| geneid | 27283 |
|---|---|
| ensemblid | ENSG00000137251.16 |
| hgncid | 14599 |
| symbol | TINAG |
| name | tubulointerstitial nephritis antigen |
| refseq_nuc | NM_014464.4 |
| refseq_prot | NP_055279.3 |
| ensembl_nuc | ENST00000259782.9 |
| ensembl_prot | ENSP00000259782.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 54308441 |
| end | 54390142 |
| strand | + |
| ver | v1.2 |
| region | chr6:54308441-54390142 |
| region5000 | chr6:54303441-54395142 |
| regionname0 | TINAG_chr6_54308441_54390142 |
| regionname5000 | TINAG_chr6_54303441_54395142 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 476 | 178 | 42 | 33 | 86 | 5 | 11 | 70 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0002 | 0/0 | 476 | 64 | 8 | 2 | 49 | 0 | 5 | 42 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0003 | 1/0 | 476 | 62 | 11 | 17 | 21 | 1 | 11 | 18 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0004 | 0/0 | 476 | 17 | 1 | 4 | 8 | 2 | 2 | 5 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0005 | 0/0 | 476 | 13 | 5 | 2 | 1 | 1 | 4 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0006 | 0/0 | 476 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0007 | 0/0 | 476 | 6 | 1 | 2 | 0 | 2 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0008 | 0/0 | 476 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0009 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0010 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0011 | 0/0 | 476 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0012 | 0/0 | 476 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0013 | 0/0 | 476 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0014 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0015 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0016 | 0/0 | 476 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0017 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0018 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0019 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0020 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0021 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0022 | 0/0 | 476 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0023 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0024 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1431 | 176 | 40 | 33 | 86 | 5 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0002 | 0/0 | 1431 | 64 | 8 | 2 | 49 | 0 | 5 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0003 | 1/0 | 1431 | 62 | 11 | 17 | 21 | 1 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0004 | 0/0 | 1431 | 16 | 0 | 4 | 8 | 2 | 2 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0005 | 0/0 | 1431 | 13 | 5 | 2 | 1 | 1 | 4 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0006 | 0/0 | 1431 | 6 | 1 | 2 | 0 | 2 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0007 | 0/0 | 1431 | 6 | 6 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0008 | 0/0 | 1431 | 3 | 1 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0009 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0010 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0011 | 0/0 | 1431 | 2 | 0 | 0 | 0 | 1 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0012 | 0/0 | 1431 | 2 | 1 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0013 | 0/0 | 1431 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0014 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0015 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0016 | 0/0 | 1431 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0017 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0018 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0019 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0020 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0021 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0022 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0023 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0024 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0025 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| c0026 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 328 | 366 | 84 | 62 | 170 | 12 | 36 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| t0002 | 0/0 | 328 | 5 | 3 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| t0003 | 0/0 | 328 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| t0004 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| 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 | 3 | 0 | 1 | 0 | 2 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1431 | 176 | 40 | 33 | 86 | 5 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0001c0010 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0002c0002 | 0/0 | 1431 | 64 | 8 | 2 | 49 | 0 | 5 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0003c0003 | 1/0 | 1431 | 62 | 11 | 17 | 21 | 1 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0004c0004 | 0/0 | 1431 | 16 | 0 | 4 | 8 | 2 | 2 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0004c0021 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0005c0005 | 0/0 | 1431 | 13 | 5 | 2 | 1 | 1 | 4 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0006c0007 | 0/0 | 1431 | 6 | 6 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0007c0006 | 0/0 | 1431 | 6 | 1 | 2 | 0 | 2 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0008c0008 | 0/0 | 1431 | 3 | 1 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0009c0018 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0010c0009 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0011c0013 | 0/0 | 1431 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0012c0011 | 0/0 | 1431 | 2 | 0 | 0 | 0 | 1 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0013c0012 | 0/0 | 1431 | 2 | 1 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0014c0015 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0015c0014 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0016c0016 | 0/0 | 1431 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0017c0017 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0018c0026 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0019c0022 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0020c0019 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0021c0020 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0022c0023 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0023c0024 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0024c0025 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1758 | 176 | 40 | 33 | 86 | 5 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0001c0010t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0002c0002t0001 | 0/0 | 1758 | 64 | 8 | 2 | 49 | 0 | 5 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0003c0003t0001 | 1/0 | 1758 | 62 | 11 | 17 | 21 | 1 | 11 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0004c0004t0001 | 0/0 | 1758 | 16 | 0 | 4 | 8 | 2 | 2 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0004c0021t0004 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0005c0005t0001 | 0/0 | 1758 | 13 | 5 | 2 | 1 | 1 | 4 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0006c0007t0001 | 0/0 | 1758 | 6 | 6 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0007c0006t0001 | 0/0 | 1758 | 5 | 0 | 2 | 0 | 2 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0007c0006t0002 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0008c0008t0002 | 0/0 | 1758 | 3 | 1 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0009c0018t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0010c0009t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0011c0013t0001 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0011c0013t0002 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0012c0011t0001 | 0/0 | 1758 | 2 | 0 | 0 | 0 | 1 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0013c0012t0001 | 0/0 | 1758 | 2 | 1 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0014c0015t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0015c0014t0003 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0016c0016t0001 | 0/0 | 1758 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0017c0017t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0018c0026t0001 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0019c0022t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0020c0019t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0021c0020t0001 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0022c0023t0001 | 0/0 | 1758 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0023c0024t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| a0024c0025t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | copy fasta | chr6 | 54303441 | 54395142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0010t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0001c0010t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0003c0003t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0004c0021t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0005c0005t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0006c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0007c0006t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0008c0008t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0008c0008t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0008c0008t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0009c0018t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0009c0018t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0010c0009t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0010c0009t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0011c0013t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0011c0013t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0012c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0012c0011t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0013c0012t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0013c0012t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0014c0015t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0014c0015t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0015c0014t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0015c0014t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0016c0016t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0016c0016t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0017c0017t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0017c0017t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0018c0026t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0019c0022t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0020c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0021c0020t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0022c0023t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0023c0024t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| a0024c0025t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0005 | t0001 | g0288 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00140 | hp1 | a0007 | c0006 | t0001 | g0249 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0044 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00280 | hp1 | a0007 | c0006 | t0001 | g0189 | EUR | FIN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00408 | hp2 | a0023 | c0024 | t0001 | g0013 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00438 | hp2 | a0004 | c0004 | t0001 | g0168 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0205 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0053 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00673 | hp1 | a0019 | c0022 | t0001 | g0195 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00735 | hp2 | a0016 | c0016 | t0001 | g0259 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0026 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01069 | hp1 | a0008 | c0008 | t0002 | g0171 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0220 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01099 | hp1 | a0004 | c0004 | t0001 | g0219 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01109 | hp1 | a0007 | c0006 | t0001 | g0138 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0028 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01169 | hp1 | a0007 | c0006 | t0001 | g0151 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0022 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01243 | hp1 | a0008 | c0008 | t0002 | g0172 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0051 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0024 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01258 | hp2 | a0011 | c0013 | t0001 | g0360 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0361 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01358 | hp1 | a0005 | c0005 | t0001 | g0299 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0050 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01361 | hp2 | a0005 | c0005 | t0001 | g0289 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0025 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01515 | hp2 | a0012 | c0011 | t0001 | g0060 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01516 | hp1 | a0004 | c0004 | t0001 | g0001 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01517 | hp1 | a0004 | c0004 | t0001 | g0001 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01884 | hp1 | a0006 | c0007 | t0001 | g0225 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01891 | hp1 | a0006 | c0007 | t0001 | g0229 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01928 | hp1 | a0004 | c0004 | t0001 | g0001 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0034 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02055 | hp1 | a0005 | c0005 | t0001 | g0287 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02055 | hp2 | a0006 | c0007 | t0001 | g0228 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0348 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02071 | hp2 | a0020 | c0019 | t0001 | g0085 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02074 | hp1 | a0004 | c0004 | t0001 | g0206 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02135 | hp1 | a0004 | c0004 | t0001 | g0080 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0067 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02145 | hp2 | a0016 | c0016 | t0001 | g0261 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0063 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0072 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0286 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0043 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02615 | hp1 | a0010 | c0009 | t0001 | g0211 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02615 | hp2 | a0006 | c0007 | t0001 | g0226 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0281 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0362 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02647 | hp2 | a0001 | c0010 | t0001 | g0312 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02698 | hp1 | a0007 | c0006 | t0001 | g0203 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02717 | hp2 | a0005 | c0005 | t0001 | g0290 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02738 | hp2 | a0004 | c0004 | t0001 | g0207 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02809 | hp2 | a0013 | c0012 | t0001 | g0073 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0075 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0059 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02970 | hp1 | a0015 | c0014 | t0003 | g0283 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02970 | hp2 | a0005 | c0005 | t0001 | g0285 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03017 | hp1 | a0005 | c0005 | t0001 | g0295 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0057 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03041 | hp1 | a0008 | c0008 | t0002 | g0079 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03041 | hp2 | a0006 | c0007 | t0001 | g0231 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03130 | hp1 | a0014 | c0015 | t0001 | g0298 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0071 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03209 | hp2 | a0005 | c0005 | t0001 | g0296 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03225 | hp1 | a0017 | c0017 | t0001 | g0278 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03453 | hp1 | a0011 | c0013 | t0002 | g0056 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03453 | hp2 | a0014 | c0015 | t0001 | g0297 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0202 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03516 | hp1 | a0004 | c0021 | t0004 | g0224 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0246 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0074 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0314 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0046 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0149 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03669 | hp2 | a0005 | c0005 | t0001 | g0258 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03704 | hp1 | a0005 | c0005 | t0001 | g0294 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03704 | hp2 | a0022 | c0023 | t0001 | g0042 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0049 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0353 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03834 | hp2 | a0005 | c0005 | t0001 | g0293 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0055 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0039 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03942 | hp2 | a0012 | c0011 | t0001 | g0040 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0054 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0047 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18906 | hp2 | a0021 | c0020 | t0001 | g0267 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18949 | hp2 | a0005 | c0005 | t0001 | g0291 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0357 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18966 | hp2 | a0004 | c0004 | t0001 | g0103 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0359 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0307 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18988 | hp2 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18989 | hp2 | a0004 | c0004 | t0001 | g0157 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18992 | hp1 | a0004 | c0004 | t0001 | g0204 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0363 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0254 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19054 | hp1 | a0024 | c0025 | t0001 | g0292 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19058 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19065 | hp2 | a0013 | c0012 | t0001 | g0209 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19074 | hp1 | a0004 | c0004 | t0001 | g0102 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19240 | hp1 | a0006 | c0007 | t0001 | g0230 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA19240 | hp2 | a0007 | c0006 | t0002 | g0279 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ASW | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ASW | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | GIH | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0041 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02109 | hp1 | a0010 | c0009 | t0001 | g0212 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02559 | hp1 | a0018 | c0026 | t0001 | g0227 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG03471 | hp2 | a0009 | c0018 | t0001 | g0222 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| HG06807 | hp2 | a0009 | c0018 | t0001 | g0260 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA20300 | hp2 | a0001 | c0010 | t0001 | g0244 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA21309 | hp1 | a0015 | c0014 | t0003 | g0284 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| NA21309 | hp2 | a0017 | c0017 | t0001 | g0277 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0037 | REF | REF | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54308557
|
A | G | 4 | a0006a0008a0009others(1): Show | 12 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
missense_variant | MODERATE | c.7A>G | p.Thr3Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 117/1758 | 7/1431 | 3/476 | chr6 | 54308557 | ||
| chr6:54308615
|
A | G | 6 | a0005a0014a0015others(3): Show | 22 | HG00099.hp1 HG00735.hp2 HG01358.hp1 others(19): Show |
missense_variant | MODERATE | c.65A>G | p.Gln22Arg | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 175/1758 | 65/1431 | 22/476 | chr6 | 54308615 | ||
| chr6:54308623
|
T | G | 1 | a0010 | 2 | HG02109.hp1 HG02615.hp1 |
missense_variant | MODERATE | c.73T>G | p.Ser25Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 183/1758 | 73/1431 | 25/476 | chr6 | 54308623 | ||
| chr6:54308786
|
C | T | 1 | a0023 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.236C>T | p.Ala79Val | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 346/1758 | 236/1431 | 79/476 | chr6 | 54308786 | ||
| chr6:54308875
|
C | G | 1 | a0024 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.325C>G | p.Pro109Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 435/1758 | 325/1431 | 109/476 | chr6 | 54308875 | ||
| chr6:54321349
|
T | C | 14 | a0001a0002a0004others(11): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
missense_variant | MODERATE | c.472T>C | p.Ser158Pro | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/11 | 582/1758 | 472/1431 | 158/476 | chr6 | 54321349 | ||
| chr6:54326888
|
C | T | 8 | a0004a0006a0008others(5): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
missense_variant | MODERATE | c.596C>T | p.Pro199Leu | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/11 | 706/1758 | 596/1431 | 199/476 | chr6 | 54326888 | ||
| chr6:54349787
|
G | A | 1 | a0020 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.971G>A | p.Ser324Asn | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/11 | 1081/1758 | 971/1431 | 324/476 | chr6 | 54349787 | ||
| chr6:54354528
|
G | A | 6 | a0004a0007a0008others(3): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
missense_variant | MODERATE | c.1142G>A | p.Arg381His | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/11 | 1252/1758 | 1142/1431 | 381/476 | chr6 | 54354528 | ||
| chr6:54354623
|
G | A | 2 | a0006a0021 | 7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
missense_variant | MODERATE | c.1237G>A | p.Val413Ile | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/11 | 1347/1758 | 1237/1431 | 413/476 | chr6 | 54354623 | ||
| chr6:54389791
|
A | C | 4 | a0002a0013a0017others(1): Show | 69 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(66): Show |
missense_variant&splice_region_variant | MODERATE | c.1297A>C | p.Ile433Leu | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 1407/1758 | 1297/1431 | 433/476 | chr6 | 54389791 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54347440
|
C | T | 1 | a0001c0010 | 2 | HG02647.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.822C>T | p.Ile274Ile | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/11 | 932/1758 | 822/1431 | 274/476 | chr6 | 54347440 | ||
| chr6:54389910
|
T | C | 1 | a0004c0021 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1416T>C | p.Ser472Ser | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 1526/1758 | 1416/1431 | 472/476 | chr6 | 54389910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54390001
|
G | A | 1 | a0004c0021t0004 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 76 | chr6 | 54390001 | |||||
| chr6:54390016
|
T | G | 1 | a0015c0014t0003 | 2 | HG02970.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 91 | chr6 | 54390016 | |||||
| chr6:54390062
|
C | T | 3 | a0007c0006t0002a0008c0008t0002a0011c0013t0002 | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 137 | chr6 | 54390062 | |||||
| chr6:54390130
|
G | T | 1 | a0004c0021t0004 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*205G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 205 | chr6 | 54390130 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54309091
|
A | G | 62 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(59): Show | 62 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(59): Show |
intron_variant | MODIFIER | c.355+186A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309091 | ||||||
| chr6:54309329
|
A | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.355+424A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309329 | ||||||
| chr6:54309844
|
C | CA | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.355+955dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | |||||
| chr6:54309844
|
C | CAA | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG01358.hp2 HG02135.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+954_355+955dup others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | |||||
| chr6:54309844
|
CA | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0262a0001c0001t0001g0263others(48): Show | 53 | HG00099.hp1 HG00741.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.355+955delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | |||||
| chr6:54309885
|
CA | C | 11 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(8): Show | 11 | HG00438.hp1 HG00735.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+982delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309885 | |||||
| chr6:54309920
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.355+1015G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309920 | ||||||
| chr6:54309941
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.355+1036C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309941 | ||||||
| chr6:54310018
|
T | G | 4 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG03098.hp2 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1113T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310018 | ||||||
| chr6:54310074
|
TCCGTGTG others(4): Show |
T | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1170_355+1180d others(13): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310074 | ||||||
| chr6:54310075
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1170C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310075 | ||||||
| chr6:54310076
|
C | CCGTGTGT others(4): Show |
1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1171_355+1172i others(13): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310076 | ||||||
| chr6:54310076
|
C | CGT | 8 | a0001c0001t0001g0093a0001c0001t0001g0245a0001c0001t0001g0262others(5): Show | 8 | HG01258.hp2 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+1201_355+1202d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGT | 13 | a0001c0001t0001g0076a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+1199_355+1202d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGT | 44 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0096others(41): Show | 45 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.355+1197_355+1202d others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(1): Show |
100 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0078others(97): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.355+1195_355+1202d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(3): Show |
52 | a0001c0001t0001g0008a0001c0001t0001g0173a0001c0001t0001g0174others(49): Show | 55 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.355+1193_355+1202d others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(5): Show |
19 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0221others(16): Show | 19 | HG00099.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.355+1191_355+1202d others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(7): Show |
12 | a0001c0001t0001g0223a0002c0002t0001g0081a0004c0021t0004g0224others(9): Show | 12 | HG02145.hp2 HG03017.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+1189_355+1202d others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(9): Show |
7 | a0005c0005t0001g0299a0006c0007t0001g0225a0006c0007t0001g0226others(4): Show | 7 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.355+1187_355+1202d others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
C | CGTGTGTG others(13): Show |
1 | a0006c0007t0001g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.355+1183_355+1202d others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310076
|
CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083 | 4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1195_355+1202d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | |||||
| chr6:54310087
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1182G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310087 | ||||||
| chr6:54310088
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1183T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310088 | ||||||
| chr6:54310108
|
A | T | 7 | a0001c0001t0001g0216a0001c0001t0001g0247a0001c0001t0001g0255others(4): Show | 7 | HG02080.hp2 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.355+1203A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310108 | ||||||
| chr6:54310163
|
G | A | 2 | a0008c0008t0002g0171a0008c0008t0002g0172 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.355+1258G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310163 | ||||||
| chr6:54310205
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0104 | 3 | NA19010.hp2 NA19059.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.355+1300C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310205 | ||||||
| chr6:54310265
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0247a0001c0001t0001g0255others(40): Show | 44 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.355+1360T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310265 | ||||||
| chr6:54310422
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.355+1517T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310422 | ||||||
| chr6:54310478
|
CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.355+1593_355+1618d others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310478 | |||||
| chr6:54310480
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.355+1575C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310480 | ||||||
| chr6:54310492
|
TTTC | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.355+1593_355+1595d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310492 | |||||
| chr6:54310496
|
TTC | T | 11 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(8): Show | 11 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.355+1593_355+1594d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310496 | |||||
| chr6:54310567
|
CCT | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | NA18994.hp1 NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.355+1669_355+1670d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310567 | |||||
| chr6:54310601
|
TTCTC | T | 5 | a0001c0001t0001g0280a0002c0002t0001g0009a0002c0002t0001g0281others(2): Show | 6 | HG02622.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+1704_355+1707d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310601 | |||||
| chr6:54310622
|
CCCTT | C | 78 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(75): Show | 79 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.355+1729_355+1732d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310622 | |||||
| chr6:54310642
|
CTCTT | C | 4 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG03098.hp2 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1745_355+1748d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310642 | |||||
| chr6:54310658
|
CTTTTTCT others(58): Show |
C | 19 | a0002c0002t0001g0253a0002c0002t0001g0254a0005c0005t0001g0258others(16): Show | 19 | HG00099.hp1 HG00735.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.355+1778_355+1842d others(67): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310658 | |||||
| chr6:54310715
|
CCTCTTTC others(25): Show |
C | 1 | a0007c0006t0002g0279 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.355+1830_355+1861d others(34): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310715 | |||||
| chr6:54310754
|
CTTT | C | 12 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(9): Show | 12 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+1853_355+1855d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310754 | |||||
| chr6:54310759
|
T | C | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+1854T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310759 | ||||||
| chr6:54310776
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0001g0301 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1871C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310776 | ||||||
| chr6:54310815
|
CCT | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(9): Show | 13 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.355+1913_355+1914d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310815 | |||||
| chr6:54310815
|
CCTCTTTC others(3): Show |
C | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+1921_355+1930d others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310815 | |||||
| chr6:54310838
|
TC | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1934delC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310838 | ||||||
| chr6:54310839
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1934C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310839 | ||||||
| chr6:54310856
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.355+1951G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310856 | ||||||
| chr6:54310865
|
TTC | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(8): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.355+1964_355+1965d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310865 | |||||
| chr6:54310870
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0217 | 2 | NA18945.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.355+1965T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310870 | ||||||
| chr6:54310873
|
CT | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(8): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.355+1975delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310873 | |||||
| chr6:54310874
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+1969T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310874 | ||||||
| chr6:54310887
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0001g0301 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1982C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310887 | ||||||
| chr6:54310907
|
C | CTTTCTT | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.355+2007_355+2008i others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310907 | |||||
| chr6:54311107
|
G | T | 78 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(75): Show | 79 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.355+2202G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311107 | ||||||
| chr6:54311218
|
C | T | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+2313C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311218 | ||||||
| chr6:54311221
|
G | A | 1 | a0003c0003t0001g0061 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.355+2316G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311221 | ||||||
| chr6:54311385
|
T | G | 1 | a0002c0002t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.355+2480T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311385 | ||||||
| chr6:54311401
|
T | C | 5 | a0001c0001t0001g0280a0002c0002t0001g0009a0002c0002t0001g0281others(2): Show | 6 | HG02622.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+2496T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311401 | ||||||
| chr6:54311429
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0247a0001c0001t0001g0256others(45): Show | 49 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.355+2524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311429 | ||||||
| chr6:54311516
|
A | G | 3 | a0005c0005t0001g0296a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.355+2611A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311516 | ||||||
| chr6:54311551
|
C | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.355+2646C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311551 | ||||||
| chr6:54311551
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.355+2646C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311551 | ||||||
| chr6:54311692
|
C | T | 56 | a0001c0001t0001g0010a0001c0001t0001g0210a0001c0001t0001g0247others(53): Show | 58 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+2787C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311692 | ||||||
| chr6:54311693
|
C | T | 56 | a0001c0001t0001g0010a0001c0001t0001g0210a0001c0001t0001g0247others(53): Show | 58 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+2788C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311693 | ||||||
| chr6:54311720
|
A | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(359): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.355+2815A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311720 | ||||||
| chr6:54311744
|
C | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0175a0001c0001t0001g0210others(34): Show | 39 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.355+2839C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311744 | ||||||
| chr6:54311767
|
A | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(9): Show | 13 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.355+2862A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311767 | ||||||
| chr6:54311975
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355+3070A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311975 | ||||||
| chr6:54312053
|
GTTTGTTT | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3165_355+3171d others(9): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54312053 | |||||
| chr6:54312072
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.355+3167T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312072 | ||||||
| chr6:54312290
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+3385C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312290 | ||||||
| chr6:54312321
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+3416T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312321 | ||||||
| chr6:54312322
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+3417A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312322 | ||||||
| chr6:54312378
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3473A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312378 | ||||||
| chr6:54312421
|
A | G | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+3516A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312421 | ||||||
| chr6:54312515
|
A | T | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+3610A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312515 | ||||||
| chr6:54312529
|
A | G | 2 | a0003c0003t0001g0058a0003c0003t0001g0059 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.355+3624A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312529 | ||||||
| chr6:54312590
|
A | G | 1 | a0002c0002t0001g0358 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.355+3685A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312590 | ||||||
| chr6:54312605
|
G | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.355+3700G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312605 | ||||||
| chr6:54312607
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.355+3702C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312607 | ||||||
| chr6:54312750
|
T | C | 3 | a0004c0004t0001g0102a0004c0004t0001g0103a0019c0022t0001g0195 | 3 | HG00673.hp1 NA18966.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.355+3845T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312750 | ||||||
| chr6:54312794
|
A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.355+3889A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312794 | ||||||
| chr6:54312894
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(14): Show | 19 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.355+3989A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312894 | ||||||
| chr6:54313014
|
G | A | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.355+4109G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313014 | ||||||
| chr6:54313108
|
A | T | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+4203A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313108 | ||||||
| chr6:54313151
|
T | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.355+4246T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313151 | ||||||
| chr6:54313223
|
T | C | 1 | a0004c0004t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.355+4318T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313223 | ||||||
| chr6:54313304
|
G | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.355+4399G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313304 | ||||||
| chr6:54313350
|
C | A | 1 | a0002c0002t0001g0108 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.355+4445C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313350 | ||||||
| chr6:54313420
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+4515T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313420 | ||||||
| chr6:54313431
|
G | T | 10 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.355+4526G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313431 | ||||||
| chr6:54313477
|
A | G | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4572A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313477 | ||||||
| chr6:54313489
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.355+4584A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313489 | ||||||
| chr6:54313536
|
G | A | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+4631G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313536 | ||||||
| chr6:54313543
|
CTCATTCA | C | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4640_355+4646d others(9): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54313543 | |||||
| chr6:54313546
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.355+4641A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313546 | ||||||
| chr6:54313551
|
T | A | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4646T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313551 | ||||||
| chr6:54313595
|
T | C | 1 | a0002c0002t0001g0308 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.355+4690T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313595 | ||||||
| chr6:54313623
|
C | T | 1 | a0002c0002t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.355+4718C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313623 | ||||||
| chr6:54313640
|
C | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.355+4735C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313640 | ||||||
| chr6:54313755
|
T | G | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4850T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313755 | ||||||
| chr6:54313853
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.355+4948A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313853 | ||||||
| chr6:54313920
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | NA18972.hp2 NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.355+5015G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313920 | ||||||
| chr6:54314024
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.355+5119A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314024 | ||||||
| chr6:54314041
|
G | C | 1 | a0015c0014t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.355+5136G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314041 | ||||||
| chr6:54314064
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.355+5159A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314064 | ||||||
| chr6:54314242
|
T | C | 57 | a0001c0001t0001g0109a0001c0001t0001g0302a0001c0001t0001g0311others(54): Show | 57 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+5337T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314242 | ||||||
| chr6:54314271
|
C | G | 9 | a0003c0003t0001g0068a0003c0003t0001g0069a0003c0003t0001g0070others(6): Show | 9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.355+5366C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314271 | ||||||
| chr6:54314358
|
A | G | 2 | a0002c0002t0001g0356a0002c0002t0001g0357 | 2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.355+5453A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314358 | ||||||
| chr6:54314584
|
C | A | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+5679C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314584 | ||||||
| chr6:54314595
|
A | T | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+5690A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314595 | ||||||
| chr6:54314605
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0265others(2): Show | 6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+5700C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314605 | ||||||
| chr6:54314606
|
G | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 37 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.355+5701G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314606 | ||||||
| chr6:54314638
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+5733T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314638 | ||||||
| chr6:54314704
|
G | A | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+5799G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314704 | ||||||
| chr6:54314740
|
T | G | 33 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0223others(30): Show | 35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.355+5835T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314740 | ||||||
| chr6:54314754
|
G | T | 9 | a0003c0003t0001g0068a0003c0003t0001g0069a0003c0003t0001g0070others(6): Show | 9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.356-5825G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314754 | ||||||
| chr6:54314800
|
A | G | 55 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(52): Show | 55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.356-5779A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314800 | ||||||
| chr6:54314842
|
G | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-5737G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314842 | ||||||
| chr6:54314950
|
T | A | 1 | a0004c0004t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356-5629T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314950 | ||||||
| chr6:54314972
|
A | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-5607A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314972 | ||||||
| chr6:54314976
|
T | G | 63 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(60): Show | 63 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(60): Show |
intron_variant | MODIFIER | c.356-5603T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314976 | ||||||
| chr6:54315057
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.356-5522G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315057 | ||||||
| chr6:54315183
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-5396G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315183 | ||||||
| chr6:54315211
|
G | A | 24 | a0001c0001t0001g0245a0003c0003t0001g0246a0003c0003t0001g0361others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-5368G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315211 | ||||||
| chr6:54315330
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.356-5249T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315330 | ||||||
| chr6:54315386
|
A | T | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-5193A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315386 | ||||||
| chr6:54315455
|
G | A | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-5124G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315455 | ||||||
| chr6:54315463
|
G | A | 33 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0223others(30): Show | 35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.356-5116G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315463 | ||||||
| chr6:54315547
|
A | G | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-5032A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315547 | ||||||
| chr6:54315644
|
T | G | 1 | a0007c0006t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.356-4935T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315644 | ||||||
| chr6:54315683
|
A | G | 27 | a0003c0003t0001g0012a0003c0003t0001g0014a0003c0003t0001g0015others(24): Show | 27 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.356-4896A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315683 | ||||||
| chr6:54315687
|
A | G | 1 | a0002c0002t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.356-4892A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315687 | ||||||
| chr6:54315691
|
A | G | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4888A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315691 | ||||||
| chr6:54315692
|
G | T | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4887G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315692 | ||||||
| chr6:54315693
|
T | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4886T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315693 | ||||||
| chr6:54315693
|
T | TA | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.356-4879dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54315693 | |||||
| chr6:54315723
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4856C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315723 | ||||||
| chr6:54315927
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(17): Show | 21 | HG01891.hp2 HG02027.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.356-4652A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315927 | ||||||
| chr6:54315955
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.356-4624G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315955 | ||||||
| chr6:54316163
|
G | A | 68 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(65): Show | 72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.356-4416G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316163 | ||||||
| chr6:54316298
|
T | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.356-4281T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316298 | ||||||
| chr6:54316318
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4261T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316318 | ||||||
| chr6:54316490
|
C | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.356-4089C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316490 | ||||||
| chr6:54316541
|
G | T | 3 | a0002c0002t0001g0352a0002c0002t0001g0353a0002c0002t0001g0354 | 3 | HG03831.hp1 NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.356-4038G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316541 | ||||||
| chr6:54316562
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-4017C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316562 | ||||||
| chr6:54316595
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0110 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.356-3984C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316595 | ||||||
| chr6:54316678
|
A | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.356-3901A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316678 | ||||||
| chr6:54316732
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.356-3847T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316732 | ||||||
| chr6:54316906
|
A | G | 1 | a0003c0003t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-3673A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316906 | ||||||
| chr6:54317057
|
A | G | 1 | a0015c0014t0003g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.356-3522A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317057 | ||||||
| chr6:54317084
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.356-3495G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317084 | ||||||
| chr6:54317149
|
T | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-3430T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317149 | ||||||
| chr6:54317198
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-3381T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317198 | ||||||
| chr6:54317233
|
G | A | 2 | a0002c0002t0001g0309a0002c0002t0001g0359 | 2 | NA18978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.356-3346G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317233 | ||||||
| chr6:54317241
|
GCTCT | G | 24 | a0001c0001t0001g0245a0003c0003t0001g0246a0003c0003t0001g0361others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-3333_356-3330d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54317241 | |||||
| chr6:54317341
|
C | T | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.356-3238C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317341 | ||||||
| chr6:54317376
|
AGAGG | A | 12 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(9): Show | 12 | HG00438.hp1 HG00735.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.356-3200_356-3197d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54317376 | |||||
| chr6:54317393
|
G | A | 56 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(53): Show | 56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-3186G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317393 | ||||||
| chr6:54317401
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-3178G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317401 | ||||||
| chr6:54317433
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.356-3146G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317433 | ||||||
| chr6:54317505
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.356-3074T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317505 | ||||||
| chr6:54317557
|
T | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.356-3022T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317557 | ||||||
| chr6:54317561
|
C | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.356-3018C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317561 | ||||||
| chr6:54317568
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-3011G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317568 | ||||||
| chr6:54317620
|
A | G | 1 | a0003c0003t0001g0035 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.356-2959A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317620 | ||||||
| chr6:54317728
|
A | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-2851A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317728 | ||||||
| chr6:54317838
|
A | G | 9 | a0002c0002t0001g0308a0002c0002t0001g0344a0002c0002t0001g0345others(6): Show | 9 | HG02056.hp2 NA18747.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-2741A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317838 | ||||||
| chr6:54317844
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-2735G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317844 | ||||||
| chr6:54318058
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.356-2521C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318058 | ||||||
| chr6:54318341
|
C | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-2238C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318341 | ||||||
| chr6:54318366
|
G | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-2213G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318366 | ||||||
| chr6:54318500
|
A | G | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.356-2079A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318500 | ||||||
| chr6:54318518
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.356-2061C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318518 | ||||||
| chr6:54318529
|
T | C | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-2050T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318529 | ||||||
| chr6:54318641
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.356-1938C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318641 | ||||||
| chr6:54318686
|
T | G | 355 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(352): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.356-1893T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318686 | ||||||
| chr6:54319025
|
C | T | 33 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0223others(30): Show | 35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.356-1554C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319025 | ||||||
| chr6:54319058
|
C | G | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-1521C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319058 | ||||||
| chr6:54319085
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.356-1494T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319085 | ||||||
| chr6:54319092
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.356-1487C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319092 | ||||||
| chr6:54319171
|
G | A | 2 | a0002c0002t0001g0309a0002c0002t0001g0359 | 2 | NA18978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.356-1408G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319171 | ||||||
| chr6:54319197
|
T | G | 8 | a0002c0002t0001g0264a0006c0007t0001g0225a0006c0007t0001g0226others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-1382T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319197 | ||||||
| chr6:54319258
|
T | A | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.356-1321T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319258 | ||||||
| chr6:54319405
|
G | A | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-1174G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319405 | ||||||
| chr6:54319412
|
C | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.356-1167C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319412 | ||||||
| chr6:54319499
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.356-1080A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319499 | ||||||
| chr6:54319655
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.356-924G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319655 | ||||||
| chr6:54319840
|
T | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-739T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319840 | ||||||
| chr6:54319893
|
C | T | 64 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(61): Show |
intron_variant | MODIFIER | c.356-686C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319893 | ||||||
| chr6:54319897
|
G | A | 7 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-682G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319897 | ||||||
| chr6:54319898
|
C | A | 7 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-681C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319898 | ||||||
| chr6:54319996
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.356-583A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319996 | ||||||
| chr6:54320000
|
GT | G | 54 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0014others(51): Show | 54 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.356-576delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54320000 | |||||
| chr6:54320082
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.356-497T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320082 | ||||||
| chr6:54320085
|
A | G | 57 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(54): Show | 57 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(54): Show |
intron_variant | MODIFIER | c.356-494A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320085 | ||||||
| chr6:54320519
|
T | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02258.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-60T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320519 | ||||||
| chr6:54320703
|
A | G | 1 | a0013c0012t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.419+61A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320703 | ||||||
| chr6:54320720
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.419+78C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320720 | ||||||
| chr6:54320724
|
A | T | 1 | a0002c0002t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.419+82A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320724 | ||||||
| chr6:54320745
|
A | G | 2 | a0001c0001t0001g0150a0007c0006t0001g0151 | 2 | HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.419+103A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320745 | ||||||
| chr6:54320804
|
T | C | 1 | a0006c0007t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419+162T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320804 | ||||||
| chr6:54320891
|
G | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.419+249G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320891 | ||||||
| chr6:54320907
|
C | G | 9 | a0003c0003t0001g0068a0003c0003t0001g0069a0003c0003t0001g0070others(6): Show | 9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.419+265C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320907 | ||||||
| chr6:54320917
|
A | G | 4 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+275A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320917 | ||||||
| chr6:54320947
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.419+305G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320947 | ||||||
| chr6:54320994
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.420-303C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320994 | ||||||
| chr6:54321002
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.420-295C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321002 | ||||||
| chr6:54321066
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.420-231G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321066 | ||||||
| chr6:54321072
|
G | A | 1 | a0002c0002t0001g0310 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.420-225G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321072 | ||||||
| chr6:54321091
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.420-206T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321091 | ||||||
| chr6:54321103
|
G | C | 69 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(66): Show | 69 | HG01123.hp2 HG01891.hp2 HG02056.hp2 others(66): Show |
intron_variant | MODIFIER | c.420-194G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321103 | ||||||
| chr6:54321226
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.420-71T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321226 | ||||||
| chr6:54321257
|
T | A | 1 | a0024c0025t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.420-40T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321257 | ||||||
| chr6:54321412
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.509+26T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321412 | ||||||
| chr6:54321457
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+71G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321457 | ||||||
| chr6:54321512
|
A | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.509+126A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321512 | ||||||
| chr6:54321764
|
T | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0038others(89): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.509+378T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321764 | ||||||
| chr6:54321830
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+444G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321830 | ||||||
| chr6:54321877
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.509+491C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321877 | ||||||
| chr6:54321982
|
G | A | 1 | a0020c0019t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.509+596G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321982 | ||||||
| chr6:54321986
|
C | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.509+600C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321986 | ||||||
| chr6:54322135
|
T | C | 1 | a0003c0003t0001g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.509+749T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322135 | ||||||
| chr6:54322201
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.509+815A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322201 | ||||||
| chr6:54322272
|
C | A | 1 | a0005c0005t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.509+886C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322272 | ||||||
| chr6:54322333
|
C | CA | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(48): Show | 55 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.509+957dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54322333 | |||||
| chr6:54322337
|
A | C | 67 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(64): Show | 67 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(64): Show |
intron_variant | MODIFIER | c.509+951A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322337 | ||||||
| chr6:54322343
|
A | AG | 6 | a0001c0001t0001g0210a0001c0001t0001g0280a0002c0002t0001g0009others(3): Show | 7 | HG02622.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+957_509+958ins others(1): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322343 | ||||||
| chr6:54322367
|
C | A | 2 | a0008c0008t0002g0171a0008c0008t0002g0172 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.509+981C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322367 | ||||||
| chr6:54322388
|
T | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.509+1002T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322388 | ||||||
| chr6:54322447
|
C | T | 3 | a0002c0002t0001g0009a0002c0002t0001g0281a0002c0002t0001g0282 | 4 | HG02622.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+1061C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322447 | ||||||
| chr6:54322496
|
A | G | 1 | a0003c0003t0001g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.509+1110A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322496 | ||||||
| chr6:54322684
|
C | T | 5 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1298C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322684 | ||||||
| chr6:54322806
|
A | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0210a0001c0001t0001g0245others(8): Show | 13 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+1420A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322806 | ||||||
| chr6:54322844
|
A | C | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+1458A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322844 | ||||||
| chr6:54322860
|
G | A | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1474G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322860 | ||||||
| chr6:54322995
|
C | A | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+1609C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322995 | ||||||
| chr6:54323100
|
A | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+1714A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323100 | ||||||
| chr6:54323251
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.509+1865A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323251 | ||||||
| chr6:54323290
|
A | G | 9 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(6): Show | 9 | HG03098.hp2 HG03195.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+1904A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323290 | ||||||
| chr6:54323384
|
C | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+1998C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323384 | ||||||
| chr6:54323585
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+2199C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323585 | ||||||
| chr6:54323680
|
G | A | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.509+2294G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323680 | ||||||
| chr6:54323693
|
C | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.509+2307C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323693 | ||||||
| chr6:54323703
|
C | T | 33 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0223others(30): Show | 35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.509+2317C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323703 | ||||||
| chr6:54323756
|
C | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0280a0002c0002t0001g0009others(3): Show | 7 | HG02622.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2370C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323756 | ||||||
| chr6:54323793
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0093others(47): Show | 52 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.509+2407G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323793 | ||||||
| chr6:54324086
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+2700A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324086 | ||||||
| chr6:54324177
|
T | A | 56 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(53): Show | 56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.510-2625T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324177 | ||||||
| chr6:54324194
|
T | G | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-2608T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324194 | ||||||
| chr6:54324281
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-2521G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324281 | ||||||
| chr6:54324424
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-2378T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324424 | ||||||
| chr6:54324620
|
C | T | 53 | a0001c0001t0001g0302a0001c0001t0001g0315a0001c0001t0001g0318others(50): Show | 53 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(50): Show |
intron_variant | MODIFIER | c.510-2182C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324620 | ||||||
| chr6:54324636
|
T | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(34): Show | 38 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.510-2166T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324636 | ||||||
| chr6:54324672
|
C | G | 56 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0313others(53): Show | 56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.510-2130C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324672 | ||||||
| chr6:54324678
|
G | C | 1 | a0012c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-2124G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324678 | ||||||
| chr6:54324807
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-1995T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324807 | ||||||
| chr6:54324884
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-1918C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324884 | ||||||
| chr6:54324934
|
A | G | 2 | a0010c0009t0001g0211a0010c0009t0001g0212 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.510-1868A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324934 | ||||||
| chr6:54324946
|
A | G | 11 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-1856A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324946 | ||||||
| chr6:54325275
|
A | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.510-1527A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325275 | ||||||
| chr6:54325276
|
G | A | 2 | a0001c0010t0001g0244a0009c0018t0001g0260 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-1526G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325276 | ||||||
| chr6:54325470
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.510-1332A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325470 | ||||||
| chr6:54325506
|
G | A | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.510-1296G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325506 | ||||||
| chr6:54325513
|
A | G | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-1289A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325513 | ||||||
| chr6:54325658
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.510-1144A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325658 | ||||||
| chr6:54325698
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | NA18963.hp1 NA18966.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.510-1104C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325698 | ||||||
| chr6:54325739
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.510-1063C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325739 | ||||||
| chr6:54325801
|
CTTA | C | 9 | a0002c0002t0001g0334a0002c0002t0001g0335a0002c0002t0001g0336others(6): Show | 9 | NA18612.hp2 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-998_510-996del others(3): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54325801 | |||||
| chr6:54325954
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-848C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325954 | ||||||
| chr6:54325956
|
A | G | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-846A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325956 | ||||||
| chr6:54326085
|
C | G | 10 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(7): Show | 10 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.510-717C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326085 | ||||||
| chr6:54326140
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-662A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326140 | ||||||
| chr6:54326147
|
T | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.510-655T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326147 | ||||||
| chr6:54326214
|
TTTA | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18962.hp2 NA18991.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.510-578_510-576del others(3): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54326214 | |||||
| chr6:54326350
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-452A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326350 | ||||||
| chr6:54326390
|
C | G | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-412C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326390 | ||||||
| chr6:54326492
|
T | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-310T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326492 | ||||||
| chr6:54326565
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.510-237G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326565 | ||||||
| chr6:54326655
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-147A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326655 | ||||||
| chr6:54326736
|
T | C | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-66T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326736 | ||||||
| chr6:54326956
|
T | C | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+40T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54326956 | ||||||
| chr6:54327167
|
G | A | 3 | a0001c0001t0001g0247a0015c0014t0003g0283a0015c0014t0003g0284 | 3 | HG02970.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+251G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327167 | ||||||
| chr6:54327172
|
T | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.624+256T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327172 | ||||||
| chr6:54327210
|
A | G | 48 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0084others(45): Show | 50 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.624+294A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327210 | ||||||
| chr6:54327232
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+316G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327232 | ||||||
| chr6:54327264
|
T | C | 38 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(35): Show | 39 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+348T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327264 | ||||||
| chr6:54327449
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+533G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327449 | ||||||
| chr6:54327463
|
A | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+547A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327463 | ||||||
| chr6:54327520
|
G | T | 1 | a0012c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.624+604G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327520 | ||||||
| chr6:54327557
|
G | GT | 6 | a0001c0001t0001g0245a0001c0001t0001g0247a0002c0002t0001g0342others(3): Show | 6 | HG02258.hp1 HG02970.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+651dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54327557 | |||||
| chr6:54327575
|
C | T | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0011c0013t0001g0360 | 3 | HG01258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.624+659C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327575 | ||||||
| chr6:54327675
|
C | T | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+759C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327675 | ||||||
| chr6:54327891
|
C | A | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+975C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327891 | ||||||
| chr6:54327997
|
C | G | 1 | a0002c0002t0001g0358 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.624+1081C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327997 | ||||||
| chr6:54328068
|
C | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.624+1152C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328068 | ||||||
| chr6:54328145
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252 | 3 | HG02258.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624+1229G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328145 | ||||||
| chr6:54328176
|
G | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+1260G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328176 | ||||||
| chr6:54328233
|
C | T | 1 | a0013c0012t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+1317C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328233 | ||||||
| chr6:54328274
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+1358C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328274 | ||||||
| chr6:54328370
|
G | A | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.624+1454G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328370 | ||||||
| chr6:54328431
|
A | T | 114 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0093others(111): Show | 118 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.624+1515A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328431 | ||||||
| chr6:54328558
|
T | C | 1 | a0001c0001t0001g0115 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.624+1642T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328558 | ||||||
| chr6:54328592
|
C | G | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+1676C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328592 | ||||||
| chr6:54328607
|
G | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0002c0002t0001g0253others(1): Show | 4 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+1691G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328607 | ||||||
| chr6:54328622
|
T | A | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+1706T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328622 | ||||||
| chr6:54328674
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+1758C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328674 | ||||||
| chr6:54328797
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0093others(105): Show | 112 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.624+1881A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328797 | ||||||
| chr6:54328835
|
A | G | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+1919A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328835 | ||||||
| chr6:54328928
|
T | C | 1 | a0004c0004t0001g0102 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.624+2012T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328928 | ||||||
| chr6:54328932
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2016T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328932 | ||||||
| chr6:54328957
|
A | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+2041A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328957 | ||||||
| chr6:54328973
|
G | A | 1 | a0002c0002t0001g0344 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.624+2057G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328973 | ||||||
| chr6:54329007
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2091C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329007 | ||||||
| chr6:54329022
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2106C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329022 | ||||||
| chr6:54329024
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2108A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329024 | ||||||
| chr6:54329032
|
C | A | 1 | a0004c0004t0001g0168 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.624+2116C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329032 | ||||||
| chr6:54329060
|
A | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+2144A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329060 | ||||||
| chr6:54329062
|
C | A | 144 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0093others(141): Show | 150 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.624+2146C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329062 | ||||||
| chr6:54329114
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.624+2198A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329114 | ||||||
| chr6:54329120
|
A | G | 1 | a0003c0003t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.624+2204A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329120 | ||||||
| chr6:54329143
|
G | A | 1 | a0002c0002t0001g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.624+2227G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329143 | ||||||
| chr6:54329303
|
G | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0002c0002t0001g0253others(1): Show | 4 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+2387G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329303 | ||||||
| chr6:54329364
|
C | T | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.624+2448C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329364 | ||||||
| chr6:54329407
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2491T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329407 | ||||||
| chr6:54329650
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2734A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329650 | ||||||
| chr6:54329709
|
G | T | 1 | a0022c0023t0001g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.624+2793G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329709 | ||||||
| chr6:54329727
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.624+2811C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329727 | ||||||
| chr6:54329854
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+2938G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329854 | ||||||
| chr6:54329895
|
AG | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2983delG | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54329895 | |||||
| chr6:54329904
|
A | G | 4 | a0003c0003t0001g0072a0003c0003t0001g0074a0003c0003t0001g0075others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+2988A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329904 | ||||||
| chr6:54329947
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+3031A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329947 | ||||||
| chr6:54330106
|
G | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.624+3190G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330106 | ||||||
| chr6:54330112
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.624+3196C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330112 | ||||||
| chr6:54330116
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+3200C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330116 | ||||||
| chr6:54330232
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+3316C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330232 | ||||||
| chr6:54330264
|
A | G | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+3348A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330264 | ||||||
| chr6:54330330
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+3414C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330330 | ||||||
| chr6:54330339
|
C | T | 3 | a0009c0018t0001g0222a0015c0014t0003g0283a0015c0014t0003g0284 | 3 | HG02970.hp1 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.624+3423C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330339 | ||||||
| chr6:54330395
|
C | T | 1 | a0004c0004t0001g0080 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.624+3479C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330395 | ||||||
| chr6:54330422
|
A | C | 1 | a0004c0004t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624+3506A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330422 | ||||||
| chr6:54330465
|
G | A | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+3549G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330465 | ||||||
| chr6:54330576
|
G | T | 1 | a0003c0003t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.624+3660G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330576 | ||||||
| chr6:54330588
|
C | T | 2 | a0003c0003t0001g0071a0016c0016t0001g0259 | 2 | HG00735.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.624+3672C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330588 | ||||||
| chr6:54330703
|
C | T | 1 | a0020c0019t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.624+3787C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330703 | ||||||
| chr6:54330704
|
G | A | 1 | a0013c0012t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+3788G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330704 | ||||||
| chr6:54330772
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.624+3856A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330772 | ||||||
| chr6:54330805
|
C | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+3889C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330805 | ||||||
| chr6:54330932
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+4016C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330932 | ||||||
| chr6:54330974
|
C | A | 1 | a0002c0002t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.624+4058C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330974 | ||||||
| chr6:54330999
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.624+4083C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330999 | ||||||
| chr6:54331035
|
G | A | 1 | a0002c0002t0001g0248 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.624+4119G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331035 | ||||||
| chr6:54331045
|
C | T | 111 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0093others(108): Show | 115 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(112): Show |
intron_variant | MODIFIER | c.624+4129C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331045 | ||||||
| chr6:54331087
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+4171C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331087 | ||||||
| chr6:54331131
|
A | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+4215A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331131 | ||||||
| chr6:54331208
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 5 | HG03471.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+4292A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331208 | ||||||
| chr6:54331263
|
C | T | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+4347C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331263 | ||||||
| chr6:54331342
|
A | G | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.624+4426A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331342 | ||||||
| chr6:54331366
|
A | G | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+4450A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331366 | ||||||
| chr6:54331392
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+4476C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331392 | ||||||
| chr6:54331393
|
G | A | 1 | a0002c0002t0001g0314 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.624+4477G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331393 | ||||||
| chr6:54331496
|
A | G | 32 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(29): Show | 34 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+4580A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331496 | ||||||
| chr6:54331497
|
T | G | 1 | a0006c0007t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.624+4581T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331497 | ||||||
| chr6:54331501
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+4585A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331501 | ||||||
| chr6:54331505
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+4589T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331505 | ||||||
| chr6:54331771
|
T | TA | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(155): Show | 165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+4858dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54331771 | |||||
| chr6:54331820
|
A | G | 7 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+4904A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331820 | ||||||
| chr6:54332057
|
G | C | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+5141G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332057 | ||||||
| chr6:54332117
|
C | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.624+5201C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332117 | ||||||
| chr6:54332138
|
A | G | 1 | a0007c0006t0001g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.624+5222A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332138 | ||||||
| chr6:54332300
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0300 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+5384C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332300 | ||||||
| chr6:54332301
|
C | T | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5385C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332301 | ||||||
| chr6:54332339
|
A | T | 2 | a0017c0017t0001g0277a0017c0017t0001g0278 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.624+5423A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332339 | ||||||
| chr6:54332374
|
T | G | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5458T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332374 | ||||||
| chr6:54332411
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 8 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+5495C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332411 | ||||||
| chr6:54332552
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+5636G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332552 | ||||||
| chr6:54332579
|
C | T | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5663C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332579 | ||||||
| chr6:54332618
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.624+5702G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332618 | ||||||
| chr6:54332636
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.624+5720G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332636 | ||||||
| chr6:54332682
|
A | C | 1 | a0004c0004t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+5766A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332682 | ||||||
| chr6:54332751
|
G | A | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5835G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332751 | ||||||
| chr6:54333062
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.624+6146G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333062 | ||||||
| chr6:54333368
|
C | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+6452C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333368 | ||||||
| chr6:54333462
|
T | A | 2 | a0001c0001t0001g0245a0021c0020t0001g0267 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+6546T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333462 | ||||||
| chr6:54333485
|
G | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(33): Show | 37 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.624+6569G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333485 | ||||||
| chr6:54333494
|
C | T | 2 | a0017c0017t0001g0277a0017c0017t0001g0278 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.624+6578C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333494 | ||||||
| chr6:54333513
|
T | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+6597T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333513 | ||||||
| chr6:54333544
|
C | A | 68 | a0001c0001t0001g0210a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 70 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(67): Show |
intron_variant | MODIFIER | c.624+6628C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333544 | ||||||
| chr6:54333565
|
T | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(155): Show | 165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+6649T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333565 | ||||||
| chr6:54333619
|
A | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(155): Show | 165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+6703A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333619 | ||||||
| chr6:54333626
|
A | T | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.624+6710A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333626 | ||||||
| chr6:54333649
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 34 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+6733A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333649 | ||||||
| chr6:54333669
|
T | C | 1 | a0003c0003t0001g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.624+6753T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333669 | ||||||
| chr6:54333764
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.624+6848C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333764 | ||||||
| chr6:54333884
|
G | T | 10 | a0002c0002t0001g0362a0003c0003t0001g0068a0003c0003t0001g0069others(7): Show | 10 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+6968G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333884 | ||||||
| chr6:54333894
|
CA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 8 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+6983delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54333894 | |||||
| chr6:54333980
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+7064T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333980 | ||||||
| chr6:54334122
|
C | T | 31 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(28): Show | 33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+7206C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334122 | ||||||
| chr6:54334211
|
G | A | 1 | a0005c0005t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.624+7295G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334211 | ||||||
| chr6:54334320
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(157): Show | 167 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.624+7404A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334320 | ||||||
| chr6:54334433
|
AG | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+7518delG | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334433 | ||||||
| chr6:54334504
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+7588A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334504 | ||||||
| chr6:54334511
|
T | C | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+7595T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334511 | ||||||
| chr6:54334521
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+7605G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334521 | ||||||
| chr6:54334764
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+7848G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334764 | ||||||
| chr6:54334784
|
T | C | 37 | a0001c0001t0001g0233a0001c0001t0001g0234a0002c0002t0001g0111others(34): Show | 39 | HG00438.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+7868T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334784 | ||||||
| chr6:54334948
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+8032T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334948 | ||||||
| chr6:54334982
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.624+8066T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334982 | ||||||
| chr6:54335077
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-8149C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335077 | ||||||
| chr6:54335078
|
G | T | 7 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-8148G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335078 | ||||||
| chr6:54335417
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.625-7809T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335417 | ||||||
| chr6:54335463
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.625-7763T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335463 | ||||||
| chr6:54335539
|
A | G | 9 | a0002c0002t0001g0362a0006c0007t0001g0225a0006c0007t0001g0226others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-7687A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335539 | ||||||
| chr6:54335560
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.625-7666A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335560 | ||||||
| chr6:54335561
|
A | G | 15 | a0001c0001t0001g0164a0001c0001t0001g0178a0001c0001t0001g0180others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.625-7665A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335561 | ||||||
| chr6:54335628
|
C | A | 3 | a0003c0003t0001g0043a0003c0003t0001g0046a0003c0003t0001g0047 | 3 | HG02602.hp1 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.625-7598C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335628 | ||||||
| chr6:54335649
|
A | C | 1 | a0002c0002t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.625-7577A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335649 | ||||||
| chr6:54335736
|
C | T | 68 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(65): Show | 70 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(67): Show |
intron_variant | MODIFIER | c.625-7490C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335736 | ||||||
| chr6:54335764
|
G | C | 1 | a0001c0001t0001g0315 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.625-7462G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335764 | ||||||
| chr6:54335987
|
G | T | 68 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(65): Show | 70 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(67): Show |
intron_variant | MODIFIER | c.625-7239G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335987 | ||||||
| chr6:54336028
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(15): Show | 20 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.625-7198G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336028 | ||||||
| chr6:54336051
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.625-7175G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336051 | ||||||
| chr6:54336091
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0301 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.625-7135G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336091 | ||||||
| chr6:54336316
|
T | C | 29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-6910T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336316 | ||||||
| chr6:54336408
|
A | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.625-6818A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336408 | ||||||
| chr6:54336411
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-6815G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336411 | ||||||
| chr6:54336529
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-6697A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336529 | ||||||
| chr6:54336569
|
T | A | 1 | a0004c0004t0001g0168 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.625-6657T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336569 | ||||||
| chr6:54336601
|
T | C | 1 | a0002c0002t0001g0324 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.625-6625T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336601 | ||||||
| chr6:54336772
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.625-6454C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336772 | ||||||
| chr6:54336792
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.625-6434C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336792 | ||||||
| chr6:54336845
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.625-6381C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336845 | ||||||
| chr6:54336846
|
G | A | 5 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-6380G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336846 | ||||||
| chr6:54336912
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0082others(43): Show | 47 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.625-6314G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336912 | ||||||
| chr6:54336931
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.625-6295A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336931 | ||||||
| chr6:54337015
|
T | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.625-6211T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337015 | ||||||
| chr6:54337027
|
A | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-6199A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337027 | ||||||
| chr6:54337127
|
AT | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0084others(12): Show | 16 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.625-6090delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337127 | |||||
| chr6:54337159
|
G | C | 1 | a0003c0003t0001g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.625-6067G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337159 | ||||||
| chr6:54337200
|
TTAAAG | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-6022_625-6018d others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337200 | |||||
| chr6:54337212
|
T | C | 1 | a0011c0013t0002g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.625-6014T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337212 | ||||||
| chr6:54337240
|
A | G | 1 | a0002c0002t0001g0332 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.625-5986A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337240 | ||||||
| chr6:54337246
|
A | AT | 16 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0163others(13): Show | 16 | HG00735.hp2 HG01175.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.625-5956dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | |||||
| chr6:54337246
|
A | ATTTT | 6 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0088others(3): Show | 7 | HG02074.hp2 NA18941.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-5959_625-5956d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | |||||
| chr6:54337246
|
AT | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.625-5956delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | |||||
| chr6:54337246
|
ATT | A | 30 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0156others(27): Show | 30 | HG01069.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.625-5957_625-5956d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | |||||
| chr6:54337333
|
A | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0082others(44): Show | 48 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.625-5893A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337333 | ||||||
| chr6:54337421
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.625-5805T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337421 | ||||||
| chr6:54337459
|
G | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-5767G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337459 | ||||||
| chr6:54337490
|
G | A | 1 | a0003c0003t0001g0068 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.625-5736G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337490 | ||||||
| chr6:54337496
|
C | T | 29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-5730C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337496 | ||||||
| chr6:54337626
|
A | G | 7 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-5600A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337626 | ||||||
| chr6:54337726
|
G | A | 1 | a0015c0014t0003g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.625-5500G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337726 | ||||||
| chr6:54337767
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.625-5459A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337767 | ||||||
| chr6:54337954
|
G | A | 1 | a0007c0006t0001g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.625-5272G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337954 | ||||||
| chr6:54338056
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0101others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-5170C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338056 | ||||||
| chr6:54338272
|
A | G | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-4954A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338272 | ||||||
| chr6:54338284
|
A | T | 1 | a0002c0002t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.625-4942A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338284 | ||||||
| chr6:54338313
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-4913A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338313 | ||||||
| chr6:54338376
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(359): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.625-4850T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338376 | ||||||
| chr6:54338391
|
A | G | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-4835A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338391 | ||||||
| chr6:54338473
|
G | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-4753G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338473 | ||||||
| chr6:54338487
|
C | T | 75 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(72): Show | 77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.625-4739C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338487 | ||||||
| chr6:54338497
|
G | A | 5 | a0007c0006t0002g0279a0008c0008t0002g0079a0008c0008t0002g0171others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-4729G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338497 | ||||||
| chr6:54338598
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(125): Show | 135 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.625-4628T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338598 | ||||||
| chr6:54338656
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-4570G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338656 | ||||||
| chr6:54338692
|
C | T | 1 | a0005c0005t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.625-4534C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338692 | ||||||
| chr6:54338719
|
C | CA | 38 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(35): Show | 41 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.625-4483dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | |||||
| chr6:54338719
|
CA | C | 31 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0131others(28): Show | 31 | HG01993.hp1 HG02055.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-4483delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | |||||
| chr6:54338719
|
CAA | C | 73 | a0001c0010t0001g0244a0001c0010t0001g0312a0002c0002t0001g0006others(70): Show | 77 | HG00642.hp2 HG01123.hp2 HG01516.hp1 others(74): Show |
intron_variant | MODIFIER | c.625-4484_625-4483d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | |||||
| chr6:54338719
|
CAAA | C | 31 | a0001c0001t0001g0313a0002c0002t0001g0340a0004c0004t0001g0080others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-4485_625-4483d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | |||||
| chr6:54338781
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0163others(1): Show | 4 | NA18947.hp1 NA19002.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-4445T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338781 | ||||||
| chr6:54338800
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.625-4426T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338800 | ||||||
| chr6:54338839
|
G | T | 1 | a0002c0002t0001g0331 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.625-4387G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338839 | ||||||
| chr6:54338842
|
C | T | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.625-4384C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338842 | ||||||
| chr6:54338910
|
A | G | 7 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-4316A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338910 | ||||||
| chr6:54338939
|
A | T | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.625-4287A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338939 | ||||||
| chr6:54338953
|
C | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-4273C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338953 | ||||||
| chr6:54338998
|
A | G | 2 | a0003c0003t0001g0058a0003c0003t0001g0059 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.625-4228A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338998 | ||||||
| chr6:54339140
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0001g0148a0001c0001t0001g0192others(2): Show | 5 | HG01070.hp2 HG01123.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-4086C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339140 | ||||||
| chr6:54339205
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-4021A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339205 | ||||||
| chr6:54339241
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3985T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339241 | ||||||
| chr6:54339327
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-3899T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339327 | ||||||
| chr6:54339549
|
G | A | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.625-3677G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339549 | ||||||
| chr6:54339554
|
G | C | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.625-3672G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339554 | ||||||
| chr6:54339564
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3662G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339564 | ||||||
| chr6:54339799
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-3427C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339799 | ||||||
| chr6:54339851
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.625-3375T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339851 | ||||||
| chr6:54339903
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.625-3323G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339903 | ||||||
| chr6:54340222
|
T | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-3004T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340222 | ||||||
| chr6:54340225
|
T | C | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-3001T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340225 | ||||||
| chr6:54340266
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.625-2960G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340266 | ||||||
| chr6:54340323
|
T | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-2903T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340323 | ||||||
| chr6:54340366
|
G | A | 5 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-2860G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340366 | ||||||
| chr6:54340395
|
C | CA | 48 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0076others(45): Show | 52 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.625-2817dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54340395 | |||||
| chr6:54340395
|
CA | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0300others(3): Show | 7 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-2817delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54340395 | |||||
| chr6:54340529
|
C | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-2697C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340529 | ||||||
| chr6:54340553
|
T | C | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-2673T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340553 | ||||||
| chr6:54340696
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.625-2530A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340696 | ||||||
| chr6:54340761
|
A | G | 5 | a0007c0006t0002g0279a0008c0008t0002g0079a0008c0008t0002g0171others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-2465A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340761 | ||||||
| chr6:54340964
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.625-2262C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340964 | ||||||
| chr6:54341007
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.625-2219A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341007 | ||||||
| chr6:54341073
|
A | G | 76 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(73): Show | 78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.625-2153A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341073 | ||||||
| chr6:54341148
|
C | G | 1 | a0003c0003t0001g0053 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.625-2078C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341148 | ||||||
| chr6:54341426
|
T | C | 1 | a0003c0003t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.625-1800T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341426 | ||||||
| chr6:54341459
|
T | A | 1 | a0003c0003t0001g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.625-1767T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341459 | ||||||
| chr6:54341468
|
C | A | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1758C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341468 | ||||||
| chr6:54341479
|
C | A | 1 | a0003c0003t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.625-1747C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341479 | ||||||
| chr6:54341559
|
T | TC | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1663dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54341559 | |||||
| chr6:54341779
|
C | T | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1447C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341779 | ||||||
| chr6:54341789
|
G | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-1437G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341789 | ||||||
| chr6:54341791
|
C | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1435C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341791 | ||||||
| chr6:54341851
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1375T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341851 | ||||||
| chr6:54341875
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1351T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341875 | ||||||
| chr6:54341915
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.625-1311A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341915 | ||||||
| chr6:54342033
|
A | C | 1 | a0002c0002t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.625-1193A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342033 | ||||||
| chr6:54342044
|
A | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | NA18959.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1182A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342044 | ||||||
| chr6:54342062
|
G | GGT | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0176others(6): Show | 11 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-1144_625-1143d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | |||||
| chr6:54342062
|
G | GGTGTGTG others(1): Show |
29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-1150_625-1143d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | |||||
| chr6:54342062
|
GGT | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(8): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-1144_625-1143d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | |||||
| chr6:54342066
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.625-1160T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342066 | ||||||
| chr6:54342082
|
T | A | 26 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0117others(23): Show | 26 | HG00558.hp2 HG00735.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.625-1144T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342082 | ||||||
| chr6:54342090
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.625-1136C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342090 | ||||||
| chr6:54342096
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.625-1130C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342096 | ||||||
| chr6:54342132
|
T | C | 5 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-1094T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342132 | ||||||
| chr6:54342361
|
C | CT | 17 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(14): Show | 18 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.625-850dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342361 | |||||
| chr6:54342564
|
T | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-662T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342564 | ||||||
| chr6:54342568
|
C | G | 1 | a0002c0002t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.625-658C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342568 | ||||||
| chr6:54342634
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-592C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342634 | ||||||
| chr6:54342822
|
T | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246others(2): Show | 6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-404T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342822 | ||||||
| chr6:54342833
|
T | A | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-393T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342833 | ||||||
| chr6:54342840
|
A | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(14): Show | 19 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.625-386A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342840 | ||||||
| chr6:54342906
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.625-320T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342906 | ||||||
| chr6:54342916
|
C | A | 1 | a0005c0005t0001g0288 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.625-310C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342916 | ||||||
| chr6:54342930
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-296A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342930 | ||||||
| chr6:54342947
|
A | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-279A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342947 | ||||||
| chr6:54342969
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-257T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342969 | ||||||
| chr6:54343001
|
T | C | 76 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(73): Show | 78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.625-225T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343001 | ||||||
| chr6:54343096
|
T | C | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.625-130T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343096 | ||||||
| chr6:54343113
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-113T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343113 | ||||||
| chr6:54343161
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.625-65G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343161 | ||||||
| chr6:54343374
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+25C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343374 | ||||||
| chr6:54343442
|
T | C | 75 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(72): Show | 77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.748+93T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343442 | ||||||
| chr6:54343483
|
G | T | 2 | a0017c0017t0001g0277a0017c0017t0001g0278 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748+134G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343483 | ||||||
| chr6:54343495
|
C | A | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.748+146C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343495 | ||||||
| chr6:54343527
|
C | A | 7 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.748+178C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343527 | ||||||
| chr6:54343533
|
G | GT | 42 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(39): Show | 45 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.748+196dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | |||||
| chr6:54343533
|
G | GTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0245a0001c0001t0001g0300others(3): Show | 7 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.748+195_748+196dup others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | |||||
| chr6:54343533
|
GT | G | 68 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(65): Show | 70 | HG00099.hp1 HG00642.hp2 HG01123.hp2 others(67): Show |
intron_variant | MODIFIER | c.748+196delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | |||||
| chr6:54343555
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(74): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.748+206T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343555 | ||||||
| chr6:54343575
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+226G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343575 | ||||||
| chr6:54343620
|
A | G | 2 | a0002c0002t0001g0242a0002c0002t0001g0358 | 2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.748+271A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343620 | ||||||
| chr6:54343632
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246others(2): Show | 6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+283G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343632 | ||||||
| chr6:54343657
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.748+308G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343657 | ||||||
| chr6:54343673
|
A | T | 1 | a0002c0002t0001g0327 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.748+324A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343673 | ||||||
| chr6:54343712
|
C | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+363C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343712 | ||||||
| chr6:54343731
|
C | T | 1 | a0003c0003t0001g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.748+382C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343731 | ||||||
| chr6:54343740
|
T | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(51): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.748+391T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343740 | ||||||
| chr6:54343751
|
AAC | A | 75 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(72): Show | 77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.748+404_748+405del others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343751 | |||||
| chr6:54343793
|
C | A | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+444C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343793 | ||||||
| chr6:54343843
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+494G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343843 | ||||||
| chr6:54344433
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.748+1084T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344433 | ||||||
| chr6:54344646
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+1297T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344646 | ||||||
| chr6:54344677
|
G | A | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+1328G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344677 | ||||||
| chr6:54344806
|
G | T | 18 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0301others(15): Show | 18 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.748+1457G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344806 | ||||||
| chr6:54344915
|
G | A | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.748+1566G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344915 | ||||||
| chr6:54344931
|
T | TA | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+1583dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54344931 | |||||
| chr6:54345030
|
A | G | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.748+1681A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345030 | ||||||
| chr6:54345093
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.748+1744A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345093 | ||||||
| chr6:54345343
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.748+1994C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345343 | ||||||
| chr6:54345418
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.749-1949C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345418 | ||||||
| chr6:54345517
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-1850T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345517 | ||||||
| chr6:54345527
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-1840A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345527 | ||||||
| chr6:54345634
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(210): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.749-1733C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345634 | ||||||
| chr6:54345712
|
G | C | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-1655G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345712 | ||||||
| chr6:54345727
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.749-1640G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345727 | ||||||
| chr6:54345940
|
A | G | 7 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.749-1427A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345940 | ||||||
| chr6:54345945
|
AT | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.749-1421delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345945 | ||||||
| chr6:54346012
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.749-1355G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346012 | ||||||
| chr6:54346208
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(17): Show | 22 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.749-1159A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346208 | ||||||
| chr6:54346259
|
G | A | 2 | a0004c0004t0001g0219a0004c0004t0001g0220 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.749-1108G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346259 | ||||||
| chr6:54346528
|
GTA | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-830_749-829del others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54346528 | |||||
| chr6:54346565
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.749-802A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346565 | ||||||
| chr6:54346576
|
T | C | 12 | a0001c0001t0001g0093a0001c0001t0001g0117a0001c0001t0001g0118others(9): Show | 12 | HG00558.hp2 NA18947.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.749-791T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346576 | ||||||
| chr6:54346576
|
T | G | 1 | a0001c0001t0001g0319 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.749-791T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346576 | ||||||
| chr6:54346607
|
C | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-760C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346607 | ||||||
| chr6:54346610
|
CAGTT | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | NA18959.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-753_749-750del others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54346610 | |||||
| chr6:54346652
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.749-715T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346652 | ||||||
| chr6:54346732
|
T | A | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-635T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346732 | ||||||
| chr6:54346781
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-586A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346781 | ||||||
| chr6:54346820
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0082others(43): Show | 47 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.749-547C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346820 | ||||||
| chr6:54347325
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.749-42C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54347325 | ||||||
| chr6:54347326
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.749-41G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54347326 | ||||||
| chr6:54347586
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.899+69T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347586 | ||||||
| chr6:54347591
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.899+74C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347591 | ||||||
| chr6:54347774
|
G | A | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.899+257G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347774 | ||||||
| chr6:54347816
|
A | C | 1 | a0001c0001t0001g0007 | 2 | NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.899+299A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347816 | ||||||
| chr6:54347972
|
C | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.899+455C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347972 | ||||||
| chr6:54348088
|
G | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.899+571G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348088 | ||||||
| chr6:54348166
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.899+649C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348166 | ||||||
| chr6:54348207
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(14): Show | 19 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.899+690G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348207 | ||||||
| chr6:54348215
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.899+698T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348215 | ||||||
| chr6:54348220
|
T | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(129): Show | 139 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.899+703T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348220 | ||||||
| chr6:54348269
|
C | T | 66 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0009others(63): Show | 68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.899+752C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348269 | ||||||
| chr6:54348398
|
A | C | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.899+881A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348398 | ||||||
| chr6:54348739
|
CATATGAA others(5): Show |
C | 1 | a0002c0002t0001g0309 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.900-975_900-964del others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 54348739 | |||||
| chr6:54348816
|
T | C | 2 | a0002c0002t0001g0116a0002c0002t0001g0165 | 2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.900-900T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348816 | ||||||
| chr6:54348996
|
T | G | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-720T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348996 | ||||||
| chr6:54349004
|
T | C | 76 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(73): Show | 78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.900-712T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349004 | ||||||
| chr6:54349087
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.900-629T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349087 | ||||||
| chr6:54349106
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.900-610C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349106 | ||||||
| chr6:54349107
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.900-609A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349107 | ||||||
| chr6:54349240
|
A | T | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0270 | 3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.900-476A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349240 | ||||||
| chr6:54349335
|
T | C | 76 | a0001c0001t0001g0210a0001c0001t0001g0311a0001c0001t0001g0313others(73): Show | 78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.900-381T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349335 | ||||||
| chr6:54349394
|
G | A | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.900-322G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349394 | ||||||
| chr6:54349395
|
G | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.900-321G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349395 | ||||||
| chr6:54349672
|
A | T | 1 | a0002c0002t0001g0362 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.900-44A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349672 | ||||||
| chr6:54349674
|
T | A | 1 | a0002c0002t0001g0324 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.900-42T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349674 | ||||||
| chr6:54349677
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.900-39C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349677 | ||||||
| chr6:54349685
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-31T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349685 | ||||||
| chr6:54349694
|
C | T | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-22C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349694 | ||||||
| chr6:54349981
|
A | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1080+85A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54349981 | ||||||
| chr6:54350086
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+190G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350086 | ||||||
| chr6:54350130
|
A | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.1080+234A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350130 | ||||||
| chr6:54350162
|
A | G | 13 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(10): Show | 13 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1080+266A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350162 | ||||||
| chr6:54350218
|
C | CT | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1080+328dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 54350218 | |||||
| chr6:54350366
|
T | C | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1080+470T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350366 | ||||||
| chr6:54350391
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1080+495A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350391 | ||||||
| chr6:54350420
|
T | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1080+524T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350420 | ||||||
| chr6:54350451
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1080+555A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350451 | ||||||
| chr6:54350488
|
A | G | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1080+592A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350488 | ||||||
| chr6:54350530
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+634C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350530 | ||||||
| chr6:54350645
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1081-707C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350645 | ||||||
| chr6:54350645
|
C | G | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-707C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350645 | ||||||
| chr6:54350705
|
T | C | 4 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-647T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350705 | ||||||
| chr6:54350743
|
T | C | 1 | a0020c0019t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1081-609T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350743 | ||||||
| chr6:54350758
|
C | T | 7 | a0006c0007t0001g0225a0006c0007t0001g0226a0006c0007t0001g0228others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081-594C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350758 | ||||||
| chr6:54350771
|
G | A | 2 | a0004c0004t0001g0168a0004c0004t0001g0169 | 2 | HG00438.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1081-581G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350771 | ||||||
| chr6:54350912
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(211): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1081-440T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350912 | ||||||
| chr6:54350997
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081-355A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350997 | ||||||
| chr6:54351075
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081-277C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351075 | ||||||
| chr6:54351129
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1081-223A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351129 | ||||||
| chr6:54351139
|
G | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1081-213G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351139 | ||||||
| chr6:54351418
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0104 | 3 | NA19010.hp2 NA19059.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1126+21G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351418 | ||||||
| chr6:54351472
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1126+75G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351472 | ||||||
| chr6:54351513
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1126+116C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351513 | ||||||
| chr6:54351607
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+210C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351607 | ||||||
| chr6:54351772
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1126+375A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351772 | ||||||
| chr6:54351810
|
G | A | 2 | a0008c0008t0002g0171a0008c0008t0002g0172 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1126+413G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351810 | ||||||
| chr6:54352049
|
A | G | 1 | a0010c0009t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1126+652A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352049 | ||||||
| chr6:54352062
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1126+665T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352062 | ||||||
| chr6:54352064
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126+667T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352064 | ||||||
| chr6:54352111
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1126+714G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352111 | ||||||
| chr6:54352169
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1126+772C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352169 | ||||||
| chr6:54352291
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0300a0003c0003t0001g0246 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+894G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352291 | ||||||
| chr6:54352635
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1126+1238A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352635 | ||||||
| chr6:54352720
|
G | GT | 6 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 7 | HG02258.hp1 HG03471.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126+1333dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 54352720 | |||||
| chr6:54352780
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1126+1383A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352780 | ||||||
| chr6:54352949
|
G | A | 3 | a0001c0001t0001g0247a0014c0015t0001g0297a0014c0015t0001g0298 | 3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1126+1552G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352949 | ||||||
| chr6:54352989
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1127-1524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352989 | ||||||
| chr6:54353014
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | NA18959.hp2 NA19064.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1127-1499G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353014 | ||||||
| chr6:54353170
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127-1343C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353170 | ||||||
| chr6:54353246
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1127-1267A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353246 | ||||||
| chr6:54353373
|
C | T | 1 | a0007c0006t0001g0189 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1127-1140C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353373 | ||||||
| chr6:54353526
|
A | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1127-987A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353526 | ||||||
| chr6:54353602
|
G | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1127-911G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353602 | ||||||
| chr6:54353634
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1127-879A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353634 | ||||||
| chr6:54353673
|
T | C | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1127-840T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353673 | ||||||
| chr6:54353755
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127-758T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353755 | ||||||
| chr6:54353776
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1127-737G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353776 | ||||||
| chr6:54353863
|
C | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1127-650C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353863 | ||||||
| chr6:54353877
|
G | C | 7 | a0003c0003t0001g0014a0003c0003t0001g0015a0003c0003t0001g0016others(4): Show | 7 | HG00621.hp1 HG02056.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127-636G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353877 | ||||||
| chr6:54354111
|
A | C | 1 | a0011c0013t0001g0360 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1127-402A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354111 | ||||||
| chr6:54354117
|
A | G | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1127-396A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354117 | ||||||
| chr6:54354270
|
G | A | 5 | a0007c0006t0002g0279a0008c0008t0002g0079a0008c0008t0002g0171others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-243G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354270 | ||||||
| chr6:54354385
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1127-128A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354385 | ||||||
| chr6:54354492
|
T | C | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1127-21T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354492 | ||||||
| chr6:54354716
|
A | C | 1 | a0006c0007t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1250+80A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354716 | ||||||
| chr6:54354757
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+121T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354757 | ||||||
| chr6:54354823
|
G | T | 4 | a0003c0003t0001g0068a0003c0003t0001g0069a0003c0003t0001g0070others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+187G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354823 | ||||||
| chr6:54354958
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0176others(7): Show | 12 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1250+322G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354958 | ||||||
| chr6:54354972
|
G | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+336G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354972 | ||||||
| chr6:54355263
|
T | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+627T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355263 | ||||||
| chr6:54355352
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1250+716A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355352 | ||||||
| chr6:54355385
|
A | G | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+749A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355385 | ||||||
| chr6:54355397
|
T | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(74): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1250+761T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355397 | ||||||
| chr6:54355398
|
G | T | 29 | a0002c0002t0001g0006a0002c0002t0001g0108a0002c0002t0001g0111others(26): Show | 30 | HG02056.hp2 HG03831.hp1 NA18612.hp2 others(27): Show |
intron_variant | MODIFIER | c.1250+762G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355398 | ||||||
| chr6:54355445
|
C | T | 63 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(60): Show | 65 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(62): Show |
intron_variant | MODIFIER | c.1250+809C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355445 | ||||||
| chr6:54355448
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+812A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355448 | ||||||
| chr6:54355466
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+830T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355466 | ||||||
| chr6:54355500
|
C | G | 1 | a0001c0001t0001g0007 | 2 | NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1250+864C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355500 | ||||||
| chr6:54355522
|
G | A | 8 | a0001c0001t0001g0262a0006c0007t0001g0225a0006c0007t0001g0226others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+886G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355522 | ||||||
| chr6:54355597
|
A | G | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+961A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355597 | ||||||
| chr6:54355617
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+981G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355617 | ||||||
| chr6:54355714
|
C | CGT | 14 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0139others(11): Show | 14 | HG01496.hp1 HG01515.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250+1109_1250+111 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
C | CGTGT | 26 | a0001c0001t0001g0105a0001c0001t0001g0123a0001c0001t0001g0129others(23): Show | 26 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1250+1107_1250+111 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
C | CGTGTGT | 58 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0077others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1250+1105_1250+111 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
C | CGTGTGTG others(1): Show |
11 | a0001c0001t0001g0038a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 11 | HG01261.hp2 HG01934.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1250+1103_1250+111 others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
C | CGTGTGTG others(3): Show |
7 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+1101_1250+111 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
CGT | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0100a0001c0001t0001g0162others(84): Show | 90 | HG00438.hp2 HG00642.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1250+1109_1250+111 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
CGTGT | C | 5 | a0001c0010t0001g0244a0001c0010t0001g0312a0002c0002t0001g0264others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+1107_1250+111 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355714
|
CGTGTGTG others(5): Show |
C | 1 | a0002c0002t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1250+1099_1250+111 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | |||||
| chr6:54355764
|
C | T | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+1128C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355764 | ||||||
| chr6:54355765
|
C | T | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+1129C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355765 | ||||||
| chr6:54355897
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1261T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355897 | ||||||
| chr6:54355915
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+1279T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355915 | ||||||
| chr6:54355937
|
T | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+1301T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355937 | ||||||
| chr6:54356261
|
G | T | 5 | a0007c0006t0002g0279a0008c0008t0002g0079a0008c0008t0002g0171others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+1625G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356261 | ||||||
| chr6:54356306
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1250+1670G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356306 | ||||||
| chr6:54356307
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250+1671A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356307 | ||||||
| chr6:54356420
|
C | G | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+1784C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356420 | ||||||
| chr6:54356432
|
G | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+1796G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356432 | ||||||
| chr6:54356435
|
G | A | 2 | a0010c0009t0001g0211a0010c0009t0001g0212 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1250+1799G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356435 | ||||||
| chr6:54356527
|
A | T | 30 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+1891A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356527 | ||||||
| chr6:54356657
|
A | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+2021A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356657 | ||||||
| chr6:54356674
|
G | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+2038G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356674 | ||||||
| chr6:54356687
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(48): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1250+2051G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356687 | ||||||
| chr6:54356847
|
T | C | 1 | a0004c0004t0001g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1250+2211T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356847 | ||||||
| chr6:54356888
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1250+2252C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356888 | ||||||
| chr6:54356918
|
T | TA | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(263): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1250+2293dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54356918 | |||||
| chr6:54357008
|
G | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+2372G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357008 | ||||||
| chr6:54357015
|
A | G | 1 | a0003c0003t0001g0012 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1250+2379A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357015 | ||||||
| chr6:54357089
|
A | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1250+2453A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357089 | ||||||
| chr6:54357129
|
T | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+2493T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357129 | ||||||
| chr6:54357311
|
G | T | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+2675G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357311 | ||||||
| chr6:54357616
|
C | G | 1 | a0005c0005t0001g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1250+2980C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357616 | ||||||
| chr6:54357670
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+3034G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357670 | ||||||
| chr6:54357834
|
G | A | 2 | a0007c0006t0001g0138a0007c0006t0001g0249 | 2 | HG00140.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1250+3198G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357834 | ||||||
| chr6:54357955
|
G | A | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+3319G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357955 | ||||||
| chr6:54358059
|
G | A | 1 | a0003c0003t0001g0023 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1250+3423G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358059 | ||||||
| chr6:54358126
|
T | G | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+3490T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358126 | ||||||
| chr6:54358156
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+3520G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358156 | ||||||
| chr6:54358218
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1250+3582C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358218 | ||||||
| chr6:54358340
|
C | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+3704C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358340 | ||||||
| chr6:54358534
|
C | CA | 92 | a0001c0001t0001g0077a0001c0001t0001g0156a0001c0001t0001g0158others(89): Show | 94 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.1250+3915dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | |||||
| chr6:54358534
|
C | CAAA | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(7): Show | 11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1250+3913_1250+391 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | |||||
| chr6:54358534
|
CA | C | 33 | a0001c0001t0001g0119a0001c0001t0001g0199a0001c0001t0001g0232others(30): Show | 35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1250+3915delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | |||||
| chr6:54358578
|
C | T | 1 | a0003c0003t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1250+3942C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358578 | ||||||
| chr6:54358654
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1250+4018C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358654 | ||||||
| chr6:54358702
|
A | C | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0270 | 3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1250+4066A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358702 | ||||||
| chr6:54358729
|
G | T | 3 | a0004c0004t0001g0001a0004c0004t0001g0202a0004c0004t0001g0205 | 5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+4093G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358729 | ||||||
| chr6:54358796
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+4160T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358796 | ||||||
| chr6:54358801
|
A | G | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+4165A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358801 | ||||||
| chr6:54358858
|
G | C | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+4222G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358858 | ||||||
| chr6:54358867
|
T | C | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1250+4231T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358867 | ||||||
| chr6:54359067
|
G | T | 30 | a0002c0002t0001g0006a0002c0002t0001g0108a0002c0002t0001g0111others(27): Show | 31 | HG02056.hp2 HG02523.hp1 HG03831.hp1 others(28): Show |
intron_variant | MODIFIER | c.1250+4431G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359067 | ||||||
| chr6:54359415
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+4779C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359415 | ||||||
| chr6:54359451
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1250+4815C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359451 | ||||||
| chr6:54359969
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1250+5333G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359969 | ||||||
| chr6:54360056
|
AAGG | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+5425_1250+542 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360056 | |||||
| chr6:54360079
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1250+5443C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360079 | ||||||
| chr6:54360162
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+5526A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360162 | ||||||
| chr6:54360169
|
T | G | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+5533T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360169 | ||||||
| chr6:54360211
|
A | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1250+5575A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360211 | ||||||
| chr6:54360233
|
T | TC | 37 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(34): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+5603dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360233 | |||||
| chr6:54360294
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+5658G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360294 | ||||||
| chr6:54360435
|
A | C | 3 | a0004c0004t0001g0001a0004c0004t0001g0202a0004c0004t0001g0205 | 5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+5799A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360435 | ||||||
| chr6:54360566
|
AT | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0218 | 3 | NA19012.hp1 NA19080.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1250+5932delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360566 | |||||
| chr6:54360609
|
T | C | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+5973T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360609 | ||||||
| chr6:54360708
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+6072C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360708 | ||||||
| chr6:54360754
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1250+6118C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360754 | ||||||
| chr6:54360839
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6204_1250+620 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360839 | |||||
| chr6:54360841
|
G | GT | 30 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0001g0126others(27): Show | 30 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1250+6236dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTT | 9 | a0001c0001t0001g0121a0001c0001t0001g0174a0001c0001t0001g0181others(6): Show | 9 | HG00741.hp2 HG01109.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1250+6235_1250+623 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0192a0001c0001t0001g0262a0002c0002t0001g0347 | 3 | HG01993.hp2 HG02109.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1250+6227_1250+623 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(4): Show |
11 | a0002c0002t0001g0006a0002c0002t0001g0108a0002c0002t0001g0310others(8): Show | 12 | HG02056.hp2 NA18945.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1250+6226_1250+623 others(15): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(5): Show |
19 | a0001c0001t0001g0311a0002c0002t0001g0141a0002c0002t0001g0142others(16): Show | 19 | HG02523.hp1 HG03540.hp2 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.1250+6225_1250+623 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(6): Show |
7 | a0001c0001t0001g0105a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG01934.hp1 HG02451.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250+6224_1250+623 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(7): Show |
14 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0119others(11): Show | 15 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250+6223_1250+623 others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(8): Show |
14 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0104others(11): Show | 15 | HG00438.hp1 HG00738.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250+6222_1250+623 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(9): Show |
8 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0306others(5): Show | 8 | HG02109.hp1 HG02698.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1250+6221_1250+623 others(20): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(10): Show |
4 | a0002c0002t0001g0309a0002c0002t0001g0314a0002c0002t0001g0326others(1): Show | 4 | HG03654.hp1 HG03669.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+6220_1250+623 others(21): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(11): Show |
14 | a0001c0001t0001g0089a0001c0001t0001g0154a0001c0001t0001g0198others(11): Show | 15 | HG01433.hp1 HG02165.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250+6219_1250+623 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(12): Show |
14 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0110others(11): Show | 14 | HG00280.hp2 HG00642.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250+6218_1250+623 others(23): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(13): Show |
13 | a0001c0001t0001g0099a0001c0001t0001g0123a0001c0001t0001g0127others(10): Show | 13 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1250+6217_1250+623 others(24): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(14): Show |
6 | a0001c0001t0001g0096a0001c0001t0001g0128a0001c0001t0001g0302others(3): Show | 6 | HG01258.hp1 HG02300.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+6216_1250+623 others(25): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(15): Show |
6 | a0001c0001t0001g0114a0001c0001t0001g0153a0001c0001t0001g0272others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+6215_1250+623 others(26): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(16): Show |
2 | a0001c0001t0001g0271a0002c0002t0001g0270 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1250+6214_1250+623 others(27): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(17): Show |
1 | a0006c0007t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1250+6213_1250+623 others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(18): Show |
1 | a0021c0020t0001g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1250+6212_1250+623 others(29): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | GTTTTTTT others(20): Show |
1 | a0006c0007t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1250+6210_1250+623 others(31): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
G | T | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6205G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360841 | ||||||
| chr6:54360841
|
GT | G | 32 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0095others(29): Show | 33 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1250+6236delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTT | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(45): Show | 49 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1250+6235_1250+623 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTT | G | 17 | a0001c0001t0001g0319a0003c0003t0001g0067a0004c0004t0001g0001others(14): Show | 19 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1250+6234_1250+623 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0146a0015c0014t0003g0283a0015c0014t0003g0284 | 3 | HG01192.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+6227_1250+623 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0001g0077a0020c0019t0001g0085 | 2 | HG02071.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1250+6225_1250+623 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(5): Show | 9 | HG02027.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+6224_1250+623 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0124 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1250+6222_1250+623 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360841
|
GTTTTTTT others(11): Show |
G | 7 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0010t0001g0244others(4): Show | 7 | HG02258.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+6219_1250+623 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | |||||
| chr6:54360852
|
T | A | 2 | a0005c0005t0001g0291a0024c0025t0001g0292 | 2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1250+6216T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360852 | ||||||
| chr6:54360861
|
T | A | 2 | a0005c0005t0001g0291a0024c0025t0001g0292 | 2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1250+6225T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360861 | ||||||
| chr6:54360872
|
T | TTTTTTTT others(10): Show |
1 | a0002c0002t0001g0248 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1250+6236_1250+623 others(21): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360872 | ||||||
| chr6:54361146
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1250+6510C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361146 | ||||||
| chr6:54361159
|
C | T | 1 | a0003c0003t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1250+6523C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361159 | ||||||
| chr6:54361369
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0198 | 3 | HG01261.hp2 HG02683.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1250+6733A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361369 | ||||||
| chr6:54361475
|
AC | A | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+6840delC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361475 | ||||||
| chr6:54361515
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+6879A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361515 | ||||||
| chr6:54361541
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+6905C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361541 | ||||||
| chr6:54361542
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(50): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1250+6906T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361542 | ||||||
| chr6:54361566
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6930G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361566 | ||||||
| chr6:54361623
|
G | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+6987G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361623 | ||||||
| chr6:54361801
|
A | T | 1 | a0001c0001t0001g0306 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1250+7165A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361801 | ||||||
| chr6:54361806
|
A | G | 8 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+7170A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361806 | ||||||
| chr6:54362009
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1250+7373T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362009 | ||||||
| chr6:54362017
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1250+7381T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362017 | ||||||
| chr6:54362120
|
G | T | 1 | a0003c0003t0001g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1250+7484G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362120 | ||||||
| chr6:54362169
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+7533G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362169 | ||||||
| chr6:54362174
|
A | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+7538A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362174 | ||||||
| chr6:54362229
|
T | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+7593T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362229 | ||||||
| chr6:54362342
|
G | C | 77 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(74): Show | 79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1250+7706G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362342 | ||||||
| chr6:54362365
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+7729T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362365 | ||||||
| chr6:54362624
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1250+7988T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362624 | ||||||
| chr6:54362786
|
G | A | 77 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(74): Show | 79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1250+8150G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362786 | ||||||
| chr6:54362805
|
G | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(74): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1250+8169G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362805 | ||||||
| chr6:54362822
|
A | G | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+8186A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362822 | ||||||
| chr6:54362856
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1250+8220C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362856 | ||||||
| chr6:54362863
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1250+8227T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362863 | ||||||
| chr6:54362893
|
G | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+8257G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362893 | ||||||
| chr6:54363051
|
C | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+8415C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363051 | ||||||
| chr6:54363123
|
G | C | 1 | a0002c0002t0001g0248 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1250+8487G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363123 | ||||||
| chr6:54363129
|
A | T | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1250+8493A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363129 | ||||||
| chr6:54363193
|
T | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(43): Show | 50 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1250+8557T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363193 | ||||||
| chr6:54363354
|
T | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(43): Show | 50 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1250+8718T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363354 | ||||||
| chr6:54363364
|
G | C | 2 | a0001c0001t0001g0245a0009c0018t0001g0222 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1250+8728G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363364 | ||||||
| chr6:54363451
|
A | C | 2 | a0002c0002t0001g0356a0002c0002t0001g0357 | 2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1250+8815A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363451 | ||||||
| chr6:54363482
|
G | A | 1 | a0005c0005t0001g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1250+8846G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363482 | ||||||
| chr6:54363493
|
G | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+8857G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363493 | ||||||
| chr6:54363533
|
T | C | 6 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(3): Show | 6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+8897T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363533 | ||||||
| chr6:54363540
|
C | A | 1 | a0002c0002t0001g0324 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1250+8904C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363540 | ||||||
| chr6:54363548
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+8912T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363548 | ||||||
| chr6:54363612
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1250+8976C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363612 | ||||||
| chr6:54363615
|
G | A | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(211): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1250+8979G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363615 | ||||||
| chr6:54363619
|
C | CA | 94 | a0001c0001t0001g0077a0001c0001t0001g0125a0001c0001t0001g0147others(91): Show | 96 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1250+8999dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54363619 | |||||
| chr6:54363619
|
CA | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(56): Show | 63 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1250+8999delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54363619 | |||||
| chr6:54363664
|
G | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+9028G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363664 | ||||||
| chr6:54363710
|
C | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+9074C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363710 | ||||||
| chr6:54363832
|
C | T | 2 | a0004c0004t0001g0080a0004c0004t0001g0206 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1250+9196C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363832 | ||||||
| chr6:54364044
|
G | A | 2 | a0002c0002t0001g0362a0013c0012t0001g0073 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1250+9408G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364044 | ||||||
| chr6:54364044
|
G | T | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+9408G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364044 | ||||||
| chr6:54364125
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(211): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1250+9489A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364125 | ||||||
| chr6:54364493
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0150 | 2 | HG01261.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1250+9857A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364493 | ||||||
| chr6:54364585
|
T | C | 1 | a0012c0011t0001g0060 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1250+9949T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364585 | ||||||
| chr6:54364724
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1250+10088C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364724 | ||||||
| chr6:54364726
|
A | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA18612.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1250+10090A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364726 | ||||||
| chr6:54364769
|
T | G | 1 | a0002c0002t0001g0347 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10133T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364769 | ||||||
| chr6:54364771
|
T | G | 1 | a0002c0002t0001g0347 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10135T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364771 | ||||||
| chr6:54364772
|
C | A | 1 | a0002c0002t0001g0347 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10136C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364772 | ||||||
| chr6:54365051
|
TTCATGCT others(3): Show |
T | 1 | a0006c0007t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1250+10417_1250+10 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54365051 | |||||
| chr6:54365086
|
A | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1250+10450A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365086 | ||||||
| chr6:54365160
|
C | T | 1 | a0007c0006t0002g0279 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1250+10524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365160 | ||||||
| chr6:54365206
|
A | G | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+10570A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365206 | ||||||
| chr6:54365250
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1250+10614C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365250 | ||||||
| chr6:54365383
|
C | T | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+10747C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365383 | ||||||
| chr6:54365418
|
G | A | 4 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(1): Show | 4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+10782G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365418 | ||||||
| chr6:54365479
|
T | C | 1 | a0003c0003t0001g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1250+10843T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365479 | ||||||
| chr6:54365495
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+10859G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365495 | ||||||
| chr6:54365516
|
C | T | 4 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+10880C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365516 | ||||||
| chr6:54365554
|
C | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+10918C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365554 | ||||||
| chr6:54365724
|
T | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(34): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11088T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365724 | ||||||
| chr6:54365766
|
T | G | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1250+11130T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365766 | ||||||
| chr6:54365833
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1250+11197G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365833 | ||||||
| chr6:54365844
|
C | A | 1 | a0004c0004t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1250+11208C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365844 | ||||||
| chr6:54365861
|
T | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+11225T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365861 | ||||||
| chr6:54365905
|
C | A | 1 | a0017c0017t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1250+11269C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365905 | ||||||
| chr6:54365905
|
C | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+11269C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365905 | ||||||
| chr6:54365982
|
T | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+11346T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365982 | ||||||
| chr6:54366091
|
A | T | 37 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(34): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11455A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366091 | ||||||
| chr6:54366138
|
A | C | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+11502A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366138 | ||||||
| chr6:54366246
|
G | T | 37 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177others(34): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11610G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366246 | ||||||
| chr6:54366254
|
A | ATG | 122 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(119): Show | 127 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1250+11641_1250+11 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54366254 | |||||
| chr6:54366254
|
A | ATGTG | 5 | a0001c0001t0001g0313a0002c0002t0001g0187a0002c0002t0001g0330others(2): Show | 5 | HG00735.hp2 HG02145.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+11639_1250+11 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54366254 | |||||
| chr6:54366288
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+11652G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366288 | ||||||
| chr6:54366520
|
C | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0300 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1250+11884C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366520 | ||||||
| chr6:54366690
|
G | A | 66 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(63): Show | 68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1250+12054G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366690 | ||||||
| chr6:54366759
|
A | G | 1 | a0003c0003t0001g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1250+12123A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366759 | ||||||
| chr6:54366773
|
G | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+12137G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366773 | ||||||
| chr6:54366891
|
G | A | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+12255G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366891 | ||||||
| chr6:54366956
|
A | C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1250+12320A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366956 | ||||||
| chr6:54367073
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+12437A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367073 | ||||||
| chr6:54367206
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1250+12570C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367206 | ||||||
| chr6:54367214
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1250+12578A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367214 | ||||||
| chr6:54367240
|
T | C | 1 | a0012c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1250+12604T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367240 | ||||||
| chr6:54367406
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+12770A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367406 | ||||||
| chr6:54367406
|
A | G | 8 | a0001c0001t0001g0078a0001c0001t0001g0119a0001c0001t0001g0120others(5): Show | 8 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+12770A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367406 | ||||||
| chr6:54367440
|
G | T | 64 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(61): Show | 66 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(63): Show |
intron_variant | MODIFIER | c.1250+12804G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367440 | ||||||
| chr6:54367453
|
G | A | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1250+12817G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367453 | ||||||
| chr6:54367597
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-12929G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367597 | ||||||
| chr6:54367873
|
G | A | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-12653G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367873 | ||||||
| chr6:54367905
|
G | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0315 | 3 | NA18955.hp2 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1251-12621G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367905 | ||||||
| chr6:54368020
|
A | G | 4 | a0006c0007t0001g0225a0006c0007t0001g0229a0006c0007t0001g0230others(1): Show | 4 | HG01884.hp1 HG01891.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-12506A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368020 | ||||||
| chr6:54368049
|
G | A | 29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-12477G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368049 | ||||||
| chr6:54368080
|
G | A | 4 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(1): Show | 4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-12446G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368080 | ||||||
| chr6:54368112
|
TA | T | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251-12411delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54368112 | |||||
| chr6:54368330
|
A | T | 3 | a0003c0003t0001g0074a0003c0003t0001g0075a0005c0005t0001g0296 | 3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1251-12196A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368330 | ||||||
| chr6:54368359
|
A | C | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-12167A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368359 | ||||||
| chr6:54368464
|
T | C | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-12062T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368464 | ||||||
| chr6:54368605
|
T | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-11921T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368605 | ||||||
| chr6:54368739
|
TA | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-11781delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54368739 | |||||
| chr6:54368755
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1251-11771A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368755 | ||||||
| chr6:54368960
|
A | G | 2 | a0017c0017t0001g0277a0017c0017t0001g0278 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251-11566A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368960 | ||||||
| chr6:54368975
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-11551T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368975 | ||||||
| chr6:54369055
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-11471G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369055 | ||||||
| chr6:54369093
|
G | T | 1 | a0002c0002t0001g0314 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1251-11433G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369093 | ||||||
| chr6:54369105
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1251-11421T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369105 | ||||||
| chr6:54369311
|
A | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-11215A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369311 | ||||||
| chr6:54369532
|
T | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-10994T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369532 | ||||||
| chr6:54369606
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(49): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1251-10920C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369606 | ||||||
| chr6:54369656
|
C | A | 4 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(1): Show | 4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-10870C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369656 | ||||||
| chr6:54369676
|
A | G | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0280others(8): Show | 11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251-10850A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369676 | ||||||
| chr6:54369780
|
A | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-10746A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369780 | ||||||
| chr6:54369815
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1251-10711A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369815 | ||||||
| chr6:54369833
|
T | C | 1 | a0006c0007t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-10693T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369833 | ||||||
| chr6:54370071
|
T | C | 9 | a0001c0001t0001g0271a0001c0001t0001g0272a0006c0007t0001g0225others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-10455T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370071 | ||||||
| chr6:54370086
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10440A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370086 | ||||||
| chr6:54370131
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0132others(4): Show | 8 | HG02083.hp2 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1251-10395G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370131 | ||||||
| chr6:54370193
|
A | G | 6 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(3): Show | 6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-10333A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370193 | ||||||
| chr6:54370544
|
A | G | 6 | a0001c0001t0001g0247a0003c0003t0001g0246a0014c0015t0001g0297others(3): Show | 6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-9982A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370544 | ||||||
| chr6:54370738
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-9788G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370738 | ||||||
| chr6:54370819
|
T | C | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9707T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370819 | ||||||
| chr6:54370847
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG00558.hp2 NA18980.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1251-9679A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370847 | ||||||
| chr6:54370883
|
G | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1251-9643G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370883 | ||||||
| chr6:54370983
|
G | T | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1251-9543G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370983 | ||||||
| chr6:54371024
|
C | A | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9502C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371024 | ||||||
| chr6:54371105
|
G | A | 1 | a0003c0003t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1251-9421G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371105 | ||||||
| chr6:54371110
|
C | CTG | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1251-9388_1251-938 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | |||||
| chr6:54371110
|
C | CTGTG | 17 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0119others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1251-9390_1251-938 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | |||||
| chr6:54371110
|
C | CTGTGTGT others(3): Show |
1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-9396_1251-938 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | |||||
| chr6:54371110
|
CTG | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(41): Show | 49 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1251-9388_1251-938 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | |||||
| chr6:54371110
|
CTGTG | C | 10 | a0001c0001t0001g0176a0001c0001t0001g0210a0001c0001t0001g0311others(7): Show | 10 | HG00408.hp2 HG01069.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1251-9390_1251-938 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | |||||
| chr6:54371148
|
GAGAA | G | 66 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(63): Show | 68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1251-9373_1251-937 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371148 | |||||
| chr6:54371213
|
A | T | 1 | a0003c0003t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1251-9313A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371213 | ||||||
| chr6:54371214
|
G | T | 1 | a0003c0003t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1251-9312G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371214 | ||||||
| chr6:54371224
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-9302C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371224 | ||||||
| chr6:54371271
|
G | A | 34 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9255G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371271 | ||||||
| chr6:54371304
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1251-9222C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371304 | ||||||
| chr6:54371343
|
A | C | 4 | a0001c0001t0001g0245a0001c0010t0001g0244a0001c0010t0001g0312others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-9183A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371343 | ||||||
| chr6:54371435
|
C | T | 1 | a0007c0006t0001g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1251-9091C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371435 | ||||||
| chr6:54371522
|
T | C | 1 | a0005c0005t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1251-9004T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371522 | ||||||
| chr6:54371556
|
T | C | 29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-8970T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371556 | ||||||
| chr6:54371599
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1251-8927A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371599 | ||||||
| chr6:54371599
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-8927A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371599 | ||||||
| chr6:54371641
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-8885G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371641 | ||||||
| chr6:54371684
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1251-8842G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371684 | ||||||
| chr6:54371701
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1251-8825T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371701 | ||||||
| chr6:54371981
|
G | GT | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0084others(36): Show | 41 | HG00621.hp1 HG01167.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1251-8518dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371981
|
G | GTT | 70 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1251-8519_1251-851 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371981
|
G | GTTT | 21 | a0001c0001t0001g0078a0001c0001t0001g0120a0001c0001t0001g0124others(18): Show | 21 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1251-8520_1251-851 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371981
|
GT | G | 8 | a0001c0001t0001g0135a0001c0001t0001g0232a0001c0001t0001g0300others(5): Show | 8 | HG01070.hp1 HG01167.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1251-8518delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371981
|
GTTT | G | 26 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(23): Show | 28 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1251-8520_1251-851 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371981
|
GTTTTTT | G | 72 | a0001c0001t0001g0245a0001c0001t0001g0271a0001c0001t0001g0272others(69): Show | 74 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(71): Show |
intron_variant | MODIFIER | c.1251-8523_1251-851 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | |||||
| chr6:54371986
|
T | TTTTTTTT others(14): Show |
1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-8532_1251-853 others(25): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371986 | |||||
| chr6:54371987
|
T | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-8539T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371987 | ||||||
| chr6:54371996
|
T | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-8530T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371996 | ||||||
| chr6:54372025
|
C | T | 3 | a0001c0001t0001g0245a0003c0003t0001g0246a0009c0018t0001g0222 | 3 | HG02258.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1251-8501C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372025 | ||||||
| chr6:54372145
|
C | A | 1 | a0005c0005t0001g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1251-8381C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372145 | ||||||
| chr6:54372189
|
A | C | 82 | a0001c0001t0001g0210a0001c0001t0001g0245a0001c0001t0001g0247others(79): Show | 84 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(81): Show |
intron_variant | MODIFIER | c.1251-8337A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372189 | ||||||
| chr6:54372239
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-8287A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372239 | ||||||
| chr6:54372268
|
A | G | 1 | a0003c0003t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1251-8258A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372268 | ||||||
| chr6:54372284
|
G | A | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-8242G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372284 | ||||||
| chr6:54372641
|
G | A | 77 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(74): Show | 79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1251-7885G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372641 | ||||||
| chr6:54372668
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(214): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1251-7858C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372668 | ||||||
| chr6:54372696
|
C | T | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-7830C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372696 | ||||||
| chr6:54372697
|
G | A | 2 | a0003c0003t0001g0039a0003c0003t0001g0057 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-7829G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372697 | ||||||
| chr6:54372723
|
CATACATA others(27): Show |
C | 16 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0301others(13): Show | 16 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251-7799_1251-776 others(38): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372723 | |||||
| chr6:54372727
|
C | CAT | 12 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0163others(9): Show | 12 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-7755_1251-775 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
C | CATAT | 7 | a0001c0001t0001g0167a0003c0003t0001g0027a0003c0003t0001g0029others(4): Show | 7 | HG00639.hp1 HG01255.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-7757_1251-775 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
C | CATATAT | 6 | a0001c0001t0001g0180a0001c0001t0001g0181a0003c0003t0001g0020others(3): Show | 6 | HG00741.hp2 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-7759_1251-775 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
C | CATATATA others(3): Show |
1 | a0003c0003t0001g0011 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1251-7763_1251-775 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CAT | C | 18 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0134others(15): Show | 18 | HG00642.hp1 HG01109.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1251-7755_1251-775 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATAT | C | 5 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01993.hp1 HG02080.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-7757_1251-775 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(3): Show |
C | 7 | a0001c0001t0001g0107a0001c0001t0001g0162a0001c0001t0001g0217others(4): Show | 7 | HG02027.hp2 HG02257.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-7763_1251-775 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(5): Show |
C | 14 | a0001c0001t0001g0076a0001c0001t0001g0176a0001c0001t0001g0177others(11): Show | 14 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-7765_1251-775 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(7): Show |
C | 12 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(9): Show | 14 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1251-7767_1251-775 others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(9): Show |
C | 11 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0210others(8): Show | 11 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1251-7769_1251-775 others(20): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(11): Show |
C | 107 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(104): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1251-7771_1251-775 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(13): Show |
C | 6 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0251others(3): Show | 6 | HG01261.hp2 HG02109.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-7773_1251-775 others(24): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(15): Show |
C | 77 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(74): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1251-7775_1251-775 others(26): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(17): Show |
C | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-7777_1251-775 others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372727
|
CATATATA others(21): Show |
C | 1 | a0001c0001t0001g0198 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1251-7781_1251-775 others(32): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | |||||
| chr6:54372730
|
ATATATAT others(8): Show |
A | 1 | a0003c0003t0001g0059 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1251-7795_1251-778 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372730 | ||||||
| chr6:54372731
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1251-7795T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372731 | ||||||
| chr6:54372733
|
T | C | 1 | a0003c0003t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1251-7793T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372733 | ||||||
| chr6:54372747
|
TATATATA others(8): Show |
T | 1 | a0003c0003t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1251-7778_1251-776 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372747 | ||||||
| chr6:54372749
|
TATATATA others(6): Show |
T | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0003c0003t0001g0068others(1): Show | 4 | HG02818.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-7776_1251-776 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372749 | ||||||
| chr6:54372751
|
TATATATA others(4): Show |
T | 5 | a0003c0003t0001g0070a0003c0003t0001g0072a0003c0003t0001g0074others(2): Show | 5 | HG02280.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-7774_1251-776 others(15): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372751 | ||||||
| chr6:54372761
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-7765T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372761 | ||||||
| chr6:54372763
|
T | C | 38 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0210others(35): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1251-7763T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372763 | ||||||
| chr6:54372765
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(131): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7761T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372765 | ||||||
| chr6:54372767
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(131): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7759T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372767 | ||||||
| chr6:54372769
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(131): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7757T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372769 | ||||||
| chr6:54372771
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(132): Show | 141 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1251-7755T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372771 | ||||||
| chr6:54372778
|
A | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(131): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7748A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372778 | ||||||
| chr6:54372854
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1251-7672T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372854 | ||||||
| chr6:54372920
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1251-7606A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372920 | ||||||
| chr6:54372946
|
TA | T | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(3): Show | 6 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-7575delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372946 | |||||
| chr6:54373035
|
G | A | 78 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(75): Show | 80 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.1251-7491G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373035 | ||||||
| chr6:54373052
|
C | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(9): Show | 14 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-7474C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373052 | ||||||
| chr6:54373210
|
T | TTTA | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(214): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1251-7315_1251-731 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54373210 | |||||
| chr6:54373395
|
C | T | 1 | a0004c0004t0001g0204 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1251-7131C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373395 | ||||||
| chr6:54373415
|
A | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG02027.hp1 HG02074.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1251-7111A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373415 | ||||||
| chr6:54373620
|
C | T | 1 | a0002c0002t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1251-6906C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373620 | ||||||
| chr6:54373724
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1251-6802C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373724 | ||||||
| chr6:54373765
|
A | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-6761A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373765 | ||||||
| chr6:54373893
|
C | G | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-6633C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373893 | ||||||
| chr6:54374053
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1251-6473T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374053 | ||||||
| chr6:54374064
|
T | C | 31 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(28): Show | 33 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1251-6462T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374064 | ||||||
| chr6:54374110
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-6416T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374110 | ||||||
| chr6:54374129
|
T | C | 1 | a0003c0003t0001g0044 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1251-6397T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374129 | ||||||
| chr6:54374171
|
T | C | 1 | a0011c0013t0001g0360 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1251-6355T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374171 | ||||||
| chr6:54374215
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-6311C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374215 | ||||||
| chr6:54374257
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(88): Show | 95 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(92): Show |
intron_variant | MODIFIER | c.1251-6269T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374257 | ||||||
| chr6:54374334
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1251-6192G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374334 | ||||||
| chr6:54374348
|
A | G | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-6178A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374348 | ||||||
| chr6:54374365
|
C | A | 3 | a0004c0004t0001g0001a0004c0004t0001g0202a0004c0004t0001g0205 | 5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-6161C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374365 | ||||||
| chr6:54374411
|
T | C | 36 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0210others(33): Show | 38 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1251-6115T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374411 | ||||||
| chr6:54374452
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(88): Show | 95 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(92): Show |
intron_variant | MODIFIER | c.1251-6074G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374452 | ||||||
| chr6:54374507
|
C | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(9): Show | 14 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-6019C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374507 | ||||||
| chr6:54374711
|
T | C | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-5815T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374711 | ||||||
| chr6:54374904
|
G | GT | 9 | a0001c0001t0001g0271a0001c0001t0001g0272a0006c0007t0001g0225others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-5614dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54374904 | |||||
| chr6:54374987
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1251-5539G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374987 | ||||||
| chr6:54375032
|
A | G | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-5494A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375032 | ||||||
| chr6:54375250
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(214): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1251-5276C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375250 | ||||||
| chr6:54375267
|
G | A | 1 | a0004c0004t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1251-5259G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375267 | ||||||
| chr6:54375383
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1251-5143G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375383 | ||||||
| chr6:54375493
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1251-5033T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375493 | ||||||
| chr6:54375555
|
A | G | 2 | a0003c0003t0001g0039a0003c0003t0001g0057 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-4971A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375555 | ||||||
| chr6:54375571
|
C | T | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-4955C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375571 | ||||||
| chr6:54375843
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1251-4683T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375843 | ||||||
| chr6:54375878
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1251-4648C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375878 | ||||||
| chr6:54375907
|
G | T | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-4619G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375907 | ||||||
| chr6:54375918
|
C | T | 2 | a0002c0002t0001g0242a0002c0002t0001g0358 | 2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1251-4608C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375918 | ||||||
| chr6:54375936
|
C | T | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-4590C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375936 | ||||||
| chr6:54375974
|
C | T | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1251-4552C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375974 | ||||||
| chr6:54376017
|
A | G | 2 | a0003c0003t0001g0039a0003c0003t0001g0057 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-4509A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376017 | ||||||
| chr6:54376112
|
T | C | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-4414T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376112 | ||||||
| chr6:54376245
|
A | G | 6 | a0002c0002t0001g0006a0002c0002t0001g0141a0002c0002t0001g0329others(3): Show | 7 | NA18951.hp2 NA18963.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-4281A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376245 | ||||||
| chr6:54376317
|
A | G | 4 | a0001c0010t0001g0244a0001c0010t0001g0312a0015c0014t0003g0283others(1): Show | 4 | HG02647.hp2 HG02970.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-4209A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376317 | ||||||
| chr6:54376565
|
T | C | 2 | a0008c0008t0002g0171a0008c0008t0002g0172 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1251-3961T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376565 | ||||||
| chr6:54376688
|
A | T | 2 | a0001c0001t0001g0247a0009c0018t0001g0260 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1251-3838A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376688 | ||||||
| chr6:54376751
|
C | T | 2 | a0001c0001t0001g0245a0009c0018t0001g0222 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1251-3775C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376751 | ||||||
| chr6:54376786
|
G | T | 2 | a0001c0001t0001g0247a0009c0018t0001g0260 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1251-3740G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376786 | ||||||
| chr6:54376795
|
T | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(80): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-3731T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376795 | ||||||
| chr6:54376831
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252 | 3 | HG02258.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1251-3695A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376831 | ||||||
| chr6:54376883
|
T | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-3643T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376883 | ||||||
| chr6:54376955
|
G | A | 4 | a0003c0003t0001g0072a0003c0003t0001g0074a0003c0003t0001g0075others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-3571G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376955 | ||||||
| chr6:54376985
|
C | T | 1 | a0003c0003t0001g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1251-3541C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376985 | ||||||
| chr6:54377117
|
T | C | 29 | a0004c0004t0001g0001a0004c0004t0001g0080a0004c0004t0001g0102others(26): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-3409T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377117 | ||||||
| chr6:54377373
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(127): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1251-3153A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377373 | ||||||
| chr6:54377387
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1251-3139T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377387 | ||||||
| chr6:54377443
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1251-3083C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377443 | ||||||
| chr6:54377454
|
A | G | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1251-3072A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377454 | ||||||
| chr6:54377513
|
G | GAAAT | 48 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0252others(45): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-2994_1251-299 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54377513 | |||||
| chr6:54377531
|
A | T | 1 | a0002c0002t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1251-2995A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377531 | ||||||
| chr6:54377661
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-2865A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377661 | ||||||
| chr6:54377702
|
A | G | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-2824A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377702 | ||||||
| chr6:54377883
|
T | C | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-2643T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377883 | ||||||
| chr6:54377947
|
G | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0275others(1): Show | 4 | HG02572.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-2579G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377947 | ||||||
| chr6:54377967
|
A | AT | 6 | a0001c0001t0001g0038a0001c0001t0001g0110a0001c0001t0001g0306others(3): Show | 6 | HG02647.hp2 HG03831.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-2549dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54377967 | |||||
| chr6:54378107
|
T | C | 1 | a0006c0007t0001g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1251-2419T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378107 | ||||||
| chr6:54378226
|
T | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0281 | 3 | HG02622.hp1 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1251-2300T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378226 | ||||||
| chr6:54378233
|
A | T | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-2293A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378233 | ||||||
| chr6:54378253
|
T | C | 1 | a0006c0007t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1251-2273T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378253 | ||||||
| chr6:54378354
|
G | A | 4 | a0002c0002t0001g0345a0002c0002t0001g0349a0002c0002t0001g0350others(1): Show | 4 | NA18939.hp1 NA18988.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-2172G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378354 | ||||||
| chr6:54378385
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1251-2141C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378385 | ||||||
| chr6:54378429
|
A | G | 2 | a0017c0017t0001g0277a0017c0017t0001g0278 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251-2097A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378429 | ||||||
| chr6:54378443
|
T | C | 2 | a0003c0003t0001g0020a0003c0003t0001g0021 | 2 | NA18967.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1251-2083T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378443 | ||||||
| chr6:54378604
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(82): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1251-1922G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378604 | ||||||
| chr6:54378607
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1251-1919C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378607 | ||||||
| chr6:54378817
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1251-1709C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378817 | ||||||
| chr6:54378896
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1251-1630A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378896 | ||||||
| chr6:54379123
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-1403T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379123 | ||||||
| chr6:54379200
|
A | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(86): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1251-1326A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379200 | ||||||
| chr6:54379256
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1251-1270G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379256 | ||||||
| chr6:54379330
|
A | G | 77 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(74): Show | 79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1251-1196A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379330 | ||||||
| chr6:54379394
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(85): Show | 92 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(89): Show |
intron_variant | MODIFIER | c.1251-1132A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379394 | ||||||
| chr6:54379414
|
G | A | 1 | a0002c0002t0001g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1251-1112G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379414 | ||||||
| chr6:54379516
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1251-1010C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379516 | ||||||
| chr6:54379762
|
T | A | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1251-764T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379762 | ||||||
| chr6:54379785
|
T | A | 14 | a0001c0001t0001g0107a0001c0001t0001g0162a0001c0001t0001g0217others(11): Show | 14 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-741T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379785 | ||||||
| chr6:54379829
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1251-697G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379829 | ||||||
| chr6:54379986
|
G | A | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-540G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379986 | ||||||
| chr6:54380034
|
G | A | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-492G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380034 | ||||||
| chr6:54380034
|
G | T | 1 | a0003c0003t0001g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1251-492G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380034 | ||||||
| chr6:54380167
|
C | T | 4 | a0003c0003t0001g0068a0003c0003t0001g0069a0003c0003t0001g0070others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-359C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380167 | ||||||
| chr6:54380177
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(7): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1251-349T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380177 | ||||||
| chr6:54380267
|
T | TC | 86 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(83): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1251-258dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54380267 | |||||
| chr6:54380381
|
G | A | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-145G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380381 | ||||||
| chr6:54380472
|
A | G | 15 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0301others(12): Show | 15 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1251-54A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380472 | ||||||
| chr6:54380484
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-42C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380484 | ||||||
| chr6:54380594
|
A | T | 1 | a0016c0016t0001g0259 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1296+23A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380594 | ||||||
| chr6:54380650
|
T | C | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0270 | 3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1296+79T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380650 | ||||||
| chr6:54380667
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1296+96C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380667 | ||||||
| chr6:54380705
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(87): Show | 94 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(91): Show |
intron_variant | MODIFIER | c.1296+134G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380705 | ||||||
| chr6:54380892
|
A | G | 1 | a0002c0002t0001g0344 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1296+321A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380892 | ||||||
| chr6:54380894
|
A | G | 33 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0001g0178others(30): Show | 33 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1296+323A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380894 | ||||||
| chr6:54380963
|
T | C | 3 | a0001c0001t0001g0247a0004c0021t0004g0224a0009c0018t0001g0260 | 3 | HG03516.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1296+392T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380963 | ||||||
| chr6:54380980
|
G | GAT | 23 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(20): Show | 25 | HG01884.hp1 HG01891.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1296+422_1296+423d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54380980 | |||||
| chr6:54380980
|
G | GATAT | 66 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(63): Show | 68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1296+420_1296+423d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54380980 | |||||
| chr6:54381006
|
A | G | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+435A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381006 | ||||||
| chr6:54381042
|
A | G | 1 | a0005c0005t0001g0289 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1296+471A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381042 | ||||||
| chr6:54381059
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(90): Show | 97 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(94): Show |
intron_variant | MODIFIER | c.1296+488C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381059 | ||||||
| chr6:54381094
|
G | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(95): Show | 102 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(99): Show |
intron_variant | MODIFIER | c.1296+523G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381094 | ||||||
| chr6:54381103
|
T | C | 1 | a0003c0003t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1296+532T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381103 | ||||||
| chr6:54381110
|
A | ATATGTAA others(51): Show |
1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1296+550_1296+551i others(60): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381110 | |||||
| chr6:54381122
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(129): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1296+551C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381122 | ||||||
| chr6:54381170
|
CT | C | 79 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(76): Show | 81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+609delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381170 | |||||
| chr6:54381358
|
CT | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1296+794delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381358 | |||||
| chr6:54381384
|
C | T | 1 | a0008c0008t0002g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1296+813C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381384 | ||||||
| chr6:54381408
|
A | G | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+837A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381408 | ||||||
| chr6:54381685
|
T | G | 3 | a0003c0003t0001g0018a0003c0003t0001g0019a0003c0003t0001g0035 | 3 | NA18941.hp2 NA18953.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1296+1114T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381685 | ||||||
| chr6:54381721
|
T | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+1150T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381721 | ||||||
| chr6:54381727
|
A | G | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+1156A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381727 | ||||||
| chr6:54381761
|
T | C | 1 | a0010c0009t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1296+1190T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381761 | ||||||
| chr6:54381789
|
G | A | 1 | a0011c0013t0001g0360 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1296+1218G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381789 | ||||||
| chr6:54381854
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1296+1283A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381854 | ||||||
| chr6:54381866
|
T | A | 5 | a0007c0006t0002g0279a0008c0008t0002g0079a0008c0008t0002g0171others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+1295T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381866 | ||||||
| chr6:54381867
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1296+1296C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381867 | ||||||
| chr6:54381915
|
T | A | 33 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(30): Show | 35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1296+1344T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381915 | ||||||
| chr6:54381967
|
A | T | 78 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(75): Show | 80 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.1296+1396A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381967 | ||||||
| chr6:54382025
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0305 | 3 | HG01515.hp1 HG01517.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1296+1454G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382025 | ||||||
| chr6:54382114
|
C | T | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+1543C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382114 | ||||||
| chr6:54382198
|
T | C | 1 | a0016c0016t0001g0261 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1296+1627T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382198 | ||||||
| chr6:54382254
|
T | G | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+1683T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382254 | ||||||
| chr6:54382382
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1296+1811G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382382 | ||||||
| chr6:54382482
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(7): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1296+1911A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382482 | ||||||
| chr6:54382489
|
C | T | 1 | a0002c0002t0001g0338 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1296+1918C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382489 | ||||||
| chr6:54382536
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1296+1965T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382536 | ||||||
| chr6:54382669
|
A | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(95): Show | 102 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(99): Show |
intron_variant | MODIFIER | c.1296+2098A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382669 | ||||||
| chr6:54382743
|
A | G | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+2172A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382743 | ||||||
| chr6:54382751
|
T | A | 2 | a0010c0009t0001g0211a0010c0009t0001g0212 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1296+2180T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382751 | ||||||
| chr6:54382771
|
G | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(91): Show | 98 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(95): Show |
intron_variant | MODIFIER | c.1296+2200G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382771 | ||||||
| chr6:54382886
|
G | C | 2 | a0014c0015t0001g0297a0014c0015t0001g0298 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+2315G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382886 | ||||||
| chr6:54383063
|
G | A | 1 | a0005c0005t0001g0289 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1296+2492G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383063 | ||||||
| chr6:54383157
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1296+2586A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383157 | ||||||
| chr6:54383370
|
T | C | 15 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0301others(12): Show | 15 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1296+2799T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383370 | ||||||
| chr6:54383384
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1296+2813T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383384 | ||||||
| chr6:54383416
|
A | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+2845A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383416 | ||||||
| chr6:54383504
|
C | T | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+2933C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383504 | ||||||
| chr6:54383881
|
C | G | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+3310C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383881 | ||||||
| chr6:54384001
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+3430C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384001 | ||||||
| chr6:54384009
|
A | T | 83 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(80): Show | 85 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(82): Show |
intron_variant | MODIFIER | c.1296+3438A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384009 | ||||||
| chr6:54384016
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1296+3445C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384016 | ||||||
| chr6:54384098
|
C | T | 79 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(76): Show | 81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+3527C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384098 | ||||||
| chr6:54384255
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0301 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1296+3684T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384255 | ||||||
| chr6:54384284
|
G | A | 33 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(30): Show | 35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1296+3713G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384284 | ||||||
| chr6:54384314
|
G | T | 2 | a0004c0004t0001g0202a0004c0004t0001g0205 | 2 | HG00639.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1296+3743G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384314 | ||||||
| chr6:54384417
|
G | A | 3 | a0001c0010t0001g0244a0001c0010t0001g0312a0002c0002t0001g0353 | 3 | HG02647.hp2 HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+3846G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384417 | ||||||
| chr6:54384480
|
T | C | 2 | a0001c0001t0001g0100a0005c0005t0001g0258 | 2 | HG01243.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1296+3909T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384480 | ||||||
| chr6:54384646
|
T | C | 2 | a0015c0014t0003g0283a0015c0014t0003g0284 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1296+4075T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384646 | ||||||
| chr6:54384839
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1296+4268T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384839 | ||||||
| chr6:54384871
|
A | G | 79 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(76): Show | 81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+4300A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384871 | ||||||
| chr6:54384956
|
A | G | 1 | a0003c0003t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1296+4385A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384956 | ||||||
| chr6:54385031
|
A | G | 1 | a0005c0005t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1296+4460A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385031 | ||||||
| chr6:54385056
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1296+4485A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385056 | ||||||
| chr6:54385070
|
T | C | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+4499T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385070 | ||||||
| chr6:54385226
|
G | T | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-4565G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385226 | ||||||
| chr6:54385296
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1297-4495G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385296 | ||||||
| chr6:54385359
|
T | G | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-4432T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385359 | ||||||
| chr6:54385480
|
G | GA | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1297-4301dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385480 | |||||
| chr6:54385480
|
GA | G | 46 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(43): Show | 48 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1297-4301delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385480 | |||||
| chr6:54385674
|
A | G | 2 | a0002c0002t0001g0137a0002c0002t0001g0355 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1297-4117A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385674 | ||||||
| chr6:54385704
|
G | A | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1297-4087G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385704 | ||||||
| chr6:54385778
|
A | C | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-4013A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385778 | ||||||
| chr6:54385801
|
T | C | 1 | a0018c0026t0001g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1297-3990T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385801 | ||||||
| chr6:54385879
|
A | AT | 112 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(109): Show | 116 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.1297-3887dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | |||||
| chr6:54385879
|
A | ATT | 66 | a0001c0001t0001g0002a0001c0001t0001g0083a0001c0001t0001g0094others(63): Show | 67 | HG00280.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1297-3888_1297-388 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | |||||
| chr6:54385879
|
A | ATTT | 18 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0001g0223others(15): Show | 18 | HG00642.hp2 HG01243.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.1297-3889_1297-388 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | |||||
| chr6:54385879
|
AT | A | 6 | a0001c0001t0001g0091a0001c0001t0001g0170a0001c0001t0001g0245others(3): Show | 6 | HG02258.hp1 HG03471.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297-3887delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | |||||
| chr6:54385880
|
T | A | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-3911T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385880 | ||||||
| chr6:54386040
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-3751C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386040 | ||||||
| chr6:54386063
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(97): Show | 104 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(101): Show |
intron_variant | MODIFIER | c.1297-3728C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386063 | ||||||
| chr6:54386095
|
C | T | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-3696C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386095 | ||||||
| chr6:54386103
|
C | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0110 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1297-3688C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386103 | ||||||
| chr6:54386187
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1297-3604G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386187 | ||||||
| chr6:54386264
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-3527T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386264 | ||||||
| chr6:54386358
|
A | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1297-3433A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386358 | ||||||
| chr6:54386360
|
G | C | 3 | a0003c0003t0001g0074a0003c0003t0001g0075a0005c0005t0001g0296 | 3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1297-3431G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386360 | ||||||
| chr6:54386526
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(7): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-3265C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386526 | ||||||
| chr6:54386557
|
A | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0110 | 2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1297-3234A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386557 | ||||||
| chr6:54386699
|
G | A | 1 | a0002c0002t0001g0336 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1297-3092G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386699 | ||||||
| chr6:54386719
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1297-3072C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386719 | ||||||
| chr6:54386744
|
A | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(96): Show | 103 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(100): Show |
intron_variant | MODIFIER | c.1297-3047A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386744 | ||||||
| chr6:54386748
|
C | A | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-3043C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386748 | ||||||
| chr6:54386893
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(7): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-2898T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386893 | ||||||
| chr6:54387272
|
G | T | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-2519G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387272 | ||||||
| chr6:54387323
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0301 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1297-2468G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387323 | ||||||
| chr6:54387426
|
G | T | 2 | a0010c0009t0001g0211a0010c0009t0001g0212 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1297-2365G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387426 | ||||||
| chr6:54387464
|
TA | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(91): Show | 98 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(95): Show |
intron_variant | MODIFIER | c.1297-2319delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54387464 | |||||
| chr6:54387494
|
A | G | 82 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(79): Show | 84 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(81): Show |
intron_variant | MODIFIER | c.1297-2297A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387494 | ||||||
| chr6:54387531
|
C | G | 4 | a0014c0015t0001g0297a0014c0015t0001g0298a0015c0014t0003g0283others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2260C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387531 | ||||||
| chr6:54387653
|
T | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(75): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1297-2138T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387653 | ||||||
| chr6:54387762
|
C | T | 1 | a0009c0018t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1297-2029C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387762 | ||||||
| chr6:54387800
|
A | G | 1 | a0004c0021t0004g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-1991A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387800 | ||||||
| chr6:54387918
|
T | G | 2 | a0001c0010t0001g0244a0001c0010t0001g0312 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-1873T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387918 | ||||||
| chr6:54387975
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1297-1816G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387975 | ||||||
| chr6:54388241
|
A | G | 1 | a0003c0003t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1297-1550A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388241 | ||||||
| chr6:54388283
|
C | T | 79 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0311others(76): Show | 81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1297-1508C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388283 | ||||||
| chr6:54388359
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1297-1432G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388359 | ||||||
| chr6:54388398
|
C | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(128): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1297-1393C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388398 | ||||||
| chr6:54388580
|
C | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02451.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-1211C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388580 | ||||||
| chr6:54388581
|
G | A | 9 | a0003c0003t0001g0043a0003c0003t0001g0046a0003c0003t0001g0047others(6): Show | 9 | HG00099.hp1 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1297-1210G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388581 | ||||||
| chr6:54388731
|
C | T | 2 | a0001c0001t0001g0245a0009c0018t0001g0222 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1297-1060C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388731 | ||||||
| chr6:54388821
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-970A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388821 | ||||||
| chr6:54389132
|
A | G | 37 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(34): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1297-659A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389132 | ||||||
| chr6:54389175
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-616T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389175 | ||||||
| chr6:54389227
|
C | T | 1 | a0003c0003t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1297-564C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389227 | ||||||
| chr6:54389301
|
T | C | 38 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0252others(35): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1297-490T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389301 | ||||||
| chr6:54389325
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0084others(7): Show | 12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-466C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389325 | ||||||
| chr6:54389537
|
C | T | 1 | a0009c0018t0001g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1297-254C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389537 | ||||||
| chr6:54389776
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1297-15T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389776 | ||||||
| chr6:54389782
|
T | G | 67 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0081others(64): Show | 69 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(66): Show |
intron_variant | MODIFIER | c.1297-9T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389782 |