 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0042 | 0/0 | 18283 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0043 | 0/0 | 18284 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0044 | 0/0 | 18284 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0045 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0046 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0047 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0048 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0049 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0050 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0051 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0052 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0053 | 0/0 | 18283 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0054 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0055 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0056 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0057 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0058 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0061 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0062 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0063 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0064 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0065 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0066 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0067 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0068 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0069 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0071 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0072 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0073 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0074 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0075 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0076 | 0/0 | 18282 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0077 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0078 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0080 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0081 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0082 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0086 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0088 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0089 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0093 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0108 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0109 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0113 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0114 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0115 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0116 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0117 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0118 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0119 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0120 | 0/0 | 18288 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0121 | 0/0 | 18287 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0122 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0123 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0124 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0125 | 0/0 | 18288 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0126 | 0/0 | 18281 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0127 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0128 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0129 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0130 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0131 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0132 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0133 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0134 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0135 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0137 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0138 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0139 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0140 | 0/0 | 18288 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0142 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0143 | 0/0 | 18288 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0144 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0145 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0146 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0148 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0001t0149 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0005t0004 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0005t0141 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0008t0002 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0008t0070 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0013t0005 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0015t0024 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0017t0079 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0001c0020t0023 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0006 | 0/0 | 18282 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0009 | 0/0 | 18279 | 6 | 1 | 3 | 0 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0032 | 0/0 | 18279 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0033 | 0/0 | 18282 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0034 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0036 | 0/0 | 18283 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0041 | 0/0 | 18280 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0083 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0084 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0085 | 0/0 | 18285 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0087 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0090 | 0/0 | 18282 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0091 | 0/0 | 18283 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0092 | 0/0 | 18283 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0094 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0096 | 0/0 | 18281 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0097 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0098 | 0/0 | 18278 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0099 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0100 | 0/0 | 18278 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0101 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0102 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0103 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0104 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0105 | 0/0 | 18280 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0106 | 0/0 | 18279 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0107 | 0/0 | 18281 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0110 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0151 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0152 | 0/0 | 18283 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0153 | 0/0 | 18282 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0154 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0155 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0156 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0002c0002t0157 | 0/0 | 18281 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0003c0003t0001 | 0/0 | 18285 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0004c0004t0019 | 0/0 | 18287 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0004c0004t0136 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0005c0007t0059 | 0/0 | 18278 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0005c0007t0060 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0006c0006t0111 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0006c0006t0112 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0007c0018t0005 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0008c0016t0147 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0009c0014t0004 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0010c0012t0006 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0011c0011t0006 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0012c0010t0150 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0013c0019t0095 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| a0014c0009t0002 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | copy fasta | chr22 | 40172925 | 40340808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0023g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0024g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0025g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0025g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0026g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0026g0303 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0027g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0028g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0028g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0029g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0029g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0030g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0030g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0031g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0031g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0033g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0034g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0035g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0035g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0037g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0037g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0038g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0038g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0039g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0039g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0040g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0040g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0042g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0043g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0044g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0045g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0046g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0047g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0048g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0049g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0050g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0052g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0053g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0054g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0055g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0056g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0057g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0058g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0061g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0062g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0063g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0064g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0065g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0066g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0067g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0068g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0069g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0071g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0072g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0073g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0074g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0075g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0076g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0077g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0078g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0080g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0081g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0082g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0086g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0088g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0089g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0093g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0108g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0109g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0113g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0114g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0115g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0116g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0117g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0118g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0119g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0120g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0121g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0122g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0123g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0124g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0125g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0126g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0127g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0128g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0129g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0130g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0131g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0132g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0133g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0134g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0135g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0137g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0138g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0139g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0140g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0142g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0143g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0144g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0145g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0146g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0148g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0149g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0005t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0005t0141g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0008t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0008t0070g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0013t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0015t0024g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0017t0079g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0020t0023g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0032g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0032g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0033g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0034g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0036g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0036g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0041g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0083g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0084g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0085g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0087g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0090g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0091g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0092g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0094g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0096g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0097g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0098g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0099g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0100g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0101g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0102g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0103g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0104g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0105g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0106g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0107g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0110g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0151g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0152g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0153g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0154g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0155g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0156g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0157g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0004t0019g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0004t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0004t0136g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0005c0007t0059g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0005c0007t0060g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0006c0006t0111g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0006c0006t0112g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0007c0018t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0008c0016t0147g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0009c0014t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0010c0012t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0011c0011t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0012c0010t0150g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0013c0019t0095g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0014c0009t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0026 | g0280 | EUR | GBR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00140 | hp2 | a0002 | c0002 | t0009 | g0120 | EUR | GBR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00280 | hp1 | a0001 | c0001 | t0045 | g0075 | EUR | FIN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00280 | hp2 | a0001 | c0001 | t0020 | g0273 | EUR | FIN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00408 | hp1 | a0001 | c0001 | t0131 | g0027 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00408 | hp2 | a0001 | c0001 | t0013 | g0267 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00423 | hp1 | a0001 | c0001 | t0137 | g0179 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00423 | hp2 | a0001 | c0020 | t0023 | g0067 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00438 | hp2 | a0001 | c0001 | t0068 | g0241 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00544 | hp1 | a0001 | c0001 | t0029 | g0243 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00639 | hp2 | a0002 | c0002 | t0083 | g0093 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00642 | hp1 | a0002 | c0002 | t0009 | g0117 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00733 | hp1 | a0001 | c0001 | t0040 | g0061 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00733 | hp2 | a0001 | c0001 | t0031 | g0299 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0289 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0069 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01069 | hp1 | a0001 | c0001 | t0030 | g0220 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01069 | hp2 | a0001 | c0001 | t0038 | g0044 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01070 | hp1 | a0002 | c0002 | t0009 | g0119 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0234 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01071 | hp1 | a0002 | c0002 | t0009 | g0122 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01106 | hp2 | a0001 | c0001 | t0143 | g0184 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01109 | hp1 | a0001 | c0001 | t0093 | g0147 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01109 | hp2 | a0002 | c0002 | t0099 | g0125 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01167 | hp1 | a0005 | c0007 | t0060 | g0270 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01167 | hp2 | a0002 | c0002 | t0085 | g0124 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01169 | hp1 | a0005 | c0007 | t0059 | g0231 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01175 | hp1 | a0004 | c0004 | t0019 | g0207 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01175 | hp2 | a0001 | c0017 | t0079 | g0269 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01243 | hp1 | a0002 | c0002 | t0090 | g0092 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01243 | hp2 | a0002 | c0002 | t0152 | g0096 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0265 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0272 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01257 | hp2 | a0002 | c0002 | t0104 | g0118 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01258 | hp1 | a0001 | c0001 | t0025 | g0271 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01258 | hp2 | a0001 | c0001 | t0121 | g0306 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01261 | hp1 | a0001 | c0001 | t0040 | g0062 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01261 | hp2 | a0002 | c0002 | t0087 | g0114 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01346 | hp2 | a0001 | c0001 | t0114 | g0081 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0295 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01361 | hp2 | a0002 | c0002 | t0098 | g0121 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01496 | hp1 | a0001 | c0001 | t0039 | g0040 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01496 | hp2 | a0002 | c0002 | t0153 | g0101 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0215 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0279 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0235 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01516 | hp2 | a0001 | c0005 | t0004 | g0171 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01517 | hp1 | a0001 | c0001 | t0072 | g0276 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01517 | hp2 | a0001 | c0005 | t0141 | g0172 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01884 | hp1 | a0006 | c0006 | t0112 | g0001 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01884 | hp2 | a0013 | c0019 | t0095 | g0166 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01891 | hp1 | a0001 | c0001 | t0065 | g0224 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01891 | hp2 | a0001 | c0001 | t0035 | g0142 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0064 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01934 | hp1 | a0002 | c0002 | t0107 | g0105 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01934 | hp2 | a0001 | c0001 | t0017 | g0033 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01943 | hp1 | a0001 | c0001 | t0013 | g0287 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02015 | hp2 | a0001 | c0001 | t0028 | g0246 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02027 | hp1 | a0001 | c0001 | t0140 | g0204 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02027 | hp2 | a0001 | c0001 | t0125 | g0022 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0176 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02040 | hp2 | a0001 | c0001 | t0029 | g0249 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02055 | hp1 | a0001 | c0001 | t0120 | g0088 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02055 | hp2 | a0002 | c0002 | t0100 | g0108 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02071 | hp2 | a0001 | c0001 | t0144 | g0053 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0308 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02129 | hp1 | a0001 | c0001 | t0130 | g0162 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02135 | hp2 | a0001 | c0001 | t0073 | g0225 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02145 | hp1 | a0002 | c0002 | t0094 | g0010 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02145 | hp2 | a0001 | c0001 | t0115 | g0090 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02165 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | CDX | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CDX | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0206 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02257 | hp2 | a0006 | c0006 | t0111 | g0214 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02258 | hp1 | a0002 | c0002 | t0110 | g0112 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02258 | hp2 | a0001 | c0001 | t0035 | g0148 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02280 | hp1 | a0004 | c0004 | t0019 | g0208 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02280 | hp2 | a0002 | c0002 | t0102 | g0097 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02293 | hp1 | a0001 | c0001 | t0014 | g0065 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02293 | hp2 | a0001 | c0001 | t0126 | g0305 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0251 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02523 | hp2 | a0001 | c0001 | t0020 | g0211 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02602 | hp1 | a0001 | c0001 | t0022 | g0177 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02615 | hp1 | a0002 | c0002 | t0034 | g0009 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02615 | hp2 | a0011 | c0011 | t0006 | g0094 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02622 | hp1 | a0002 | c0002 | t0154 | g0155 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02622 | hp2 | a0001 | c0001 | t0049 | g0141 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02630 | hp1 | a0001 | c0001 | t0042 | g0003 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02647 | hp1 | a0001 | c0001 | t0078 | g0277 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02647 | hp2 | a0001 | c0001 | t0034 | g0091 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02698 | hp1 | a0001 | c0001 | t0146 | g0173 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02698 | hp2 | a0001 | c0001 | t0043 | g0157 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0111 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02717 | hp2 | a0001 | c0001 | t0052 | g0002 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02723 | hp1 | a0001 | c0001 | t0054 | g0132 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02809 | hp1 | a0002 | c0002 | t0084 | g0008 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02818 | hp1 | a0001 | c0001 | t0089 | g0151 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0140 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0107 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02895 | hp2 | a0001 | c0015 | t0024 | g0131 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02896 | hp1 | a0002 | c0002 | t0006 | g0095 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02896 | hp2 | a0001 | c0001 | t0127 | g0085 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02976 | hp2 | a0001 | c0001 | t0108 | g0145 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03017 | hp1 | a0001 | c0001 | t0122 | g0056 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03017 | hp2 | a0002 | c0002 | t0009 | g0116 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03041 | hp1 | a0001 | c0001 | t0024 | g0136 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03041 | hp2 | a0002 | c0002 | t0006 | g0144 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0086 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03139 | hp2 | a0002 | c0002 | t0156 | g0104 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03195 | hp1 | a0002 | c0002 | t0155 | g0156 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03195 | hp2 | a0001 | c0001 | t0086 | g0213 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0139 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03225 | hp2 | a0002 | c0002 | t0096 | g0005 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03239 | hp2 | a0002 | c0002 | t0032 | g0127 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03491 | hp1 | a0001 | c0001 | t0128 | g0084 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03491 | hp2 | a0001 | c0001 | t0037 | g0059 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03492 | hp1 | a0001 | c0001 | t0037 | g0060 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03492 | hp2 | a0001 | c0001 | t0039 | g0165 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0089 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03516 | hp2 | a0002 | c0002 | t0103 | g0100 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03540 | hp1 | a0002 | c0002 | t0097 | g0103 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03540 | hp2 | a0001 | c0001 | t0033 | g0146 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03579 | hp1 | a0012 | c0010 | t0150 | g0102 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03579 | hp2 | a0001 | c0001 | t0046 | g0153 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03669 | hp1 | a0002 | c0002 | t0105 | g0115 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03669 | hp2 | a0001 | c0001 | t0030 | g0221 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03704 | hp1 | a0001 | c0001 | t0117 | g0042 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0238 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03710 | hp1 | a0001 | c0001 | t0148 | g0041 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03710 | hp2 | a0001 | c0001 | t0074 | g0222 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03831 | hp2 | a0002 | c0002 | t0041 | g0129 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03834 | hp1 | a0001 | c0001 | t0031 | g0216 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03834 | hp2 | a0001 | c0001 | t0022 | g0126 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03927 | hp1 | a0001 | c0001 | t0123 | g0054 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0200 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0058 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04115 | hp1 | a0002 | c0002 | t0032 | g0128 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04115 | hp2 | a0001 | c0001 | t0022 | g0199 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0202 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04199 | hp1 | a0002 | c0002 | t0106 | g0154 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04204 | hp1 | a0001 | c0001 | t0076 | g0268 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04204 | hp2 | a0002 | c0002 | t0033 | g0159 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0087 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18522 | hp2 | a0002 | c0002 | t0036 | g0012 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18906 | hp1 | a0002 | c0002 | t0151 | g0106 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18906 | hp2 | a0001 | c0001 | t0047 | g0152 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18939 | hp1 | a0001 | c0001 | t0028 | g0239 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18941 | hp2 | a0009 | c0014 | t0004 | g0189 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18942 | hp2 | a0001 | c0013 | t0005 | g0195 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18943 | hp2 | a0014 | c0009 | t0002 | g0229 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18944 | hp1 | a0002 | c0002 | t0092 | g0110 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18945 | hp1 | a0001 | c0001 | t0061 | g0301 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18945 | hp2 | a0001 | c0001 | t0149 | g0021 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18946 | hp1 | a0001 | c0001 | t0124 | g0030 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18946 | hp2 | a0001 | c0001 | t0066 | g0290 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18947 | hp1 | a0001 | c0001 | t0082 | g0253 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18947 | hp2 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18949 | hp1 | a0001 | c0001 | t0057 | g0244 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18951 | hp2 | a0001 | c0001 | t0119 | g0068 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0247 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18954 | hp2 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18959 | hp1 | a0001 | c0001 | t0062 | g0233 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18959 | hp2 | a0001 | c0001 | t0142 | g0201 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18960 | hp1 | a0001 | c0001 | t0109 | g0130 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18961 | hp1 | a0001 | c0001 | t0064 | g0298 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18962 | hp1 | a0001 | c0001 | t0134 | g0182 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18963 | hp1 | a0001 | c0001 | t0019 | g0210 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18973 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18973 | hp2 | a0001 | c0001 | t0063 | g0275 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18974 | hp2 | a0002 | c0002 | t0091 | g0109 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18979 | hp2 | a0001 | c0001 | t0077 | g0286 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18981 | hp1 | a0001 | c0001 | t0129 | g0036 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18981 | hp2 | a0001 | c0001 | t0071 | g0236 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0055 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18984 | hp2 | a0001 | c0001 | t0069 | g0297 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18986 | hp1 | a0001 | c0001 | t0058 | g0261 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0293 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18993 | hp1 | a0001 | c0001 | t0138 | g0167 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0291 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0045 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18995 | hp1 | a0007 | c0018 | t0005 | g0205 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18995 | hp2 | a0001 | c0001 | t0027 | g0232 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19004 | hp2 | a0001 | c0001 | t0012 | g0186 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19005 | hp1 | a0001 | c0001 | t0132 | g0004 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19005 | hp2 | a0001 | c0001 | t0113 | g0263 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19007 | hp1 | a0001 | c0001 | t0145 | g0168 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19007 | hp2 | a0001 | c0001 | t0081 | g0256 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19010 | hp2 | a0001 | c0001 | t0027 | g0284 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19012 | hp1 | a0001 | c0001 | t0080 | g0257 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19043 | hp1 | a0001 | c0001 | t0088 | g0143 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19043 | hp2 | a0001 | c0001 | t0055 | g0134 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19058 | hp2 | a0001 | c0001 | t0135 | g0183 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19062 | hp1 | a0001 | c0001 | t0018 | g0047 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19062 | hp2 | a0001 | c0001 | t0139 | g0175 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0283 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19068 | hp2 | a0001 | c0001 | t0067 | g0282 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19070 | hp1 | a0001 | c0001 | t0118 | g0083 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19077 | hp1 | a0001 | c0001 | t0011 | g0051 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19077 | hp2 | a0001 | c0001 | t0050 | g0242 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19080 | hp1 | a0001 | c0001 | t0021 | g0181 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0292 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19081 | hp1 | a0001 | c0001 | t0075 | g0164 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19082 | hp1 | a0001 | c0001 | t0017 | g0017 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19082 | hp2 | a0001 | c0008 | t0002 | g0259 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19085 | hp1 | a0001 | c0001 | t0018 | g0063 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0262 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19088 | hp2 | a0001 | c0001 | t0133 | g0031 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19091 | hp1 | a0001 | c0008 | t0070 | g0250 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19240 | hp1 | a0001 | c0001 | t0056 | g0133 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19240 | hp2 | a0001 | c0001 | t0021 | g0170 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20805 | hp1 | a0001 | c0001 | t0116 | g0161 | EUR | TSI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0245 | EUR | TSI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20905 | hp1 | a0008 | c0016 | t0147 | g0198 | SAS | GIH | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | GIH | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01123 | hp1 | a0001 | c0001 | t0044 | g0066 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0278 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02559 | hp1 | a0010 | c0012 | t0006 | g0113 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02559 | hp2 | a0001 | c0001 | t0048 | g0138 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03471 | hp1 | a0002 | c0002 | t0036 | g0098 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03471 | hp2 | a0004 | c0004 | t0136 | g0209 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20300 | hp1 | a0002 | c0002 | t0157 | g0099 | AFR | USA | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20300 | hp2 | a0002 | c0002 | t0101 | g0123 | AFR | USA | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA21309 | hp1 | a0001 | c0001 | t0051 | g0149 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA21309 | hp2 | a0001 | c0001 | t0053 | g0137 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0023 | g0158 | REF | REF | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0026 | g0303 | REF | REF | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40262125
|
G | A | 1 | a0014 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.409G>A | p.Ala137Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 620/18280 | 409/5502 | 137/1833 | chr22 | 40262125 | ||
| chr22:40262141
|
C | T | 1 | a0013 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.425C>T | p.Ala142Val | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 636/18280 | 425/5502 | 142/1833 | chr22 | 40262141 | ||
| chr22:40264769
|
C | G | 1 | a0007 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.539C>G | p.Ser180Cys | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 750/18280 | 539/5502 | 180/1833 | chr22 | 40264769 | ||
| chr22:40266436
|
C | T | 1 | a0008 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2206C>T | p.Arg736Cys | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2417/18280 | 2206/5502 | 736/1833 | chr22 | 40266436 | ||
| chr22:40266599
|
G | A | 1 | a0003 | 3 | NA18962.hp2 NA18963.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.2369G>A | p.Ser790Asn | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2580/18280 | 2369/5502 | 790/1833 | chr22 | 40266599 | ||
| chr22:40266839
|
A | C | 1 | a0005 | 2 | HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.2609A>C | p.Glu870Ala | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2820/18280 | 2609/5502 | 870/1833 | chr22 | 40266839 | ||
| chr22:40270226
|
T | C | 1 | a0004 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.2911T>C | p.Ser971Pro | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/23 | 3122/18280 | 2911/5502 | 971/1833 | chr22 | 40270226 | ||
| chr22:40273478
|
G | A | 2 | a0006a0012 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.3019G>A | p.Ala1007Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/23 | 3230/18280 | 3019/5502 | 1007/1833 | chr22 | 40273478 | ||
| chr22:40281188
|
T | A | 1 | a0011 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3481T>A | p.Ser1161Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/23 | 3692/18280 | 3481/5502 | 1161/1833 | chr22 | 40281188 | ||
| chr22:40301172
|
TGCA | T | 5 | a0002a0010a0011others(2): Show | 48 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
conservative_inframe_deletion | MODERATE | c.3982_3984delCAG | p.Gln1328del | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/23 | 4193/18280 | 3982/5502 | 1328/1833 | INFO_REALIGN_3_PRIME | chr22 | 40301172 | |
| chr22:40301315
|
A | G | 1 | a0009 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.4102A>G | p.Ile1368Val | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/23 | 4313/18280 | 4102/5502 | 1368/1833 | chr22 | 40301315 | ||
| chr22:40323074
|
G | A | 1 | a0010 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.5335G>A | p.Ala1779Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5546/18280 | 5335/5502 | 1779/1833 | chr22 | 40323074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40261962
|
C | T | 1 | a0001c0020 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.246C>T | p.Ser82Ser | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 457/18280 | 246/5502 | 82/1833 | chr22 | 40261962 | ||
| chr22:40264809
|
C | T | 1 | a0001c0008 | 2 | NA19082.hp2 NA19091.hp1 |
synonymous_variant | LOW | c.579C>T | p.Asp193Asp | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 790/18280 | 579/5502 | 193/1833 | chr22 | 40264809 | ||
| chr22:40265145
|
T | C | 1 | a0001c0005 | 2 | HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.915T>C | p.Asn305Asn | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 1126/18280 | 915/5502 | 305/1833 | chr22 | 40265145 | ||
| chr22:40266009
|
C | T | 1 | a0001c0017 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1779C>T | p.Tyr593Tyr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 1990/18280 | 1779/5502 | 593/1833 | chr22 | 40266009 | ||
| chr22:40266936
|
T | C | 2 | a0006c0006a0012c0010 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.2706T>C | p.Tyr902Tyr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2917/18280 | 2706/5502 | 902/1833 | chr22 | 40266936 | ||
| chr22:40300463
|
C | T | 1 | a0001c0015 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.3717C>T | p.Ala1239Ala | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 13/23 | 3928/18280 | 3717/5502 | 1239/1833 | chr22 | 40300463 | ||
| chr22:40315308
|
A | G | 1 | a0001c0013 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.4704A>G | p.Thr1568Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/23 | 4915/18280 | 4704/5502 | 1568/1833 | chr22 | 40315308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40177976
|
T | G | 1 | a0002c0002t0041 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/23 | 160 | chr22 | 40177976 | |||||
| chr22:40178093
|
C | T | 1 | a0001c0001t0040 | 2 | HG00733.hp1 HG01261.hp1 |
5_prime_UTR_variant | MODIFIER | c.-43C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/23 | 43 | chr22 | 40178093 | |||||
| chr22:40323732
|
G | C | 7 | a0001c0001t0014a0001c0001t0023a0001c0001t0042others(4): Show | 9 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*491G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 491 | chr22 | 40323732 | |||||
| chr22:40324023
|
G | A | 5 | a0001c0001t0015a0001c0001t0046a0001c0001t0047others(2): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 782 | chr22 | 40324023 | |||||
| chr22:40324290
|
G | GT | 8 | a0002c0002t0151a0002c0002t0152a0002c0002t0153others(5): Show | 8 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1064dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1065 | INFO_REALIGN_3_PRIME | chr22 | 40324290 | ||||
| chr22:40324598
|
C | T | 1 | a0001c0001t0149 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1357 | chr22 | 40324598 | |||||
| chr22:40324606
|
G | A | 1 | a0001c0001t0050 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1365 | chr22 | 40324606 | |||||
| chr22:40324630
|
G | A | 1 | a0001c0001t0051 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1389 | chr22 | 40324630 | |||||
| chr22:40324671
|
C | T | 1 | a0001c0001t0148 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1430 | chr22 | 40324671 | |||||
| chr22:40324700
|
A | G | 66 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(63): Show | 142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1459A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1459 | chr22 | 40324700 | |||||
| chr22:40324949
|
G | C | 7 | a0001c0001t0024a0001c0001t0052a0001c0001t0053others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1708 | chr22 | 40324949 | |||||
| chr22:40324959
|
C | T | 129 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(126): Show | 218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1718C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1718 | chr22 | 40324959 | |||||
| chr22:40325058
|
G | A | 63 | a0001c0001t0006a0001c0001t0015a0001c0001t0024others(60): Show | 76 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1817G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1817 | chr22 | 40325058 | |||||
| chr22:40325350
|
T | C | 1 | a0002c0002t0083 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2109 | chr22 | 40325350 | |||||
| chr22:40325523
|
C | T | 1 | a0002c0002t0110 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2282 | chr22 | 40325523 | |||||
| chr22:40325575
|
A | G | 2 | a0006c0006t0111a0006c0006t0112 | 2 | HG01884.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2334A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2334 | chr22 | 40325575 | |||||
| chr22:40326741
|
A | G | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(64): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3500A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3500 | chr22 | 40326741 | |||||
| chr22:40326807
|
G | A | 7 | a0001c0001t0024a0001c0001t0052a0001c0001t0053others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3566G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3566 | chr22 | 40326807 | |||||
| chr22:40326844
|
G | A | 1 | a0001c0001t0115 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3603G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3603 | chr22 | 40326844 | |||||
| chr22:40326930
|
T | C | 1 | a0002c0002t0084 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3689T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3689 | chr22 | 40326930 | |||||
| chr22:40327350
|
G | A | 3 | a0001c0001t0010a0001c0001t0057a0001c0001t0058 | 7 | HG01361.hp1 HG02074.hp2 NA18949.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4109G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4109 | chr22 | 40327350 | |||||
| chr22:40327705
|
A | G | 168 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(165): Show | 302 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*4464A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4464 | chr22 | 40327705 | |||||
| chr22:40327775
|
C | G | 26 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(23): Show | 48 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4534C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4534 | chr22 | 40327775 | |||||
| chr22:40327916
|
A | G | 1 | a0001c0001t0133 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4675 | chr22 | 40327916 | |||||
| chr22:40328153
|
A | G | 2 | a0001c0001t0022a0008c0016t0147 | 4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4912A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4912 | chr22 | 40328153 | |||||
| chr22:40328417
|
A | G | 3 | a0001c0001t0080a0001c0001t0081a0001c0001t0082 | 3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5176A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5176 | chr22 | 40328417 | |||||
| chr22:40328579
|
A | T | 1 | a0001c0001t0132 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5338A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5338 | chr22 | 40328579 | |||||
| chr22:40328693
|
C | T | 1 | a0001c0001t0108 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5452C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5452 | chr22 | 40328693 | |||||
| chr22:40329019
|
CA | C | 59 | a0001c0001t0006a0001c0001t0015a0001c0001t0024others(56): Show | 72 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5790delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5790 | INFO_REALIGN_3_PRIME | chr22 | 40329019 | ||||
| chr22:40329032
|
C | A | 1 | a0001c0001t0061 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5791C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5791 | chr22 | 40329032 | |||||
| chr22:40329043
|
C | A | 3 | a0001c0001t0027a0001c0001t0062a0001c0001t0063 | 4 | NA18959.hp1 NA18973.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5802C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5802 | chr22 | 40329043 | |||||
| chr22:40329113
|
C | T | 1 | a0001c0001t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5872C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5872 | chr22 | 40329113 | |||||
| chr22:40329137
|
T | A | 2 | a0002c0002t0032a0002c0002t0041 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5896T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5896 | chr22 | 40329137 | |||||
| chr22:40329145
|
A | G | 1 | a0001c0017t0079 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5904A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5904 | chr22 | 40329145 | |||||
| chr22:40329196
|
C | G | 2 | a0002c0002t0107a0002c0002t0157 | 2 | HG01934.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5955C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5955 | chr22 | 40329196 | |||||
| chr22:40329561
|
C | T | 1 | a0002c0002t0106 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6320C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6320 | chr22 | 40329561 | |||||
| chr22:40329590
|
T | G | 1 | a0001c0001t0042 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6349T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6349 | chr22 | 40329590 | |||||
| chr22:40329688
|
G | A | 2 | a0001c0001t0134a0001c0001t0135 | 2 | NA18962.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6447G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6447 | chr22 | 40329688 | |||||
| chr22:40329849
|
A | G | 2 | a0001c0001t0146a0002c0002t0105 | 2 | HG02698.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6608A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6608 | chr22 | 40329849 | |||||
| chr22:40329899
|
A | C | 1 | a0002c0002t0104 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6658A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6658 | chr22 | 40329899 | |||||
| chr22:40330179
|
T | C | 46 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(43): Show | 95 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*6938T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6938 | chr22 | 40330179 | |||||
| chr22:40330485
|
C | T | 1 | a0001c0001t0145 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7244C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7244 | chr22 | 40330485 | |||||
| chr22:40330745
|
C | T | 122 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(119): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*7504C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7504 | chr22 | 40330745 | |||||
| chr22:40330758
|
A | G | 122 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(119): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*7517A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7517 | chr22 | 40330758 | |||||
| chr22:40331319
|
T | G | 7 | a0001c0001t0034a0001c0001t0093a0001c0001t0127others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8078T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8078 | chr22 | 40331319 | |||||
| chr22:40331385
|
T | A | 1 | a0013c0019t0095 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8144T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8144 | chr22 | 40331385 | |||||
| chr22:40331639
|
T | G | 1 | a0001c0001t0122 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8398T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8398 | chr22 | 40331639 | |||||
| chr22:40331645
|
AT | A | 77 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(74): Show | 146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*8429delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | ||||
| chr22:40331645
|
ATT | A | 40 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(37): Show | 87 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*8428_*8429delTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8428 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | ||||
| chr22:40331645
|
ATTT | A | 10 | a0001c0001t0042a0001c0001t0043a0001c0001t0046others(7): Show | 10 | HG01261.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8427_*8429delTTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8427 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | ||||
| chr22:40331668
|
T | C | 2 | a0001c0001t0093a0012c0010t0150 | 2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8427T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8427 | chr22 | 40331668 | |||||
| chr22:40331669
|
T | A | 2 | a0001c0001t0093a0012c0010t0150 | 2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8428T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8428 | chr22 | 40331669 | |||||
| chr22:40331670
|
T | A | 2 | a0001c0001t0093a0012c0010t0150 | 2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8429T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | chr22 | 40331670 | |||||
| chr22:40331670
|
T | C | 1 | a0002c0002t0087 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8429T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | chr22 | 40331670 | |||||
| chr22:40331671
|
C | A | 3 | a0001c0001t0093a0002c0002t0087a0012c0010t0150 | 3 | HG01109.hp1 HG01261.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8430C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8430 | chr22 | 40331671 | |||||
| chr22:40331788
|
G | T | 4 | a0001c0001t0042a0001c0001t0051a0001c0001t0093others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8547G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8547 | chr22 | 40331788 | |||||
| chr22:40331895
|
T | A | 1 | a0001c0001t0142 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8654T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8654 | chr22 | 40331895 | |||||
| chr22:40332541
|
ATTC | A | 19 | a0001c0001t0039a0001c0001t0076a0001c0001t0144others(16): Show | 26 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*9306_*9308delCTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9306 | INFO_REALIGN_3_PRIME | chr22 | 40332541 | ||||
| chr22:40332578
|
A | G | 1 | a0001c0001t0139 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9337 | chr22 | 40332578 | |||||
| chr22:40332831
|
C | T | 2 | a0001c0001t0029a0001c0001t0050 | 3 | HG00544.hp1 HG02040.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9590C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9590 | chr22 | 40332831 | |||||
| chr22:40333071
|
C | T | 5 | a0001c0001t0034a0001c0001t0127a0002c0002t0034others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9830C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9830 | chr22 | 40333071 | |||||
| chr22:40333150
|
C | T | 1 | a0001c0001t0117 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9909C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9909 | chr22 | 40333150 | |||||
| chr22:40333194
|
G | A | 5 | a0001c0001t0034a0001c0001t0127a0002c0002t0034others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9953G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9953 | chr22 | 40333194 | |||||
| chr22:40333209
|
C | T | 2 | a0001c0001t0044a0001c0001t0075 | 2 | HG01123.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9968C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9968 | chr22 | 40333209 | |||||
| chr22:40333210
|
G | A | 4 | a0001c0001t0034a0002c0002t0034a0002c0002t0084others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9969G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9969 | chr22 | 40333210 | |||||
| chr22:40333331
|
C | T | 2 | a0001c0001t0093a0012c0010t0150 | 2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10090C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10090 | chr22 | 40333331 | |||||
| chr22:40333559
|
G | C | 1 | a0001c0001t0149 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10318G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10318 | chr22 | 40333559 | |||||
| chr22:40333610
|
A | G | 40 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(37): Show | 86 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*10369A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10369 | chr22 | 40333610 | |||||
| chr22:40333705
|
C | T | 2 | a0005c0007t0059a0005c0007t0060 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10464C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10464 | chr22 | 40333705 | |||||
| chr22:40333895
|
C | G | 1 | a0001c0001t0073 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10654C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10654 | chr22 | 40333895 | |||||
| chr22:40334079
|
A | T | 1 | a0001c0001t0131 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10838A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10838 | chr22 | 40334079 | |||||
| chr22:40334137
|
A | G | 2 | a0001c0001t0093a0012c0010t0150 | 2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10896A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10896 | chr22 | 40334137 | |||||
| chr22:40334942
|
A | C | 1 | a0002c0002t0092 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11701A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11701 | chr22 | 40334942 | |||||
| chr22:40335130
|
C | A | 1 | a0002c0002t0099 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11889C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11889 | chr22 | 40335130 | |||||
| chr22:40335162
|
C | CT | 26 | a0001c0001t0011a0001c0001t0013a0001c0001t0016others(23): Show | 37 | HG00408.hp2 HG01106.hp2 HG01516.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*11948dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11949 | INFO_REALIGN_3_PRIME | chr22 | 40335162 | ||||
| chr22:40335162
|
CT | C | 18 | a0001c0001t0028a0001c0001t0030a0001c0001t0035others(15): Show | 22 | HG01069.hp1 HG01243.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*11948delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11948 | INFO_REALIGN_3_PRIME | chr22 | 40335162 | ||||
| chr22:40335189
|
T | A | 1 | a0001c0001t0071 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11948T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11948 | chr22 | 40335189 | |||||
| chr22:40335307
|
T | C | 1 | a0001c0001t0066 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12066T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12066 | chr22 | 40335307 | |||||
| chr22:40335477
|
C | CA | 13 | a0001c0001t0034a0001c0001t0051a0001c0001t0068others(10): Show | 13 | HG00438.hp2 HG01109.hp1 HG01167.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12252dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12253 | INFO_REALIGN_3_PRIME | chr22 | 40335477 | ||||
| chr22:40335477
|
CA | C | 7 | a0001c0001t0067a0001c0001t0118a0001c0001t0119others(4): Show | 7 | NA18945.hp2 NA18946.hp1 NA18951.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12252delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12252 | INFO_REALIGN_3_PRIME | chr22 | 40335477 | ||||
| chr22:40335540
|
G | A | 1 | a0001c0001t0123 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12299G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12299 | chr22 | 40335540 | |||||
| chr22:40335557
|
G | C | 1 | a0006c0006t0112 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12316G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12316 | chr22 | 40335557 | |||||
| chr22:40335570
|
C | T | 1 | a0002c0002t0091 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12329C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12329 | chr22 | 40335570 | |||||
| chr22:40335764
|
G | GAAAAAA | 9 | a0001c0001t0014a0001c0001t0044a0001c0001t0047others(6): Show | 11 | HG00741.hp2 HG01123.hp1 HG01496.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*12526_*12531dupAA others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12532 | INFO_REALIGN_3_PRIME | chr22 | 40335764 | ||||
| chr22:40335764
|
G | GAAAAAAA | 158 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(155): Show | 291 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*12525_*12531dupAA others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12532 | INFO_REALIGN_3_PRIME | chr22 | 40335764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40178166
|
T | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+26T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40178166 | ||||||
| chr22:40178764
|
C | T | 1 | a0001c0001t0010g0308 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5+624C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40178764 | ||||||
| chr22:40179168
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5+1028C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179168 | ||||||
| chr22:40179180
|
T | A | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+1040T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179180 | ||||||
| chr22:40179943
|
A | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+1803A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179943 | ||||||
| chr22:40179976
|
A | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+1836A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179976 | ||||||
| chr22:40180059
|
T | G | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5+1919T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180059 | ||||||
| chr22:40180298
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2158T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180298 | ||||||
| chr22:40180392
|
A | T | 1 | a0001c0001t0002g0307 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5+2252A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180392 | ||||||
| chr22:40180449
|
T | A | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.5+2309T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180449 | ||||||
| chr22:40180600
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2460C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180600 | ||||||
| chr22:40180791
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2651C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180791 | ||||||
| chr22:40180868
|
G | T | 47 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.5+2728G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180868 | ||||||
| chr22:40180928
|
A | T | 1 | a0013c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+2788A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180928 | ||||||
| chr22:40181188
|
C | T | 1 | a0001c0001t0039g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5+3048C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181188 | ||||||
| chr22:40181340
|
G | GTCCTCAC others(13): Show |
1 | a0001c0001t0075g0164 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.5+3224_5+3243dupTC others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40181340 | |||||
| chr22:40181444
|
A | G | 1 | a0001c0001t0126g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.5+3304A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181444 | ||||||
| chr22:40181555
|
A | T | 1 | a0001c0001t0004g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5+3415A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181555 | ||||||
| chr22:40181948
|
G | GA | 212 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(209): Show | 212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.5+3820dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40181948 | |||||
| chr22:40181967
|
C | T | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5+3827C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181967 | ||||||
| chr22:40182137
|
C | G | 1 | a0001c0001t0116g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5+3997C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182137 | ||||||
| chr22:40182339
|
T | G | 2 | a0001c0001t0030g0220a0001c0001t0030g0221 | 2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.5+4199T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182339 | ||||||
| chr22:40182404
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5+4264C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182404 | ||||||
| chr22:40182405
|
G | A | 1 | a0001c0001t0052g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5+4265G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182405 | ||||||
| chr22:40182471
|
G | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+4331G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182471 | ||||||
| chr22:40182494
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+4354A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182494 | ||||||
| chr22:40182626
|
G | A | 1 | a0001c0001t0039g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5+4486G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182626 | ||||||
| chr22:40182653
|
T | C | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5+4513T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182653 | ||||||
| chr22:40182760
|
A | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+4620A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182760 | ||||||
| chr22:40182794
|
G | A | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+4654G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182794 | ||||||
| chr22:40182798
|
G | A | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+4658G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182798 | ||||||
| chr22:40182830
|
T | G | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5+4690T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182830 | ||||||
| chr22:40182896
|
G | A | 2 | a0001c0001t0008g0223a0001c0001t0074g0222 | 2 | HG00735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5+4756G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182896 | ||||||
| chr22:40182954
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+4814A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182954 | ||||||
| chr22:40183071
|
C | CAG | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+4931_5+4932insAG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183071 | ||||||
| chr22:40183081
|
G | T | 1 | a0001c0001t0002g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5+4941G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183081 | ||||||
| chr22:40183086
|
G | A | 306 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(303): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.5+4946G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183086 | ||||||
| chr22:40183217
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5077G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183217 | ||||||
| chr22:40183419
|
C | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+5279C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183419 | ||||||
| chr22:40183422
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5+5282T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183422 | ||||||
| chr22:40183431
|
C | T | 1 | a0001c0001t0061g0301 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5+5291C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183431 | ||||||
| chr22:40183510
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+5370G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183510 | ||||||
| chr22:40183649
|
G | A | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5+5509G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183649 | ||||||
| chr22:40183668
|
G | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5528G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183668 | ||||||
| chr22:40183696
|
G | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5556G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183696 | ||||||
| chr22:40183801
|
G | T | 225 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.5+5661G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183801 | ||||||
| chr22:40183893
|
C | T | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+5753C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183893 | ||||||
| chr22:40184157
|
G | A | 3 | a0002c0002t0034g0009a0002c0002t0084g0008a0002c0002t0094g0010 | 3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5+6017G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184157 | ||||||
| chr22:40184730
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+6590T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184730 | ||||||
| chr22:40184797
|
G | A | 1 | a0001c0001t0075g0164 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.5+6657G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184797 | ||||||
| chr22:40184804
|
T | G | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5+6664T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184804 | ||||||
| chr22:40184918
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5+6778G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184918 | ||||||
| chr22:40185005
|
G | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+6865G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185005 | ||||||
| chr22:40185017
|
A | G | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5+6877A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185017 | ||||||
| chr22:40185147
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+7007C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185147 | ||||||
| chr22:40185210
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+7070T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185210 | ||||||
| chr22:40185221
|
C | G | 2 | a0001c0001t0023g0158a0001c0001t0043g0157 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5+7081C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185221 | ||||||
| chr22:40185579
|
C | G | 2 | a0002c0002t0154g0155a0002c0002t0155g0156 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5+7439C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185579 | ||||||
| chr22:40185594
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+7454T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185594 | ||||||
| chr22:40185663
|
G | A | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+7523G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185663 | ||||||
| chr22:40185724
|
G | A | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5+7584G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185724 | ||||||
| chr22:40185818
|
A | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+7678A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185818 | ||||||
| chr22:40186231
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8091C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186231 | ||||||
| chr22:40186369
|
C | T | 1 | a0002c0002t0106g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5+8229C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186369 | ||||||
| chr22:40186394
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8254G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186394 | ||||||
| chr22:40186471
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8331G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186471 | ||||||
| chr22:40186480
|
C | T | 131 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.5+8340C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186480 | ||||||
| chr22:40186505
|
C | T | 1 | a0001c0001t0118g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5+8365C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186505 | ||||||
| chr22:40186506
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8366G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186506 | ||||||
| chr22:40186517
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5+8377A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186517 | ||||||
| chr22:40186525
|
G | A | 8 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+8385G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186525 | ||||||
| chr22:40186607
|
G | A | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5+8467G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186607 | ||||||
| chr22:40186737
|
C | CA | 50 | a0001c0001t0022g0126a0001c0001t0073g0225a0001c0001t0109g0130others(47): Show | 50 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.5+8611dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40186737 | |||||
| chr22:40186762
|
A | G | 1 | a0001c0001t0031g0299 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5+8622A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186762 | ||||||
| chr22:40186866
|
G | GT | 7 | a0001c0001t0002g0296a0001c0001t0064g0298a0001c0001t0069g0297others(4): Show | 7 | HG01346.hp2 HG02293.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+8734dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40186866 | |||||
| chr22:40186964
|
C | T | 17 | a0001c0001t0022g0126a0002c0002t0009g0116a0002c0002t0009g0117others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.5+8824C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186964 | ||||||
| chr22:40187533
|
C | T | 2 | a0001c0001t0046g0153a0001c0001t0047g0152 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5+9393C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187533 | ||||||
| chr22:40187640
|
G | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+9500G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187640 | ||||||
| chr22:40187657
|
G | A | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5+9517G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187657 | ||||||
| chr22:40187676
|
G | A | 2 | a0001c0001t0012g0169a0001c0001t0021g0170 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5+9536G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187676 | ||||||
| chr22:40187783
|
A | G | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5+9643A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187783 | ||||||
| chr22:40187881
|
G | T | 1 | a0001c0001t0010g0295 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5+9741G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187881 | ||||||
| chr22:40187991
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5+9851G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187991 | ||||||
| chr22:40188124
|
G | A | 4 | a0001c0001t0054g0132a0001c0001t0055g0134a0001c0001t0056g0133others(1): Show | 4 | HG02723.hp1 HG02895.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+9984G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188124 | ||||||
| chr22:40188147
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 14 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.5+10007T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188147 | ||||||
| chr22:40188358
|
C | T | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5+10218C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188358 | ||||||
| chr22:40188387
|
G | A | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+10247G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188387 | ||||||
| chr22:40188619
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5+10479C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188619 | ||||||
| chr22:40188958
|
T | C | 77 | a0001c0001t0006g0135a0001c0001t0015g0139a0001c0001t0015g0140others(74): Show | 77 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.5+10818T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188958 | ||||||
| chr22:40189191
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5+11051G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189191 | ||||||
| chr22:40189498
|
C | CA | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0226others(11): Show | 14 | HG00735.hp2 HG01106.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.5+11375dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40189498 | |||||
| chr22:40189498
|
CA | C | 91 | a0001c0001t0006g0150a0001c0001t0007g0292a0001c0001t0007g0293others(88): Show | 91 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.5+11375delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40189498 | |||||
| chr22:40189518
|
G | T | 4 | a0001c0001t0022g0126a0002c0002t0032g0127a0002c0002t0032g0128others(1): Show | 4 | HG03239.hp2 HG03831.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+11378G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189518 | ||||||
| chr22:40189740
|
A | G | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+11600A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189740 | ||||||
| chr22:40189834
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5+11694A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189834 | ||||||
| chr22:40189978
|
A | T | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5+11838A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189978 | ||||||
| chr22:40190052
|
T | G | 1 | a0001c0001t0109g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5+11912T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190052 | ||||||
| chr22:40190065
|
C | G | 42 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.5+11925C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190065 | ||||||
| chr22:40190100
|
G | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+11960G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190100 | ||||||
| chr22:40190230
|
C | A | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+12090C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190230 | ||||||
| chr22:40190250
|
C | T | 1 | a0001c0001t0012g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5+12110C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190250 | ||||||
| chr22:40190735
|
C | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+12595C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190735 | ||||||
| chr22:40190747
|
C | T | 4 | a0001c0001t0006g0150a0001c0001t0034g0091a0001c0001t0051g0149others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+12607C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190747 | ||||||
| chr22:40190823
|
T | C | 1 | a0002c0002t0090g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5+12683T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190823 | ||||||
| chr22:40191079
|
G | A | 1 | a0001c0001t0124g0030 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5+12939G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191079 | ||||||
| chr22:40191096
|
G | T | 49 | a0001c0001t0109g0130a0002c0002t0006g0095a0002c0002t0006g0107others(46): Show | 49 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.5+12956G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191096 | ||||||
| chr22:40191114
|
G | A | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5+12974G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191114 | ||||||
| chr22:40191240
|
A | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+13100A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191240 | ||||||
| chr22:40191280
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+13140T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191280 | ||||||
| chr22:40191292
|
G | A | 2 | a0001c0005t0004g0171a0001c0005t0141g0172 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5+13152G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191292 | ||||||
| chr22:40191713
|
C | G | 2 | a0001c0001t0008g0289a0001c0001t0126g0305 | 2 | HG00741.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.5+13573C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191713 | ||||||
| chr22:40191843
|
T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5+13703T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191843 | ||||||
| chr22:40192197
|
G | A | 1 | a0001c0001t0133g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5+14057G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192197 | ||||||
| chr22:40192349
|
G | A | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5+14209G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192349 | ||||||
| chr22:40192446
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14306G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192446 | ||||||
| chr22:40192478
|
A | G | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5+14338A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192478 | ||||||
| chr22:40192531
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14391T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192531 | ||||||
| chr22:40192616
|
CA | C | 46 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.5+14487delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40192616 | |||||
| chr22:40192645
|
G | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14505G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192645 | ||||||
| chr22:40192800
|
G | A | 1 | a0001c0001t0027g0232 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5+14660G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192800 | ||||||
| chr22:40192864
|
C | T | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5+14724C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192864 | ||||||
| chr22:40192881
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14741A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192881 | ||||||
| chr22:40192936
|
G | T | 4 | a0001c0001t0002g0226a0001c0001t0002g0230a0001c0001t0002g0307others(1): Show | 4 | NA18943.hp2 NA18965.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+14796G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192936 | ||||||
| chr22:40193049
|
C | G | 1 | a0001c0001t0118g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5+14909C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193049 | ||||||
| chr22:40193123
|
A | G | 2 | a0001c0001t0008g0288a0001c0001t0069g0297 | 2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.5+14983A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193123 | ||||||
| chr22:40193246
|
G | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+15106G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193246 | ||||||
| chr22:40193342
|
A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+15202A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193342 | ||||||
| chr22:40193865
|
AAAAG | A | 43 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.5+15731_5+15734del others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40193865 | |||||
| chr22:40193927
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+15787C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193927 | ||||||
| chr22:40194090
|
A | G | 1 | a0001c0001t0035g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5+15950A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194090 | ||||||
| chr22:40194115
|
C | T | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+15975C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194115 | ||||||
| chr22:40194122
|
G | T | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+15982G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194122 | ||||||
| chr22:40194225
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+16085T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194225 | ||||||
| chr22:40195254
|
T | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+17114T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195254 | ||||||
| chr22:40195308
|
T | A | 132 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.5+17168T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195308 | ||||||
| chr22:40195376
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+17236G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195376 | ||||||
| chr22:40195521
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+17381G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195521 | ||||||
| chr22:40195620
|
T | G | 2 | a0001c0001t0046g0153a0001c0001t0047g0152 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5+17480T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195620 | ||||||
| chr22:40195751
|
G | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+17611G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195751 | ||||||
| chr22:40195919
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0003g0163 | 2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.5+17779G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195919 | ||||||
| chr22:40195979
|
G | A | 1 | a0001c0001t0073g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5+17839G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195979 | ||||||
| chr22:40196020
|
G | C | 1 | a0011c0011t0006g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5+17880G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196020 | ||||||
| chr22:40196076
|
CT | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(211): Show | 214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.5+17948delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196076 | |||||
| chr22:40196210
|
A | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.5+18070A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196210 | ||||||
| chr22:40196237
|
C | G | 1 | a0001c0001t0013g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5+18097C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196237 | ||||||
| chr22:40196244
|
GGCTCAAG others(7460): Show |
G | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5+18107_5+25573del | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196244 | |||||
| chr22:40196321
|
T | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+18181T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196321 | ||||||
| chr22:40196454
|
G | A | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5+18314G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196454 | ||||||
| chr22:40196533
|
G | A | 1 | a0002c0002t0105g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5+18393G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196533 | ||||||
| chr22:40196621
|
A | G | 1 | a0001c0001t0046g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5+18481A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196621 | ||||||
| chr22:40196624
|
ATGGAACT others(18): Show |
A | 216 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+18513_5+18537del others(25): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196624 | |||||
| chr22:40196705
|
A | T | 1 | a0002c0002t0087g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5+18565A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196705 | ||||||
| chr22:40196990
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+18850T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196990 | ||||||
| chr22:40197226
|
C | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19086C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197226 | ||||||
| chr22:40197257
|
C | T | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5+19117C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197257 | ||||||
| chr22:40197288
|
G | GT | 54 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.5+19157dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197288 | |||||
| chr22:40197288
|
GT | G | 7 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+19157delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197288 | |||||
| chr22:40197310
|
C | T | 1 | a0001c0001t0077g0286 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5+19170C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197310 | ||||||
| chr22:40197316
|
G | A | 45 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.5+19176G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197316 | ||||||
| chr22:40197334
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19194G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197334 | ||||||
| chr22:40197344
|
G | A | 1 | a0001c0001t0022g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5+19204G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197344 | ||||||
| chr22:40197531
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5+19391C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197531 | ||||||
| chr22:40197541
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19401C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197541 | ||||||
| chr22:40197576
|
C | T | 1 | a0001c0001t0023g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5+19436C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197576 | ||||||
| chr22:40197606
|
C | CT | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG00280.hp1 NA18612.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+19481dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197606 | |||||
| chr22:40197606
|
CT | C | 60 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0008g0234others(57): Show | 60 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5+19481delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197606 | |||||
| chr22:40197721
|
C | T | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5+19581C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197721 | ||||||
| chr22:40198417
|
C | T | 1 | a0001c0001t0008g0234 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5+20277C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198417 | ||||||
| chr22:40198558
|
C | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+20418C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198558 | ||||||
| chr22:40198629
|
A | G | 1 | a0001c0001t0027g0284 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5+20489A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198629 | ||||||
| chr22:40198698
|
A | G | 84 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(81): Show | 84 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.5+20558A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198698 | ||||||
| chr22:40198777
|
G | A | 1 | a0001c0001t0013g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5+20637G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198777 | ||||||
| chr22:40198816
|
C | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+20676C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198816 | ||||||
| chr22:40199267
|
C | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+21127C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199267 | ||||||
| chr22:40199371
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+21231A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199371 | ||||||
| chr22:40199549
|
T | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+21409T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199549 | ||||||
| chr22:40199558
|
A | G | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0076others(4): Show | 7 | NA18612.hp2 NA18943.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+21418A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199558 | ||||||
| chr22:40199654
|
T | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+21514T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199654 | ||||||
| chr22:40199870
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+21730C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199870 | ||||||
| chr22:40199879
|
C | G | 2 | a0002c0002t0154g0155a0002c0002t0155g0156 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5+21739C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199879 | ||||||
| chr22:40199887
|
T | A | 1 | a0001c0001t0071g0236 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5+21747T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199887 | ||||||
| chr22:40200027
|
G | A | 2 | a0002c0002t0034g0009a0002c0002t0084g0008 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5+21887G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200027 | ||||||
| chr22:40200046
|
G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+21906G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200046 | ||||||
| chr22:40200278
|
C | CT | 181 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0018others(178): Show | 181 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.5+22162dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | |||||
| chr22:40200278
|
C | CTT | 34 | a0001c0001t0001g0034a0001c0001t0001g0074a0001c0001t0002g0217others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.5+22161_5+22162dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | |||||
| chr22:40200278
|
C | CTTT | 49 | a0001c0001t0001g0029a0001c0001t0014g0069a0001c0001t0015g0139others(46): Show | 49 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.5+22160_5+22162dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | |||||
| chr22:40200278
|
C | CTTTT | 15 | a0001c0001t0035g0142a0001c0001t0046g0153a0002c0002t0006g0107others(12): Show | 15 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+22159_5+22162dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | |||||
| chr22:40200278
|
CTTTTT | C | 6 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0054g0132others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+22158_5+22162del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | |||||
| chr22:40200380
|
G | A | 3 | a0001c0001t0002g0240a0001c0001t0008g0289a0001c0001t0013g0235 | 3 | HG00741.hp1 HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.5+22240G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200380 | ||||||
| chr22:40200381
|
G | A | 1 | a0001c0001t0013g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5+22241G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200381 | ||||||
| chr22:40200508
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+22368T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200508 | ||||||
| chr22:40200535
|
G | A | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5+22395G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200535 | ||||||
| chr22:40200583
|
C | T | 3 | a0002c0002t0032g0127a0002c0002t0032g0128a0002c0002t0041g0129 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5+22443C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200583 | ||||||
| chr22:40200620
|
A | T | 48 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.5+22480A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200620 | ||||||
| chr22:40200884
|
T | A | 83 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(80): Show | 83 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5+22744T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200884 | ||||||
| chr22:40201663
|
G | A | 85 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(82): Show | 85 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.5+23523G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201663 | ||||||
| chr22:40201869
|
G | C | 1 | a0001c0001t0068g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+23729G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201869 | ||||||
| chr22:40201964
|
C | G | 1 | a0002c0002t0151g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5+23824C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201964 | ||||||
| chr22:40202249
|
G | GTTGTTTT others(7): Show |
81 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(78): Show | 81 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.5+24112_5+24125dup others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202249 | |||||
| chr22:40202260
|
G | GTTTTTGT others(8): Show |
4 | a0002c0002t0041g0129a0002c0002t0107g0105a0006c0006t0111g0214others(1): Show | 4 | HG01884.hp1 HG01934.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+24125_5+24126ins others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202260 | |||||
| chr22:40202260
|
G | T | 2 | a0001c0001t0007g0283a0001c0001t0067g0282 | 2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.5+24120G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40202260 | ||||||
| chr22:40202260
|
GT | G | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.5+24134delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202260 | |||||
| chr22:40203328
|
A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+25188A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203328 | ||||||
| chr22:40203379
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+25239G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203379 | ||||||
| chr22:40203414
|
G | A | 1 | a0002c0002t0105g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5+25274G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203414 | ||||||
| chr22:40203532
|
A | C | 26 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0016g0086others(23): Show | 26 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.5+25392A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203532 | ||||||
| chr22:40203627
|
G | A | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+25487G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203627 | ||||||
| chr22:40203700
|
C | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+25560C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203700 | ||||||
| chr22:40203873
|
T | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+25733T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203873 | ||||||
| chr22:40203875
|
C | T | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+25735C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203875 | ||||||
| chr22:40204114
|
C | T | 1 | a0001c0001t0018g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5+25974C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204114 | ||||||
| chr22:40204326
|
A | C | 1 | a0001c0001t0004g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5+26186A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204326 | ||||||
| chr22:40204483
|
G | A | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+26343G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204483 | ||||||
| chr22:40204542
|
G | A | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+26402G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204542 | ||||||
| chr22:40204774
|
TCTGCTG | T | 3 | a0001c0001t0007g0292a0001c0001t0007g0293a0001c0001t0066g0290 | 3 | NA18946.hp2 NA18991.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5+26646_5+26651del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40204774 | |||||
| chr22:40205437
|
A | C | 1 | a0001c0001t0039g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5+27297A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205437 | ||||||
| chr22:40205438
|
T | C | 1 | a0001c0001t0050g0242 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5+27298T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205438 | ||||||
| chr22:40205445
|
A | G | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+27305A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205445 | ||||||
| chr22:40205635
|
A | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+27495A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205635 | ||||||
| chr22:40206068
|
T | A | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+27928T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206068 | ||||||
| chr22:40206181
|
T | C | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+28041T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206181 | ||||||
| chr22:40206466
|
ATG | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.5+28328_5+28329del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40206466 | |||||
| chr22:40206616
|
G | A | 83 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(80): Show | 83 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5+28476G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206616 | ||||||
| chr22:40206811
|
G | T | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+28671G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206811 | ||||||
| chr22:40206944
|
G | A | 86 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(83): Show | 86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+28804G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206944 | ||||||
| chr22:40207285
|
A | G | 86 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(83): Show | 86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+29145A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207285 | ||||||
| chr22:40207359
|
G | C | 86 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(83): Show | 86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+29219G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207359 | ||||||
| chr22:40207399
|
C | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.5+29259C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207399 | ||||||
| chr22:40207406
|
C | CA | 46 | a0001c0001t0001g0023a0001c0001t0001g0219a0001c0001t0002g0285others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.5+29279dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | |||||
| chr22:40207406
|
C | CAA | 59 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.5+29278_5+29279dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | |||||
| chr22:40207406
|
C | CAAA | 22 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0039others(19): Show | 22 | HG00733.hp1 HG01346.hp2 NA18941.hp1 others(19): Show |
intron_variant | MODIFIER | c.5+29277_5+29279dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | |||||
| chr22:40207406
|
C | CAAAA | 8 | a0001c0001t0001g0035a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG01261.hp1 HG02129.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+29276_5+29279dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | |||||
| chr22:40207413
|
AAAAAAAT others(4): Show |
A | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+29275_5+29285del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207413 | |||||
| chr22:40207415
|
AAAAATAT others(4): Show |
A | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5+29277_5+29287del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207415 | |||||
| chr22:40207416
|
AAAATATA others(5): Show |
A | 3 | a0002c0002t0036g0012a0002c0002t0156g0104a0011c0011t0006g0094 | 3 | HG02615.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5+29278_5+29289del others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207416 | |||||
| chr22:40207417
|
AAATATAT others(4): Show |
A | 4 | a0001c0001t0006g0135a0001c0001t0022g0126a0002c0002t0096g0005others(1): Show | 4 | HG01934.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+29279_5+29289del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207417 | |||||
| chr22:40207417
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+29279_5+29291del others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207417 | |||||
| chr22:40207418
|
A | T | 1 | a0001c0001t0026g0280 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5+29278A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207418 | ||||||
| chr22:40207418
|
AATATATA others(5): Show |
A | 67 | a0001c0001t0006g0150a0001c0001t0015g0139a0001c0001t0015g0140others(64): Show | 67 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.5+29293_5+29304del others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207418 | |||||
| chr22:40207419
|
ATATATAT others(4): Show |
A | 8 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+29280_5+29290del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207419 | ||||||
| chr22:40207419
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5+29280_5+29292del others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207419 | ||||||
| chr22:40207420
|
T | A | 172 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.5+29280T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207420 | ||||||
| chr22:40207422
|
T | A | 126 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.5+29282T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207422 | ||||||
| chr22:40207424
|
T | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 41 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.5+29284T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207424 | ||||||
| chr22:40207426
|
T | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0003g0019others(2): Show | 5 | HG00544.hp2 HG02083.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+29286T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207426 | ||||||
| chr22:40207432
|
T | A | 5 | a0001c0001t0086g0213a0001c0001t0088g0143a0002c0002t0006g0095others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+29292T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207432 | ||||||
| chr22:40207533
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+29393T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207533 | ||||||
| chr22:40207576
|
C | A | 220 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.5+29436C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207576 | ||||||
| chr22:40207728
|
A | G | 134 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.5+29588A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207728 | ||||||
| chr22:40207939
|
C | T | 1 | a0001c0001t0128g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5+29799C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207939 | ||||||
| chr22:40207975
|
A | G | 220 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.5+29835A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207975 | ||||||
| chr22:40208006
|
C | T | 1 | a0013c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+29866C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208006 | ||||||
| chr22:40208031
|
G | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5+29891G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208031 | ||||||
| chr22:40208070
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5+29930G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208070 | ||||||
| chr22:40208110
|
T | A | 6 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+29970T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208110 | ||||||
| chr22:40208111
|
C | CA | 20 | a0001c0001t0002g0240a0001c0001t0002g0252a0001c0001t0002g0254others(17): Show | 20 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.5+29992dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208111 | |||||
| chr22:40208115
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5+29983_5+30000del others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208115 | |||||
| chr22:40208119
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0012g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5+29987_5+30000del others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208119 | |||||
| chr22:40208120
|
A | C | 85 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(82): Show | 85 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.5+29980A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208120 | ||||||
| chr22:40208126
|
AAAAAAAC | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.5+29993_5+29999del others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208126 | |||||
| chr22:40208127
|
A | C | 130 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(127): Show | 130 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.5+29987A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208127 | ||||||
| chr22:40208127
|
AAAAAAC | A | 10 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0073others(7): Show | 10 | HG01346.hp2 HG01928.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.5+29993_5+29998del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208127 | |||||
| chr22:40208128
|
A | C | 1 | a0001c0001t0002g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5+29988A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208128 | ||||||
| chr22:40208133
|
C | A | 48 | a0001c0001t0002g0217a0001c0001t0004g0178a0001c0001t0004g0180others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.5+29993C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208133 | ||||||
| chr22:40208435
|
G | A | 1 | a0001c0001t0013g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5+30295G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208435 | ||||||
| chr22:40208542
|
C | T | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+30402C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208542 | ||||||
| chr22:40208712
|
T | C | 220 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.5+30572T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208712 | ||||||
| chr22:40208878
|
C | T | 2 | a0001c0001t0037g0059a0001c0001t0037g0060 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5+30738C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208878 | ||||||
| chr22:40208941
|
T | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+30801T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208941 | ||||||
| chr22:40209159
|
G | A | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+31019G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209159 | ||||||
| chr22:40209263
|
GC | G | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+31128delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40209263 | |||||
| chr22:40209360
|
A | T | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+31220A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209360 | ||||||
| chr22:40209500
|
G | C | 1 | a0001c0001t0117g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5+31360G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209500 | ||||||
| chr22:40209569
|
G | A | 1 | a0001c0001t0029g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5+31429G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209569 | ||||||
| chr22:40209677
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+31537C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209677 | ||||||
| chr22:40209696
|
G | A | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+31556G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209696 | ||||||
| chr22:40209821
|
C | G | 4 | a0001c0001t0022g0126a0001c0001t0022g0177a0001c0001t0022g0199others(1): Show | 4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+31681C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209821 | ||||||
| chr22:40209875
|
C | T | 1 | a0013c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+31735C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209875 | ||||||
| chr22:40209997
|
A | G | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+31857A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209997 | ||||||
| chr22:40210017
|
C | CA | 210 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(207): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.5+31892dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40210017 | |||||
| chr22:40210017
|
C | CAA | 7 | a0001c0001t0001g0070a0001c0001t0004g0180a0001c0001t0039g0165others(4): Show | 7 | HG00544.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+31891_5+31892dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40210017 | |||||
| chr22:40210127
|
G | C | 1 | a0010c0012t0006g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5+31987G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210127 | ||||||
| chr22:40210150
|
C | G | 1 | a0001c0001t0068g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+32010C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210150 | ||||||
| chr22:40210289
|
A | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+32149A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210289 | ||||||
| chr22:40210473
|
G | T | 3 | a0001c0001t0022g0126a0001c0001t0022g0177a0001c0001t0022g0199 | 3 | HG02602.hp1 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5+32333G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210473 | ||||||
| chr22:40210526
|
C | A | 3 | a0002c0002t0006g0107a0002c0002t0100g0108a0010c0012t0006g0113 | 3 | HG02055.hp2 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.5+32386C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210526 | ||||||
| chr22:40210693
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+32553T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210693 | ||||||
| chr22:40211041
|
C | G | 1 | a0001c0001t0038g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5+32901C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211041 | ||||||
| chr22:40211113
|
ATCT | A | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+32984_5+32986del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40211113 | |||||
| chr22:40211138
|
G | T | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5+32998G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211138 | ||||||
| chr22:40211208
|
G | T | 1 | a0001c0001t0017g0033 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5+33068G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211208 | ||||||
| chr22:40211375
|
G | A | 1 | a0001c0001t0003g0038 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.5+33235G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211375 | ||||||
| chr22:40211383
|
C | CT | 219 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+33251dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40211383 | |||||
| chr22:40211620
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+33480G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211620 | ||||||
| chr22:40211625
|
G | A | 47 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.5+33485G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211625 | ||||||
| chr22:40211829
|
G | A | 3 | a0001c0001t0012g0206a0001c0001t0121g0306a0001c0001t0143g0184 | 3 | HG01106.hp2 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5+33689G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211829 | ||||||
| chr22:40212118
|
T | C | 1 | a0002c0002t0107g0105 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6-33897T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212118 | ||||||
| chr22:40212296
|
G | T | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6-33719G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212296 | ||||||
| chr22:40212482
|
A | G | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.6-33533A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212482 | ||||||
| chr22:40212669
|
A | G | 1 | a0002c0002t0097g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6-33346A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212669 | ||||||
| chr22:40212773
|
C | T | 2 | a0001c0001t0137g0179a0007c0018t0005g0205 | 2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-33242C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212773 | ||||||
| chr22:40212892
|
T | C | 210 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(207): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.6-33123T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212892 | ||||||
| chr22:40212942
|
C | T | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-33073C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212942 | ||||||
| chr22:40213074
|
G | A | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-32941G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213074 | ||||||
| chr22:40213123
|
T | A | 1 | a0001c0001t0021g0181 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6-32892T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213123 | ||||||
| chr22:40213147
|
A | G | 210 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(207): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.6-32868A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213147 | ||||||
| chr22:40213300
|
G | T | 1 | a0001c0001t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-32715G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213300 | ||||||
| chr22:40213338
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-32677C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213338 | ||||||
| chr22:40213557
|
C | G | 1 | a0001c0001t0049g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6-32458C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213557 | ||||||
| chr22:40213645
|
A | G | 8 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0033g0146others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-32370A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213645 | ||||||
| chr22:40213705
|
A | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-32310A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213705 | ||||||
| chr22:40214282
|
A | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-31733A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214282 | ||||||
| chr22:40214322
|
C | T | 7 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0034g0091others(4): Show | 7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-31693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214322 | ||||||
| chr22:40214394
|
C | A | 101 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0076others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.6-31621C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214394 | ||||||
| chr22:40214439
|
A | C | 1 | a0001c0001t0119g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-31576A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214439 | ||||||
| chr22:40214549
|
G | GTT | 168 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.6-31456_6-31455dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40214549 | |||||
| chr22:40214549
|
G | GTTT | 40 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(37): Show | 40 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.6-31457_6-31455dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40214549 | |||||
| chr22:40214596
|
G | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.6-31419G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214596 | ||||||
| chr22:40214862
|
T | C | 1 | a0002c0002t0085g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.6-31153T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214862 | ||||||
| chr22:40214892
|
T | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-31123T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214892 | ||||||
| chr22:40215008
|
G | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.6-31007G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215008 | ||||||
| chr22:40215010
|
AAT | A | 96 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.6-31004_6-31003del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215010 | ||||||
| chr22:40215077
|
T | C | 4 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0069others(1): Show | 4 | HG00741.hp2 HG01123.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-30938T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215077 | ||||||
| chr22:40215106
|
TAAC | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(3): Show | 6 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-30906_6-30904del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40215106 | |||||
| chr22:40215188
|
T | C | 1 | a0001c0001t0089g0151 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6-30827T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215188 | ||||||
| chr22:40215284
|
A | AT | 207 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.6-30726dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40215284 | |||||
| chr22:40215484
|
A | G | 1 | a0001c0001t0003g0038 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6-30531A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215484 | ||||||
| chr22:40215624
|
A | G | 207 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.6-30391A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215624 | ||||||
| chr22:40216127
|
A | G | 223 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-29888A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216127 | ||||||
| chr22:40216152
|
C | T | 7 | a0002c0002t0009g0119a0002c0002t0009g0120a0002c0002t0009g0122others(4): Show | 7 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-29863C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216152 | ||||||
| chr22:40216166
|
C | T | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-29849C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216166 | ||||||
| chr22:40216167
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6-29848G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216167 | ||||||
| chr22:40216319
|
G | A | 1 | a0001c0017t0079g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6-29696G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216319 | ||||||
| chr22:40216765
|
G | C | 1 | a0007c0018t0005g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.6-29250G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216765 | ||||||
| chr22:40216820
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-29195T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216820 | ||||||
| chr22:40216937
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6-29078C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216937 | ||||||
| chr22:40216970
|
G | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-29045G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216970 | ||||||
| chr22:40217032
|
A | G | 225 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.6-28983A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217032 | ||||||
| chr22:40217069
|
A | G | 223 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-28946A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217069 | ||||||
| chr22:40217145
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-28870A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217145 | ||||||
| chr22:40217278
|
A | C | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-28737A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217278 | ||||||
| chr22:40217407
|
G | A | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-28608G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217407 | ||||||
| chr22:40217458
|
G | A | 3 | a0002c0002t0034g0009a0002c0002t0084g0008a0002c0002t0094g0010 | 3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.6-28557G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217458 | ||||||
| chr22:40217843
|
C | T | 1 | a0002c0002t0152g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-28172C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217843 | ||||||
| chr22:40217929
|
C | T | 3 | a0002c0002t0034g0009a0002c0002t0084g0008a0002c0002t0094g0010 | 3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.6-28086C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217929 | ||||||
| chr22:40217972
|
C | CA | 8 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0003g0052others(5): Show | 8 | HG02698.hp2 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-28025dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | |||||
| chr22:40217972
|
C | CAA | 128 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 128 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.6-28026_6-28025dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | |||||
| chr22:40217972
|
C | CAAA | 83 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.6-28027_6-28025dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | |||||
| chr22:40218129
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-27886A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218129 | ||||||
| chr22:40218186
|
G | T | 3 | a0001c0001t0007g0265a0001c0001t0007g0278a0001c0001t0007g0300 | 3 | HG01123.hp2 HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.6-27829G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218186 | ||||||
| chr22:40218226
|
A | G | 1 | a0001c0001t0030g0221 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6-27789A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218226 | ||||||
| chr22:40218314
|
TTTTTCTT others(3): Show |
T | 3 | a0001c0001t0002g0279a0001c0001t0072g0276a0001c0001t0078g0277 | 3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.6-27696_6-27687del others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218314 | |||||
| chr22:40218324
|
C | CT | 135 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.6-27671dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | |||||
| chr22:40218324
|
C | CTT | 87 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-27672_6-27671dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | |||||
| chr22:40218324
|
C | CTTT | 7 | a0001c0001t0002g0266a0001c0001t0002g0302a0001c0001t0007g0265others(4): Show | 7 | HG01123.hp2 HG01255.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-27673_6-27671dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | |||||
| chr22:40218445
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-27570G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218445 | ||||||
| chr22:40218508
|
T | G | 133 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 133 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.6-27507T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218508 | ||||||
| chr22:40218623
|
G | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-27392G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218623 | ||||||
| chr22:40218671
|
A | T | 3 | a0001c0001t0002g0240a0001c0001t0008g0289a0001c0001t0013g0235 | 3 | HG00741.hp1 HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6-27344A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218671 | ||||||
| chr22:40219272
|
G | T | 133 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 133 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.6-26743G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40219272 | ||||||
| chr22:40219757
|
C | T | 1 | a0001c0001t0134g0182 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6-26258C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40219757 | ||||||
| chr22:40220064
|
T | G | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-25951T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220064 | ||||||
| chr22:40220069
|
T | C | 1 | a0001c0001t0127g0085 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6-25946T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220069 | ||||||
| chr22:40220108
|
G | A | 221 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(218): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.6-25907G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220108 | ||||||
| chr22:40220120
|
C | T | 1 | a0001c0001t0005g0197 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6-25895C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220120 | ||||||
| chr22:40220241
|
C | A | 1 | a0001c0001t0007g0300 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.6-25774C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220241 | ||||||
| chr22:40220699
|
C | T | 43 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.6-25316C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220699 | ||||||
| chr22:40220703
|
A | G | 224 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.6-25312A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220703 | ||||||
| chr22:40220707
|
A | G | 1 | a0001c0001t0117g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6-25308A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220707 | ||||||
| chr22:40220844
|
T | G | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-25171T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220844 | ||||||
| chr22:40221090
|
A | G | 1 | a0001c0001t0116g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6-24925A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221090 | ||||||
| chr22:40221096
|
G | A | 224 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.6-24919G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221096 | ||||||
| chr22:40221715
|
A | T | 1 | a0001c0001t0057g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.6-24300A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221715 | ||||||
| chr22:40221751
|
G | GC | 15 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(12): Show | 15 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.6-24254dupC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221751 | |||||
| chr22:40221751
|
G | GCCCCC | 15 | a0001c0001t0001g0219a0001c0001t0004g0187a0001c0001t0004g0203others(12): Show | 15 | HG00423.hp1 HG00438.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-24258_6-24254dup others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221751 | |||||
| chr22:40221761
|
C | CCT | 13 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0037others(10): Show | 13 | HG00738.hp2 HG01934.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.6-24254_6-24253ins others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221761 | ||||||
| chr22:40221761
|
C | CT | 82 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.6-24242dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221761 | |||||
| chr22:40221761
|
CT | C | 73 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0228others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.6-24242delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221761 | |||||
| chr22:40221762
|
T | C | 16 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0252others(13): Show | 16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.6-24253T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221762 | ||||||
| chr22:40222059
|
A | G | 48 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.6-23956A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222059 | ||||||
| chr22:40222089
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-23926A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222089 | ||||||
| chr22:40222094
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-23921T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222094 | ||||||
| chr22:40222210
|
T | C | 6 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-23805T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222210 | ||||||
| chr22:40222411
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-23604G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222411 | ||||||
| chr22:40222567
|
G | A | 26 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0016g0086others(23): Show | 26 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.6-23448G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222567 | ||||||
| chr22:40222625
|
C | T | 1 | a0001c0001t0021g0181 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6-23390C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222625 | ||||||
| chr22:40222728
|
C | CT | 13 | a0001c0001t0093g0147a0002c0002t0036g0012a0002c0002t0036g0098others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-23254dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTT | 9 | a0001c0001t0042g0003a0001c0001t0052g0002a0002c0002t0032g0127others(6): Show | 9 | HG01257.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-23255_6-23254dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTT | 13 | a0001c0001t0024g0136a0001c0001t0053g0137a0001c0001t0054g0132others(10): Show | 13 | HG01243.hp2 HG01496.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-23256_6-23254dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT | 29 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(26): Show | 29 | HG00733.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.6-23260_6-23254dup others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(1): Show |
30 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0071others(27): Show | 30 | HG00280.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.6-23261_6-23254dup others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(2): Show |
22 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0020others(19): Show | 22 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.6-23262_6-23254dup others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0016a0001c0001t0004g0185a0001c0001t0004g0203others(11): Show | 14 | HG00438.hp1 HG01346.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-23263_6-23254dup others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0005g0192a0001c0001t0037g0060a0001c0001t0140g0204others(1): Show | 4 | HG02027.hp1 HG03492.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-23264_6-23254dup others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0193a0001c0001t0139g0175a0001c0001t0149g0021 | 3 | HG02074.hp1 NA18945.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.6-23265_6-23254dup others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(7): Show |
6 | a0001c0001t0003g0019a0001c0001t0003g0043a0001c0001t0004g0178others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-23267_6-23254dup others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0012g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6-23268_6-23254dup others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
C | T | 2 | a0001c0001t0012g0169a0001c0001t0015g0174 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.6-23287C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222728 | ||||||
| chr22:40222728
|
CT | C | 12 | a0001c0001t0006g0150a0001c0001t0015g0139a0001c0001t0015g0140others(9): Show | 12 | HG00639.hp2 HG01070.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-23254delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTT | C | 8 | a0001c0001t0011g0011a0001c0001t0016g0086a0001c0001t0016g0087others(5): Show | 8 | HG02145.hp2 HG02896.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-23255_6-23254del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTT | C | 8 | a0001c0001t0001g0080a0001c0001t0008g0238a0001c0001t0057g0244others(5): Show | 8 | HG00423.hp1 HG03704.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-23259_6-23254del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT | C | 77 | a0001c0001t0001g0219a0001c0001t0002g0217a0001c0001t0002g0218others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.6-23260_6-23254del others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0002g0285a0001c0001t0010g0237a0001c0001t0062g0233others(4): Show | 7 | HG02129.hp2 HG02896.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-23261_6-23254del others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-23262_6-23254del others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6-23263_6-23254del others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6-23264_6-23254del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222728
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0011g0055a0001c0001t0018g0047 | 2 | NA18984.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.6-23267_6-23254del others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | |||||
| chr22:40222737
|
T | C | 4 | a0001c0001t0002g0226a0001c0001t0002g0230a0001c0001t0002g0307others(1): Show | 4 | NA18943.hp2 NA18965.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-23278T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222737 | ||||||
| chr22:40222807
|
A | G | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-23208A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222807 | ||||||
| chr22:40222871
|
G | C | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-23144G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222871 | ||||||
| chr22:40222888
|
G | A | 1 | a0001c0001t0077g0286 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6-23127G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222888 | ||||||
| chr22:40223005
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-23010C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223005 | ||||||
| chr22:40223023
|
A | G | 1 | a0001c0001t0064g0298 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.6-22992A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223023 | ||||||
| chr22:40223074
|
C | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22941C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223074 | ||||||
| chr22:40223210
|
G | A | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6-22805G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223210 | ||||||
| chr22:40223235
|
T | C | 307 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.6-22780T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223235 | ||||||
| chr22:40223381
|
C | T | 1 | a0001c0001t0063g0275 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6-22634C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223381 | ||||||
| chr22:40223407
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-22608G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223407 | ||||||
| chr22:40223451
|
TGTTTC | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22563_6-22559del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223451 | ||||||
| chr22:40223651
|
A | G | 1 | a0001c0001t0015g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6-22364A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223651 | ||||||
| chr22:40223704
|
A | G | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22311A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223704 | ||||||
| chr22:40223775
|
C | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22240C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223775 | ||||||
| chr22:40223923
|
A | G | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6-22092A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223923 | ||||||
| chr22:40224171
|
A | C | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.6-21844A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224171 | ||||||
| chr22:40224194
|
G | A | 2 | a0001c0001t0008g0288a0001c0001t0069g0297 | 2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6-21821G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224194 | ||||||
| chr22:40224463
|
C | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-21552C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224463 | ||||||
| chr22:40224526
|
A | G | 1 | a0001c0001t0013g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6-21489A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224526 | ||||||
| chr22:40224561
|
G | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-21454G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224561 | ||||||
| chr22:40224664
|
C | T | 1 | a0002c0002t0087g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6-21351C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224664 | ||||||
| chr22:40224897
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-21118C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224897 | ||||||
| chr22:40224928
|
G | A | 2 | a0001c0001t0008g0288a0001c0001t0069g0297 | 2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6-21087G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224928 | ||||||
| chr22:40225284
|
G | A | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20731G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225284 | ||||||
| chr22:40225400
|
C | G | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20615C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225400 | ||||||
| chr22:40225641
|
G | A | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20374G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225641 | ||||||
| chr22:40225738
|
G | A | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6-20277G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225738 | ||||||
| chr22:40225742
|
C | CA | 18 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0016g0089others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.6-20248dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | |||||
| chr22:40225742
|
C | CAAA | 6 | a0001c0001t0002g0245a0001c0001t0002g0255a0001c0001t0008g0234others(3): Show | 6 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-20250_6-20248dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | |||||
| chr22:40225742
|
C | CAAAA | 57 | a0001c0001t0002g0217a0001c0001t0002g0240a0001c0001t0002g0248others(54): Show | 57 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.6-20251_6-20248dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | |||||
| chr22:40225742
|
C | CAAAAA | 23 | a0001c0001t0002g0218a0001c0001t0002g0227a0001c0001t0002g0228others(20): Show | 23 | HG00140.hp1 HG00438.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.6-20252_6-20248dup others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | |||||
| chr22:40225742
|
CA | C | 117 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(114): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.6-20248delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | |||||
| chr22:40225873
|
T | G | 44 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.6-20142T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225873 | ||||||
| chr22:40226221
|
T | C | 3 | a0001c0001t0012g0169a0001c0001t0015g0174a0001c0001t0021g0170 | 3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6-19794T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226221 | ||||||
| chr22:40226476
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-19539C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226476 | ||||||
| chr22:40226940
|
T | TA | 12 | a0001c0001t0003g0057a0001c0001t0003g0160a0001c0001t0003g0215others(9): Show | 12 | HG00733.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-19074dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40226940 | |||||
| chr22:40226973
|
A | C | 2 | a0001c0001t0013g0267a0001c0001t0073g0225 | 2 | HG00408.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.6-19042A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226973 | ||||||
| chr22:40227075
|
A | AATT | 36 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0039others(33): Show | 36 | HG01243.hp1 HG01346.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.6-18900_6-18898dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | |||||
| chr22:40227075
|
AATT | A | 169 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.6-18900_6-18898del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | |||||
| chr22:40227075
|
AATTATT | A | 19 | a0001c0001t0006g0135a0001c0001t0015g0139a0001c0001t0015g0140others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-18903_6-18898del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | |||||
| chr22:40227075
|
AATTATTA others(2): Show |
A | 10 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 10 | HG02055.hp1 HG02896.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.6-18906_6-18898del others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | |||||
| chr22:40227188
|
C | T | 1 | a0001c0001t0014g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6-18827C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227188 | ||||||
| chr22:40227245
|
T | C | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-18770T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227245 | ||||||
| chr22:40227277
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-18738G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227277 | ||||||
| chr22:40227323
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.6-18692A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227323 | ||||||
| chr22:40227358
|
C | CT | 92 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0048others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.6-18632dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | |||||
| chr22:40227358
|
C | CTT | 33 | a0001c0001t0002g0218a0001c0001t0002g0227a0001c0001t0002g0230others(30): Show | 33 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.6-18633_6-18632dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | |||||
| chr22:40227358
|
CT | C | 42 | a0001c0001t0001g0020a0001c0001t0004g0178a0001c0001t0004g0180others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.6-18632delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | |||||
| chr22:40227392
|
G | T | 1 | a0001c0017t0079g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6-18623G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227392 | ||||||
| chr22:40227426
|
T | C | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-18589T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227426 | ||||||
| chr22:40227427
|
G | A | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-18588G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227427 | ||||||
| chr22:40227520
|
T | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6-18495T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227520 | ||||||
| chr22:40227678
|
A | G | 2 | a0001c0001t0137g0179a0007c0018t0005g0205 | 2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-18337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227678 | ||||||
| chr22:40228035
|
G | A | 1 | a0002c0002t0154g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-17980G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228035 | ||||||
| chr22:40228212
|
G | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-17803G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228212 | ||||||
| chr22:40228543
|
A | G | 250 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(247): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.6-17472A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228543 | ||||||
| chr22:40228585
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-17430T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228585 | ||||||
| chr22:40228804
|
A | G | 303 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(300): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.6-17211A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228804 | ||||||
| chr22:40228992
|
GACCTAAG others(11): Show |
G | 1 | a0001c0001t0123g0054 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6-17003_6-16986del others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40228992 | |||||
| chr22:40229042
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6-16973C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229042 | ||||||
| chr22:40229046
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6-16969A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229046 | ||||||
| chr22:40229445
|
CT | C | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-16558delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40229445 | |||||
| chr22:40229456
|
T | C | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6-16559T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229456 | ||||||
| chr22:40229520
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6-16495G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229520 | ||||||
| chr22:40229573
|
C | CT | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16441dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40229573 | |||||
| chr22:40229905
|
A | G | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16110A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229905 | ||||||
| chr22:40229947
|
C | T | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16068C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229947 | ||||||
| chr22:40230282
|
CT | C | 99 | a0001c0001t0001g0016a0001c0001t0002g0217a0001c0001t0002g0218others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.6-15709delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40230282 | |||||
| chr22:40230282
|
CTT | C | 8 | a0001c0001t0008g0234a0001c0001t0010g0237a0001c0001t0028g0246others(5): Show | 8 | HG01070.hp2 HG01167.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-15710_6-15709del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40230282 | |||||
| chr22:40230329
|
G | A | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-15686G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230329 | ||||||
| chr22:40230479
|
A | G | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-15536A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230479 | ||||||
| chr22:40230511
|
C | G | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-15504C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230511 | ||||||
| chr22:40230588
|
G | A | 6 | a0002c0002t0151g0106a0002c0002t0152g0096a0002c0002t0153g0101others(3): Show | 6 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-15427G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230588 | ||||||
| chr22:40230647
|
G | C | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-15368G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230647 | ||||||
| chr22:40230684
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6-15331T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230684 | ||||||
| chr22:40231001
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-15014C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231001 | ||||||
| chr22:40231053
|
C | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.6-14962C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231053 | ||||||
| chr22:40231053
|
C | CTA | 5 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0034g0091others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-14948_6-14947dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40231053 | |||||
| chr22:40231055
|
A | C | 137 | a0001c0001t0001g0219a0001c0001t0002g0217a0001c0001t0002g0218others(134): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.6-14960A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231055 | ||||||
| chr22:40231057
|
A | C | 76 | a0001c0001t0002g0226a0001c0001t0002g0228a0001c0001t0002g0230others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.6-14958A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231057 | ||||||
| chr22:40231083
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6-14932A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231083 | ||||||
| chr22:40231265
|
C | T | 3 | a0001c0001t0012g0169a0001c0001t0015g0174a0001c0001t0021g0170 | 3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6-14750C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231265 | ||||||
| chr22:40231315
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-14700C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231315 | ||||||
| chr22:40231525
|
CT | C | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-14483delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40231525 | |||||
| chr22:40231767
|
T | C | 1 | a0001c0001t0002g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6-14248T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231767 | ||||||
| chr22:40231872
|
C | T | 7 | a0001c0001t0002g0258a0001c0001t0002g0260a0001c0001t0002g0264others(4): Show | 7 | HG00408.hp2 HG02083.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-14143C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231872 | ||||||
| chr22:40231998
|
T | C | 1 | a0008c0016t0147g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6-14017T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231998 | ||||||
| chr22:40232046
|
G | C | 25 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0016g0086others(22): Show | 25 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.6-13969G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232046 | ||||||
| chr22:40232062
|
A | T | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-13953A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232062 | ||||||
| chr22:40232224
|
T | C | 2 | a0001c0001t0039g0165a0001c0001t0128g0084 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6-13791T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232224 | ||||||
| chr22:40232229
|
C | T | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6-13786C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232229 | ||||||
| chr22:40232230
|
G | A | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6-13785G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232230 | ||||||
| chr22:40232330
|
G | A | 1 | a0001c0001t0003g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6-13685G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232330 | ||||||
| chr22:40232383
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6-13632T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232383 | ||||||
| chr22:40232562
|
C | T | 2 | a0001c0001t0046g0153a0001c0001t0047g0152 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6-13453C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232562 | ||||||
| chr22:40232591
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-13424T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232591 | ||||||
| chr22:40232750
|
C | T | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-13265C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232750 | ||||||
| chr22:40232922
|
C | T | 3 | a0001c0001t0025g0271a0001c0001t0025g0272a0001c0001t0026g0280 | 3 | HG00140.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6-13093C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232922 | ||||||
| chr22:40233134
|
T | C | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-12881T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233134 | ||||||
| chr22:40233295
|
C | G | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6-12720C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233295 | ||||||
| chr22:40233316
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-12699G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233316 | ||||||
| chr22:40233441
|
G | T | 47 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.6-12574G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233441 | ||||||
| chr22:40233537
|
G | A | 1 | a0002c0002t0085g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.6-12478G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233537 | ||||||
| chr22:40233620
|
C | CA | 8 | a0001c0001t0002g0285a0001c0001t0014g0065a0001c0001t0028g0246others(5): Show | 8 | HG00544.hp1 HG02015.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-12381dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40233620 | |||||
| chr22:40233719
|
G | A | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6-12296G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233719 | ||||||
| chr22:40233801
|
A | G | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-12214A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233801 | ||||||
| chr22:40233965
|
G | C | 2 | a0001c0001t0137g0179a0007c0018t0005g0205 | 2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-12050G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233965 | ||||||
| chr22:40233976
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(4): Show | 7 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-12039C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233976 | ||||||
| chr22:40234009
|
G | A | 1 | a0010c0012t0006g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6-12006G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234009 | ||||||
| chr22:40234268
|
C | T | 1 | a0002c0002t0101g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6-11747C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234268 | ||||||
| chr22:40234404
|
A | G | 1 | a0002c0002t0087g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6-11611A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234404 | ||||||
| chr22:40234670
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6-11345A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234670 | ||||||
| chr22:40234945
|
A | T | 27 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0187others(24): Show | 27 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.6-11070A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234945 | ||||||
| chr22:40235029
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10986C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235029 | ||||||
| chr22:40235106
|
G | C | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10909G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235106 | ||||||
| chr22:40235335
|
G | A | 87 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-10680G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235335 | ||||||
| chr22:40235433
|
C | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10582C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235433 | ||||||
| chr22:40235448
|
G | A | 1 | a0001c0001t0004g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.6-10567G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235448 | ||||||
| chr22:40235491
|
C | T | 1 | a0002c0002t0100g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6-10524C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235491 | ||||||
| chr22:40235613
|
G | A | 90 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.6-10402G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235613 | ||||||
| chr22:40235735
|
A | G | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10280A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235735 | ||||||
| chr22:40235755
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0023others(2): Show | 5 | HG02083.hp1 NA18944.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-10260C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235755 | ||||||
| chr22:40235791
|
T | C | 6 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-10224T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235791 | ||||||
| chr22:40235917
|
A | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-10098A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235917 | ||||||
| chr22:40236043
|
A | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.6-9972A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236043 | ||||||
| chr22:40236079
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-9936C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236079 | ||||||
| chr22:40236506
|
C | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.6-9509C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236506 | ||||||
| chr22:40236768
|
A | G | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-9247A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236768 | ||||||
| chr22:40237057
|
C | T | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-8958C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237057 | ||||||
| chr22:40237214
|
A | G | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(11): Show | 14 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-8801A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237214 | ||||||
| chr22:40237305
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6-8710A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237305 | ||||||
| chr22:40237459
|
A | C | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-8556A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237459 | ||||||
| chr22:40237487
|
G | A | 2 | a0001c0001t0013g0267a0002c0002t0009g0120 | 2 | HG00140.hp2 HG00408.hp2 |
intron_variant | MODIFIER | c.6-8528G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237487 | ||||||
| chr22:40237508
|
G | A | 1 | a0001c0001t0019g0210 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6-8507G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237508 | ||||||
| chr22:40237687
|
T | A | 3 | a0002c0002t0083g0093a0002c0002t0097g0103a0013c0019t0095g0166 | 3 | HG00639.hp2 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6-8328T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237687 | ||||||
| chr22:40237778
|
C | T | 1 | a0002c0002t0036g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6-8237C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237778 | ||||||
| chr22:40237829
|
T | TG | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-8184dupG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40237829 | |||||
| chr22:40238049
|
C | T | 1 | a0001c0001t0055g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6-7966C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238049 | ||||||
| chr22:40238409
|
A | G | 1 | a0002c0002t0032g0128 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6-7606A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238409 | ||||||
| chr22:40238503
|
A | G | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-7512A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238503 | ||||||
| chr22:40239063
|
C | T | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6-6952C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239063 | ||||||
| chr22:40239109
|
G | A | 1 | a0002c0002t0094g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6-6906G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239109 | ||||||
| chr22:40239122
|
G | A | 7 | a0002c0002t0151g0106a0002c0002t0152g0096a0002c0002t0153g0101others(4): Show | 7 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-6893G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239122 | ||||||
| chr22:40239167
|
C | T | 1 | a0001c0001t0119g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-6848C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239167 | ||||||
| chr22:40239194
|
C | A | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6-6821C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239194 | ||||||
| chr22:40239272
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0070others(24): Show | 27 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.6-6743G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239272 | ||||||
| chr22:40239479
|
A | G | 1 | a0001c0001t0117g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6-6536A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239479 | ||||||
| chr22:40239717
|
T | C | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-6298T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239717 | ||||||
| chr22:40240072
|
T | C | 242 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.6-5943T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240072 | ||||||
| chr22:40240254
|
T | C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-5761T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240254 | ||||||
| chr22:40240329
|
A | T | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-5686A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240329 | ||||||
| chr22:40240590
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6-5425C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240590 | ||||||
| chr22:40240611
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-5404C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240611 | ||||||
| chr22:40240795
|
A | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.6-5220A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240795 | ||||||
| chr22:40240888
|
T | C | 1 | a0001c0001t0026g0280 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6-5127T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240888 | ||||||
| chr22:40241031
|
C | T | 2 | a0001c0001t0015g0139a0001c0001t0049g0141 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.6-4984C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241031 | ||||||
| chr22:40241096
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-4919G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241096 | ||||||
| chr22:40241308
|
A | G | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6-4707A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241308 | ||||||
| chr22:40241333
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6-4682C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241333 | ||||||
| chr22:40241346
|
G | A | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-4669G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241346 | ||||||
| chr22:40241723
|
T | C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-4292T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241723 | ||||||
| chr22:40241800
|
T | G | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-4215T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241800 | ||||||
| chr22:40242094
|
A | G | 1 | a0002c0002t0105g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6-3921A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242094 | ||||||
| chr22:40242112
|
T | C | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6-3903T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242112 | ||||||
| chr22:40242179
|
A | AGT | 114 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.6-3806_6-3805dupTG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | |||||
| chr22:40242179
|
A | AGTGT | 13 | a0001c0001t0001g0035a0001c0001t0003g0163a0001c0001t0037g0059others(10): Show | 13 | HG00423.hp1 HG02293.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-3808_6-3805dupTG others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | |||||
| chr22:40242179
|
AGT | A | 27 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(24): Show | 27 | HG00438.hp1 HG01884.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.6-3806_6-3805delTG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | |||||
| chr22:40242179
|
AGTGT | A | 5 | a0001c0001t0001g0071a0001c0001t0006g0150a0001c0001t0065g0224others(2): Show | 5 | HG01891.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-3808_6-3805delTG others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | |||||
| chr22:40242179
|
AGTGTGTG others(1): Show |
A | 86 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.6-3812_6-3805delTG others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | |||||
| chr22:40242219
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-3796C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242219 | ||||||
| chr22:40242329
|
A | G | 1 | a0001c0001t0005g0191 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6-3686A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242329 | ||||||
| chr22:40242394
|
A | G | 1 | a0002c0002t0152g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-3621A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242394 | ||||||
| chr22:40242517
|
G | A | 6 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0039g0165others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-3498G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242517 | ||||||
| chr22:40242520
|
TC | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 4 | NA18612.hp2 NA18943.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-3492delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242520 | |||||
| chr22:40242675
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-3340C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242675 | ||||||
| chr22:40242710
|
G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6-3305G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242710 | ||||||
| chr22:40242930
|
C | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-3085C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242930 | ||||||
| chr22:40243120
|
C | T | 7 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0034g0091others(4): Show | 7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-2895C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243120 | ||||||
| chr22:40243291
|
G | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-2724G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243291 | ||||||
| chr22:40243419
|
C | G | 90 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.6-2596C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243419 | ||||||
| chr22:40243513
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-2502A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243513 | ||||||
| chr22:40243702
|
C | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.6-2313C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243702 | ||||||
| chr22:40243726
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.6-2289A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243726 | ||||||
| chr22:40244276
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 10 | HG02083.hp1 NA18944.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.6-1739A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244276 | ||||||
| chr22:40244281
|
G | A | 249 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.6-1734G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244281 | ||||||
| chr22:40244481
|
A | G | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6-1534A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244481 | ||||||
| chr22:40244512
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.6-1503C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244512 | ||||||
| chr22:40244716
|
G | T | 4 | a0001c0001t0022g0126a0001c0001t0022g0177a0001c0001t0022g0199others(1): Show | 4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-1299G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244716 | ||||||
| chr22:40244765
|
C | T | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6-1250C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244765 | ||||||
| chr22:40245074
|
C | CATTT | 48 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0187others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.6-912_6-909dupATTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | |||||
| chr22:40245074
|
C | CATTTATT others(1): Show |
12 | a0001c0001t0004g0185a0001c0001t0004g0188a0001c0001t0012g0186others(9): Show | 12 | HG01258.hp2 HG01346.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-916_6-909dupATTT others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | |||||
| chr22:40245074
|
C | CATTTATT others(5): Show |
1 | a0001c0001t0143g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6-920_6-909dupATTT others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | |||||
| chr22:40245074
|
CATTT | C | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-912_6-909delATTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | |||||
| chr22:40245074
|
CATTTATT others(5): Show |
C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-920_6-909delATTT others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | |||||
| chr22:40245160
|
G | T | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-855G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245160 | ||||||
| chr22:40245375
|
G | A | 1 | a0001c0001t0119g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-640G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245375 | ||||||
| chr22:40245378
|
A | C | 2 | a0001c0001t0016g0086a0001c0001t0016g0087 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6-637A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245378 | ||||||
| chr22:40245438
|
AAAATAG | A | 3 | a0001c0001t0039g0165a0001c0001t0115g0090a0001c0001t0128g0084 | 3 | HG02145.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6-561_6-556delTAGA others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245438 | |||||
| chr22:40245711
|
CGT | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.6-285_6-284delGT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245711 | |||||
| chr22:40245711
|
CGTGT | C | 87 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-287_6-284delGTGT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245711 | |||||
| chr22:40245793
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-222C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245793 | ||||||
| chr22:40245888
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(3): Show | 6 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-127T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245888 | ||||||
| chr22:40245976
|
G | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-39G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245976 | ||||||
| chr22:40246121
|
G | A | 1 | a0014c0009t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.93+19G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246121 | ||||||
| chr22:40246334
|
T | C | 307 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.93+232T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246334 | ||||||
| chr22:40246364
|
G | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.93+262G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246364 | ||||||
| chr22:40246448
|
G | A | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.93+346G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246448 | ||||||
| chr22:40246457
|
G | C | 1 | a0001c0001t0002g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.93+355G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246457 | ||||||
| chr22:40246648
|
C | G | 91 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.93+546C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246648 | ||||||
| chr22:40246739
|
G | A | 3 | a0002c0002t0034g0009a0002c0002t0084g0008a0002c0002t0094g0010 | 3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.93+637G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246739 | ||||||
| chr22:40246795
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.93+693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246795 | ||||||
| chr22:40247003
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.93+901G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247003 | ||||||
| chr22:40247203
|
A | G | 1 | a0001c0001t0018g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.93+1101A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247203 | ||||||
| chr22:40247462
|
A | G | 51 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.93+1360A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247462 | ||||||
| chr22:40247543
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.93+1441A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247543 | ||||||
| chr22:40247791
|
CTGGTG | C | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.93+1695_93+1699del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40247791 | |||||
| chr22:40247835
|
C | T | 89 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.93+1733C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247835 | ||||||
| chr22:40247868
|
C | T | 80 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0228others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.93+1766C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247868 | ||||||
| chr22:40248076
|
A | G | 7 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0034g0091others(4): Show | 7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1974A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248076 | ||||||
| chr22:40248077
|
G | GA | 10 | a0001c0001t0002g0218a0001c0001t0002g0228a0001c0001t0002g0252others(7): Show | 10 | HG00642.hp2 HG02258.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+1990dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40248077 | |||||
| chr22:40248142
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0003g0163 | 2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.93+2040C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248142 | ||||||
| chr22:40248151
|
A | G | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.93+2049A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248151 | ||||||
| chr22:40248242
|
C | G | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.93+2140C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248242 | ||||||
| chr22:40248471
|
T | G | 1 | a0009c0014t0004g0189 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.93+2369T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248471 | ||||||
| chr22:40248707
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-2472G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248707 | ||||||
| chr22:40248713
|
G | A | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-2466G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248713 | ||||||
| chr22:40249568
|
G | A | 1 | a0001c0001t0008g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.94-1611G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40249568 | ||||||
| chr22:40249591
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-1588A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40249591 | ||||||
| chr22:40250046
|
C | T | 2 | a0001c0001t0015g0139a0001c0001t0049g0141 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.94-1133C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250046 | ||||||
| chr22:40250066
|
T | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-1113T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250066 | ||||||
| chr22:40250068
|
C | T | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-1111C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250068 | ||||||
| chr22:40250433
|
C | T | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-746C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250433 | ||||||
| chr22:40250458
|
ACTTT | A | 6 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0039g0165others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-716_94-713delCT others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40250458 | |||||
| chr22:40250797
|
A | G | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94-382A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250797 | ||||||
| chr22:40250933
|
CT | C | 252 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(249): Show | 252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.94-228delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40250933 | |||||
| chr22:40251163
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-16T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40251163 | ||||||
| chr22:40251214
|
T | C | 1 | a0001c0001t0015g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.115+14T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251214 | ||||||
| chr22:40251218
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115+18T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251218 | ||||||
| chr22:40251400
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.115+200G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251400 | ||||||
| chr22:40251419
|
C | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115+219C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251419 | ||||||
| chr22:40251435
|
A | G | 1 | a0001c0001t0024g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.115+235A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251435 | ||||||
| chr22:40251456
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+256G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251456 | ||||||
| chr22:40251495
|
G | T | 6 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0039g0165others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+295G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251495 | ||||||
| chr22:40251735
|
A | G | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115+535A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251735 | ||||||
| chr22:40251893
|
C | T | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115+693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251893 | ||||||
| chr22:40252036
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG02280.hp1 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+836A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252036 | ||||||
| chr22:40252194
|
A | G | 46 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.115+994A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252194 | ||||||
| chr22:40252418
|
G | A | 1 | a0001c0001t0013g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.115+1218G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252418 | ||||||
| chr22:40252968
|
C | T | 4 | a0002c0002t0009g0119a0002c0002t0009g0120a0002c0002t0009g0122others(1): Show | 4 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1768C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252968 | ||||||
| chr22:40253005
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.115+1805A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253005 | ||||||
| chr22:40253102
|
CT | C | 33 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(30): Show | 33 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.115+1915delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253102 | |||||
| chr22:40253245
|
C | A | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.115+2045C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253245 | ||||||
| chr22:40253248
|
A | AT | 6 | a0001c0001t0001g0074a0001c0001t0002g0302a0001c0001t0022g0199others(3): Show | 6 | HG01261.hp2 HG03017.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+2063dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253248 | |||||
| chr22:40253333
|
G | A | 2 | a0001c0001t0030g0220a0001c0001t0030g0221 | 2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.115+2133G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253333 | ||||||
| chr22:40253336
|
T | C | 234 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.115+2136T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253336 | ||||||
| chr22:40253516
|
T | C | 3 | a0001c0001t0033g0146a0001c0001t0035g0148a0001c0001t0093g0147 | 3 | HG01109.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.115+2316T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253516 | ||||||
| chr22:40253668
|
T | C | 1 | a0001c0001t0005g0192 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.115+2468T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253668 | ||||||
| chr22:40253691
|
C | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+2491C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253691 | ||||||
| chr22:40253699
|
C | T | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+2499C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253699 | ||||||
| chr22:40253811
|
G | A | 1 | a0001c0001t0119g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.115+2611G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253811 | ||||||
| chr22:40253819
|
CCTT | C | 91 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 91 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.115+2628_115+2630d others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253819 | |||||
| chr22:40254200
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | NA18979.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.115+3000C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254200 | ||||||
| chr22:40254280
|
G | A | 5 | a0002c0002t0009g0119a0002c0002t0009g0120a0002c0002t0009g0122others(2): Show | 5 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+3080G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254280 | ||||||
| chr22:40254613
|
C | T | 3 | a0001c0001t0002g0279a0001c0001t0072g0276a0001c0001t0078g0277 | 3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.115+3413C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254613 | ||||||
| chr22:40254748
|
G | A | 3 | a0002c0002t0032g0127a0002c0002t0032g0128a0002c0002t0041g0129 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.115+3548G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254748 | ||||||
| chr22:40254931
|
A | G | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.115+3731A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254931 | ||||||
| chr22:40255004
|
G | T | 1 | a0001c0001t0055g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115+3804G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255004 | ||||||
| chr22:40255037
|
A | G | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+3837A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255037 | ||||||
| chr22:40255141
|
T | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115+3941T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255141 | ||||||
| chr22:40255358
|
G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.115+4158G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255358 | ||||||
| chr22:40255414
|
A | C | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115+4214A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255414 | ||||||
| chr22:40255460
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115+4260C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255460 | ||||||
| chr22:40255604
|
A | T | 1 | a0001c0001t0002g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+4404A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255604 | ||||||
| chr22:40255716
|
T | G | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115+4516T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255716 | ||||||
| chr22:40255723
|
A | G | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115+4523A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255723 | ||||||
| chr22:40255794
|
T | C | 5 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(2): Show | 5 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+4594T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255794 | ||||||
| chr22:40255843
|
CTTGTTTG others(5): Show |
C | 147 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(144): Show | 147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.115+4658_115+4669d others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40255843 | |||||
| chr22:40256470
|
C | A | 6 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+5270C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256470 | ||||||
| chr22:40256573
|
G | A | 1 | a0001c0001t0067g0282 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.116-5259G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256573 | ||||||
| chr22:40256797
|
A | G | 235 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.116-5035A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256797 | ||||||
| chr22:40256869
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 95 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.116-4963A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256869 | ||||||
| chr22:40256920
|
A | G | 2 | a0002c0002t0085g0124a0002c0002t0099g0125 | 2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.116-4912A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256920 | ||||||
| chr22:40257783
|
G | A | 2 | a0002c0002t0107g0105a0002c0002t0157g0099 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.116-4049G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257783 | ||||||
| chr22:40257878
|
T | C | 235 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.116-3954T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257878 | ||||||
| chr22:40257943
|
G | A | 1 | a0002c0002t0009g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116-3889G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257943 | ||||||
| chr22:40258064
|
A | G | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116-3768A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258064 | ||||||
| chr22:40258071
|
C | CT | 54 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.116-3731dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTT | 12 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0003g0163others(9): Show | 12 | HG00735.hp2 HG01261.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.116-3732_116-3731d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-3741_116-3731d others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(5): Show |
17 | a0001c0001t0002g0230a0001c0001t0002g0266a0001c0001t0002g0296others(14): Show | 17 | HG00140.hp1 HG00280.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-3742_116-3731d others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(6): Show |
26 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0245others(23): Show | 26 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.116-3743_116-3731d others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(7): Show |
14 | a0001c0001t0002g0240a0001c0001t0002g0258a0001c0001t0002g0279others(11): Show | 14 | HG00408.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-3744_116-3731d others(16): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(8): Show |
11 | a0001c0001t0002g0217a0001c0001t0002g0248a0001c0001t0008g0223others(8): Show | 11 | HG00438.hp2 HG00544.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.116-3745_116-3731d others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0002g0218a0001c0001t0010g0295a0001c0001t0013g0291others(1): Show | 4 | HG01361.hp1 HG01517.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3746_116-3731d others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0027g0232a0001c0001t0057g0244 | 2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.116-3747_116-3731d others(19): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0028g0239 | 3 | HG02165.hp2 NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.116-3748_116-3731d others(20): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0010g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116-3750_116-3731d others(22): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0010g0308a0001c0001t0063g0275 | 2 | HG02074.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.116-3751_116-3731d others(23): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.116-3754_116-3731d others(26): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
CT | C | 14 | a0001c0001t0002g0285a0001c0001t0034g0091a0001c0001t0035g0148others(11): Show | 14 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.116-3731delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
CTT | C | 53 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0015g0139others(50): Show | 53 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.116-3732_116-3731d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258071
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0007g0265a0001c0001t0007g0278a0001c0001t0007g0300 | 3 | HG01123.hp2 HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.116-3741_116-3731d others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | |||||
| chr22:40258101
|
T | TTTTTTTT others(3): Show |
1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-3731_116-3730i others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258101 | ||||||
| chr22:40258272
|
T | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.116-3560T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258272 | ||||||
| chr22:40258306
|
T | G | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-3526T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258306 | ||||||
| chr22:40258601
|
C | A | 1 | a0002c0002t0009g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.116-3231C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258601 | ||||||
| chr22:40259025
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.116-2807C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259025 | ||||||
| chr22:40259304
|
A | G | 3 | a0001c0001t0012g0206a0001c0001t0121g0306a0001c0001t0143g0184 | 3 | HG01106.hp2 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.116-2528A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259304 | ||||||
| chr22:40259444
|
G | A | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116-2388G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259444 | ||||||
| chr22:40259500
|
G | A | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.116-2332G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259500 | ||||||
| chr22:40259736
|
G | A | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.116-2096G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259736 | ||||||
| chr22:40259830
|
C | T | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.116-2002C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259830 | ||||||
| chr22:40260087
|
A | G | 1 | a0001c0001t0011g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.116-1745A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260087 | ||||||
| chr22:40260094
|
G | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-1738G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260094 | ||||||
| chr22:40260201
|
C | CT | 142 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.116-1617dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40260201 | |||||
| chr22:40260308
|
A | T | 1 | a0001c0001t0028g0239 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.116-1524A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260308 | ||||||
| chr22:40260473
|
A | G | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-1359A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260473 | ||||||
| chr22:40260540
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-1292G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260540 | ||||||
| chr22:40260736
|
C | G | 1 | a0001c0001t0029g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.116-1096C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260736 | ||||||
| chr22:40260884
|
G | A | 287 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(284): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.116-948G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260884 | ||||||
| chr22:40260892
|
G | A | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-940G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260892 | ||||||
| chr22:40260923
|
G | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.116-909G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260923 | ||||||
| chr22:40261414
|
T | G | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.116-418T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40261414 | ||||||
| chr22:40262521
|
GA | G | 21 | a0002c0002t0006g0107a0002c0002t0009g0111a0002c0002t0009g0116others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.457+350delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40262521 | |||||
| chr22:40262665
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.457+492T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262665 | ||||||
| chr22:40262687
|
T | C | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.457+514T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262687 | ||||||
| chr22:40262762
|
G | C | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.457+589G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262762 | ||||||
| chr22:40262824
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.457+651G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262824 | ||||||
| chr22:40262907
|
G | A | 3 | a0001c0001t0012g0169a0001c0001t0015g0174a0001c0001t0021g0170 | 3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.457+734G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262907 | ||||||
| chr22:40263016
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.457+843G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263016 | ||||||
| chr22:40263034
|
C | T | 2 | a0001c0001t0015g0174a0001c0001t0139g0175 | 2 | HG02809.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.457+861C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263034 | ||||||
| chr22:40263039
|
T | TA | 7 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0034g0091others(4): Show | 7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+884dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | |||||
| chr22:40263039
|
TA | T | 78 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(75): Show | 78 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.457+884delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | |||||
| chr22:40263039
|
TAA | T | 7 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(4): Show | 7 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+883_457+884del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | |||||
| chr22:40263169
|
A | G | 1 | a0001c0001t0004g0187 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.457+996A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263169 | ||||||
| chr22:40263222
|
T | C | 1 | a0001c0001t0123g0054 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.457+1049T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263222 | ||||||
| chr22:40263247
|
T | A | 94 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.457+1074T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263247 | ||||||
| chr22:40263279
|
A | T | 1 | a0001c0001t0013g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+1106A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263279 | ||||||
| chr22:40263457
|
G | A | 1 | a0001c0001t0046g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.458-1231G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263457 | ||||||
| chr22:40263569
|
T | C | 164 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.458-1119T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263569 | ||||||
| chr22:40263579
|
C | T | 1 | a0001c0001t0007g0265 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.458-1109C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263579 | ||||||
| chr22:40263580
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-1108G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263580 | ||||||
| chr22:40263753
|
G | A | 1 | a0009c0014t0004g0189 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.458-935G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263753 | ||||||
| chr22:40263777
|
A | G | 90 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.458-911A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263777 | ||||||
| chr22:40264005
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-683T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264005 | ||||||
| chr22:40264110
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-578C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264110 | ||||||
| chr22:40264185
|
A | G | 1 | a0001c0001t0029g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.458-503A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264185 | ||||||
| chr22:40264257
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-431A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264257 | ||||||
| chr22:40267399
|
G | A | 85 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2806+363G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267399 | ||||||
| chr22:40267749
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2806+713G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267749 | ||||||
| chr22:40267857
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2806+821G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267857 | ||||||
| chr22:40267870
|
C | CA | 96 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.2806+844dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40267870 | |||||
| chr22:40267884
|
C | T | 8 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0033g0146others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2806+848C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267884 | ||||||
| chr22:40268008
|
A | G | 1 | a0001c0001t0109g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2806+972A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268008 | ||||||
| chr22:40268046
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2806+1010G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268046 | ||||||
| chr22:40268079
|
A | G | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2806+1043A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268079 | ||||||
| chr22:40268156
|
C | T | 1 | a0002c0002t0094g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2806+1120C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268156 | ||||||
| chr22:40268161
|
C | T | 86 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2806+1125C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268161 | ||||||
| chr22:40268186
|
A | C | 1 | a0001c0001t0017g0033 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2806+1150A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268186 | ||||||
| chr22:40268236
|
C | T | 1 | a0002c0002t0009g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2806+1200C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268236 | ||||||
| chr22:40268379
|
C | T | 1 | a0001c0001t0117g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2806+1343C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268379 | ||||||
| chr22:40268640
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-1482G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268640 | ||||||
| chr22:40268674
|
G | T | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2807-1448G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268674 | ||||||
| chr22:40268756
|
G | A | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2807-1366G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268756 | ||||||
| chr22:40268785
|
A | G | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-1337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268785 | ||||||
| chr22:40268907
|
C | T | 5 | a0001c0001t0015g0139a0001c0001t0049g0141a0006c0006t0111g0214others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2807-1215C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268907 | ||||||
| chr22:40268912
|
C | CAAAAAAA others(4): Show |
1 | a0012c0010t0150g0102 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2807-1204_2807-120 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268912 | |||||
| chr22:40268916
|
A | AAAAAAAA others(4): Show |
2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2807-1204_2807-120 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | |||||
| chr22:40268916
|
A | AAAT | 12 | a0001c0001t0002g0218a0001c0001t0012g0186a0001c0001t0012g0202others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.2807-1178_2807-117 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | |||||
| chr22:40268916
|
AAATAATA others(2): Show |
A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2807-1184_2807-117 others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | |||||
| chr22:40268919
|
T | A | 8 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2807-1203T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268919 | ||||||
| chr22:40268922
|
T | A | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2807-1200T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268922 | ||||||
| chr22:40269053
|
C | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2807-1069C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269053 | ||||||
| chr22:40269063
|
T | C | 88 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2807-1059T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269063 | ||||||
| chr22:40269126
|
C | CT | 7 | a0002c0002t0009g0122a0002c0002t0091g0109a0002c0002t0092g0110others(4): Show | 7 | HG01071.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2807-969dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | |||||
| chr22:40269126
|
CT | C | 104 | a0001c0001t0001g0050a0001c0001t0001g0073a0001c0001t0002g0217others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2807-969delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | |||||
| chr22:40269126
|
CTT | C | 126 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2807-970_2807-969d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | |||||
| chr22:40269221
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2807-901C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269221 | ||||||
| chr22:40269706
|
C | A | 2 | a0001c0001t0037g0059a0001c0001t0037g0060 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2807-416C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269706 | ||||||
| chr22:40269786
|
G | T | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-336G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269786 | ||||||
| chr22:40269887
|
C | CA | 168 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 168 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.2807-213dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269887 | |||||
| chr22:40269887
|
C | CAA | 15 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0001t0001g0077others(12): Show | 15 | HG01123.hp1 HG02027.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.2807-214_2807-213d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269887 | |||||
| chr22:40270313
|
CT | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(16): Show | 19 | HG01884.hp1 HG02027.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2965+51delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr22 | 40270313 | |||||
| chr22:40270393
|
C | T | 2 | a0002c0002t0090g0092a0002c0002t0152g0096 | 2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2965+113C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270393 | ||||||
| chr22:40270469
|
G | A | 1 | a0001c0015t0024g0131 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2965+189G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270469 | ||||||
| chr22:40270481
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0045g0075 | 2 | HG00280.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.2965+201G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270481 | ||||||
| chr22:40270693
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+413G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270693 | ||||||
| chr22:40270852
|
G | C | 2 | a0001c0005t0004g0171a0001c0005t0141g0172 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2965+572G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270852 | ||||||
| chr22:40270918
|
G | C | 48 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.2965+638G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270918 | ||||||
| chr22:40270940
|
C | T | 1 | a0002c0002t0085g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2965+660C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270940 | ||||||
| chr22:40270966
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+686G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270966 | ||||||
| chr22:40271087
|
G | A | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+807G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271087 | ||||||
| chr22:40271436
|
C | G | 1 | a0013c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2965+1156C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271436 | ||||||
| chr22:40271573
|
G | A | 2 | a0001c0001t0010g0262a0001c0001t0058g0261 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2965+1293G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271573 | ||||||
| chr22:40271767
|
C | G | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+1487C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271767 | ||||||
| chr22:40271988
|
CT | C | 259 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(256): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2966-1434delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr22 | 40271988 | |||||
| chr22:40271992
|
A | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(256): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2966-1433A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271992 | ||||||
| chr22:40272070
|
G | A | 233 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2966-1355G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272070 | ||||||
| chr22:40272087
|
G | T | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2966-1338G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272087 | ||||||
| chr22:40272227
|
C | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2966-1198C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272227 | ||||||
| chr22:40272237
|
A | G | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2966-1188A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272237 | ||||||
| chr22:40272384
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2966-1041T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272384 | ||||||
| chr22:40272631
|
G | A | 46 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2966-794G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272631 | ||||||
| chr22:40272789
|
C | T | 1 | a0001c0001t0022g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2966-636C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272789 | ||||||
| chr22:40272984
|
C | G | 92 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(89): Show | 92 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2966-441C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272984 | ||||||
| chr22:40273644
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 95 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.3141+44A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273644 | ||||||
| chr22:40273794
|
G | A | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3141+194G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273794 | ||||||
| chr22:40273826
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3141+226T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273826 | ||||||
| chr22:40274354
|
C | T | 3 | a0006c0006t0111g0214a0006c0006t0112g0001a0012c0010t0150g0102 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3141+754C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274354 | ||||||
| chr22:40274422
|
C | CT | 42 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.3141+838dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40274422 | |||||
| chr22:40274422
|
C | CTTTTTTT others(15): Show |
2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3141+838_3141+839i others(24): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40274422 | |||||
| chr22:40274554
|
G | T | 5 | a0002c0002t0151g0106a0002c0002t0153g0101a0002c0002t0154g0155others(2): Show | 5 | HG01496.hp2 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3141+954G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274554 | ||||||
| chr22:40274810
|
A | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3141+1210A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274810 | ||||||
| chr22:40274890
|
A | G | 3 | a0001c0001t0002g0279a0001c0001t0072g0276a0001c0001t0078g0277 | 3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3141+1290A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274890 | ||||||
| chr22:40274971
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3141+1371C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274971 | ||||||
| chr22:40275106
|
T | C | 1 | a0002c0002t0105g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3141+1506T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275106 | ||||||
| chr22:40275126
|
A | G | 1 | a0001c0001t0126g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3141+1526A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275126 | ||||||
| chr22:40275494
|
G | A | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3142-1583G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275494 | ||||||
| chr22:40275584
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3142-1493A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275584 | ||||||
| chr22:40275680
|
T | C | 1 | a0001c0001t0014g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3142-1397T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275680 | ||||||
| chr22:40275704
|
A | C | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3142-1373A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275704 | ||||||
| chr22:40275716
|
T | C | 2 | a0001c0001t0015g0139a0001c0001t0049g0141 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3142-1361T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275716 | ||||||
| chr22:40275915
|
C | T | 2 | a0002c0002t0107g0105a0002c0002t0157g0099 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3142-1162C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275915 | ||||||
| chr22:40275959
|
C | CA | 9 | a0001c0001t0001g0077a0001c0001t0002g0217a0001c0001t0003g0038others(6): Show | 9 | HG00639.hp1 HG02145.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.3142-1107dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40275959 | |||||
| chr22:40276057
|
A | G | 2 | a0002c0002t0091g0109a0002c0002t0092g0110 | 2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3142-1020A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276057 | ||||||
| chr22:40276074
|
A | G | 232 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.3142-1003A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276074 | ||||||
| chr22:40276076
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3142-1001G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276076 | ||||||
| chr22:40276122
|
C | T | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3142-955C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276122 | ||||||
| chr22:40276203
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3142-874C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276203 | ||||||
| chr22:40276204
|
G | A | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3142-873G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276204 | ||||||
| chr22:40276826
|
A | C | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3142-251A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276826 | ||||||
| chr22:40277521
|
A | G | 2 | a0001c0001t0004g0185a0001c0001t0004g0188 | 2 | HG01346.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3216+370A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277521 | ||||||
| chr22:40277577
|
C | T | 1 | a0001c0001t0067g0282 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3217-422C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277577 | ||||||
| chr22:40277681
|
T | C | 233 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.3217-318T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277681 | ||||||
| chr22:40277728
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3217-271G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277728 | ||||||
| chr22:40277823
|
A | T | 1 | a0001c0001t0026g0280 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3217-176A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277823 | ||||||
| chr22:40277995
|
C | T | 225 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
splice_region_variant&intron_variant | LOW | c.3217-4C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277995 | ||||||
| chr22:40278281
|
C | T | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3262+237C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278281 | ||||||
| chr22:40278341
|
C | T | 1 | a0001c0001t0005g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3262+297C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278341 | ||||||
| chr22:40278555
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3262+511T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278555 | ||||||
| chr22:40278556
|
C | CA | 20 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0035others(17): Show | 20 | HG00642.hp2 HG01106.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3262+530dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr22 | 40278556 | |||||
| chr22:40278583
|
G | A | 7 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0187others(4): Show | 7 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.3262+539G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278583 | ||||||
| chr22:40278589
|
G | A | 86 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3262+545G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278589 | ||||||
| chr22:40278776
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3262+732G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278776 | ||||||
| chr22:40278811
|
C | T | 2 | a0001c0001t0030g0220a0001c0001t0030g0221 | 2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3262+767C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278811 | ||||||
| chr22:40279087
|
A | G | 145 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3263-908A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279087 | ||||||
| chr22:40279195
|
C | T | 1 | a0001c0001t0020g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3263-800C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279195 | ||||||
| chr22:40279528
|
C | G | 1 | a0001c0001t0027g0284 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3263-467C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279528 | ||||||
| chr22:40279557
|
A | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3263-438A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279557 | ||||||
| chr22:40279947
|
G | A | 2 | a0001c0001t0012g0169a0001c0001t0021g0170 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3263-48G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279947 | ||||||
| chr22:40279953
|
A | G | 2 | a0002c0002t0107g0105a0002c0002t0157g0099 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3263-42A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279953 | ||||||
| chr22:40280433
|
G | A | 2 | a0001c0001t0019g0210a0001c0001t0038g0058 | 2 | HG03942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.3411+290G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280433 | ||||||
| chr22:40280658
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3412-461A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280658 | ||||||
| chr22:40280668
|
T | G | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3412-451T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280668 | ||||||
| chr22:40280742
|
G | A | 2 | a0001c0001t0012g0186a0001c0001t0142g0201 | 2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3412-377G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280742 | ||||||
| chr22:40280844
|
G | A | 3 | a0002c0002t0151g0106a0002c0002t0153g0101a0002c0002t0156g0104 | 3 | HG01496.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3412-275G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280844 | ||||||
| chr22:40280857
|
G | A | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3412-262G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280857 | ||||||
| chr22:40280947
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3412-172T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280947 | ||||||
| chr22:40280982
|
T | A | 85 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.3412-137T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280982 | ||||||
| chr22:40280992
|
A | G | 5 | a0001c0001t0003g0043a0001c0001t0037g0059a0001c0001t0037g0060others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.3412-127A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280992 | ||||||
| chr22:40280997
|
T | C | 225 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.3412-122T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280997 | ||||||
| chr22:40281491
|
C | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3582+202C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281491 | ||||||
| chr22:40281495
|
A | AT | 135 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3582+217dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281495 | |||||
| chr22:40281495
|
AT | A | 6 | a0001c0001t0002g0296a0001c0001t0002g0304a0001c0001t0086g0213others(3): Show | 6 | HG02615.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3582+217delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281495 | |||||
| chr22:40281511
|
C | T | 225 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.3582+222C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281511 | ||||||
| chr22:40281679
|
A | G | 8 | a0001c0001t0024g0136a0001c0001t0035g0142a0001c0001t0052g0002others(5): Show | 8 | HG01891.hp2 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3582+390A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281679 | ||||||
| chr22:40281717
|
TGG | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.3582+430_3582+431d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281717 | |||||
| chr22:40282017
|
AC | A | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3582+730delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40282017 | |||||
| chr22:40282147
|
T | G | 1 | a0001c0001t0020g0273 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3582+858T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282147 | ||||||
| chr22:40282693
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3582+1404A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282693 | ||||||
| chr22:40282736
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3582+1447A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282736 | ||||||
| chr22:40282783
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3582+1494T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282783 | ||||||
| chr22:40282945
|
A | G | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3582+1656A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282945 | ||||||
| chr22:40283195
|
C | T | 83 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.3582+1906C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283195 | ||||||
| chr22:40283200
|
G | A | 1 | a0001c0001t0038g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3582+1911G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283200 | ||||||
| chr22:40283229
|
G | A | 83 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.3582+1940G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283229 | ||||||
| chr22:40283261
|
A | T | 1 | a0002c0002t0105g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3582+1972A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283261 | ||||||
| chr22:40283302
|
T | C | 1 | a0001c0001t0019g0210 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3582+2013T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283302 | ||||||
| chr22:40283327
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3582+2038C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283327 | ||||||
| chr22:40283329
|
T | C | 1 | a0001c0001t0066g0290 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3582+2040T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283329 | ||||||
| chr22:40283330
|
G | A | 1 | a0001c0001t0062g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3582+2041G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283330 | ||||||
| chr22:40283358
|
C | G | 145 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3582+2069C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283358 | ||||||
| chr22:40283365
|
G | A | 1 | a0001c0001t0144g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3582+2076G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283365 | ||||||
| chr22:40283931
|
A | G | 1 | a0001c0001t0050g0242 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3583-1714A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283931 | ||||||
| chr22:40284186
|
T | C | 2 | a0001c0001t0012g0169a0001c0001t0021g0170 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3583-1459T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284186 | ||||||
| chr22:40284541
|
A | G | 6 | a0001c0001t0002g0258a0001c0001t0002g0260a0001c0001t0002g0264others(3): Show | 6 | HG02083.hp2 NA18947.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.3583-1104A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284541 | ||||||
| chr22:40284646
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0023others(5): Show | 8 | HG02083.hp1 NA18944.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.3583-999A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284646 | ||||||
| chr22:40284696
|
C | T | 258 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(255): Show | 258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.3583-949C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284696 | ||||||
| chr22:40284697
|
C | T | 8 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0033g0146others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3583-948C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284697 | ||||||
| chr22:40284809
|
C | T | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3583-836C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284809 | ||||||
| chr22:40284858
|
C | T | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3583-787C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284858 | ||||||
| chr22:40285015
|
T | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3583-630T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285015 | ||||||
| chr22:40285265
|
A | G | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3583-380A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285265 | ||||||
| chr22:40285330
|
A | G | 2 | a0001c0001t0002g0227a0001c0001t0008g0238 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3583-315A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285330 | ||||||
| chr22:40285415
|
C | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3583-230C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285415 | ||||||
| chr22:40285481
|
T | C | 1 | a0001c0001t0015g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3583-164T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285481 | ||||||
| chr22:40285784
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3708+14C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40285784 | ||||||
| chr22:40286052
|
A | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3708+282A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286052 | ||||||
| chr22:40286114
|
C | A | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+344C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286114 | ||||||
| chr22:40286394
|
C | T | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3708+624C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286394 | ||||||
| chr22:40286459
|
A | G | 1 | a0002c0002t0097g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3708+689A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286459 | ||||||
| chr22:40286624
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+854A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286624 | ||||||
| chr22:40286651
|
T | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+881T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286651 | ||||||
| chr22:40286847
|
A | G | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1077A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286847 | ||||||
| chr22:40286915
|
T | C | 1 | a0001c0001t0040g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3708+1145T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286915 | ||||||
| chr22:40286923
|
G | C | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1153G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286923 | ||||||
| chr22:40287117
|
C | T | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1347C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287117 | ||||||
| chr22:40287184
|
T | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+1414T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287184 | ||||||
| chr22:40287209
|
A | G | 2 | a0001c0001t0012g0186a0001c0001t0142g0201 | 2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3708+1439A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287209 | ||||||
| chr22:40287334
|
A | AAGACCAG others(30): Show |
1 | a0001c0001t0072g0276 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3708+1565_3708+160 others(41): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40287334 | |||||
| chr22:40287464
|
G | A | 1 | a0001c0001t0013g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3708+1694G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287464 | ||||||
| chr22:40287497
|
C | A | 50 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(47): Show | 50 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3708+1727C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287497 | ||||||
| chr22:40287710
|
A | G | 1 | a0001c0017t0079g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3708+1940A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287710 | ||||||
| chr22:40287836
|
G | A | 50 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(47): Show | 50 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3708+2066G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287836 | ||||||
| chr22:40287881
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+2111A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287881 | ||||||
| chr22:40288056
|
C | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 144 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3708+2286C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288056 | ||||||
| chr22:40288203
|
A | G | 8 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0033g0146others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3708+2433A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288203 | ||||||
| chr22:40288275
|
T | TCCA | 148 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.3708+2506_3708+250 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288275 | |||||
| chr22:40288279
|
G | A | 259 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(256): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.3708+2509G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288279 | ||||||
| chr22:40288561
|
G | T | 7 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0069others(4): Show | 7 | HG00423.hp2 HG00741.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.3708+2791G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288561 | ||||||
| chr22:40288732
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3708+2962G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288732 | ||||||
| chr22:40288762
|
C | A | 4 | a0001c0001t0006g0150a0001c0001t0034g0091a0001c0001t0051g0149others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3708+2992C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288762 | ||||||
| chr22:40288839
|
C | CT | 88 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0035others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.3708+3089dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288839 | |||||
| chr22:40288839
|
C | CTT | 16 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0188others(13): Show | 16 | HG00438.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.3708+3088_3708+308 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288839 | |||||
| chr22:40288846
|
T | TC | 4 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0048g0138others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3708+3076_3708+307 others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288846 | ||||||
| chr22:40288941
|
G | A | 1 | a0002c0002t0009g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3708+3171G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288941 | ||||||
| chr22:40288963
|
G | A | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3708+3193G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288963 | ||||||
| chr22:40289015
|
T | C | 2 | a0005c0007t0059g0231a0005c0007t0060g0270 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3708+3245T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289015 | ||||||
| chr22:40289414
|
G | T | 1 | a0001c0001t0004g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3708+3644G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289414 | ||||||
| chr22:40289567
|
T | G | 1 | a0001c0001t0023g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3708+3797T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289567 | ||||||
| chr22:40289899
|
G | T | 1 | a0011c0011t0006g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3708+4129G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289899 | ||||||
| chr22:40290122
|
C | A | 307 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3708+4352C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290122 | ||||||
| chr22:40290141
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3708+4371C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290141 | ||||||
| chr22:40290378
|
C | T | 1 | a0001c0013t0005g0195 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3708+4608C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290378 | ||||||
| chr22:40290382
|
G | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(138): Show | 141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3708+4612G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290382 | ||||||
| chr22:40291114
|
G | C | 3 | a0001c0001t0012g0169a0001c0001t0015g0174a0001c0001t0021g0170 | 3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3708+5344G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291114 | ||||||
| chr22:40291614
|
C | T | 6 | a0002c0002t0151g0106a0002c0002t0153g0101a0002c0002t0154g0155others(3): Show | 6 | HG01496.hp2 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.3708+5844C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291614 | ||||||
| chr22:40291753
|
C | T | 259 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(256): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.3708+5983C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291753 | ||||||
| chr22:40292167
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.3708+6397T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292167 | ||||||
| chr22:40292193
|
C | CA | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.3708+6432dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292193 | |||||
| chr22:40292271
|
T | C | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3708+6501T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292271 | ||||||
| chr22:40292352
|
CA | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02976.hp1 NA18939.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.3708+6599delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292352 | |||||
| chr22:40292352
|
CAA | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.3708+6598_3708+659 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292352 | |||||
| chr22:40292405
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3708+6635A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292405 | ||||||
| chr22:40292633
|
A | C | 2 | a0001c0001t0039g0165a0001c0001t0128g0084 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3708+6863A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292633 | ||||||
| chr22:40292686
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+6916G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292686 | ||||||
| chr22:40292713
|
G | A | 5 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(2): Show | 5 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3708+6943G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292713 | ||||||
| chr22:40292913
|
A | G | 87 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.3708+7143A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292913 | ||||||
| chr22:40292946
|
T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3708+7176T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292946 | ||||||
| chr22:40293190
|
C | CT | 22 | a0001c0001t0004g0178a0001c0001t0006g0135a0001c0001t0033g0146others(19): Show | 22 | HG01071.hp1 HG01109.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.3709-7242dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | |||||
| chr22:40293190
|
C | CTT | 117 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(114): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.3709-7243_3709-724 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | |||||
| chr22:40293190
|
C | CTTT | 90 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0032others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.3709-7244_3709-724 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | |||||
| chr22:40293190
|
C | CTTTT | 16 | a0001c0001t0001g0050a0001c0001t0001g0281a0001c0001t0002g0258others(13): Show | 16 | HG01123.hp2 HG01255.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.3709-7245_3709-724 others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | |||||
| chr22:40293256
|
C | T | 49 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-7199C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293256 | ||||||
| chr22:40293375
|
G | A | 86 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0226others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3709-7080G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293375 | ||||||
| chr22:40293816
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0130g0162 | 2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.3709-6639A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293816 | ||||||
| chr22:40293930
|
G | A | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3709-6525G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293930 | ||||||
| chr22:40294070
|
C | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3709-6385C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294070 | ||||||
| chr22:40294073
|
C | CA | 15 | a0001c0001t0002g0240a0002c0002t0009g0111a0002c0002t0032g0128others(12): Show | 15 | HG01167.hp2 HG01175.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.3709-6360dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | |||||
| chr22:40294073
|
CA | C | 228 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.3709-6360delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | |||||
| chr22:40294073
|
CAAAAAAA others(3): Show |
C | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3709-6369_3709-636 others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | |||||
| chr22:40294074
|
A | C | 1 | a0002c0002t0087g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3709-6381A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294074 | ||||||
| chr22:40294108
|
C | T | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3709-6347C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294108 | ||||||
| chr22:40294286
|
A | G | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3709-6169A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294286 | ||||||
| chr22:40294381
|
A | G | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.3709-6074A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294381 | ||||||
| chr22:40294582
|
A | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3709-5873A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294582 | ||||||
| chr22:40294620
|
A | G | 4 | a0001c0001t0027g0232a0001c0001t0027g0284a0001c0001t0062g0233others(1): Show | 4 | NA18959.hp1 NA18973.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.3709-5835A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294620 | ||||||
| chr22:40294830
|
G | A | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-5625G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294830 | ||||||
| chr22:40294937
|
G | A | 2 | a0001c0001t0033g0146a0001c0001t0093g0147 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3709-5518G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294937 | ||||||
| chr22:40295146
|
G | T | 7 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0008g0223others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.3709-5309G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295146 | ||||||
| chr22:40295201
|
C | A | 1 | a0001c0001t0057g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3709-5254C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295201 | ||||||
| chr22:40295213
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3709-5242C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295213 | ||||||
| chr22:40295287
|
C | T | 3 | a0002c0002t0032g0127a0002c0002t0032g0128a0002c0002t0041g0129 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3709-5168C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295287 | ||||||
| chr22:40295335
|
G | A | 2 | a0001c0001t0006g0150a0001c0001t0089g0151 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3709-5120G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295335 | ||||||
| chr22:40295351
|
G | A | 4 | a0002c0002t0006g0107a0002c0002t0009g0111a0002c0002t0100g0108others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-5104G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295351 | ||||||
| chr22:40295398
|
C | T | 4 | a0001c0001t0046g0153a0001c0001t0047g0152a0001c0001t0086g0213others(1): Show | 4 | HG02976.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3709-5057C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295398 | ||||||
| chr22:40295474
|
CA | C | 133 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.3709-4964delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40295474 | |||||
| chr22:40295487
|
A | G | 2 | a0002c0002t0091g0109a0002c0002t0092g0110 | 2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3709-4968A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295487 | ||||||
| chr22:40295583
|
G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3709-4872G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295583 | ||||||
| chr22:40295683
|
A | C | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3709-4772A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295683 | ||||||
| chr22:40295702
|
A | G | 50 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.3709-4753A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295702 | ||||||
| chr22:40295729
|
C | CA | 49 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-4717dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40295729 | |||||
| chr22:40295999
|
G | C | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3709-4456G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295999 | ||||||
| chr22:40296326
|
A | AT | 40 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0020others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.3709-4106dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296326 | |||||
| chr22:40296326
|
A | ATT | 6 | a0001c0001t0016g0089a0001c0001t0030g0220a0001c0001t0030g0221others(3): Show | 6 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3709-4107_3709-410 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296326 | |||||
| chr22:40296602
|
G | A | 2 | a0001c0001t0020g0273a0001c0017t0079g0269 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3709-3853G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40296602 | ||||||
| chr22:40296631
|
C | CT | 33 | a0001c0001t0001g0048a0001c0001t0004g0188a0001c0001t0143g0184others(30): Show | 33 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3709-3811dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296631 | |||||
| chr22:40297072
|
T | C | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3709-3383T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297072 | ||||||
| chr22:40297088
|
A | G | 1 | a0001c0001t0005g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3709-3367A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297088 | ||||||
| chr22:40297172
|
G | A | 1 | a0001c0001t0040g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3709-3283G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297172 | ||||||
| chr22:40297267
|
C | T | 1 | a0001c0001t0117g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3709-3188C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297267 | ||||||
| chr22:40297358
|
G | A | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3709-3097G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297358 | ||||||
| chr22:40297660
|
A | G | 1 | a0001c0001t0038g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3709-2795A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297660 | ||||||
| chr22:40297770
|
C | T | 1 | a0001c0001t0123g0054 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3709-2685C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297770 | ||||||
| chr22:40297905
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3709-2550A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297905 | ||||||
| chr22:40297986
|
A | T | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3709-2469A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297986 | ||||||
| chr22:40298009
|
C | T | 1 | a0001c0001t0013g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3709-2446C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298009 | ||||||
| chr22:40298018
|
G | T | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-2437G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298018 | ||||||
| chr22:40298125
|
AAAAAAT | A | 10 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(7): Show | 10 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3709-2308_3709-230 others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40298125 | |||||
| chr22:40298164
|
AT | A | 3 | a0001c0001t0012g0169a0001c0001t0015g0174a0001c0001t0021g0170 | 3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3709-2289delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40298164 | |||||
| chr22:40298166
|
T | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.3709-2289T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298166 | ||||||
| chr22:40298174
|
A | C | 3 | a0002c0002t0032g0127a0002c0002t0032g0128a0002c0002t0041g0129 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3709-2281A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298174 | ||||||
| chr22:40298311
|
C | A | 302 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 302 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.3709-2144C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298311 | ||||||
| chr22:40298456
|
A | T | 1 | a0001c0001t0133g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3709-1999A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298456 | ||||||
| chr22:40298458
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0038g0044 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3709-1997G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298458 | ||||||
| chr22:40298590
|
T | C | 1 | a0001c0001t0035g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3709-1865T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298590 | ||||||
| chr22:40298594
|
G | A | 6 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0046g0153others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3709-1861G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298594 | ||||||
| chr22:40298715
|
T | C | 231 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(228): Show | 231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.3709-1740T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298715 | ||||||
| chr22:40298723
|
T | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3709-1732T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298723 | ||||||
| chr22:40298794
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3709-1661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298794 | ||||||
| chr22:40298822
|
C | T | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3709-1633C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298822 | ||||||
| chr22:40298839
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3709-1616G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298839 | ||||||
| chr22:40299144
|
C | CA | 12 | a0001c0001t0002g0266a0001c0001t0005g0191a0001c0001t0015g0140others(9): Show | 12 | HG00140.hp2 HG00438.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.3709-1298dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299144 | |||||
| chr22:40299152
|
A | C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3709-1303A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299152 | ||||||
| chr22:40299153
|
A | C | 9 | a0001c0001t0002g0258a0001c0001t0002g0260a0001c0001t0002g0264others(6): Show | 9 | HG01884.hp1 HG02083.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3709-1302A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299153 | ||||||
| chr22:40299154
|
A | C | 2 | a0001c0001t0089g0151a0002c0002t0151g0106 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3709-1301A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299154 | ||||||
| chr22:40299158
|
C | A | 2 | a0001c0001t0002g0266a0001c0001t0143g0184 | 2 | HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3709-1297C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299158 | ||||||
| chr22:40299158
|
C | CA | 9 | a0001c0001t0002g0302a0001c0001t0010g0308a0001c0001t0042g0003others(6): Show | 9 | HG00438.hp2 HG02074.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.3709-1281dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299158 | |||||
| chr22:40299162
|
A | C | 4 | a0001c0001t0002g0254a0001c0001t0002g0307a0001c0001t0033g0146others(1): Show | 4 | HG01109.hp1 HG03540.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-1293A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299162 | ||||||
| chr22:40299163
|
A | C | 152 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(149): Show | 152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.3709-1292A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299163 | ||||||
| chr22:40299165
|
A | C | 2 | a0001c0001t0015g0139a0001c0001t0049g0141 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3709-1290A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299165 | ||||||
| chr22:40299168
|
A | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3709-1287A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299168 | ||||||
| chr22:40299170
|
A | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3709-1285A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299170 | ||||||
| chr22:40299175
|
C | A | 1 | a0001c0001t0078g0277 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3709-1280C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299175 | ||||||
| chr22:40299240
|
C | CT | 8 | a0001c0001t0014g0069a0001c0001t0030g0221a0001c0001t0035g0142others(5): Show | 8 | HG00741.hp2 HG01175.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.3709-1199dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299240 | |||||
| chr22:40299360
|
C | G | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3709-1095C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299360 | ||||||
| chr22:40299375
|
G | T | 1 | a0002c0002t0009g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3709-1080G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299375 | ||||||
| chr22:40299436
|
T | G | 4 | a0001c0001t0002g0254a0001c0001t0002g0296a0001c0001t0002g0304others(1): Show | 4 | NA18977.hp2 NA19005.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-1019T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299436 | ||||||
| chr22:40299510
|
A | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3709-945A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299510 | ||||||
| chr22:40299555
|
A | G | 1 | a0001c0001t0045g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3709-900A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299555 | ||||||
| chr22:40299625
|
G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3709-830G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299625 | ||||||
| chr22:40299657
|
T | G | 2 | a0002c0002t0107g0105a0002c0002t0157g0099 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3709-798T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299657 | ||||||
| chr22:40299751
|
G | A | 44 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(41): Show | 44 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3709-704G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299751 | ||||||
| chr22:40300019
|
T | G | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3709-436T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40300019 | ||||||
| chr22:40300877
|
T | A | 3 | a0001c0001t0039g0165a0001c0001t0115g0090a0001c0001t0128g0084 | 3 | HG02145.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3841-33T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 13/22 | chr22 | 40300877 | ||||||
| chr22:40301077
|
A | G | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3936+72A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301077 | ||||||
| chr22:40301086
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3937-64C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301086 | ||||||
| chr22:40301109
|
G | A | 4 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0048g0138others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3937-41G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301109 | ||||||
| chr22:40301373
|
A | G | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.4120+40A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301373 | ||||||
| chr22:40301401
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4120+68A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301401 | ||||||
| chr22:40301529
|
T | C | 1 | a0001c0001t0076g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4120+196T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301529 | ||||||
| chr22:40301577
|
C | T | 227 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.4120+244C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301577 | ||||||
| chr22:40301585
|
T | G | 145 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.4120+252T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301585 | ||||||
| chr22:40301587
|
G | T | 9 | a0001c0001t0006g0150a0001c0001t0010g0295a0001c0001t0033g0146others(6): Show | 9 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.4120+254G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301587 | ||||||
| chr22:40301603
|
C | G | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4120+270C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301603 | ||||||
| chr22:40301691
|
A | G | 4 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0048g0138others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4120+358A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301691 | ||||||
| chr22:40302089
|
C | A | 1 | a0001c0001t0018g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4120+756C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302089 | ||||||
| chr22:40302260
|
C | A | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4120+927C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302260 | ||||||
| chr22:40302277
|
T | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4120+944T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302277 | ||||||
| chr22:40302278
|
C | A | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4120+945C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302278 | ||||||
| chr22:40302309
|
T | TAAATGTA others(30): Show |
1 | a0002c0002t0032g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4120+976_4120+977i others(39): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302309 | ||||||
| chr22:40302358
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4120+1025C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302358 | ||||||
| chr22:40302361
|
G | A | 1 | a0001c0001t0026g0280 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4120+1028G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302361 | ||||||
| chr22:40302389
|
C | G | 4 | a0001c0001t0016g0086a0001c0001t0016g0087a0001c0001t0016g0089others(1): Show | 4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4120+1056C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302389 | ||||||
| chr22:40302431
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4120+1098G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302431 | ||||||
| chr22:40302564
|
C | T | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4120+1231C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302564 | ||||||
| chr22:40302632
|
CAAAAAAA others(2): Show |
C | 43 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.4120+1310_4120+131 others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40302632 | |||||
| chr22:40302714
|
G | A | 2 | a0001c0001t0015g0140a0001c0001t0048g0138 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4120+1381G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302714 | ||||||
| chr22:40303021
|
C | CCTT | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0076others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG03195.hp2 others(11): Show |
intron_variant | MODIFIER | c.4120+1713_4120+171 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303021 | |||||
| chr22:40303021
|
CCTTCTT | C | 39 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.4120+1710_4120+171 others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303021 | |||||
| chr22:40303041
|
TTCTTC | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 11 | HG02071.hp2 HG02083.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.4120+1710_4120+171 others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303041 | |||||
| chr22:40303046
|
C | CT | 8 | a0001c0001t0001g0050a0001c0001t0002g0285a0001c0001t0003g0052others(5): Show | 8 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.4120+1734dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303046 | |||||
| chr22:40303046
|
CT | C | 65 | a0001c0001t0001g0281a0001c0001t0006g0135a0001c0001t0006g0150others(62): Show | 65 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.4120+1734delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303046 | |||||
| chr22:40303089
|
G | A | 49 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.4120+1756G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303089 | ||||||
| chr22:40303133
|
G | T | 1 | a0002c0002t0032g0128 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4120+1800G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303133 | ||||||
| chr22:40303261
|
G | A | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1928G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303261 | ||||||
| chr22:40303273
|
A | T | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1940A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303273 | ||||||
| chr22:40303276
|
G | T | 4 | a0001c0001t0086g0213a0001c0001t0108g0145a0002c0002t0036g0012others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4120+1943G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303276 | ||||||
| chr22:40303277
|
T | C | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1944T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303277 | ||||||
| chr22:40303278
|
G | C | 2 | a0002c0002t0036g0012a0011c0011t0006g0094 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1945G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303278 | ||||||
| chr22:40303586
|
T | C | 1 | a0001c0001t0122g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4120+2253T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303586 | ||||||
| chr22:40304349
|
G | A | 1 | a0001c0001t0018g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4120+3016G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304349 | ||||||
| chr22:40304433
|
A | G | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4120+3100A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304433 | ||||||
| chr22:40304530
|
G | A | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4120+3197G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304530 | ||||||
| chr22:40304610
|
C | T | 3 | a0002c0002t0034g0009a0002c0002t0084g0008a0002c0002t0094g0010 | 3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4120+3277C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304610 | ||||||
| chr22:40304894
|
A | G | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4120+3561A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304894 | ||||||
| chr22:40304932
|
C | T | 1 | a0007c0018t0005g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4121-3580C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304932 | ||||||
| chr22:40305225
|
G | A | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4121-3287G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305225 | ||||||
| chr22:40305431
|
G | A | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4121-3081G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305431 | ||||||
| chr22:40305512
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4121-3000A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305512 | ||||||
| chr22:40305833
|
A | G | 47 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(44): Show | 47 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.4121-2679A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305833 | ||||||
| chr22:40306044
|
G | A | 1 | a0002c0002t0103g0100 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4121-2468G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306044 | ||||||
| chr22:40306059
|
G | A | 1 | a0001c0001t0074g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4121-2453G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306059 | ||||||
| chr22:40306070
|
C | T | 1 | a0001c0001t0013g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4121-2442C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306070 | ||||||
| chr22:40306119
|
C | T | 2 | a0001c0001t0035g0142a0001c0001t0075g0164 | 2 | HG01891.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4121-2393C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306119 | ||||||
| chr22:40306252
|
G | A | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4121-2260G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306252 | ||||||
| chr22:40306291
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4121-2209_4121-219 others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40306291 | |||||
| chr22:40306815
|
G | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4121-1697G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306815 | ||||||
| chr22:40307071
|
T | G | 96 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.4121-1441T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307071 | ||||||
| chr22:40307089
|
T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4121-1423T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307089 | ||||||
| chr22:40307241
|
A | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4121-1271A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307241 | ||||||
| chr22:40307279
|
C | G | 6 | a0001c0001t0006g0150a0001c0001t0033g0146a0001c0001t0035g0148others(3): Show | 6 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4121-1233C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307279 | ||||||
| chr22:40307566
|
G | A | 3 | a0001c0001t0033g0146a0001c0001t0035g0148a0001c0001t0093g0147 | 3 | HG01109.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4121-946G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307566 | ||||||
| chr22:40307884
|
C | G | 55 | a0001c0001t0024g0136a0001c0001t0034g0091a0001c0001t0052g0002others(52): Show | 55 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.4121-628C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307884 | ||||||
| chr22:40307885
|
G | A | 1 | a0001c0001t0007g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4121-627G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307885 | ||||||
| chr22:40307954
|
T | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4121-558T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307954 | ||||||
| chr22:40307971
|
C | G | 1 | a0001c0001t0005g0192 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4121-541C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307971 | ||||||
| chr22:40308048
|
C | T | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.4121-464C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308048 | ||||||
| chr22:40308167
|
G | T | 3 | a0002c0002t0032g0127a0002c0002t0032g0128a0002c0002t0041g0129 | 3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4121-345G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308167 | ||||||
| chr22:40308265
|
G | C | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4121-247G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308265 | ||||||
| chr22:40308467
|
A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4121-45A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308467 | ||||||
| chr22:40308895
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4258+246C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40308895 | ||||||
| chr22:40309086
|
T | G | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4258+437T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40309086 | ||||||
| chr22:40310035
|
C | T | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4259-782C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310035 | ||||||
| chr22:40310071
|
C | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0003g0163 | 3 | NA18986.hp2 NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4259-746C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310071 | ||||||
| chr22:40310101
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4259-716C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310101 | ||||||
| chr22:40310261
|
G | A | 1 | a0001c0001t0014g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4259-556G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310261 | ||||||
| chr22:40310632
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0076others(4): Show | 7 | NA18612.hp2 NA18943.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.4259-185G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310632 | ||||||
| chr22:40310677
|
G | A | 2 | a0002c0002t0104g0118a0002c0002t0105g0115 | 2 | HG01257.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4259-140G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310677 | ||||||
| chr22:40311227
|
T | C | 1 | a0001c0001t0088g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4435+234T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311227 | ||||||
| chr22:40311654
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4435+661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311654 | ||||||
| chr22:40311687
|
G | A | 1 | a0001c0001t0044g0066 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4435+694G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311687 | ||||||
| chr22:40311824
|
T | C | 48 | a0001c0001t0001g0219a0001c0001t0004g0178a0001c0001t0004g0180others(45): Show | 48 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.4436-681T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311824 | ||||||
| chr22:40311835
|
G | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4436-670G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311835 | ||||||
| chr22:40311839
|
G | A | 15 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0174others(12): Show | 15 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.4436-666G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311839 | ||||||
| chr22:40311909
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4436-596G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311909 | ||||||
| chr22:40312309
|
T | C | 2 | a0002c0002t0083g0093a0002c0002t0097g0103 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4436-196T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40312309 | ||||||
| chr22:40312403
|
G | A | 1 | a0001c0001t0135g0183 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4436-102G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40312403 | ||||||
| chr22:40312675
|
T | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.4582+24T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 18/22 | chr22 | 40312675 | ||||||
| chr22:40312784
|
T | G | 7 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0174others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4583-118T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 18/22 | chr22 | 40312784 | ||||||
| chr22:40313107
|
G | A | 1 | a0002c0002t0034g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4678+110G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313107 | ||||||
| chr22:40313196
|
C | T | 1 | a0001c0001t0012g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4678+199C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313196 | ||||||
| chr22:40313339
|
C | A | 1 | a0001c0001t0020g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4678+342C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313339 | ||||||
| chr22:40313655
|
T | C | 1 | a0001c0001t0068g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4678+658T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313655 | ||||||
| chr22:40313905
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4678+908C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313905 | ||||||
| chr22:40314191
|
C | T | 6 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0069others(3): Show | 6 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.4679-1092C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314191 | ||||||
| chr22:40314309
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4679-974C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314309 | ||||||
| chr22:40314651
|
T | C | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4679-632T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314651 | ||||||
| chr22:40314715
|
A | T | 1 | a0001c0001t0013g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4679-568A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314715 | ||||||
| chr22:40314948
|
C | T | 1 | a0001c0001t0148g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4679-335C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314948 | ||||||
| chr22:40315113
|
A | G | 7 | a0001c0001t0024g0136a0001c0001t0052g0002a0001c0001t0053g0137others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4679-170A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40315113 | ||||||
| chr22:40315223
|
A | AT | 103 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.4679-57dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr22 | 40315223 | |||||
| chr22:40315244
|
G | A | 7 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0187others(4): Show | 7 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.4679-39G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40315244 | ||||||
| chr22:40315602
|
A | C | 2 | a0001c0001t0001g0219a0001c0001t0130g0162 | 2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.4903+95A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315602 | ||||||
| chr22:40315616
|
G | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4903+109G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315616 | ||||||
| chr22:40315685
|
A | AAAGGGAC others(12): Show |
307 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.4903+185_4903+186i others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr22 | 40315685 | |||||
| chr22:40315862
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4904-80A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315862 | ||||||
| chr22:40316126
|
G | A | 1 | a0001c0001t0043g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4974+114G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316126 | ||||||
| chr22:40316196
|
T | TA | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.4974+185dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40316196 | |||||
| chr22:40316227
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4974+215G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316227 | ||||||
| chr22:40316278
|
C | T | 1 | a0001c0001t0143g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4974+266C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316278 | ||||||
| chr22:40316353
|
C | CA | 12 | a0001c0001t0005g0192a0001c0001t0015g0139a0001c0001t0015g0140others(9): Show | 12 | HG01884.hp1 HG02015.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4974+352dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40316353 | |||||
| chr22:40316435
|
G | A | 5 | a0001c0001t0003g0043a0001c0001t0037g0059a0001c0001t0037g0060others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.4974+423G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316435 | ||||||
| chr22:40316455
|
C | T | 1 | a0001c0001t0123g0054 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4974+443C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316455 | ||||||
| chr22:40316470
|
A | C | 3 | a0004c0004t0019g0207a0004c0004t0019g0208a0004c0004t0136g0209 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4974+458A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316470 | ||||||
| chr22:40316488
|
C | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4974+476C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316488 | ||||||
| chr22:40316633
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.4974+621G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316633 | ||||||
| chr22:40316649
|
A | G | 2 | a0001c0001t0027g0284a0001c0001t0028g0239 | 2 | NA18939.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.4974+637A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316649 | ||||||
| chr22:40316764
|
G | T | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4974+752G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316764 | ||||||
| chr22:40317041
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4974+1029C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317041 | ||||||
| chr22:40317077
|
A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1065A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317077 | ||||||
| chr22:40317555
|
C | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1543C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317555 | ||||||
| chr22:40317612
|
T | C | 4 | a0002c0002t0006g0107a0002c0002t0009g0111a0002c0002t0100g0108others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4974+1600T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317612 | ||||||
| chr22:40317616
|
C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1604C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317616 | ||||||
| chr22:40317801
|
G | A | 41 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.4974+1789G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317801 | ||||||
| chr22:40317857
|
T | A | 221 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(218): Show | 221 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.4974+1845T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317857 | ||||||
| chr22:40317879
|
A | G | 1 | a0001c0001t0010g0295 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4974+1867A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317879 | ||||||
| chr22:40317911
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4974+1899A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317911 | ||||||
| chr22:40318105
|
C | T | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4974+2093C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318105 | ||||||
| chr22:40318130
|
G | T | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4974+2118G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318130 | ||||||
| chr22:40318148
|
C | T | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4974+2136C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318148 | ||||||
| chr22:40318177
|
A | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4974+2165A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318177 | ||||||
| chr22:40318274
|
A | G | 1 | a0001c0001t0029g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4974+2262A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318274 | ||||||
| chr22:40318352
|
C | G | 2 | a0001c0001t0003g0043a0001c0001t0038g0044 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.4974+2340C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318352 | ||||||
| chr22:40318363
|
T | C | 6 | a0001c0001t0022g0126a0001c0001t0022g0177a0001c0001t0022g0199others(3): Show | 6 | HG02602.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.4974+2351T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318363 | ||||||
| chr22:40318560
|
T | A | 1 | a0013c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4975-2530T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318560 | ||||||
| chr22:40318771
|
A | G | 1 | a0001c0001t0011g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4975-2319A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318771 | ||||||
| chr22:40318869
|
C | T | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-2221C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318869 | ||||||
| chr22:40318964
|
C | T | 7 | a0002c0002t0151g0106a0002c0002t0152g0096a0002c0002t0153g0101others(4): Show | 7 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4975-2126C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318964 | ||||||
| chr22:40319024
|
T | C | 46 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.4975-2066T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319024 | ||||||
| chr22:40319026
|
G | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-2064G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319026 | ||||||
| chr22:40319226
|
C | A | 1 | a0002c0002t0087g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4975-1864C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319226 | ||||||
| chr22:40319257
|
C | T | 2 | a0001c0001t0002g0240a0001c0001t0013g0235 | 2 | HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4975-1833C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319257 | ||||||
| chr22:40319276
|
A | C | 1 | a0001c0001t0029g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4975-1814A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319276 | ||||||
| chr22:40319299
|
A | G | 220 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.4975-1791A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319299 | ||||||
| chr22:40319411
|
ACTTTT | A | 45 | a0001c0001t0004g0178a0001c0001t0004g0180a0001c0001t0004g0185others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4975-1668_4975-166 others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319411 | |||||
| chr22:40319422
|
C | CT | 15 | a0001c0001t0002g0227a0001c0001t0002g0266a0001c0001t0014g0065others(12): Show | 15 | HG01261.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4975-1649dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319422 | |||||
| chr22:40319422
|
CT | C | 7 | a0001c0001t0003g0013a0001c0001t0017g0006a0001c0001t0028g0239others(4): Show | 7 | HG01167.hp2 HG02165.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.4975-1649delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319422 | |||||
| chr22:40319624
|
C | T | 1 | a0001c0001t0012g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4975-1466C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319624 | ||||||
| chr22:40319643
|
C | T | 1 | a0001c0001t0035g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4975-1447C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319643 | ||||||
| chr22:40319661
|
T | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(12): Show | 15 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.4975-1429T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319661 | ||||||
| chr22:40319845
|
A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4975-1245A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319845 | ||||||
| chr22:40319873
|
C | T | 1 | a0001c0001t0054g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4975-1217C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319873 | ||||||
| chr22:40319899
|
G | A | 6 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0255others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4975-1191G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319899 | ||||||
| chr22:40319918
|
C | T | 2 | a0001c0001t0010g0262a0001c0001t0058g0261 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4975-1172C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319918 | ||||||
| chr22:40319937
|
G | A | 1 | a0001c0001t0007g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4975-1153G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319937 | ||||||
| chr22:40320053
|
G | A | 4 | a0002c0002t0006g0144a0002c0002t0036g0098a0002c0002t0102g0097others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4975-1037G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320053 | ||||||
| chr22:40320251
|
G | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4975-839G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320251 | ||||||
| chr22:40320304
|
A | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-786A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320304 | ||||||
| chr22:40320352
|
C | T | 2 | a0001c0001t0033g0146a0001c0001t0093g0147 | 2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4975-738C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320352 | ||||||
| chr22:40320429
|
G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4975-661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320429 | ||||||
| chr22:40320484
|
C | A | 132 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.4975-606C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320484 | ||||||
| chr22:40320618
|
G | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 131 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.4975-472G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320618 | ||||||
| chr22:40320618
|
G | C | 59 | a0001c0001t0006g0135a0001c0001t0006g0150a0001c0001t0033g0146others(56): Show | 59 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.4975-472G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320618 | ||||||
| chr22:40320680
|
G | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4975-410G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320680 | ||||||
| chr22:40320952
|
C | A | 1 | a0001c0001t0054g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4975-138C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320952 | ||||||
| chr22:40321239
|
C | T | 2 | a0002c0002t0107g0105a0002c0002t0157g0099 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5114+10C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321239 | ||||||
| chr22:40321347
|
C | T | 1 | a0001c0001t0008g0288 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5114+118C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321347 | ||||||
| chr22:40321380
|
G | A | 1 | a0001c0001t0067g0282 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5114+151G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321380 | ||||||
| chr22:40321573
|
G | A | 4 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0048g0138others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5114+344G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321573 | ||||||
| chr22:40321655
|
G | A | 2 | a0001c0001t0086g0213a0001c0001t0108g0145 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5114+426G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321655 | ||||||
| chr22:40321819
|
C | T | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5114+590C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321819 | ||||||
| chr22:40321890
|
G | A | 1 | a0001c0001t0007g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.5114+661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321890 | ||||||
| chr22:40321976
|
C | T | 1 | a0001c0001t0007g0300 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5114+747C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321976 | ||||||
| chr22:40321979
|
A | T | 16 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0174others(13): Show | 16 | HG01891.hp2 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.5114+750A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321979 | ||||||
| chr22:40322096
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.5115-758G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322096 | ||||||
| chr22:40322349
|
T | A | 2 | a0006c0006t0111g0214a0006c0006t0112g0001 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5115-505T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322349 | ||||||
| chr22:40322495
|
C | T | 4 | a0001c0001t0022g0126a0001c0001t0022g0177a0001c0001t0022g0199others(1): Show | 4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.5115-359C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322495 | ||||||
| chr22:40322768
|
T | C | 1 | a0001c0001t0004g0187 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5115-86T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322768 |