Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1297 |
|---|---|
| ensemblid | ENSG00000112280.18 |
| hgncid | 2217 |
| symbol | COL9A1 |
| name | collagen type IX alpha 1 chain |
| refseq_nuc | NM_001851.6 |
| refseq_prot | NP_001842.3 |
| ensembl_nuc | ENST00000357250.11 |
| ensembl_prot | ENSP00000349790.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 70216126 |
| end | 70303084 |
| strand | - |
| ver | v1.2 |
| region | chr6:70216126-70303084 |
| region5000 | chr6:70211126-70308084 |
| regionname0 | COL9A1_chr6_70216126_70303084 |
| regionname5000 | COL9A1_chr6_70211126_70308084 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 921 | 119 | 5 | 20 | 74 | 4 | 14 | 46 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002 | 0/0 | 921 | 104 | 35 | 24 | 32 | 1 | 12 | 30 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003 | 0/0 | 921 | 63 | 19 | 9 | 24 | 3 | 8 | 21 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004 | 0/0 | 921 | 28 | 5 | 4 | 19 | 0 | 0 | 12 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005 | 0/0 | 921 | 21 | 4 | 9 | 3 | 3 | 2 | 3 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0006 | 0/0 | 921 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0007 | 0/0 | 921 | 5 | 3 | 0 | 2 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0008 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0009 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0010 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0011 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0012 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0013 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0014 | 0/0 | 921 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0015 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0016 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0017 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2766 | 106 | 4 | 16 | 69 | 4 | 11 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0002 | 0/0 | 2766 | 62 | 20 | 12 | 24 | 0 | 6 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0003 | 0/0 | 2766 | 30 | 9 | 8 | 3 | 3 | 7 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0004 | 0/0 | 2766 | 25 | 7 | 7 | 6 | 1 | 4 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0005 | 0/0 | 2766 | 19 | 4 | 9 | 1 | 3 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0006 | 0/0 | 2766 | 17 | 0 | 0 | 16 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0007 | 0/0 | 2766 | 15 | 5 | 3 | 7 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0008 | 0/0 | 2766 | 13 | 6 | 5 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0009 | 0/0 | 2766 | 13 | 0 | 1 | 12 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0010 | 0/0 | 2766 | 11 | 10 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0011 | 0/0 | 2766 | 9 | 9 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0012 | 0/0 | 2766 | 7 | 0 | 4 | 1 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0013 | 0/0 | 2766 | 5 | 0 | 0 | 5 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0014 | 0/0 | 2766 | 5 | 3 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0015 | 0/0 | 2766 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0016 | 0/0 | 2766 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0017 | 0/0 | 2766 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0018 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0019 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0020 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0021 | 0/0 | 2766 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0022 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0023 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0024 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0025 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0026 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0027 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0028 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0029 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0030 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0031 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0032 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0033 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0034 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| c0035 | 0/0 | 2766 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 932 | 130 | 29 | 34 | 49 | 4 | 14 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0002 | 0/0 | 933 | 100 | 7 | 25 | 54 | 3 | 11 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0003 | 1/1 | 932 | 83 | 15 | 5 | 50 | 5 | 6 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0004 | 0/0 | 934 | 18 | 11 | 1 | 1 | 0 | 5 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0005 | 0/0 | 934 | 9 | 6 | 3 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0006 | 0/0 | 932 | 7 | 7 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0007 | 0/0 | 932 | 5 | 5 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0008 | 0/0 | 932 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0009 | 0/0 | 933 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0010 | 0/0 | 933 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0011 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0012 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| t0013 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2766 | 106 | 4 | 16 | 69 | 4 | 11 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0012 | 0/0 | 2766 | 7 | 0 | 4 | 1 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0017 | 0/0 | 2766 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0019 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0029 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0030 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0031 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0002 | 0/0 | 2766 | 62 | 20 | 12 | 24 | 0 | 6 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004 | 0/0 | 2766 | 25 | 7 | 7 | 6 | 1 | 4 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0008 | 0/0 | 2766 | 13 | 6 | 5 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0016 | 0/0 | 2766 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0018 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0022 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003 | 0/0 | 2766 | 30 | 9 | 8 | 3 | 3 | 7 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0006 | 0/0 | 2766 | 17 | 0 | 0 | 16 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0010 | 0/0 | 2766 | 11 | 10 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0013 | 0/0 | 2766 | 5 | 0 | 0 | 5 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0007 | 0/0 | 2766 | 15 | 5 | 3 | 7 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0009 | 0/0 | 2766 | 13 | 0 | 1 | 12 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0005 | 0/0 | 2766 | 19 | 4 | 9 | 1 | 3 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0028 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0034 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0006c0011 | 0/0 | 2766 | 9 | 9 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0007c0014 | 0/0 | 2766 | 5 | 3 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0008c0015 | 0/0 | 2766 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0008c0023 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0009c0020 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0010c0021 | 0/0 | 2766 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0011c0024 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0012c0025 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0013c0026 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0014c0033 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0015c0032 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0016c0027 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0017c0035 | 0/0 | 2766 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3698 | 59 | 2 | 12 | 40 | 1 | 4 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0001t0003 | 1/1 | 3697 | 42 | 1 | 4 | 29 | 3 | 3 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0001t0004 | 0/0 | 3699 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0001t0006 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0001t0009 | 0/0 | 3698 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0012t0001 | 0/0 | 3697 | 7 | 0 | 4 | 1 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0017t0002 | 0/0 | 3698 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0019t0006 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0029t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0030t0003 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0001c0031t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0002t0001 | 0/0 | 3697 | 58 | 18 | 11 | 24 | 0 | 5 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0002t0002 | 0/0 | 3698 | 2 | 0 | 1 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0002t0003 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0002t0006 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0001 | 0/0 | 3697 | 3 | 1 | 1 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0002 | 0/0 | 3698 | 15 | 2 | 5 | 5 | 0 | 3 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0003 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0004 | 0/0 | 3699 | 4 | 2 | 1 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0008 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0004t0011 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0008t0002 | 0/0 | 3698 | 4 | 0 | 2 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0008t0005 | 0/0 | 3699 | 9 | 6 | 3 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0016t0004 | 0/0 | 3699 | 2 | 0 | 0 | 0 | 0 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0018t0006 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0002c0022t0001 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0001 | 0/0 | 3697 | 14 | 2 | 4 | 3 | 2 | 3 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0002 | 0/0 | 3698 | 9 | 1 | 4 | 0 | 1 | 3 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0004 | 0/0 | 3699 | 2 | 1 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0007 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0008 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0003t0010 | 0/0 | 3698 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0006t0003 | 0/0 | 3697 | 17 | 0 | 0 | 16 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0010t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0010t0003 | 0/0 | 3697 | 8 | 7 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0010t0007 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0010t0008 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0003c0013t0003 | 0/0 | 3697 | 5 | 0 | 0 | 5 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0007t0001 | 0/0 | 3697 | 11 | 1 | 3 | 7 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0007t0006 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0007t0007 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0009t0001 | 0/0 | 3697 | 12 | 0 | 1 | 11 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0004c0009t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0005t0001 | 0/0 | 3697 | 15 | 2 | 8 | 1 | 2 | 2 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0005t0002 | 0/0 | 3698 | 2 | 0 | 1 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0005t0003 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0005t0006 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0028t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0005c0034t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0006c0011t0003 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0006c0011t0004 | 0/0 | 3699 | 8 | 8 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0007c0014t0001 | 0/0 | 3697 | 4 | 2 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0007c0014t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0008c0015t0003 | 0/0 | 3697 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0008c0023t0012 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0009c0020t0003 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0010c0021t0001 | 0/0 | 3697 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0011c0024t0001 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0012c0025t0001 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0013c0026t0001 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0014c0033t0003 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0015c0032t0013 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0016c0027t0003 | 0/0 | 3697 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| a0017c0035t0001 | 0/0 | 3697 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | copy fasta | chr6 | 70211126 | 70308084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0006g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0012t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0017t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0017t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0019t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0029t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0030t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0001c0031t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0002t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0004t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0008t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0016t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0016t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0018t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0002c0022t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0003t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0006t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0010t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0013t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0013t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0013t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0013t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0003c0013t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0007t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0004c0009t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0005t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0028t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0005c0034t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0006c0011t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0007c0014t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0007c0014t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0007c0014t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0007c0014t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0007c0014t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0008c0015t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0008c0023t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0009c0020t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0010c0021t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0011c0024t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0012c0025t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0013c0026t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0014c0033t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0015c0032t0013g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0016c0027t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| a0017c0035t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0005 | t0001 | g0108 | EUR | GBR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0046 | EUR | GBR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00323 | hp2 | a0005 | c0005 | t0002 | g0015 | EUR | FIN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00408 | hp2 | a0001 | c0031 | t0002 | g0175 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00438 | hp1 | a0004 | c0007 | t0001 | g0023 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00597 | hp1 | a0001 | c0012 | t0001 | g0233 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00621 | hp1 | a0004 | c0009 | t0001 | g0325 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00639 | hp2 | a0017 | c0035 | t0001 | g0152 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00673 | hp1 | a0001 | c0017 | t0002 | g0185 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00733 | hp2 | a0002 | c0004 | t0002 | g0050 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00738 | hp2 | a0005 | c0005 | t0001 | g0016 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00741 | hp1 | a0002 | c0008 | t0005 | g0337 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG00741 | hp2 | a0005 | c0005 | t0001 | g0119 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01069 | hp1 | a0003 | c0010 | t0003 | g0085 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0127 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0253 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0041 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01109 | hp2 | a0005 | c0005 | t0001 | g0133 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01167 | hp1 | a0002 | c0008 | t0005 | g0009 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0047 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01169 | hp2 | a0002 | c0008 | t0005 | g0009 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0042 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01192 | hp2 | a0005 | c0005 | t0001 | g0204 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0150 | AMR | PUR | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01255 | hp2 | a0004 | c0009 | t0001 | g0239 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01256 | hp1 | a0005 | c0005 | t0001 | g0189 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01257 | hp2 | a0001 | c0012 | t0001 | g0131 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01258 | hp1 | a0001 | c0012 | t0001 | g0180 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01258 | hp2 | a0005 | c0005 | t0001 | g0151 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0105 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01361 | hp2 | a0010 | c0021 | t0001 | g0215 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0094 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01433 | hp2 | a0002 | c0004 | t0004 | g0254 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01496 | hp1 | a0002 | c0004 | t0002 | g0049 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01496 | hp2 | a0002 | c0004 | t0002 | g0217 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0232 | EUR | IBS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0110 | EUR | IBS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0104 | EUR | IBS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0226 | EUR | IBS | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01884 | hp1 | a0015 | c0032 | t0013 | g0341 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01884 | hp2 | a0007 | c0014 | t0001 | g0065 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01928 | hp1 | a0002 | c0008 | t0002 | g0069 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01934 | hp1 | a0005 | c0005 | t0001 | g0024 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01934 | hp2 | a0002 | c0004 | t0002 | g0299 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01952 | hp2 | a0004 | c0007 | t0001 | g0014 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01975 | hp2 | a0001 | c0012 | t0001 | g0191 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01978 | hp1 | a0004 | c0007 | t0001 | g0017 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02004 | hp1 | a0002 | c0004 | t0002 | g0220 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02040 | hp1 | a0003 | c0006 | t0003 | g0067 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02055 | hp1 | a0005 | c0005 | t0001 | g0022 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02074 | hp1 | a0002 | c0004 | t0004 | g0212 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02080 | hp2 | a0004 | c0009 | t0001 | g0320 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02083 | hp1 | a0004 | c0009 | t0001 | g0211 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02129 | hp2 | a0004 | c0009 | t0001 | g0319 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02132 | hp2 | a0004 | c0009 | t0001 | g0234 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02135 | hp1 | a0004 | c0009 | t0002 | g0237 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0252 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0289 | EAS | CDX | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02165 | hp1 | a0003 | c0006 | t0003 | g0236 | EAS | CDX | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CDX | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02258 | hp1 | a0004 | c0007 | t0007 | g0331 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02280 | hp1 | a0002 | c0004 | t0002 | g0242 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02280 | hp2 | a0006 | c0011 | t0004 | g0259 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02293 | hp1 | a0005 | c0005 | t0002 | g0248 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02293 | hp2 | a0002 | c0008 | t0002 | g0091 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0043 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02451 | hp1 | a0008 | c0023 | t0012 | g0329 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02451 | hp2 | a0006 | c0011 | t0004 | g0007 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02572 | hp2 | a0011 | c0024 | t0001 | g0244 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0114 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02602 | hp2 | a0002 | c0004 | t0002 | g0294 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02615 | hp1 | a0004 | c0007 | t0001 | g0256 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02615 | hp2 | a0003 | c0010 | t0003 | g0036 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02622 | hp2 | a0002 | c0008 | t0005 | g0339 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02630 | hp1 | a0006 | c0011 | t0004 | g0122 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02630 | hp2 | a0007 | c0014 | t0002 | g0270 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02647 | hp1 | a0002 | c0004 | t0004 | g0246 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02647 | hp2 | a0006 | c0011 | t0004 | g0279 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0303 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0060 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02698 | hp1 | a0001 | c0012 | t0001 | g0135 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0302 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02717 | hp1 | a0007 | c0014 | t0001 | g0066 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02723 | hp1 | a0002 | c0008 | t0005 | g0338 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02723 | hp2 | a0003 | c0003 | t0004 | g0271 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0120 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0145 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02738 | hp1 | a0002 | c0016 | t0004 | g0100 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02738 | hp2 | a0005 | c0005 | t0001 | g0260 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02809 | hp1 | a0002 | c0008 | t0005 | g0334 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02886 | hp1 | a0008 | c0015 | t0003 | g0002 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02895 | hp1 | a0008 | c0015 | t0003 | g0002 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02895 | hp2 | a0006 | c0011 | t0004 | g0277 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02896 | hp2 | a0003 | c0010 | t0003 | g0273 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02897 | hp1 | a0008 | c0015 | t0003 | g0002 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02897 | hp2 | a0003 | c0010 | t0003 | g0272 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02965 | hp1 | a0006 | c0011 | t0004 | g0007 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02965 | hp2 | a0003 | c0010 | t0003 | g0083 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02970 | hp1 | a0003 | c0010 | t0007 | g0335 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02970 | hp2 | a0003 | c0003 | t0007 | g0350 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02976 | hp1 | a0002 | c0004 | t0008 | g0123 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02976 | hp2 | a0005 | c0005 | t0003 | g0247 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03098 | hp1 | a0002 | c0004 | t0001 | g0059 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03098 | hp2 | a0005 | c0005 | t0006 | g0345 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03130 | hp1 | a0001 | c0019 | t0006 | g0344 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03139 | hp1 | a0004 | c0007 | t0007 | g0348 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0340 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03195 | hp1 | a0003 | c0010 | t0008 | g0087 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0342 | AFR | ESN | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03209 | hp1 | a0002 | c0008 | t0005 | g0333 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03225 | hp1 | a0004 | c0007 | t0006 | g0346 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0328 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03239 | hp2 | a0003 | c0003 | t0004 | g0054 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03453 | hp1 | a0003 | c0010 | t0003 | g0071 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03453 | hp2 | a0013 | c0026 | t0001 | g0249 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03486 | hp1 | a0003 | c0003 | t0010 | g0250 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03486 | hp2 | a0009 | c0020 | t0003 | g0213 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03491 | hp1 | a0016 | c0027 | t0003 | g0181 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03491 | hp2 | a0001 | c0030 | t0003 | g0121 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03540 | hp1 | a0003 | c0003 | t0010 | g0241 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03654 | hp2 | a0002 | c0016 | t0004 | g0187 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03669 | hp1 | a0002 | c0004 | t0002 | g0295 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0052 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03688 | hp2 | a0002 | c0004 | t0002 | g0051 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0309 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0285 | SAS | PJL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03831 | hp1 | a0003 | c0006 | t0003 | g0314 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03927 | hp1 | a0005 | c0005 | t0001 | g0255 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0031 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0240 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04115 | hp2 | a0012 | c0025 | t0001 | g0282 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | BEB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0011 | SAS | STU | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0265 | AFR | YRI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18522 | hp2 | a0003 | c0010 | t0002 | g0084 | AFR | YRI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | CHB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | YRI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18906 | hp2 | a0003 | c0010 | t0003 | g0081 | AFR | YRI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18940 | hp2 | a0004 | c0007 | t0001 | g0018 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18945 | hp2 | a0003 | c0006 | t0003 | g0037 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18946 | hp1 | a0004 | c0009 | t0001 | g0097 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18949 | hp2 | a0004 | c0007 | t0001 | g0028 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18962 | hp1 | a0003 | c0006 | t0003 | g0038 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18965 | hp1 | a0004 | c0009 | t0001 | g0316 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18966 | hp2 | a0003 | c0006 | t0003 | g0003 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18967 | hp1 | a0005 | c0028 | t0002 | g0324 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18967 | hp2 | a0005 | c0034 | t0002 | g0206 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18970 | hp2 | a0003 | c0006 | t0003 | g0027 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18971 | hp1 | a0003 | c0006 | t0003 | g0090 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18972 | hp2 | a0003 | c0006 | t0003 | g0026 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18973 | hp1 | a0002 | c0004 | t0002 | g0006 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18973 | hp2 | a0004 | c0007 | t0001 | g0021 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18974 | hp2 | a0004 | c0007 | t0001 | g0088 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18977 | hp1 | a0004 | c0007 | t0001 | g0196 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18977 | hp2 | a0001 | c0029 | t0002 | g0174 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18981 | hp1 | a0004 | c0009 | t0001 | g0321 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18982 | hp1 | a0004 | c0009 | t0001 | g0323 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18983 | hp1 | a0003 | c0006 | t0003 | g0158 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18983 | hp2 | a0002 | c0004 | t0002 | g0006 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18984 | hp2 | a0007 | c0014 | t0001 | g0224 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18986 | hp1 | a0003 | c0006 | t0003 | g0074 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18991 | hp2 | a0003 | c0006 | t0003 | g0073 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19000 | hp1 | a0005 | c0005 | t0001 | g0163 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19000 | hp2 | a0002 | c0004 | t0002 | g0229 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19005 | hp2 | a0004 | c0009 | t0001 | g0315 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19007 | hp2 | a0003 | c0013 | t0003 | g0160 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19009 | hp1 | a0001 | c0017 | t0002 | g0138 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19010 | hp1 | a0003 | c0013 | t0003 | g0311 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19030 | hp2 | a0002 | c0004 | t0002 | g0086 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19043 | hp1 | a0002 | c0004 | t0011 | g0330 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19043 | hp2 | a0003 | c0010 | t0003 | g0082 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19057 | hp2 | a0004 | c0007 | t0001 | g0308 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19060 | hp1 | a0003 | c0006 | t0003 | g0221 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19062 | hp1 | a0003 | c0013 | t0003 | g0197 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19066 | hp1 | a0002 | c0004 | t0002 | g0020 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19066 | hp2 | a0004 | c0009 | t0001 | g0322 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19075 | hp1 | a0002 | c0004 | t0002 | g0235 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19075 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19076 | hp1 | a0002 | c0008 | t0002 | g0092 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19076 | hp2 | a0003 | c0006 | t0003 | g0003 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19077 | hp2 | a0003 | c0006 | t0003 | g0078 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19080 | hp1 | a0003 | c0006 | t0003 | g0072 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19082 | hp2 | a0003 | c0006 | t0003 | g0080 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19088 | hp1 | a0007 | c0014 | t0001 | g0225 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19090 | hp1 | a0003 | c0013 | t0003 | g0199 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20129 | hp1 | a0002 | c0004 | t0004 | g0274 | AFR | ASW | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20129 | hp2 | a0003 | c0003 | t0007 | g0349 | AFR | ASW | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20752 | hp1 | a0005 | c0005 | t0001 | g0258 | EUR | TSI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0113 | EUR | TSI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20805 | hp1 | a0014 | c0033 | t0003 | g0159 | EUR | TSI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20805 | hp2 | a0002 | c0004 | t0003 | g0286 | EUR | TSI | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20905 | hp1 | a0003 | c0003 | t0002 | g0053 | SAS | GIH | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | GIH | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01123 | hp1 | a0004 | c0007 | t0001 | g0128 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG01123 | hp2 | a0001 | c0012 | t0001 | g0132 | AMR | CLM | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02109 | hp1 | a0006 | c0011 | t0004 | g0275 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02109 | hp2 | a0002 | c0008 | t0005 | g0336 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02486 | hp1 | a0005 | c0005 | t0001 | g0107 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02486 | hp2 | a0006 | c0011 | t0003 | g0278 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG02559 | hp2 | a0002 | c0018 | t0006 | g0343 | AFR | ACB | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03471 | hp1 | a0002 | c0008 | t0005 | g0332 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | MSL | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0057 | AFR | USA | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| HG06807 | hp2 | a0003 | c0003 | t0008 | g0280 | AFR | USA | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18955 | hp1 | a0003 | c0013 | t0003 | g0198 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA18955 | hp2 | a0002 | c0008 | t0002 | g0313 | EAS | JPT | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | USA | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA20300 | hp2 | a0006 | c0011 | t0004 | g0276 | AFR | USA | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA21309 | hp1 | a0004 | c0007 | t0006 | g0347 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| NA21309 | hp2 | a0002 | c0022 | t0001 | g0281 | AFR | LWK | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0102 | REF | REF | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0111 | REF | REF | COL9A1_chr6_70211126_70308084 | COL9A1 | chr6 | 70211126 | 70308084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70232616
|
G | T | 1 | a0006 | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.2470C>A | p.Pro824Thr | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/38 | 2630/3697 | 2470/2766 | 824/921 | chr6 | 70232616 | ||
| chr6:70232650
|
C | A | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2436G>T | p.Gln812His | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/38 | 2596/3697 | 2436/2766 | 812/921 | chr6 | 70232650 | ||
| chr6:70232688
|
G | A | 1 | a0012 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2398C>T | p.Pro800Ser | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/38 | 2558/3697 | 2398/2766 | 800/921 | chr6 | 70232688 | ||
| chr6:70234554
|
T | C | 5 | a0004a0007a0008others(2): Show | 39 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(36): Show |
missense_variant | MODERATE | c.2299A>G | p.Met767Val | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/38 | 2459/3697 | 2299/2766 | 767/921 | chr6 | 70234554 | ||
| chr6:70242023
|
T | G | 1 | a0014 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1939A>C | p.Ser647Arg | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/38 | 2099/3697 | 1939/2766 | 647/921 | chr6 | 70242023 | ||
| chr6:70252130
|
T | C | 8 | a0003a0004a0005others(5): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
missense_variant | MODERATE | c.1862A>G | p.Gln621Arg | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/38 | 2022/3697 | 1862/2766 | 621/921 | chr6 | 70252130 | ||
| chr6:70256806
|
C | G | 1 | a0016 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1465G>C | p.Asp489His | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/38 | 1625/3697 | 1465/2766 | 489/921 | chr6 | 70256806 | ||
| chr6:70260680
|
T | C | 1 | a0013 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1426A>G | p.Ile476Val | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/38 | 1586/3697 | 1426/2766 | 476/921 | chr6 | 70260680 | ||
| chr6:70263290
|
T | C | 1 | a0017 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1349A>G | p.Glu450Gly | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/38 | 1509/3697 | 1349/2766 | 450/921 | chr6 | 70263290 | ||
| chr6:70274733
|
A | G | 8 | a0002a0003a0007others(5): Show | 180 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(177): Show |
missense_variant | MODERATE | c.1015T>C | p.Ser339Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/38 | 1175/3697 | 1015/2766 | 339/921 | chr6 | 70274733 | ||
| chr6:70280828
|
C | T | 1 | a0010 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.959G>A | p.Gly320Asp | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/38 | 1119/3697 | 959/2766 | 320/921 | chr6 | 70280828 | ||
| chr6:70294510
|
C | T | 1 | a0009 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.353G>A | p.Arg118Gln | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/38 | 513/3697 | 353/2766 | 118/921 | chr6 | 70294510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70216987
|
C | T | 1 | a0001c0031 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2676G>A | p.Pro892Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 2836/3697 | 2676/2766 | 892/921 | chr6 | 70216987 | ||
| chr6:70225951
|
A | G | 1 | a0002c0016 | 2 | HG02738.hp1 HG03654.hp2 |
synonymous_variant | LOW | c.2562T>C | p.Pro854Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/38 | 2722/3697 | 2562/2766 | 854/921 | chr6 | 70225951 | ||
| chr6:70234582
|
C | T | 5 | a0001c0030a0002c0022a0003c0006others(2): Show | 25 | HG02040.hp1 HG02165.hp1 HG03491.hp2 others(22): Show |
synonymous_variant | LOW | c.2271G>A | p.Pro757Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/38 | 2431/3697 | 2271/2766 | 757/921 | chr6 | 70234582 | ||
| chr6:70241970
|
A | C | 1 | a0001c0029 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.1992T>G | p.Gly664Gly | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/38 | 2152/3697 | 1992/2766 | 664/921 | chr6 | 70241970 | ||
| chr6:70253421
|
A | C | 4 | a0001c0012a0001c0019a0002c0002others(1): Show | 71 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(68): Show |
synonymous_variant | LOW | c.1728T>G | p.Pro576Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/38 | 1888/3697 | 1728/2766 | 576/921 | chr6 | 70253421 | ||
| chr6:70254972
|
A | G | 2 | a0004c0009a0005c0028 | 14 | HG00621.hp1 HG01255.hp2 HG02080.hp2 others(11): Show |
synonymous_variant | LOW | c.1656T>C | p.Pro552Pro | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/38 | 1816/3697 | 1656/2766 | 552/921 | chr6 | 70254972 | ||
| chr6:70255192
|
A | T | 1 | a0001c0017 | 2 | HG00673.hp1 NA19009.hp1 |
synonymous_variant | LOW | c.1569T>A | p.Gly523Gly | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 23/38 | 1729/3697 | 1569/2766 | 523/921 | chr6 | 70255192 | ||
| chr6:70272083
|
A | G | 4 | a0002c0008a0003c0006a0003c0010others(1): Show | 44 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(41): Show |
synonymous_variant | LOW | c.1071T>C | p.Arg357Arg | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 13/38 | 1231/3697 | 1071/2766 | 357/921 | chr6 | 70272083 | ||
| chr6:70300337
|
C | T | 2 | a0001c0019a0002c0018 | 2 | HG02559.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.138G>A | p.Lys46Lys | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 3/38 | 298/3697 | 138/2766 | 46/921 | chr6 | 70300337 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70216359
|
A | T | 1 | a0015c0032t0013 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*538T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 538 | chr6 | 70216359 | |||||
| chr6:70216631
|
A | G | 20 | a0001c0001t0006a0001c0012t0001a0001c0019t0006others(17): Show | 137 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*266T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 266 | chr6 | 70216631 | |||||
| chr6:70216654
|
C | CT | 16 | a0001c0001t0002a0001c0001t0009a0001c0017t0002others(13): Show | 104 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*242dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 242 | chr6 | 70216654 | |||||
| chr6:70216654
|
C | CTT | 6 | a0001c0001t0004a0002c0004t0004a0002c0008t0005others(3): Show | 27 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*241_*242dupAA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 242 | chr6 | 70216654 | |||||
| chr6:70216668
|
A | G | 11 | a0001c0001t0004a0002c0004t0004a0002c0004t0008others(8): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*229T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 38/38 | 229 | chr6 | 70216668 | |||||
| chr6:70302967
|
G | A | 2 | a0002c0004t0011a0008c0023t0012 | 2 | HG02451.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-43C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/38 | 43 | chr6 | 70302967 | |||||
| chr6:70303031
|
T | C | 11 | a0001c0001t0006a0001c0019t0006a0002c0002t0006others(8): Show | 22 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-107A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/38 | 107 | chr6 | 70303031 | |||||
| chr6:70303074
|
A | G | 1 | a0001c0001t0009 | 2 | HG03704.hp1 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-150T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/38 | 150 | chr6 | 70303074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70217184
|
C | T | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-103G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217184 | ||||||
| chr6:70217195
|
G | A | 292 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(289): Show | 303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.2582-114C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217195 | ||||||
| chr6:70217230
|
G | C | 71 | a0001c0012t0001g0120a0001c0012t0001g0131a0001c0012t0001g0132others(68): Show | 73 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.2582-149C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217230 | ||||||
| chr6:70217245
|
A | G | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-164T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217245 | ||||||
| chr6:70217276
|
A | G | 1 | a0002c0004t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2582-195T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217276 | ||||||
| chr6:70217312
|
T | A | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2582-231A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217312 | ||||||
| chr6:70217449
|
G | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-368C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217449 | ||||||
| chr6:70217627
|
G | A | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-546C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217627 | ||||||
| chr6:70217712
|
T | C | 1 | a0001c0001t0002g0176 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2582-631A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217712 | ||||||
| chr6:70217731
|
G | A | 31 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(28): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2582-650C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217731 | ||||||
| chr6:70217805
|
T | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(126): Show | 135 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2582-724A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70217805 | ||||||
| chr6:70218086
|
T | C | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2582-1005A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218086 | ||||||
| chr6:70218264
|
T | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-1183A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218264 | ||||||
| chr6:70218689
|
C | T | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(94): Show | 101 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2582-1608G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218689 | ||||||
| chr6:70218737
|
C | CAGTGGTC others(5): Show |
133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-1657_2582-165 others(16): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218737 | ||||||
| chr6:70218739
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-1658A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218739 | ||||||
| chr6:70218802
|
T | C | 24 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0004t0008g0123others(21): Show | 26 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2582-1721A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218802 | ||||||
| chr6:70218803
|
T | A | 8 | a0003c0003t0004g0271a0006c0011t0004g0007a0006c0011t0004g0122others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2582-1722A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218803 | ||||||
| chr6:70218897
|
A | G | 2 | a0003c0003t0007g0349a0003c0003t0007g0350 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2582-1816T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70218897 | ||||||
| chr6:70219141
|
A | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(94): Show | 101 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2582-2060T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219141 | ||||||
| chr6:70219179
|
C | T | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2582-2098G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219179 | ||||||
| chr6:70219180
|
G | A | 2 | a0001c0001t0003g0079a0001c0001t0003g0117 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2582-2099C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219180 | ||||||
| chr6:70219211
|
C | A | 31 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(28): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2582-2130G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219211 | ||||||
| chr6:70219294
|
TG | T | 3 | a0002c0004t0008g0123a0002c0004t0011g0330a0003c0010t0008g0087 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2582-2214delC | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219294 | ||||||
| chr6:70219708
|
C | T | 64 | a0001c0012t0001g0120a0001c0012t0001g0191a0001c0012t0001g0233others(61): Show | 66 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2582-2627G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219708 | ||||||
| chr6:70219709
|
A | G | 269 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(266): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.2582-2628T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219709 | ||||||
| chr6:70219712
|
G | A | 2 | a0003c0003t0001g0226a0003c0003t0001g0232 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2582-2631C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219712 | ||||||
| chr6:70219819
|
T | G | 13 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(10): Show | 13 | HG00099.hp1 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2582-2738A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70219819 | ||||||
| chr6:70220139
|
G | GTCA | 36 | a0001c0001t0002g0098a0001c0001t0003g0032a0001c0001t0003g0040others(33): Show | 36 | HG00558.hp2 HG00673.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.2582-3061_2582-305 others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220139 | ||||||
| chr6:70220139
|
G | GTCATCA | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2582-3064_2582-305 others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220139 | ||||||
| chr6:70220139
|
GTCA | G | 24 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0004t0008g0123others(21): Show | 26 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2582-3061_2582-305 others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220139 | ||||||
| chr6:70220207
|
G | GT | 133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-3127_2582-312 others(5): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220207 | ||||||
| chr6:70220209
|
G | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(130): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2582-3128C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220209 | ||||||
| chr6:70220230
|
G | A | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2582-3149C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220230 | ||||||
| chr6:70220246
|
T | C | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2582-3165A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220246 | ||||||
| chr6:70220318
|
A | G | 1 | a0003c0010t0008g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2582-3237T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220318 | ||||||
| chr6:70220322
|
C | A | 1 | a0001c0001t0003g0171 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2582-3241G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220322 | ||||||
| chr6:70220370
|
G | T | 29 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(26): Show | 31 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2582-3289C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220370 | ||||||
| chr6:70220373
|
T | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2582-3292A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220373 | ||||||
| chr6:70220373
|
T | TG | 22 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0004t0008g0123others(19): Show | 24 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2582-3293dupC | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220373 | ||||||
| chr6:70220376
|
A | G | 36 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(33): Show | 40 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.2582-3295T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220376 | ||||||
| chr6:70220385
|
G | T | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2582-3304C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220385 | ||||||
| chr6:70220389
|
G | GGTGT | 22 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0004t0008g0123others(19): Show | 24 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2582-3312_2582-330 others(8): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220389 | ||||||
| chr6:70220389
|
GGT | G | 61 | a0001c0001t0002g0167a0001c0001t0003g0004a0001c0001t0003g0012others(58): Show | 64 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2582-3310_2582-330 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220389 | ||||||
| chr6:70220389
|
GGTGT | G | 112 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(109): Show | 116 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2582-3312_2582-330 others(8): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220389 | ||||||
| chr6:70220389
|
GGTGTGT | G | 125 | a0001c0001t0006g0342a0001c0012t0001g0120a0001c0012t0001g0131others(122): Show | 127 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.2582-3314_2582-330 others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220389 | ||||||
| chr6:70220389
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2582-3318_2582-330 others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220389 | ||||||
| chr6:70220464
|
C | G | 1 | a0002c0002t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2582-3383G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220464 | ||||||
| chr6:70220585
|
CAT | C | 31 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(28): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2582-3506_2582-350 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220585 | ||||||
| chr6:70220718
|
C | T | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(94): Show | 101 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2582-3637G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220718 | ||||||
| chr6:70220892
|
T | G | 1 | a0002c0002t0001g0223 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2582-3811A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220892 | ||||||
| chr6:70220897
|
T | C | 31 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(28): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2582-3816A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70220897 | ||||||
| chr6:70221098
|
GT | G | 31 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(28): Show | 33 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2582-4018delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221098 | ||||||
| chr6:70221108
|
T | A | 1 | a0001c0012t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2582-4027A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221108 | ||||||
| chr6:70221189
|
G | A | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-4108C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221189 | ||||||
| chr6:70221191
|
A | C | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(94): Show | 101 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2582-4110T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221191 | ||||||
| chr6:70221194
|
A | T | 1 | a0002c0002t0001g0200 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2582-4113T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221194 | ||||||
| chr6:70221232
|
G | A | 9 | a0003c0003t0004g0271a0003c0003t0008g0280a0006c0011t0004g0007others(6): Show | 10 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2582-4151C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221232 | ||||||
| chr6:70221292
|
G | C | 1 | a0003c0003t0001g0293 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2582-4211C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221292 | ||||||
| chr6:70221314
|
G | T | 1 | a0005c0005t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2582-4233C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221314 | ||||||
| chr6:70221342
|
G | A | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-4261C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221342 | ||||||
| chr6:70221408
|
A | G | 36 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(33): Show | 40 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.2582-4327T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221408 | ||||||
| chr6:70221493
|
C | T | 1 | a0001c0001t0006g0342 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2582-4412G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221493 | ||||||
| chr6:70221723
|
T | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(99): Show | 108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2581+4209A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221723 | ||||||
| chr6:70221809
|
A | G | 1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2581+4123T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70221809 | ||||||
| chr6:70222030
|
T | G | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2581+3902A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222030 | ||||||
| chr6:70222546
|
G | A | 1 | a0002c0002t0002g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2581+3386C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222546 | ||||||
| chr6:70222576
|
C | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(94): Show | 101 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2581+3356G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222576 | ||||||
| chr6:70222693
|
G | A | 1 | a0004c0009t0001g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2581+3239C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222693 | ||||||
| chr6:70222739
|
C | CT | 99 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(96): Show | 103 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2581+3192dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222739 | ||||||
| chr6:70222742
|
T | TTC | 5 | a0003c0003t0007g0349a0003c0003t0007g0350a0008c0015t0003g0002others(2): Show | 7 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2581+3189_2581+319 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222742 | ||||||
| chr6:70222789
|
A | G | 1 | a0003c0006t0003g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2581+3143T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222789 | ||||||
| chr6:70222832
|
A | C | 327 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(324): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.2581+3100T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222832 | ||||||
| chr6:70222901
|
A | C | 85 | a0001c0012t0001g0120a0001c0012t0001g0131a0001c0012t0001g0132others(82): Show | 87 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2581+3031T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70222901 | ||||||
| chr6:70223089
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2581+2843A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223089 | ||||||
| chr6:70223115
|
C | A | 1 | a0002c0002t0001g0297 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2581+2817G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223115 | ||||||
| chr6:70223158
|
G | A | 29 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(26): Show | 31 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2581+2774C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223158 | ||||||
| chr6:70223181
|
G | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2581+2751C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223181 | ||||||
| chr6:70223208
|
A | G | 28 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(25): Show | 30 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.2581+2724T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223208 | ||||||
| chr6:70223360
|
A | G | 1 | a0002c0002t0002g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2581+2572T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223360 | ||||||
| chr6:70223387
|
T | A | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2581+2545A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223387 | ||||||
| chr6:70223466
|
A | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(100): Show | 109 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2581+2466T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223466 | ||||||
| chr6:70223472
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(100): Show | 109 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2581+2460C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223472 | ||||||
| chr6:70223595
|
G | A | 2 | a0003c0003t0007g0349a0003c0003t0007g0350 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2581+2337C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223595 | ||||||
| chr6:70223683
|
A | C | 4 | a0007c0014t0002g0270a0008c0015t0003g0002a0008c0023t0012g0329others(1): Show | 6 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2581+2249T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223683 | ||||||
| chr6:70223687
|
G | A | 5 | a0001c0012t0001g0233a0002c0002t0001g0222a0002c0002t0001g0227others(2): Show | 5 | HG00597.hp1 HG00609.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.2581+2245C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70223687 | ||||||
| chr6:70224016
|
G | C | 1 | a0001c0001t0002g0130 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2581+1916C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224016 | ||||||
| chr6:70224188
|
G | T | 2 | a0008c0015t0003g0002a0008c0023t0012g0329 | 4 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581+1744C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224188 | ||||||
| chr6:70224234
|
T | G | 3 | a0001c0001t0002g0126a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | NA18962.hp2 NA18985.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2581+1698A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224234 | ||||||
| chr6:70224415
|
G | A | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2581+1517C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224415 | ||||||
| chr6:70224473
|
T | C | 10 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2581+1459A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224473 | ||||||
| chr6:70224543
|
GAGA | G | 5 | a0004c0009t0001g0315a0004c0009t0001g0316a0004c0009t0001g0321others(2): Show | 5 | NA18965.hp1 NA18981.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2581+1386_2581+138 others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224543 | ||||||
| chr6:70224579
|
T | C | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2581+1353A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224579 | ||||||
| chr6:70224588
|
A | C | 44 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.2581+1344T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224588 | ||||||
| chr6:70224610
|
G | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2581+1322C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224610 | ||||||
| chr6:70224675
|
T | C | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2581+1257A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224675 | ||||||
| chr6:70224677
|
T | G | 3 | a0008c0015t0003g0002a0008c0023t0012g0329a0015c0032t0013g0341 | 5 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2581+1255A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224677 | ||||||
| chr6:70224894
|
GT | G | 36 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2581+1037delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224894 | ||||||
| chr6:70224907
|
A | T | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2581+1025T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224907 | ||||||
| chr6:70224908
|
T | A | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2581+1024A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224908 | ||||||
| chr6:70224994
|
T | G | 1 | a0002c0002t0001g0238 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2581+938A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224994 | ||||||
| chr6:70224997
|
A | T | 1 | a0001c0001t0002g0164 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2581+935T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70224997 | ||||||
| chr6:70225131
|
A | G | 23 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(20): Show | 24 | HG02040.hp1 HG02165.hp1 HG03491.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581+801T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225131 | ||||||
| chr6:70225153
|
C | G | 71 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(68): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2581+779G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225153 | ||||||
| chr6:70225167
|
G | C | 8 | a0004c0007t0001g0256a0004c0007t0006g0346a0004c0007t0006g0347others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2581+765C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225167 | ||||||
| chr6:70225265
|
T | C | 326 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(323): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.2581+667A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225265 | ||||||
| chr6:70225430
|
G | A | 8 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0122others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2581+502C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225430 | ||||||
| chr6:70225443
|
TTTTC | T | 25 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2581+485_2581+488d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225443 | ||||||
| chr6:70225501
|
G | A | 1 | a0002c0004t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2581+431C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225501 | ||||||
| chr6:70225587
|
TA | T | 33 | a0001c0001t0002g0205a0001c0001t0004g0145a0001c0001t0004g0257others(30): Show | 33 | HG01069.hp1 HG01433.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.2581+344delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225587 | ||||||
| chr6:70225587
|
TAA | T | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2581+343_2581+344d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225587 | ||||||
| chr6:70225598
|
A | C | 1 | a0004c0007t0006g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2581+334T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225598 | ||||||
| chr6:70225620
|
A | G | 1 | a0001c0017t0002g0138 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2581+312T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 37/37 | chr6 | 70225620 | ||||||
| chr6:70226014
|
A | G | 1 | a0002c0002t0001g0303 | 1 | HG02683.hp1 | splice_region_variant&intron_variant | LOW | c.2504-5T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226014 | ||||||
| chr6:70226056
|
T | C | 15 | a0001c0001t0006g0342a0003c0003t0004g0271a0003c0003t0008g0280others(12): Show | 15 | HG01069.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.2504-47A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226056 | ||||||
| chr6:70226303
|
C | T | 1 | a0002c0004t0002g0299 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2504-294G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226303 | ||||||
| chr6:70226395
|
C | T | 2 | a0008c0015t0003g0002a0008c0023t0012g0329 | 4 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-386G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226395 | ||||||
| chr6:70226412
|
A | T | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2504-403T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226412 | ||||||
| chr6:70226464
|
T | C | 1 | a0003c0010t0003g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2504-455A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226464 | ||||||
| chr6:70226470
|
T | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2504-461A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226470 | ||||||
| chr6:70226515
|
A | G | 2 | a0008c0015t0003g0002a0008c0023t0012g0329 | 4 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-506T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226515 | ||||||
| chr6:70226518
|
G | A | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2504-509C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226518 | ||||||
| chr6:70226661
|
A | C | 2 | a0002c0002t0001g0063a0002c0002t0001g0269 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2504-652T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226661 | ||||||
| chr6:70226774
|
TCTC | T | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2504-768_2504-766d others(5): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226774 | ||||||
| chr6:70226857
|
T | C | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2504-848A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226857 | ||||||
| chr6:70226977
|
C | A | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2504-968G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70226977 | ||||||
| chr6:70227139
|
A | G | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2504-1130T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227139 | ||||||
| chr6:70227178
|
C | G | 1 | a0004c0007t0001g0308 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2504-1169G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227178 | ||||||
| chr6:70227208
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2504-1199T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227208 | ||||||
| chr6:70227414
|
A | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2504-1405T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227414 | ||||||
| chr6:70227424
|
T | TA | 56 | a0001c0001t0002g0095a0001c0001t0002g0098a0001c0001t0002g0126others(53): Show | 59 | HG00438.hp2 HG00609.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.2504-1416dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAA | 12 | a0001c0001t0003g0032a0001c0001t0003g0039a0001c0012t0001g0233others(9): Show | 12 | HG00597.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.2504-1417_2504-141 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAA | 37 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0254others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.2504-1418_2504-141 others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAA | 8 | a0002c0004t0004g0212a0004c0007t0001g0256a0004c0007t0006g0346others(5): Show | 8 | HG02074.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-1419_2504-141 others(8): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(3): Show |
2 | a0003c0003t0001g0328a0004c0007t0001g0196 | 2 | HG03225.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2504-1425_2504-141 others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(4): Show |
3 | a0003c0006t0003g0038a0003c0006t0003g0078a0003c0006t0003g0090 | 3 | NA18962.hp1 NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2504-1426_2504-141 others(15): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(5): Show |
2 | a0003c0003t0007g0349a0005c0034t0002g0206 | 2 | NA18967.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2504-1427_2504-141 others(16): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(6): Show |
1 | a0003c0003t0007g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2504-1428_2504-141 others(17): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(7): Show |
2 | a0003c0003t0010g0241a0013c0026t0001g0249 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2504-1429_2504-141 others(18): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(9): Show |
1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2504-1431_2504-141 others(20): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(11): Show |
3 | a0002c0008t0005g0332a0004c0009t0001g0319a0004c0009t0001g0320 | 3 | HG02080.hp2 HG02129.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2504-1433_2504-141 others(22): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(12): Show |
3 | a0002c0008t0005g0333a0002c0008t0005g0334a0002c0008t0005g0336 | 3 | HG02109.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2504-1434_2504-141 others(23): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(13): Show |
1 | a0002c0004t0004g0274 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2504-1435_2504-141 others(24): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(14): Show |
1 | a0002c0008t0005g0009 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2504-1436_2504-141 others(25): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(15): Show |
5 | a0002c0004t0004g0246a0002c0004t0011g0330a0002c0008t0005g0337others(2): Show | 5 | HG00741.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-1437_2504-141 others(26): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(16): Show |
4 | a0004c0009t0001g0097a0004c0009t0001g0239a0004c0009t0001g0315others(1): Show | 4 | HG01255.hp2 NA18946.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-1438_2504-141 others(27): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(17): Show |
4 | a0004c0009t0001g0322a0004c0009t0001g0323a0004c0009t0001g0325others(1): Show | 4 | HG00621.hp1 HG02135.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-1439_2504-141 others(28): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(18): Show |
3 | a0002c0004t0008g0123a0003c0013t0003g0197a0004c0009t0001g0316 | 3 | HG02976.hp1 NA18965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(29): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(19): Show |
11 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(8): Show | 12 | HG02040.hp1 HG03491.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(30): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(20): Show |
11 | a0003c0006t0003g0072a0003c0006t0003g0236a0003c0013t0003g0198others(8): Show | 11 | HG01123.hp1 HG01978.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(31): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(21): Show |
5 | a0002c0002t0001g0064a0002c0004t0001g0059a0003c0006t0003g0080others(2): Show | 5 | HG00438.hp1 HG01952.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(32): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(22): Show |
3 | a0002c0002t0001g0030a0002c0002t0001g0055a0002c0002t0001g0056 | 3 | HG02055.hp2 HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(33): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(25): Show |
2 | a0007c0014t0001g0065a0007c0014t0001g0066 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(36): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(26): Show |
2 | a0003c0006t0003g0073a0004c0007t0001g0018 | 2 | NA18940.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(37): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(27): Show |
2 | a0002c0002t0001g0045a0002c0002t0001g0058 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2504-1416_2504-141 others(38): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
T | TAAAAAAA others(28): Show |
1 | a0003c0006t0003g0221 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2504-1416_2504-141 others(39): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227424
|
TA | T | 7 | a0001c0001t0002g0062a0001c0001t0002g0124a0001c0001t0002g0139others(4): Show | 7 | HG01257.hp2 HG03491.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.2504-1416delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227424 | ||||||
| chr6:70227473
|
C | T | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2504-1464G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227473 | ||||||
| chr6:70227474
|
G | A | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2504-1465C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227474 | ||||||
| chr6:70227500
|
G | C | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2504-1491C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227500 | ||||||
| chr6:70227510
|
C | T | 3 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350 | 3 | HG02970.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2504-1501G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227510 | ||||||
| chr6:70227957
|
C | T | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2504-1948G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70227957 | ||||||
| chr6:70228109
|
A | T | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2504-2100T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70228109 | ||||||
| chr6:70228273
|
G | A | 1 | a0014c0033t0003g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2504-2264C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70228273 | ||||||
| chr6:70228422
|
C | T | 10 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2504-2413G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70228422 | ||||||
| chr6:70228423
|
G | A | 2 | a0008c0015t0003g0002a0008c0023t0012g0329 | 4 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-2414C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70228423 | ||||||
| chr6:70228608
|
T | A | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2504-2599A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70228608 | ||||||
| chr6:70229033
|
G | A | 64 | a0001c0012t0001g0120a0001c0012t0001g0131a0001c0012t0001g0132others(61): Show | 66 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2504-3024C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229033 | ||||||
| chr6:70229089
|
A | G | 8 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0122others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2504-3080T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229089 | ||||||
| chr6:70229434
|
T | C | 1 | a0002c0004t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2503+3149A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229434 | ||||||
| chr6:70229439
|
G | A | 1 | a0002c0004t0002g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2503+3144C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229439 | ||||||
| chr6:70229633
|
A | G | 1 | a0003c0003t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2503+2950T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229633 | ||||||
| chr6:70229725
|
A | G | 8 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2503+2858T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229725 | ||||||
| chr6:70229787
|
T | C | 2 | a0001c0001t0002g0166a0005c0028t0002g0324 | 2 | NA18967.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2503+2796A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229787 | ||||||
| chr6:70229794
|
G | T | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2503+2789C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229794 | ||||||
| chr6:70229864
|
T | C | 36 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2503+2719A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229864 | ||||||
| chr6:70229872
|
C | A | 7 | a0001c0001t0003g0004a0001c0001t0003g0034a0001c0001t0003g0039others(4): Show | 8 | HG00408.hp1 HG00597.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.2503+2711G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70229872 | ||||||
| chr6:70230238
|
G | A | 3 | a0008c0015t0003g0002a0008c0023t0012g0329a0015c0032t0013g0341 | 5 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2503+2345C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230238 | ||||||
| chr6:70230378
|
A | T | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2503+2205T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230378 | ||||||
| chr6:70230448
|
G | A | 127 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2503+2135C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230448 | ||||||
| chr6:70230793
|
G | C | 42 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.2503+1790C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230793 | ||||||
| chr6:70230808
|
G | C | 36 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2503+1775C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230808 | ||||||
| chr6:70230838
|
G | A | 36 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2503+1745C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230838 | ||||||
| chr6:70230843
|
G | A | 42 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.2503+1740C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230843 | ||||||
| chr6:70230874
|
C | T | 56 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(53): Show | 57 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.2503+1709G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230874 | ||||||
| chr6:70230949
|
C | T | 42 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.2503+1634G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230949 | ||||||
| chr6:70230976
|
T | C | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2503+1607A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70230976 | ||||||
| chr6:70231000
|
T | G | 45 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(42): Show | 47 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.2503+1583A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231000 | ||||||
| chr6:70231029
|
T | A | 6 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(3): Show | 6 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2503+1554A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231029 | ||||||
| chr6:70231061
|
G | C | 1 | a0005c0005t0001g0150 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2503+1522C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231061 | ||||||
| chr6:70231092
|
G | A | 42 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.2503+1491C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231092 | ||||||
| chr6:70231119
|
T | C | 152 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(149): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2503+1464A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231119 | ||||||
| chr6:70231228
|
G | T | 46 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(43): Show | 46 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.2503+1355C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231228 | ||||||
| chr6:70231244
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2503+1339G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231244 | ||||||
| chr6:70231427
|
T | G | 1 | a0003c0003t0004g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2503+1156A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231427 | ||||||
| chr6:70231458
|
T | C | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2503+1125A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231458 | ||||||
| chr6:70231512
|
T | C | 348 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(345): Show | 360 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.2503+1071A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231512 | ||||||
| chr6:70231528
|
G | T | 22 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(19): Show | 22 | HG01069.hp1 HG01433.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2503+1055C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231528 | ||||||
| chr6:70231546
|
T | C | 33 | a0004c0007t0001g0014a0004c0007t0001g0017a0004c0007t0001g0018others(30): Show | 33 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2503+1037A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231546 | ||||||
| chr6:70231563
|
C | CA | 46 | a0001c0001t0002g0125a0001c0012t0001g0120a0001c0012t0001g0135others(43): Show | 48 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.2503+1019dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231563 | ||||||
| chr6:70231715
|
T | TA | 96 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2503+867dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231715 | ||||||
| chr6:70231730
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2503+853G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231730 | ||||||
| chr6:70231771
|
T | C | 46 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(43): Show | 48 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.2503+812A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231771 | ||||||
| chr6:70231775
|
G | A | 19 | a0001c0001t0002g0019a0001c0001t0002g0033a0001c0001t0002g0068others(16): Show | 19 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2503+808C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231775 | ||||||
| chr6:70231791
|
T | C | 36 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2503+792A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231791 | ||||||
| chr6:70231904
|
A | G | 153 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2503+679T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70231904 | ||||||
| chr6:70232064
|
G | GA | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2503+518dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70232064 | ||||||
| chr6:70232069
|
A | G | 1 | a0002c0004t0008g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2503+514T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70232069 | ||||||
| chr6:70232262
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2503+321T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70232262 | ||||||
| chr6:70232269
|
T | C | 6 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2503+314A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70232269 | ||||||
| chr6:70232514
|
G | A | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2503+69C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 36/37 | chr6 | 70232514 | ||||||
| chr6:70232834
|
A | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2315-63T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70232834 | ||||||
| chr6:70232886
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2315-115T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70232886 | ||||||
| chr6:70232949
|
G | A | 1 | a0003c0003t0001g0328 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2315-178C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70232949 | ||||||
| chr6:70232957
|
T | A | 1 | a0001c0001t0006g0342 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2315-186A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70232957 | ||||||
| chr6:70232957
|
T | G | 87 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(84): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2315-186A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70232957 | ||||||
| chr6:70233014
|
G | C | 5 | a0002c0002t0001g0223a0002c0002t0001g0288a0002c0002t0001g0290others(2): Show | 5 | NA18946.hp2 NA18960.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.2315-243C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233014 | ||||||
| chr6:70233038
|
G | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2315-267C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233038 | ||||||
| chr6:70233081
|
C | T | 153 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2315-310G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233081 | ||||||
| chr6:70233166
|
TG | T | 33 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(30): Show | 33 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2315-396delC | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233166 | ||||||
| chr6:70233244
|
G | A | 3 | a0003c0006t0003g0003a0003c0006t0003g0072a0003c0006t0003g0080 | 4 | NA18966.hp2 NA19076.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2315-473C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233244 | ||||||
| chr6:70233334
|
T | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2315-563A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233334 | ||||||
| chr6:70233338
|
C | T | 34 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(31): Show | 34 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2315-567G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233338 | ||||||
| chr6:70233359
|
A | G | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2315-588T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233359 | ||||||
| chr6:70233804
|
T | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2314+735A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233804 | ||||||
| chr6:70233872
|
A | G | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2314+667T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233872 | ||||||
| chr6:70233874
|
G | A | 91 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(88): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.2314+665C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233874 | ||||||
| chr6:70233875
|
G | A | 1 | a0004c0007t0006g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2314+664C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233875 | ||||||
| chr6:70233989
|
G | A | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2314+550C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70233989 | ||||||
| chr6:70234083
|
C | T | 2 | a0002c0008t0005g0009a0002c0008t0005g0337 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2314+456G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234083 | ||||||
| chr6:70234103
|
C | T | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2314+436G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234103 | ||||||
| chr6:70234235
|
A | AGT | 10 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2314+302_2314+303d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234235 | ||||||
| chr6:70234235
|
AGT | A | 46 | a0002c0004t0001g0105a0002c0008t0002g0092a0003c0003t0001g0029others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.2314+302_2314+303d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234235 | ||||||
| chr6:70234257
|
T | TGTGTGTG others(1): Show |
1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2314+281_2314+282i others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234257 | ||||||
| chr6:70234299
|
C | CAAAAA | 24 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2314+239_2314+240i others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234299 | ||||||
| chr6:70234304
|
C | A | 24 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2314+235G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234304 | ||||||
| chr6:70234304
|
C | CAAAA | 26 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0004g0212others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.2314+231_2314+234d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234304 | ||||||
| chr6:70234305
|
A | AAAAC | 4 | a0002c0004t0003g0286a0002c0004t0004g0254a0003c0003t0008g0280others(1): Show | 4 | HG01433.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2314+233_2314+234i others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234305 | ||||||
| chr6:70234374
|
T | C | 2 | a0003c0003t0001g0226a0003c0003t0001g0232 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2314+165A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234374 | ||||||
| chr6:70234376
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2314+163G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234376 | ||||||
| chr6:70234420
|
G | C | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2314+119C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 35/37 | chr6 | 70234420 | ||||||
| chr6:70234728
|
A | G | 1 | a0002c0004t0011g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2259+66T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 34/37 | chr6 | 70234728 | ||||||
| chr6:70234739
|
G | C | 24 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2259+55C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 34/37 | chr6 | 70234739 | ||||||
| chr6:70234762
|
A | G | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2259+32T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 34/37 | chr6 | 70234762 | ||||||
| chr6:70234787
|
C | A | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.2259+7G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 34/37 | chr6 | 70234787 | ||||||
| chr6:70234959
|
C | T | 1 | a0007c0014t0002g0270 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2113-19G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70234959 | ||||||
| chr6:70235030
|
G | A | 33 | a0004c0007t0001g0014a0004c0007t0001g0017a0004c0007t0001g0018others(30): Show | 33 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2113-90C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235030 | ||||||
| chr6:70235102
|
C | T | 1 | a0003c0010t0003g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2113-162G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235102 | ||||||
| chr6:70235122
|
C | T | 33 | a0004c0007t0001g0014a0004c0007t0001g0017a0004c0007t0001g0018others(30): Show | 33 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2113-182G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235122 | ||||||
| chr6:70235131
|
A | G | 3 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350 | 3 | HG02970.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2113-191T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235131 | ||||||
| chr6:70235280
|
C | T | 10 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2113-340G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235280 | ||||||
| chr6:70235409
|
T | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-469A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235409 | ||||||
| chr6:70235432
|
A | G | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-492T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235432 | ||||||
| chr6:70235459
|
TATA | T | 23 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(20): Show | 24 | HG02040.hp1 HG02165.hp1 HG03491.hp2 others(21): Show |
intron_variant | MODIFIER | c.2113-522_2113-520d others(5): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235459 | ||||||
| chr6:70235462
|
A | T | 1 | a0001c0001t0002g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2113-522T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235462 | ||||||
| chr6:70235517
|
T | C | 13 | a0004c0009t0001g0097a0004c0009t0001g0211a0004c0009t0001g0234others(10): Show | 13 | HG00621.hp1 HG01255.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2113-577A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235517 | ||||||
| chr6:70235565
|
C | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2113-625G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235565 | ||||||
| chr6:70235723
|
CT | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-784delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235723 | ||||||
| chr6:70235750
|
C | T | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-810G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235750 | ||||||
| chr6:70235842
|
C | T | 1 | a0004c0009t0001g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2113-902G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235842 | ||||||
| chr6:70235852
|
C | T | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2113-912G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235852 | ||||||
| chr6:70235889
|
C | T | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-949G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235889 | ||||||
| chr6:70235910
|
C | T | 1 | a0001c0017t0002g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2113-970G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235910 | ||||||
| chr6:70235955
|
A | C | 4 | a0008c0015t0003g0002a0008c0023t0012g0329a0013c0026t0001g0249others(1): Show | 6 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2113-1015T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70235955 | ||||||
| chr6:70236008
|
G | A | 2 | a0001c0001t0003g0102a0001c0001t0003g0104 | 2 | HG01517.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2113-1068C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236008 | ||||||
| chr6:70236099
|
C | T | 1 | a0004c0009t0001g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2113-1159G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236099 | ||||||
| chr6:70236112
|
C | CA | 60 | a0001c0001t0002g0013a0001c0001t0002g0136a0001c0001t0002g0137others(57): Show | 60 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2113-1173dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236112 | ||||||
| chr6:70236112
|
C | CAA | 13 | a0001c0001t0002g0098a0001c0001t0002g0156a0001c0001t0002g0167others(10): Show | 13 | HG00408.hp1 HG00597.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2113-1174_2113-117 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236112 | ||||||
| chr6:70236112
|
CA | C | 22 | a0001c0030t0003g0121a0002c0002t0001g0030a0002c0002t0001g0058others(19): Show | 23 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.2113-1173delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236112 | ||||||
| chr6:70236112
|
CAA | C | 74 | a0001c0001t0004g0257a0001c0001t0006g0342a0002c0002t0001g0045others(71): Show | 76 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2113-1174_2113-117 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236112 | ||||||
| chr6:70236112
|
CAAA | C | 28 | a0001c0001t0004g0145a0002c0004t0001g0105a0002c0004t0003g0286others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2113-1175_2113-117 others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236112 | ||||||
| chr6:70236140
|
A | T | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-1200T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236140 | ||||||
| chr6:70236176
|
G | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-1236C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236176 | ||||||
| chr6:70236202
|
G | A | 127 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2113-1262C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236202 | ||||||
| chr6:70236360
|
A | T | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2113-1420T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236360 | ||||||
| chr6:70236407
|
A | G | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2113-1467T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236407 | ||||||
| chr6:70236413
|
T | C | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2113-1473A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236413 | ||||||
| chr6:70236516
|
C | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2113-1576G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236516 | ||||||
| chr6:70236591
|
A | C | 8 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0122others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2113-1651T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236591 | ||||||
| chr6:70236640
|
T | C | 8 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0122others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2113-1700A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236640 | ||||||
| chr6:70236799
|
T | C | 3 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350 | 3 | HG02970.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2113-1859A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236799 | ||||||
| chr6:70236823
|
C | CT | 16 | a0001c0001t0003g0170a0001c0001t0006g0342a0002c0008t0005g0336others(13): Show | 16 | HG01069.hp1 HG02109.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.2113-1884dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236823 | ||||||
| chr6:70236825
|
T | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-1885A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236825 | ||||||
| chr6:70236832
|
T | C | 54 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2113-1892A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236832 | ||||||
| chr6:70236971
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2113-2031C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70236971 | ||||||
| chr6:70237011
|
T | C | 58 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2113-2071A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237011 | ||||||
| chr6:70237029
|
G | T | 12 | a0004c0007t0001g0014a0004c0007t0001g0017a0004c0007t0001g0018others(9): Show | 12 | HG00438.hp1 HG01123.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2113-2089C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237029 | ||||||
| chr6:70237065
|
T | C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2113-2125A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237065 | ||||||
| chr6:70237113
|
T | G | 36 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0105others(33): Show | 38 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2112+2141A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237113 | ||||||
| chr6:70237206
|
C | T | 1 | a0004c0009t0001g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2112+2048G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237206 | ||||||
| chr6:70237237
|
T | G | 1 | a0002c0002t0001g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2112+2017A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237237 | ||||||
| chr6:70237257
|
A | C | 3 | a0003c0010t0003g0081a0003c0010t0003g0082a0003c0010t0003g0085 | 3 | HG01069.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2112+1997T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237257 | ||||||
| chr6:70237409
|
A | G | 1 | a0003c0003t0001g0029 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2112+1845T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237409 | ||||||
| chr6:70237563
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2112+1691A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237563 | ||||||
| chr6:70237661
|
G | A | 1 | a0007c0014t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2112+1593C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237661 | ||||||
| chr6:70237758
|
G | T | 4 | a0008c0015t0003g0002a0008c0023t0012g0329a0013c0026t0001g0249others(1): Show | 6 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2112+1496C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237758 | ||||||
| chr6:70237789
|
G | A | 42 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(39): Show | 42 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2112+1465C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237789 | ||||||
| chr6:70237893
|
G | A | 2 | a0013c0026t0001g0249a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2112+1361C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237893 | ||||||
| chr6:70237913
|
A | G | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2112+1341T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70237913 | ||||||
| chr6:70238027
|
T | C | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2112+1227A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238027 | ||||||
| chr6:70238144
|
T | A | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2112+1110A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238144 | ||||||
| chr6:70238145
|
A | T | 24 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(21): Show | 25 | HG00741.hp2 HG02040.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.2112+1109T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238145 | ||||||
| chr6:70238186
|
T | C | 11 | a0003c0010t0002g0084a0003c0010t0003g0036a0003c0010t0003g0071others(8): Show | 11 | HG01069.hp1 HG02615.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.2112+1068A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238186 | ||||||
| chr6:70238204
|
G | A | 1 | a0002c0002t0001g0201 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2112+1050C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238204 | ||||||
| chr6:70238361
|
C | G | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2112+893G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238361 | ||||||
| chr6:70238459
|
G | A | 1 | a0005c0005t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2112+795C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238459 | ||||||
| chr6:70238467
|
C | T | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2112+787G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238467 | ||||||
| chr6:70238494
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2112+760A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238494 | ||||||
| chr6:70238534
|
C | T | 13 | a0001c0001t0006g0342a0003c0003t0004g0271a0003c0010t0002g0084others(10): Show | 13 | HG01069.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2112+720G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238534 | ||||||
| chr6:70238582
|
C | T | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2112+672G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238582 | ||||||
| chr6:70238647
|
T | C | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2112+607A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238647 | ||||||
| chr6:70238861
|
G | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2112+393C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238861 | ||||||
| chr6:70238993
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2112+261C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70238993 | ||||||
| chr6:70239138
|
C | CA | 15 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(12): Show | 15 | HG00099.hp1 HG00639.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2112+115dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70239138 | ||||||
| chr6:70239138
|
CA | C | 16 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(13): Show | 18 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2112+115delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70239138 | ||||||
| chr6:70239185
|
A | G | 10 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2112+69T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70239185 | ||||||
| chr6:70239198
|
T | C | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2112+56A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 33/37 | chr6 | 70239198 | ||||||
| chr6:70239316
|
A | G | 16 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(13): Show | 18 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2080-30T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239316 | ||||||
| chr6:70239376
|
A | G | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2080-90T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239376 | ||||||
| chr6:70239404
|
C | T | 24 | a0002c0004t0001g0105a0003c0003t0001g0226a0003c0003t0001g0231others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2080-118G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239404 | ||||||
| chr6:70239622
|
A | C | 153 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2080-336T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239622 | ||||||
| chr6:70239696
|
C | T | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2080-410G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239696 | ||||||
| chr6:70239749
|
A | G | 153 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2080-463T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239749 | ||||||
| chr6:70239777
|
T | A | 16 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(13): Show | 18 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2080-491A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239777 | ||||||
| chr6:70239784
|
C | T | 16 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(13): Show | 18 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2080-498G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239784 | ||||||
| chr6:70239975
|
T | C | 23 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(20): Show | 24 | HG02040.hp1 HG02165.hp1 HG03491.hp2 others(21): Show |
intron_variant | MODIFIER | c.2080-689A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70239975 | ||||||
| chr6:70240038
|
A | C | 1 | a0001c0031t0002g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2079+651T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240038 | ||||||
| chr6:70240048
|
C | T | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2079+641G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240048 | ||||||
| chr6:70240200
|
C | A | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2079+489G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240200 | ||||||
| chr6:70240202
|
T | C | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2079+487A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240202 | ||||||
| chr6:70240321
|
C | T | 7 | a0001c0001t0002g0035a0001c0001t0002g0126a0001c0001t0002g0134others(4): Show | 7 | NA18942.hp1 NA18962.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.2079+368G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240321 | ||||||
| chr6:70240326
|
T | A | 1 | a0001c0001t0002g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2079+363A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240326 | ||||||
| chr6:70240342
|
T | C | 23 | a0001c0030t0003g0121a0003c0006t0003g0003a0003c0006t0003g0026others(20): Show | 24 | HG02040.hp1 HG02165.hp1 HG03491.hp2 others(21): Show |
intron_variant | MODIFIER | c.2079+347A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240342 | ||||||
| chr6:70240362
|
C | T | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2079+327G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240362 | ||||||
| chr6:70240502
|
G | T | 8 | a0002c0002t0001g0025a0002c0002t0001g0218a0002c0002t0001g0219others(5): Show | 8 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.2079+187C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240502 | ||||||
| chr6:70240578
|
A | AATAT | 8 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(5): Show | 10 | HG01884.hp1 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2079+107_2079+110d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240578 | ||||||
| chr6:70240578
|
AAT | A | 138 | a0001c0001t0006g0342a0001c0030t0003g0121a0002c0002t0001g0030others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.2079+109_2079+110d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240578 | ||||||
| chr6:70240594
|
T | TATATAC | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2079+94_2079+95ins others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240594 | ||||||
| chr6:70240607
|
CTG | C | 3 | a0002c0002t0001g0044a0003c0003t0008g0280a0009c0020t0003g0213 | 3 | HG03486.hp2 HG04184.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2079+80_2079+81del others(2): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240607 | ||||||
| chr6:70240612
|
T | TTAGAAGT others(7): Show |
1 | a0002c0002t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2079+63_2079+76dup others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240612 | ||||||
| chr6:70240618
|
G | GTA | 15 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(12): Show | 17 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2079+69_2079+70dup others(2): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240618 | ||||||
| chr6:70240652
|
T | C | 15 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(12): Show | 17 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2079+37A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 32/37 | chr6 | 70240652 | ||||||
| chr6:70240838
|
G | A | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2035-105C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240838 | ||||||
| chr6:70240893
|
GT | G | 15 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(12): Show | 17 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2035-161delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240893 | ||||||
| chr6:70240895
|
T | C | 15 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(12): Show | 17 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2035-162A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240895 | ||||||
| chr6:70240902
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2035-169T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240902 | ||||||
| chr6:70240925
|
A | G | 1 | a0004c0009t0001g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2035-192T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240925 | ||||||
| chr6:70240932
|
A | T | 1 | a0003c0013t0003g0311 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2035-199T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70240932 | ||||||
| chr6:70241122
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2034+297C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241122 | ||||||
| chr6:70241176
|
G | C | 13 | a0001c0001t0006g0342a0003c0003t0004g0271a0003c0010t0002g0084others(10): Show | 13 | HG01069.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034+243C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241176 | ||||||
| chr6:70241182
|
C | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0129 | 2 | NA18949.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2034+237G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241182 | ||||||
| chr6:70241242
|
T | C | 26 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0002t0001g0030others(23): Show | 28 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.2034+177A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241242 | ||||||
| chr6:70241261
|
C | A | 2 | a0002c0004t0008g0123a0002c0004t0011g0330 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2034+158G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241261 | ||||||
| chr6:70241400
|
A | C | 6 | a0004c0007t0001g0256a0004c0007t0006g0346a0004c0007t0006g0347others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2034+19T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241400 | ||||||
| chr6:70241400
|
A | G | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2034+19T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 31/37 | chr6 | 70241400 | ||||||
| chr6:70241470
|
T | C | 1 | a0001c0001t0003g0117 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1999-16A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/37 | chr6 | 70241470 | ||||||
| chr6:70241537
|
A | G | 15 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(12): Show | 17 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1999-83T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/37 | chr6 | 70241537 | ||||||
| chr6:70241549
|
G | A | 7 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0259others(4): Show | 8 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1999-95C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/37 | chr6 | 70241549 | ||||||
| chr6:70241740
|
C | A | 12 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(9): Show | 14 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1998+224G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/37 | chr6 | 70241740 | ||||||
| chr6:70241744
|
C | A | 12 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(9): Show | 14 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1998+220G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 30/37 | chr6 | 70241744 | ||||||
| chr6:70242103
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1927-68G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 29/37 | chr6 | 70242103 | ||||||
| chr6:70242206
|
G | A | 3 | a0002c0004t0002g0049a0002c0004t0002g0050a0002c0004t0002g0051 | 3 | HG00733.hp2 HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1927-171C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 29/37 | chr6 | 70242206 | ||||||
| chr6:70242278
|
G | A | 98 | a0001c0001t0002g0179a0001c0012t0001g0120a0001c0012t0001g0131others(95): Show | 100 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1927-243C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 29/37 | chr6 | 70242278 | ||||||
| chr6:70242362
|
A | G | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1926+300T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 29/37 | chr6 | 70242362 | ||||||
| chr6:70242579
|
T | C | 1 | a0002c0004t0011g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1926+83A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 29/37 | chr6 | 70242579 | ||||||
| chr6:70242967
|
T | A | 1 | a0001c0001t0002g0162 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1873-252A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70242967 | ||||||
| chr6:70243110
|
A | G | 1 | a0003c0010t0003g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1873-395T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243110 | ||||||
| chr6:70243194
|
T | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0129 | 2 | NA18949.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1873-479A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243194 | ||||||
| chr6:70243321
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1873-606T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243321 | ||||||
| chr6:70243399
|
G | T | 23 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1873-684C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243399 | ||||||
| chr6:70243514
|
A | G | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-799T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243514 | ||||||
| chr6:70243635
|
C | A | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-920G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243635 | ||||||
| chr6:70243824
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1873-1109C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243824 | ||||||
| chr6:70243926
|
A | G | 1 | a0002c0002t0002g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1873-1211T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70243926 | ||||||
| chr6:70244450
|
G | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1873-1735C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244450 | ||||||
| chr6:70244525
|
C | T | 35 | a0001c0030t0003g0121a0003c0003t0004g0271a0003c0006t0003g0003others(32): Show | 36 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.1873-1810G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244525 | ||||||
| chr6:70244704
|
G | A | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-1989C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244704 | ||||||
| chr6:70244783
|
G | A | 4 | a0003c0006t0003g0038a0003c0006t0003g0078a0003c0006t0003g0090others(1): Show | 4 | NA18962.hp1 NA18967.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873-2068C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244783 | ||||||
| chr6:70244784
|
A | T | 1 | a0002c0002t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1873-2069T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244784 | ||||||
| chr6:70244801
|
CTT | C | 15 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(12): Show | 16 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1873-2088_1873-208 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244801 | ||||||
| chr6:70244950
|
C | G | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-2235G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70244950 | ||||||
| chr6:70245174
|
G | A | 23 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(20): Show | 23 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1873-2459C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245174 | ||||||
| chr6:70245322
|
A | T | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1873-2607T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245322 | ||||||
| chr6:70245504
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1873-2789C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245504 | ||||||
| chr6:70245513
|
A | G | 2 | a0004c0009t0001g0319a0004c0009t0001g0320 | 2 | HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1873-2798T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245513 | ||||||
| chr6:70245520
|
CAGATATG others(6): Show |
C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1873-2818_1873-280 others(17): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245520 | ||||||
| chr6:70245564
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1873-2849T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245564 | ||||||
| chr6:70245740
|
A | C | 8 | a0001c0001t0002g0019a0001c0012t0001g0131a0001c0012t0001g0180others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1873-3025T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245740 | ||||||
| chr6:70245789
|
T | TA | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1873-3075dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245789 | ||||||
| chr6:70245911
|
C | T | 1 | a0002c0004t0002g0235 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1873-3196G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70245911 | ||||||
| chr6:70246027
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1873-3312G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246027 | ||||||
| chr6:70246193
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1873-3478G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246193 | ||||||
| chr6:70246257
|
G | A | 3 | a0001c0001t0002g0287a0001c0001t0002g0318a0001c0029t0002g0174 | 3 | HG00558.hp1 NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1873-3542C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246257 | ||||||
| chr6:70246375
|
C | CA | 14 | a0001c0001t0002g0168a0001c0001t0004g0145a0001c0001t0004g0257others(11): Show | 16 | HG01433.hp2 HG01884.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.1873-3661dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246375 | ||||||
| chr6:70246379
|
A | C | 15 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(12): Show | 16 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1873-3664T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246379 | ||||||
| chr6:70246455
|
A | G | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1873-3740T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246455 | ||||||
| chr6:70246724
|
A | T | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-4009T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246724 | ||||||
| chr6:70246817
|
A | T | 1 | a0002c0002t0001g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1873-4102T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246817 | ||||||
| chr6:70246930
|
A | C | 4 | a0001c0012t0001g0131a0001c0012t0001g0132a0001c0012t0001g0135others(1): Show | 4 | HG01123.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873-4215T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70246930 | ||||||
| chr6:70247066
|
G | A | 51 | a0001c0012t0001g0120a0001c0012t0001g0131a0001c0012t0001g0132others(48): Show | 53 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1873-4351C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247066 | ||||||
| chr6:70247112
|
G | T | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1873-4397C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247112 | ||||||
| chr6:70247146
|
T | C | 2 | a0001c0001t0003g0096a0001c0001t0003g0310 | 2 | NA19004.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1873-4431A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247146 | ||||||
| chr6:70247186
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1873-4471T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247186 | ||||||
| chr6:70247329
|
G | C | 1 | a0001c0001t0002g0001 | 4 | NA18952.hp1 NA18981.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873-4614C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247329 | ||||||
| chr6:70247354
|
A | G | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1873-4639T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247354 | ||||||
| chr6:70247719
|
T | C | 13 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(10): Show | 15 | HG01433.hp2 HG01884.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1872+4401A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247719 | ||||||
| chr6:70247889
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1872+4231C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247889 | ||||||
| chr6:70247976
|
C | T | 1 | a0002c0002t0001g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1872+4144G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70247976 | ||||||
| chr6:70248069
|
C | T | 147 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1872+4051G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70248069 | ||||||
| chr6:70248357
|
G | A | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1872+3763C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70248357 | ||||||
| chr6:70248643
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(74): Show | 81 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1872+3477G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70248643 | ||||||
| chr6:70248785
|
G | A | 20 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(17): Show | 23 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1872+3335C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70248785 | ||||||
| chr6:70248942
|
C | T | 3 | a0008c0023t0012g0329a0013c0026t0001g0249a0015c0032t0013g0341 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1872+3178G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70248942 | ||||||
| chr6:70249079
|
A | G | 132 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(129): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1872+3041T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249079 | ||||||
| chr6:70249172
|
T | TCCACTGA others(321): Show |
1 | a0003c0003t0002g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(332): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(322): Show |
1 | a0003c0003t0002g0252 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(333): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(328): Show |
2 | a0003c0003t0002g0052a0003c0003t0002g0053 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1872+2947_1872+294 others(339): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(329): Show |
1 | a0003c0003t0002g0047 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(340): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(333): Show |
4 | a0003c0003t0001g0328a0003c0003t0007g0349a0003c0003t0007g0350others(1): Show | 4 | HG02572.hp2 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1872+2947_1872+294 others(344): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(343): Show |
1 | a0005c0005t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(354): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(344): Show |
2 | a0003c0003t0001g0041a0003c0003t0002g0127 | 2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1872+2947_1872+294 others(355): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(345): Show |
7 | a0003c0003t0001g0029a0003c0003t0001g0042a0003c0003t0001g0094others(4): Show | 7 | HG00099.hp2 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1872+2947_1872+294 others(356): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(346): Show |
1 | a0003c0003t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(357): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249172
|
T | TCCACTGA others(349): Show |
1 | a0003c0003t0001g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1872+2947_1872+294 others(360): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249172 | ||||||
| chr6:70249280
|
T | C | 1 | a0002c0002t0001g0218 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1872+2840A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249280 | ||||||
| chr6:70249528
|
T | C | 2 | a0001c0001t0002g0124a0002c0004t0002g0294 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1872+2592A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249528 | ||||||
| chr6:70249549
|
G | C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1872+2571C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249549 | ||||||
| chr6:70249637
|
G | A | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2483C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249637 | ||||||
| chr6:70249670
|
A | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2450T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249670 | ||||||
| chr6:70249780
|
AC | A | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2339delG | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249780 | ||||||
| chr6:70249835
|
C | T | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1872+2285G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249835 | ||||||
| chr6:70249849
|
T | A | 1 | a0002c0002t0001g0292 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1872+2271A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249849 | ||||||
| chr6:70249908
|
T | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2212A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70249908 | ||||||
| chr6:70250020
|
G | T | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2100C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250020 | ||||||
| chr6:70250043
|
C | T | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1872+2077G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250043 | ||||||
| chr6:70250096
|
A | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+2024T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250096 | ||||||
| chr6:70250127
|
G | GCCCTGC | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1872+1992_1872+199 others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250127 | ||||||
| chr6:70250128
|
G | A | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1872+1992C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250128 | ||||||
| chr6:70250172
|
G | A | 33 | a0003c0006t0003g0003a0003c0006t0003g0026a0003c0006t0003g0027others(30): Show | 34 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.1872+1948C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250172 | ||||||
| chr6:70250307
|
G | A | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1813C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250307 | ||||||
| chr6:70250358
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1872+1762C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250358 | ||||||
| chr6:70250389
|
C | T | 15 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(12): Show | 16 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1872+1731G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250389 | ||||||
| chr6:70250406
|
C | T | 5 | a0002c0002t0001g0030a0002c0002t0001g0045a0002c0002t0001g0055others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1872+1714G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250406 | ||||||
| chr6:70250532
|
C | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1588G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250532 | ||||||
| chr6:70250602
|
G | C | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1518C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250602 | ||||||
| chr6:70250624
|
T | C | 143 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1872+1496A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250624 | ||||||
| chr6:70250725
|
T | C | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1395A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250725 | ||||||
| chr6:70250738
|
T | C | 35 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(32): Show | 36 | HG01069.hp1 HG02165.hp1 HG02615.hp2 others(33): Show |
intron_variant | MODIFIER | c.1872+1382A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250738 | ||||||
| chr6:70250741
|
G | A | 35 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(32): Show | 36 | HG01069.hp1 HG02165.hp1 HG02615.hp2 others(33): Show |
intron_variant | MODIFIER | c.1872+1379C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250741 | ||||||
| chr6:70250925
|
T | A | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1195A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250925 | ||||||
| chr6:70250960
|
C | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1160G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70250960 | ||||||
| chr6:70251023
|
C | T | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1097G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251023 | ||||||
| chr6:70251088
|
C | T | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+1032G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251088 | ||||||
| chr6:70251187
|
A | C | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+933T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251187 | ||||||
| chr6:70251205
|
A | C | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+915T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251205 | ||||||
| chr6:70251288
|
T | C | 23 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1872+832A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251288 | ||||||
| chr6:70251393
|
A | T | 16 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(13): Show | 19 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1872+727T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251393 | ||||||
| chr6:70251414
|
A | G | 36 | a0003c0003t0004g0271a0003c0003t0010g0241a0003c0003t0010g0250others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1872+706T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251414 | ||||||
| chr6:70251439
|
C | T | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG01175.hp2 HG01257.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1872+681G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251439 | ||||||
| chr6:70251513
|
C | A | 25 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1872+607G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251513 | ||||||
| chr6:70251519
|
C | T | 1 | a0004c0009t0002g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1872+601G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251519 | ||||||
| chr6:70251608
|
T | A | 146 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1872+512A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251608 | ||||||
| chr6:70251633
|
T | A | 7 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(4): Show | 7 | HG01433.hp2 HG02074.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1872+487A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251633 | ||||||
| chr6:70251693
|
A | G | 35 | a0003c0003t0001g0285a0004c0007t0001g0014a0004c0007t0001g0017others(32): Show | 35 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1872+427T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251693 | ||||||
| chr6:70251783
|
T | C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1872+337A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70251783 | ||||||
| chr6:70252042
|
A | G | 96 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(93): Show | 97 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1872+78T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 28/37 | chr6 | 70252042 | ||||||
| chr6:70252336
|
C | T | 59 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(56): Show | 60 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1765-21G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252336 | ||||||
| chr6:70252341
|
A | G | 142 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0059others(139): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1765-26T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252341 | ||||||
| chr6:70252405
|
T | C | 1 | a0003c0006t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1765-90A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252405 | ||||||
| chr6:70252406
|
G | T | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1765-91C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252406 | ||||||
| chr6:70252461
|
T | C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-146A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252461 | ||||||
| chr6:70252478
|
C | T | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-163G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252478 | ||||||
| chr6:70252516
|
G | A | 59 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(56): Show | 60 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1765-201C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252516 | ||||||
| chr6:70252536
|
A | C | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1765-221T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252536 | ||||||
| chr6:70252537
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1765-222A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252537 | ||||||
| chr6:70252728
|
G | T | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-413C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252728 | ||||||
| chr6:70252736
|
G | A | 12 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(9): Show | 12 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1765-421C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252736 | ||||||
| chr6:70252764
|
G | A | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1765-449C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252764 | ||||||
| chr6:70252844
|
G | A | 68 | a0001c0012t0001g0120a0001c0012t0001g0131a0001c0012t0001g0132others(65): Show | 70 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1765-529C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252844 | ||||||
| chr6:70252887
|
A | T | 1 | a0001c0019t0006g0344 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1764+498T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70252887 | ||||||
| chr6:70253016
|
GA | G | 58 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(55): Show | 59 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1764+368delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70253016 | ||||||
| chr6:70253112
|
T | A | 4 | a0005c0005t0001g0024a0005c0005t0001g0255a0005c0005t0001g0258others(1): Show | 4 | HG01934.hp1 HG02738.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+273A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 26/37 | chr6 | 70253112 | ||||||
| chr6:70253453
|
T | G | 134 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1720-24A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253453 | ||||||
| chr6:70253529
|
A | G | 134 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1720-100T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253529 | ||||||
| chr6:70253544
|
T | C | 37 | a0003c0003t0001g0285a0003c0003t0010g0241a0003c0003t0010g0250others(34): Show | 37 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1720-115A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253544 | ||||||
| chr6:70253576
|
T | C | 134 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1720-147A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253576 | ||||||
| chr6:70253818
|
C | T | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720-389G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253818 | ||||||
| chr6:70253841
|
G | T | 142 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0059others(139): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1720-412C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70253841 | ||||||
| chr6:70254066
|
T | C | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1719+410A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254066 | ||||||
| chr6:70254078
|
C | T | 2 | a0005c0005t0001g0107a0005c0005t0001g0108 | 2 | HG00099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1719+398G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254078 | ||||||
| chr6:70254101
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1719+375A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254101 | ||||||
| chr6:70254238
|
A | T | 35 | a0003c0003t0001g0285a0004c0007t0001g0014a0004c0007t0001g0017others(32): Show | 35 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1719+238T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254238 | ||||||
| chr6:70254303
|
A | C | 1 | a0001c0001t0003g0109 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1719+173T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254303 | ||||||
| chr6:70254354
|
T | C | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1719+122A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 25/37 | chr6 | 70254354 | ||||||
| chr6:70254551
|
C | T | 1 | a0003c0003t0004g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1666-22G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254551 | ||||||
| chr6:70254561
|
C | T | 1 | a0003c0003t0001g0285 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1666-32G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254561 | ||||||
| chr6:70254594
|
G | A | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1666-65C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254594 | ||||||
| chr6:70254653
|
T | C | 1 | a0003c0003t0002g0047 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1666-124A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254653 | ||||||
| chr6:70254818
|
G | A | 1 | a0001c0001t0003g0096 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1665+145C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254818 | ||||||
| chr6:70254821
|
A | T | 2 | a0003c0003t0004g0271a0008c0015t0003g0002 | 4 | HG02723.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1665+142T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254821 | ||||||
| chr6:70254877
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1665+86A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254877 | ||||||
| chr6:70254909
|
T | C | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1665+54A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 24/37 | chr6 | 70254909 | ||||||
| chr6:70255041
|
T | C | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1612-25A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 23/37 | chr6 | 70255041 | ||||||
| chr6:70255042
|
G | T | 14 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(11): Show | 14 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612-26C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 23/37 | chr6 | 70255042 | ||||||
| chr6:70255248
|
C | T | 7 | a0003c0006t0003g0026a0003c0006t0003g0027a0003c0006t0003g0073others(4): Show | 7 | NA18970.hp2 NA18972.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-45G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 22/37 | chr6 | 70255248 | ||||||
| chr6:70255279
|
A | G | 1 | a0002c0004t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557+58T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 22/37 | chr6 | 70255279 | ||||||
| chr6:70255404
|
A | T | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1504-14T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255404 | ||||||
| chr6:70255422
|
A | C | 326 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(323): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.1504-32T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255422 | ||||||
| chr6:70255446
|
T | A | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1504-56A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255446 | ||||||
| chr6:70255559
|
C | G | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1504-169G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255559 | ||||||
| chr6:70255724
|
T | A | 26 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(23): Show | 28 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1504-334A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255724 | ||||||
| chr6:70255790
|
T | A | 1 | a0002c0002t0001g0048 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1504-400A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255790 | ||||||
| chr6:70255791
|
A | G | 1 | a0002c0004t0004g0246 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1504-401T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255791 | ||||||
| chr6:70255797
|
A | G | 102 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1504-407T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255797 | ||||||
| chr6:70255825
|
TTGATATA others(2): Show |
T | 110 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0001g0059others(107): Show | 113 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1504-444_1504-436d others(11): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255825 | ||||||
| chr6:70255843
|
G | A | 7 | a0003c0006t0003g0026a0003c0006t0003g0027a0003c0006t0003g0073others(4): Show | 7 | NA18970.hp2 NA18972.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-453C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255843 | ||||||
| chr6:70255986
|
T | G | 1 | a0002c0002t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1504-596A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70255986 | ||||||
| chr6:70256124
|
G | A | 64 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(61): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1503+644C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256124 | ||||||
| chr6:70256156
|
C | A | 1 | a0001c0001t0004g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1503+612G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256156 | ||||||
| chr6:70256181
|
G | C | 1 | a0005c0005t0002g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1503+587C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256181 | ||||||
| chr6:70256216
|
G | A | 35 | a0003c0003t0001g0285a0004c0007t0001g0014a0004c0007t0001g0017others(32): Show | 35 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1503+552C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256216 | ||||||
| chr6:70256270
|
T | C | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1503+498A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256270 | ||||||
| chr6:70256417
|
G | A | 146 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1503+351C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256417 | ||||||
| chr6:70256470
|
A | G | 102 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1503+298T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256470 | ||||||
| chr6:70256602
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1503+166G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256602 | ||||||
| chr6:70256718
|
C | CA | 24 | a0001c0001t0002g0154a0002c0002t0001g0044a0002c0004t0002g0235others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1503+49dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256718 | ||||||
| chr6:70256718
|
CA | C | 17 | a0001c0019t0006g0344a0002c0004t0001g0059a0002c0004t0004g0246others(14): Show | 18 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1503+49delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 21/37 | chr6 | 70256718 | ||||||
| chr6:70256867
|
A | G | 1 | a0002c0008t0005g0334 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1450-46T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70256867 | ||||||
| chr6:70256902
|
T | C | 1 | a0001c0001t0002g0178 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1450-81A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70256902 | ||||||
| chr6:70256905
|
T | C | 1 | a0001c0001t0003g0172 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1450-84A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70256905 | ||||||
| chr6:70256958
|
G | A | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1450-137C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70256958 | ||||||
| chr6:70256961
|
T | A | 1 | a0001c0001t0002g0178 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1450-140A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70256961 | ||||||
| chr6:70257027
|
A | G | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1450-206T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257027 | ||||||
| chr6:70257048
|
A | AT | 36 | a0001c0001t0002g0095a0001c0001t0002g0137a0001c0001t0002g0153others(33): Show | 36 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1450-228dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257048
|
AT | A | 55 | a0001c0001t0002g0156a0001c0001t0003g0079a0001c0001t0003g0310others(52): Show | 56 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.1450-228delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257048
|
ATT | A | 14 | a0002c0004t0008g0123a0002c0004t0011g0330a0002c0008t0005g0336others(11): Show | 14 | HG01069.hp1 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1450-229_1450-228d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257048
|
ATTT | A | 10 | a0002c0004t0001g0059a0002c0018t0006g0343a0003c0003t0001g0231others(7): Show | 10 | HG00741.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1450-230_1450-228d others(5): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257048
|
ATTTT | A | 30 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(27): Show | 31 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1450-231_1450-228d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257048
|
ATTTTT | A | 22 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(19): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1450-232_1450-228d others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257048 | ||||||
| chr6:70257053
|
T | A | 4 | a0003c0003t0001g0061a0003c0003t0001g0094a0003c0003t0002g0252others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-232A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257053 | ||||||
| chr6:70257054
|
T | A | 21 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(18): Show | 23 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1450-233A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257054 | ||||||
| chr6:70257091
|
G | A | 65 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(62): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1450-270C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257091 | ||||||
| chr6:70257148
|
C | T | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1450-327G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257148 | ||||||
| chr6:70257242
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | NA18962.hp2 NA18985.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1450-421C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257242 | ||||||
| chr6:70257249
|
T | C | 146 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1450-428A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257249 | ||||||
| chr6:70257424
|
G | A | 1 | a0016c0027t0003g0181 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1450-603C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257424 | ||||||
| chr6:70257481
|
G | A | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1450-660C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257481 | ||||||
| chr6:70257560
|
C | G | 23 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1450-739G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257560 | ||||||
| chr6:70257603
|
C | T | 1 | a0001c0012t0001g0191 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1450-782G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257603 | ||||||
| chr6:70257604
|
G | A | 24 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1450-783C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257604 | ||||||
| chr6:70257687
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1450-866G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257687 | ||||||
| chr6:70257771
|
A | G | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1450-950T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257771 | ||||||
| chr6:70257784
|
A | G | 3 | a0003c0003t0010g0241a0003c0003t0010g0250a0013c0026t0001g0249 | 3 | HG03453.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1450-963T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257784 | ||||||
| chr6:70257791
|
CACTCTAA others(13): Show |
C | 2 | a0001c0001t0003g0079a0001c0001t0003g0117 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1450-990_1450-971d others(22): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257791 | ||||||
| chr6:70257974
|
A | G | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1450-1153T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257974 | ||||||
| chr6:70257988
|
A | G | 3 | a0003c0006t0003g0003a0003c0006t0003g0072a0003c0006t0003g0080 | 4 | NA18966.hp2 NA19076.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-1167T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70257988 | ||||||
| chr6:70258009
|
G | C | 102 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1450-1188C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258009 | ||||||
| chr6:70258241
|
A | G | 1 | a0005c0005t0001g0204 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1450-1420T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258241 | ||||||
| chr6:70258343
|
A | G | 102 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1450-1522T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258343 | ||||||
| chr6:70258504
|
G | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1450-1683C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258504 | ||||||
| chr6:70258573
|
T | G | 102 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1450-1752A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258573 | ||||||
| chr6:70258655
|
A | ACT | 25 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1450-1836_1450-183 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258655 | ||||||
| chr6:70258957
|
T | C | 25 | a0003c0003t0001g0226a0003c0003t0001g0231a0003c0003t0001g0232others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1449+1700A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70258957 | ||||||
| chr6:70259250
|
C | T | 146 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1449+1407G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259250 | ||||||
| chr6:70259318
|
A | G | 146 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1449+1339T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259318 | ||||||
| chr6:70259344
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1449+1313C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259344 | ||||||
| chr6:70259399
|
T | C | 1 | a0002c0002t0001g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1449+1258A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259399 | ||||||
| chr6:70259724
|
A | G | 1 | a0005c0005t0001g0204 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1449+933T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259724 | ||||||
| chr6:70259814
|
G | A | 1 | a0002c0008t0002g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1449+843C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259814 | ||||||
| chr6:70259893
|
A | G | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1449+764T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259893 | ||||||
| chr6:70259949
|
A | G | 14 | a0002c0004t0001g0059a0002c0004t0004g0246a0002c0004t0004g0274others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1449+708T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70259949 | ||||||
| chr6:70260011
|
C | T | 3 | a0004c0007t0001g0021a0004c0007t0001g0088a0004c0007t0001g0196 | 3 | NA18973.hp2 NA18974.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1449+646G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260011 | ||||||
| chr6:70260237
|
C | T | 1 | a0002c0016t0004g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1449+420G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260237 | ||||||
| chr6:70260277
|
C | T | 2 | a0001c0001t0003g0113a0014c0033t0003g0159 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1449+380G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260277 | ||||||
| chr6:70260296
|
C | G | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1449+361G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260296 | ||||||
| chr6:70260403
|
C | T | 1 | a0003c0006t0003g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1449+254G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260403 | ||||||
| chr6:70260412
|
A | G | 96 | a0001c0001t0003g0195a0001c0001t0004g0145a0001c0001t0004g0257others(93): Show | 98 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.1449+245T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260412 | ||||||
| chr6:70260462
|
C | T | 1 | a0002c0004t0002g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1449+195G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260462 | ||||||
| chr6:70260548
|
C | CA | 49 | a0001c0001t0002g0095a0001c0001t0003g0195a0001c0001t0006g0342others(46): Show | 50 | HG00099.hp2 HG00323.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1449+108dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260548 | ||||||
| chr6:70260548
|
CA | C | 11 | a0001c0001t0002g0149a0001c0001t0004g0145a0001c0001t0004g0257others(8): Show | 11 | HG00733.hp1 HG01070.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1449+108delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260548 | ||||||
| chr6:70260596
|
C | T | 107 | a0001c0001t0002g0188a0001c0001t0004g0145a0001c0001t0004g0257others(104): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1449+61G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260596 | ||||||
| chr6:70260597
|
G | A | 2 | a0003c0013t0003g0198a0003c0013t0003g0199 | 2 | NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1449+60C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 20/37 | chr6 | 70260597 | ||||||
| chr6:70260767
|
A | G | 1 | a0002c0004t0004g0246 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1396-57T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70260767 | ||||||
| chr6:70260797
|
G | A | 4 | a0001c0001t0002g0148a0002c0004t0002g0049a0002c0004t0002g0050others(1): Show | 4 | HG00733.hp2 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-87C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70260797 | ||||||
| chr6:70260798
|
A | G | 31 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(28): Show | 32 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1396-88T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70260798 | ||||||
| chr6:70260896
|
T | G | 1 | a0001c0001t0003g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1396-186A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70260896 | ||||||
| chr6:70260936
|
G | T | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1396-226C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70260936 | ||||||
| chr6:70261040
|
T | C | 43 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(40): Show | 44 | HG01069.hp1 HG01070.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.1396-330A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261040 | ||||||
| chr6:70261087
|
A | T | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1396-377T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261087 | ||||||
| chr6:70261161
|
G | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1396-451C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261161 | ||||||
| chr6:70261311
|
T | C | 117 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(114): Show | 119 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.1396-601A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261311 | ||||||
| chr6:70261312
|
G | A | 34 | a0002c0004t0011g0330a0003c0003t0001g0285a0004c0007t0001g0014others(31): Show | 34 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1396-602C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261312 | ||||||
| chr6:70261364
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1396-654A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261364 | ||||||
| chr6:70261377
|
GC | G | 117 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(114): Show | 119 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.1396-668delG | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261377 | ||||||
| chr6:70261385
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1396-675T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261385 | ||||||
| chr6:70261387
|
T | A | 22 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1396-677A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261387 | ||||||
| chr6:70261427
|
G | A | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1396-717C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261427 | ||||||
| chr6:70261443
|
G | A | 2 | a0003c0003t0008g0280a0009c0020t0003g0213 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1396-733C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261443 | ||||||
| chr6:70261554
|
T | C | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1396-844A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261554 | ||||||
| chr6:70261595
|
T | A | 1 | a0001c0001t0002g0068 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1396-885A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261595 | ||||||
| chr6:70261611
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1396-901A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261611 | ||||||
| chr6:70261797
|
G | A | 2 | a0001c0001t0002g0013a0003c0003t0004g0271 | 2 | HG02723.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1396-1087C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261797 | ||||||
| chr6:70261806
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1396-1096G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261806 | ||||||
| chr6:70261885
|
G | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1396-1175C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261885 | ||||||
| chr6:70261938
|
C | T | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1396-1228G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261938 | ||||||
| chr6:70261955
|
A | G | 2 | a0003c0003t0004g0271a0008c0023t0012g0329 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1396-1245T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261955 | ||||||
| chr6:70261972
|
A | G | 2 | a0003c0003t0004g0271a0008c0023t0012g0329 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1396-1262T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261972 | ||||||
| chr6:70261974
|
G | A | 2 | a0003c0003t0004g0271a0008c0023t0012g0329 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1396-1264C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70261974 | ||||||
| chr6:70262085
|
C | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+1159G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262085 | ||||||
| chr6:70262128
|
T | A | 19 | a0003c0003t0004g0054a0003c0003t0004g0271a0005c0005t0001g0016others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1395+1116A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262128 | ||||||
| chr6:70262165
|
C | CA | 22 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1395+1078dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262165 | ||||||
| chr6:70262195
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1395+1049T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262195 | ||||||
| chr6:70262235
|
A | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+1009T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262235 | ||||||
| chr6:70262260
|
G | A | 1 | a0001c0029t0002g0174 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1395+984C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262260 | ||||||
| chr6:70262405
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+839G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262405 | ||||||
| chr6:70262425
|
G | A | 21 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1395+819C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262425 | ||||||
| chr6:70262477
|
T | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+767A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262477 | ||||||
| chr6:70262504
|
A | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+740T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262504 | ||||||
| chr6:70262533
|
G | A | 1 | a0003c0006t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1395+711C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262533 | ||||||
| chr6:70262625
|
G | A | 22 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1395+619C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262625 | ||||||
| chr6:70262679
|
G | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+565C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262679 | ||||||
| chr6:70262748
|
A | G | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1395+496T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262748 | ||||||
| chr6:70262762
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1395+482G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262762 | ||||||
| chr6:70262874
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1395+370A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262874 | ||||||
| chr6:70262899
|
T | A | 1 | a0002c0004t0004g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1395+345A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262899 | ||||||
| chr6:70262925
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+319G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262925 | ||||||
| chr6:70262943
|
G | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+301C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70262943 | ||||||
| chr6:70263005
|
T | C | 21 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1395+239A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70263005 | ||||||
| chr6:70263111
|
G | A | 27 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(24): Show | 29 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1395+133C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70263111 | ||||||
| chr6:70263230
|
A | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+14T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 19/37 | chr6 | 70263230 | ||||||
| chr6:70263324
|
G | A | 6 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342-27C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263324 | ||||||
| chr6:70263372
|
T | TAACTCAT others(333): Show |
1 | a0001c0001t0002g0130 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1342-76_1342-75ins others(340): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263372 | ||||||
| chr6:70263449
|
A | C | 5 | a0005c0005t0001g0107a0005c0005t0001g0108a0005c0005t0001g0133others(2): Show | 5 | HG00099.hp1 HG00639.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-152T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263449 | ||||||
| chr6:70263497
|
A | T | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1342-200T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263497 | ||||||
| chr6:70263500
|
C | A | 2 | a0001c0001t0002g0176a0001c0031t0002g0175 | 2 | HG00408.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1342-203G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263500 | ||||||
| chr6:70263504
|
A | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-207T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263504 | ||||||
| chr6:70263598
|
G | T | 1 | a0001c0019t0006g0344 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1342-301C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263598 | ||||||
| chr6:70263673
|
G | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1342-376C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263673 | ||||||
| chr6:70263717
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-420A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263717 | ||||||
| chr6:70263724
|
T | G | 1 | a0003c0003t0001g0285 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1342-427A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263724 | ||||||
| chr6:70263802
|
A | G | 21 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1342-505T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263802 | ||||||
| chr6:70263909
|
A | G | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1342-612T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263909 | ||||||
| chr6:70263919
|
G | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-622C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263919 | ||||||
| chr6:70263928
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-631G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263928 | ||||||
| chr6:70263940
|
G | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-643C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263940 | ||||||
| chr6:70263973
|
T | G | 1 | a0002c0004t0004g0246 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1342-676A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263973 | ||||||
| chr6:70263986
|
C | A | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1342-689G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263986 | ||||||
| chr6:70263987
|
G | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-690C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70263987 | ||||||
| chr6:70264023
|
T | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-726A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264023 | ||||||
| chr6:70264060
|
C | T | 2 | a0003c0003t0004g0271a0008c0023t0012g0329 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1342-763G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264060 | ||||||
| chr6:70264063
|
G | A | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1342-766C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264063 | ||||||
| chr6:70264063
|
G | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-766C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264063 | ||||||
| chr6:70264261
|
A | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342-964T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264261 | ||||||
| chr6:70264363
|
T | C | 23 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1342-1066A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264363 | ||||||
| chr6:70264407
|
C | T | 6 | a0004c0007t0001g0256a0004c0007t0006g0346a0004c0007t0006g0347others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1342-1110G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264407 | ||||||
| chr6:70264526
|
G | T | 25 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(22): Show | 27 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1342-1229C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264526 | ||||||
| chr6:70264545
|
C | A | 1 | a0001c0001t0006g0342 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1342-1248G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264545 | ||||||
| chr6:70264562
|
T | G | 2 | a0002c0008t0005g0338a0002c0008t0005g0339 | 2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1342-1265A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264562 | ||||||
| chr6:70264568
|
A | C | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1342-1271T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264568 | ||||||
| chr6:70264763
|
T | C | 27 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(24): Show | 29 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1342-1466A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264763 | ||||||
| chr6:70264942
|
C | T | 2 | a0001c0012t0001g0131a0001c0012t0001g0180 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1342-1645G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70264942 | ||||||
| chr6:70265021
|
C | T | 1 | a0001c0001t0009g0010 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1341+1696G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265021 | ||||||
| chr6:70265210
|
G | A | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1341+1507C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265210 | ||||||
| chr6:70265236
|
G | A | 1 | a0003c0003t0008g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1341+1481C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265236 | ||||||
| chr6:70265277
|
G | A | 33 | a0003c0006t0003g0003a0003c0006t0003g0026a0003c0006t0003g0027others(30): Show | 34 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.1341+1440C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265277 | ||||||
| chr6:70265417
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1341+1300G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265417 | ||||||
| chr6:70265428
|
GT | G | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1341+1288delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265428 | ||||||
| chr6:70265500
|
C | CT | 12 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0002t0001g0219others(9): Show | 12 | HG00738.hp1 HG01070.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1341+1216dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265500 | ||||||
| chr6:70265500
|
C | CTT | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1341+1215_1341+121 others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265500 | ||||||
| chr6:70265500
|
CT | C | 8 | a0001c0001t0002g0156a0001c0001t0002g0184a0002c0002t0001g0300others(5): Show | 8 | HG02683.hp1 HG03098.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1341+1216delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265500 | ||||||
| chr6:70265608
|
A | G | 3 | a0005c0005t0002g0248a0005c0005t0003g0247a0005c0005t0006g0345 | 3 | HG02293.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1341+1109T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265608 | ||||||
| chr6:70265658
|
C | T | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1341+1059G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265658 | ||||||
| chr6:70265688
|
A | G | 1 | a0007c0014t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1341+1029T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265688 | ||||||
| chr6:70265734
|
A | G | 1 | a0001c0001t0003g0310 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1341+983T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265734 | ||||||
| chr6:70265809
|
C | T | 214 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1341+908G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70265809 | ||||||
| chr6:70266014
|
A | G | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1341+703T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266014 | ||||||
| chr6:70266079
|
G | T | 81 | a0001c0001t0006g0342a0002c0004t0004g0246a0002c0004t0004g0274others(78): Show | 83 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.1341+638C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266079 | ||||||
| chr6:70266089
|
A | C | 46 | a0001c0001t0006g0342a0002c0004t0004g0246a0002c0004t0004g0274others(43): Show | 47 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1341+628T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266089 | ||||||
| chr6:70266207
|
A | G | 5 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341+510T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266207 | ||||||
| chr6:70266302
|
GC | G | 22 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1341+414delG | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266302 | ||||||
| chr6:70266396
|
C | T | 101 | a0001c0001t0006g0342a0002c0004t0001g0059a0002c0004t0004g0246others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1341+321G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266396 | ||||||
| chr6:70266532
|
A | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1341+185T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266532 | ||||||
| chr6:70266580
|
G | T | 2 | a0004c0009t0001g0211a0004c0009t0001g0234 | 2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1341+137C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266580 | ||||||
| chr6:70266600
|
A | T | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1341+117T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 18/37 | chr6 | 70266600 | ||||||
| chr6:70266774
|
A | T | 1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.1288-4T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266774 | ||||||
| chr6:70266835
|
A | G | 57 | a0002c0022t0001g0281a0003c0003t0001g0029a0003c0003t0001g0031others(54): Show | 58 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.1288-65T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266835 | ||||||
| chr6:70266887
|
T | C | 9 | a0001c0001t0002g0035a0001c0001t0002g0126a0001c0001t0002g0134others(6): Show | 9 | HG00408.hp2 NA18942.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288-117A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266887 | ||||||
| chr6:70266916
|
A | T | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288-146T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266916 | ||||||
| chr6:70266937
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1288-167G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266937 | ||||||
| chr6:70266958
|
T | G | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1288-188A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70266958 | ||||||
| chr6:70267083
|
C | T | 1 | a0005c0005t0006g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1288-313G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267083 | ||||||
| chr6:70267100
|
G | T | 9 | a0002c0002t0001g0243a0002c0002t0001g0261a0002c0002t0001g0262others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288-330C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267100 | ||||||
| chr6:70267110
|
G | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288-340C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267110 | ||||||
| chr6:70267115
|
G | A | 20 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1288-345C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267115 | ||||||
| chr6:70267198
|
T | C | 1 | a0002c0002t0001g0307 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1288-428A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267198 | ||||||
| chr6:70267224
|
T | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1288-454A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267224 | ||||||
| chr6:70267263
|
T | G | 3 | a0003c0003t0002g0047a0003c0003t0002g0052a0003c0003t0002g0053 | 3 | HG01169.hp1 HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1288-493A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267263 | ||||||
| chr6:70267297
|
A | AT | 6 | a0001c0001t0002g0125a0001c0001t0002g0144a0001c0001t0002g0162others(3): Show | 6 | HG00639.hp1 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288-528dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267297 | ||||||
| chr6:70267315
|
T | G | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288-545A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267315 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(2): Show |
23 | a0002c0004t0011g0330a0002c0022t0001g0281a0003c0003t0001g0285others(20): Show | 23 | HG00621.hp1 HG01123.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1288-550_1288-549i others(11): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(3): Show |
11 | a0001c0001t0006g0342a0004c0007t0001g0017a0004c0007t0001g0018others(8): Show | 11 | HG00438.hp1 HG01255.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1288-550_1288-549i others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(4): Show |
1 | a0004c0009t0001g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1288-550_1288-549i others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0004g0145a0002c0004t0004g0212a0002c0016t0004g0187others(1): Show | 4 | HG01070.hp1 HG02074.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-550_1288-549i others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(6): Show |
5 | a0001c0001t0004g0257a0002c0004t0003g0286a0002c0004t0004g0254others(2): Show | 5 | HG01433.hp2 HG02738.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288-550_1288-549i others(15): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267319
|
G | GTTTTTTT others(7): Show |
1 | a0003c0003t0002g0252 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1288-550_1288-549i others(16): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267319 | ||||||
| chr6:70267327
|
G | GGTTTTTT others(3): Show |
1 | a0002c0008t0005g0336 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1288-558_1288-557i others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GGTTTTTT others(4): Show |
8 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(5): Show | 9 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288-558_1288-557i others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GGTTTTTT others(5): Show |
1 | a0002c0008t0005g0333 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1288-558_1288-557i others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GT | 6 | a0001c0001t0002g0141a0002c0002t0001g0291a0002c0004t0002g0006others(3): Show | 7 | HG04184.hp1 NA18973.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1288-558dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTGTT others(4): Show |
1 | a0003c0003t0002g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1288-558_1288-557i others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(2): Show |
10 | a0003c0010t0002g0084a0003c0010t0003g0071a0003c0010t0003g0082others(7): Show | 10 | HG01069.hp1 HG02451.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288-566_1288-558d others(11): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(5): Show |
2 | a0008c0015t0003g0002a0013c0026t0001g0249 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-558_1288-557i others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(3): Show |
26 | a0003c0006t0003g0003a0003c0006t0003g0037a0003c0006t0003g0038others(23): Show | 27 | HG00738.hp2 HG01192.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1288-567_1288-558d others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(4): Show |
38 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1288-568_1288-558d others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(5): Show |
4 | a0003c0003t0001g0061a0005c0005t0001g0107a0007c0014t0001g0065others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-569_1288-558d others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(6): Show |
1 | a0002c0004t0008g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1288-558_1288-557i others(15): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(7): Show |
1 | a0002c0004t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1288-558_1288-557i others(16): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | GTTTTTTT others(8): Show |
1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1288-558_1288-557i others(17): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267327
|
G | T | 48 | a0001c0001t0004g0145a0001c0001t0004g0257a0001c0001t0006g0342others(45): Show | 48 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1288-557C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267327 | ||||||
| chr6:70267353
|
G | A | 3 | a0003c0003t0004g0271a0008c0015t0003g0002a0013c0026t0001g0249 | 5 | HG02723.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288-583C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267353 | ||||||
| chr6:70267368
|
G | T | 2 | a0008c0015t0003g0002a0013c0026t0001g0249 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-598C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267368 | ||||||
| chr6:70267448
|
G | A | 1 | a0004c0007t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1288-678C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267448 | ||||||
| chr6:70267467
|
C | T | 1 | a0005c0028t0002g0324 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1288-697G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267467 | ||||||
| chr6:70267617
|
C | T | 7 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(4): Show | 9 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288-847G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267617 | ||||||
| chr6:70267667
|
G | C | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1288-897C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267667 | ||||||
| chr6:70267783
|
T | C | 1 | a0001c0001t0003g0004 | 2 | HG02132.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1288-1013A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70267783 | ||||||
| chr6:70268023
|
G | GTATT | 22 | a0003c0006t0003g0003a0003c0006t0003g0026a0003c0006t0003g0027others(19): Show | 23 | HG02040.hp1 HG02165.hp1 HG03831.hp1 others(20): Show |
intron_variant | MODIFIER | c.1287+777_1287+780d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268023 | ||||||
| chr6:70268041
|
T | C | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287+763A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268041 | ||||||
| chr6:70268105
|
C | G | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1287+699G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268105 | ||||||
| chr6:70268172
|
A | G | 1 | a0001c0001t0003g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1287+632T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268172 | ||||||
| chr6:70268182
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1287+622T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268182 | ||||||
| chr6:70268212
|
T | C | 22 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1287+592A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268212 | ||||||
| chr6:70268221
|
CT | C | 9 | a0001c0001t0004g0145a0001c0001t0004g0257a0002c0004t0003g0286others(6): Show | 9 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+582delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268221 | ||||||
| chr6:70268308
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1287+496C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268308 | ||||||
| chr6:70268325
|
C | A | 5 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287+479G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268325 | ||||||
| chr6:70268353
|
T | G | 1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1287+451A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268353 | ||||||
| chr6:70268429
|
G | T | 4 | a0002c0004t0002g0006a0002c0004t0002g0020a0002c0004t0002g0229others(1): Show | 5 | NA18973.hp1 NA18983.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+375C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268429 | ||||||
| chr6:70268576
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1287+228A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268576 | ||||||
| chr6:70268660
|
C | A | 2 | a0008c0015t0003g0002a0013c0026t0001g0249 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+144G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268660 | ||||||
| chr6:70268694
|
T | C | 11 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287+110A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 17/37 | chr6 | 70268694 | ||||||
| chr6:70268937
|
A | G | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1231-77T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70268937 | ||||||
| chr6:70268939
|
C | A | 5 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-79G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70268939 | ||||||
| chr6:70269001
|
C | T | 7 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(4): Show | 9 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-141G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269001 | ||||||
| chr6:70269250
|
C | T | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1230+383G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269250 | ||||||
| chr6:70269341
|
G | A | 34 | a0003c0006t0003g0003a0003c0006t0003g0026a0003c0006t0003g0027others(31): Show | 35 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(32): Show |
intron_variant | MODIFIER | c.1230+292C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269341 | ||||||
| chr6:70269422
|
A | G | 346 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(343): Show | 358 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.1230+211T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269422 | ||||||
| chr6:70269440
|
T | C | 1 | a0002c0004t0011g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1230+193A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269440 | ||||||
| chr6:70269490
|
C | T | 145 | a0001c0001t0002g0179a0001c0001t0004g0145a0001c0001t0004g0257others(142): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1230+143G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269490 | ||||||
| chr6:70269580
|
G | A | 41 | a0002c0004t0001g0059a0002c0004t0008g0123a0002c0018t0006g0343others(38): Show | 44 | HG01069.hp1 HG01884.hp2 HG02040.hp1 others(41): Show |
intron_variant | MODIFIER | c.1230+53C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269580 | ||||||
| chr6:70269580
|
G | T | 10 | a0002c0004t0004g0246a0002c0004t0004g0274a0002c0008t0005g0009others(7): Show | 11 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1230+53C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269580 | ||||||
| chr6:70269621
|
A | G | 22 | a0003c0003t0001g0029a0003c0003t0001g0031a0003c0003t0001g0041others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1230+12T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 16/37 | chr6 | 70269621 | ||||||
| chr6:70269709
|
T | C | 2 | a0005c0005t0001g0151a0005c0005t0001g0189 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1198-44A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70269709 | ||||||
| chr6:70269829
|
G | A | 1 | a0002c0022t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1198-164C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70269829 | ||||||
| chr6:70269833
|
T | C | 1 | a0002c0002t0001g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1198-168A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70269833 | ||||||
| chr6:70269888
|
C | T | 36 | a0002c0004t0004g0274a0003c0003t0001g0231a0003c0006t0003g0003others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-223G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70269888 | ||||||
| chr6:70269897
|
A | G | 36 | a0002c0004t0004g0274a0003c0003t0001g0231a0003c0006t0003g0003others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-232T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70269897 | ||||||
| chr6:70270049
|
G | A | 36 | a0002c0004t0004g0274a0003c0003t0001g0231a0003c0006t0003g0003others(33): Show | 37 | HG01069.hp1 HG02040.hp1 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1197+265C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70270049 | ||||||
| chr6:70270139
|
C | T | 1 | a0003c0003t0002g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1197+175G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70270139 | ||||||
| chr6:70270209
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1197+105A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70270209 | ||||||
| chr6:70270303
|
A | G | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1197+11T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 15/37 | chr6 | 70270303 | ||||||
| chr6:70270387
|
C | T | 1 | a0003c0006t0003g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1144-20G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270387 | ||||||
| chr6:70270504
|
C | T | 2 | a0004c0009t0001g0319a0004c0009t0001g0320 | 2 | HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1144-137G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270504 | ||||||
| chr6:70270544
|
A | G | 67 | a0001c0001t0002g0318a0001c0001t0003g0106a0001c0001t0004g0257others(64): Show | 67 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1144-177T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270544 | ||||||
| chr6:70270631
|
A | G | 11 | a0002c0004t0011g0330a0006c0011t0003g0278a0006c0011t0004g0007others(8): Show | 12 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1144-264T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270631 | ||||||
| chr6:70270665
|
G | A | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1144-298C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270665 | ||||||
| chr6:70270685
|
G | A | 213 | a0001c0001t0002g0019a0001c0001t0002g0318a0001c0001t0003g0012others(210): Show | 219 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.1144-318C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270685 | ||||||
| chr6:70270755
|
T | C | 109 | a0001c0001t0002g0019a0001c0001t0002g0098a0001c0001t0002g0318others(106): Show | 113 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1144-388A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270755 | ||||||
| chr6:70270759
|
C | T | 1 | a0002c0004t0008g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1144-392G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270759 | ||||||
| chr6:70270906
|
C | T | 3 | a0007c0014t0001g0065a0007c0014t0001g0066a0013c0026t0001g0249 | 3 | HG01884.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1144-539G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270906 | ||||||
| chr6:70270921
|
G | C | 2 | a0002c0004t0004g0212a0002c0016t0004g0187 | 2 | HG02074.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1144-554C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70270921 | ||||||
| chr6:70271018
|
A | T | 10 | a0003c0010t0002g0084a0003c0010t0003g0036a0003c0010t0003g0071others(7): Show | 10 | HG01069.hp1 HG02615.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1143+637T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271018 | ||||||
| chr6:70271138
|
A | G | 3 | a0007c0014t0001g0065a0007c0014t0001g0066a0013c0026t0001g0249 | 3 | HG01884.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1143+517T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271138 | ||||||
| chr6:70271145
|
G | A | 3 | a0004c0007t0001g0021a0004c0007t0001g0088a0004c0007t0001g0196 | 3 | NA18973.hp2 NA18974.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1143+510C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271145 | ||||||
| chr6:70271153
|
A | G | 42 | a0001c0001t0002g0208a0002c0004t0004g0274a0002c0008t0002g0069others(39): Show | 46 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.1143+502T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271153 | ||||||
| chr6:70271171
|
C | G | 2 | a0007c0014t0001g0065a0007c0014t0001g0066 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1143+484G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271171 | ||||||
| chr6:70271231
|
A | G | 20 | a0002c0008t0002g0069a0002c0008t0002g0091a0002c0008t0002g0092others(17): Show | 21 | HG01928.hp1 HG02040.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.1143+424T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271231 | ||||||
| chr6:70271337
|
T | G | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+318A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271337 | ||||||
| chr6:70271347
|
G | C | 7 | a0002c0004t0001g0059a0002c0004t0002g0242a0002c0004t0008g0123others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+308C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271347 | ||||||
| chr6:70271464
|
G | A | 1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1143+191C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271464 | ||||||
| chr6:70271494
|
A | C | 1 | a0004c0009t0001g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1143+161T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271494 | ||||||
| chr6:70271495
|
T | C | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+160A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271495 | ||||||
| chr6:70271559
|
T | G | 1 | a0004c0009t0001g0097 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1143+96A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271559 | ||||||
| chr6:70271627
|
G | A | 2 | a0007c0014t0001g0065a0007c0014t0001g0066 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1143+28C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 14/37 | chr6 | 70271627 | ||||||
| chr6:70271942
|
A | T | 1 | a0004c0009t0001g0097 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1089+123T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 13/37 | chr6 | 70271942 | ||||||
| chr6:70272018
|
G | A | 1 | a0001c0001t0003g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1089+47C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 13/37 | chr6 | 70272018 | ||||||
| chr6:70272091
|
A | G | 36 | a0001c0001t0002g0019a0001c0001t0002g0318a0001c0001t0002g0327others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.1066-3T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272091 | ||||||
| chr6:70272108
|
A | G | 1 | a0001c0030t0003g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1066-20T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272108 | ||||||
| chr6:70272123
|
G | T | 1 | a0001c0001t0002g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1066-35C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272123 | ||||||
| chr6:70272124
|
G | T | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066-36C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272124 | ||||||
| chr6:70272198
|
A | G | 1 | a0002c0008t0002g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1066-110T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272198 | ||||||
| chr6:70272294
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1066-206A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272294 | ||||||
| chr6:70272306
|
T | A | 7 | a0002c0004t0001g0059a0002c0004t0002g0242a0002c0004t0008g0123others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066-218A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272306 | ||||||
| chr6:70272325
|
CT | C | 128 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(125): Show | 131 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(128): Show |
intron_variant | MODIFIER | c.1066-238delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272325 | ||||||
| chr6:70272361
|
T | G | 128 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(125): Show | 131 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(128): Show |
intron_variant | MODIFIER | c.1066-273A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272361 | ||||||
| chr6:70272404
|
G | T | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066-316C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272404 | ||||||
| chr6:70272412
|
C | G | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1066-324G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272412 | ||||||
| chr6:70272412
|
C | T | 7 | a0002c0004t0001g0059a0002c0004t0002g0242a0002c0004t0008g0123others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066-324G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272412 | ||||||
| chr6:70272448
|
A | G | 128 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(125): Show | 131 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(128): Show |
intron_variant | MODIFIER | c.1066-360T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272448 | ||||||
| chr6:70272610
|
C | A | 1 | a0002c0002t0001g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1066-522G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272610 | ||||||
| chr6:70272820
|
A | G | 1 | a0002c0004t0004g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1066-732T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272820 | ||||||
| chr6:70272916
|
C | T | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1066-828G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272916 | ||||||
| chr6:70272917
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1066-829G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70272917 | ||||||
| chr6:70273003
|
T | C | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1066-915A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273003 | ||||||
| chr6:70273079
|
A | T | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1065+968T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273079 | ||||||
| chr6:70273114
|
A | C | 7 | a0001c0001t0003g0040a0001c0001t0003g0079a0001c0001t0003g0089others(4): Show | 7 | HG02015.hp1 HG02135.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065+933T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273114 | ||||||
| chr6:70273117
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1065+930G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273117 | ||||||
| chr6:70273226
|
G | A | 130 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(127): Show | 133 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.1065+821C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273226 | ||||||
| chr6:70273354
|
A | G | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1065+693T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273354 | ||||||
| chr6:70273576
|
T | C | 172 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(169): Show | 179 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(176): Show |
intron_variant | MODIFIER | c.1065+471A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273576 | ||||||
| chr6:70273583
|
C | A | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1065+464G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273583 | ||||||
| chr6:70273714
|
A | T | 130 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(127): Show | 133 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.1065+333T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273714 | ||||||
| chr6:70273776
|
G | A | 130 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(127): Show | 133 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.1065+271C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273776 | ||||||
| chr6:70273941
|
T | TAATA | 48 | a0001c0001t0002g0019a0001c0001t0002g0125a0001c0001t0002g0141others(45): Show | 51 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1065+102_1065+105d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273941 | ||||||
| chr6:70273941
|
T | TAATAAAT others(1): Show |
21 | a0001c0001t0002g0327a0001c0001t0003g0012a0002c0008t0005g0332others(18): Show | 22 | HG00609.hp1 HG01255.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1065+98_1065+105du others(9): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273941 | ||||||
| chr6:70273941
|
T | TAATAAAT others(5): Show |
3 | a0004c0007t0001g0021a0004c0007t0006g0346a0005c0005t0002g0015 | 3 | HG00323.hp2 HG03225.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1065+94_1065+105du others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273941 | ||||||
| chr6:70273941
|
TAATA | T | 129 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0208others(126): Show | 132 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.1065+102_1065+105d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273941 | ||||||
| chr6:70273941
|
TAATAAAT others(5): Show |
T | 4 | a0001c0001t0006g0342a0002c0002t0001g0044a0002c0002t0001g0186others(1): Show | 4 | HG01884.hp1 HG03195.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+94_1065+105de others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273941 | ||||||
| chr6:70273963
|
A | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1065+84T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273963 | ||||||
| chr6:70273972
|
T | TAAATAAA others(5): Show |
3 | a0004c0007t0007g0331a0004c0007t0007g0348a0006c0011t0004g0259 | 3 | HG02258.hp1 HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1065+74_1065+75ins others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 12/37 | chr6 | 70273972 | ||||||
| chr6:70274102
|
C | A | 7 | a0002c0004t0001g0059a0002c0004t0002g0242a0002c0004t0008g0123others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-20G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274102 | ||||||
| chr6:70274185
|
GT | G | 45 | a0001c0019t0006g0344a0002c0004t0004g0274a0002c0004t0011g0330others(42): Show | 49 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.1030-104delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274185 | ||||||
| chr6:70274188
|
T | G | 1 | a0001c0001t0002g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1030-106A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274188 | ||||||
| chr6:70274226
|
G | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1030-144C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274226 | ||||||
| chr6:70274247
|
AG | A | 8 | a0001c0001t0003g0040a0001c0001t0003g0079a0001c0001t0003g0089others(5): Show | 8 | HG02015.hp1 HG02135.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-166delC | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274247 | ||||||
| chr6:70274260
|
A | G | 48 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(45): Show | 52 | HG00741.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1030-178T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274260 | ||||||
| chr6:70274383
|
C | T | 7 | a0002c0004t0001g0059a0002c0004t0002g0242a0002c0004t0008g0123others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-301G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274383 | ||||||
| chr6:70274526
|
T | C | 1 | a0002c0002t0001g0238 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1029+193A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274526 | ||||||
| chr6:70274548
|
CT | C | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1029+170delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274548 | ||||||
| chr6:70274583
|
T | C | 2 | a0007c0014t0001g0065a0007c0014t0001g0066 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1029+136A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 11/37 | chr6 | 70274583 | ||||||
| chr6:70274859
|
T | C | 211 | a0001c0001t0002g0019a0001c0001t0002g0318a0001c0001t0002g0327others(208): Show | 218 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.976-87A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70274859 | ||||||
| chr6:70274860
|
G | A | 116 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(113): Show | 119 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.976-88C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70274860 | ||||||
| chr6:70274917
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.976-145A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70274917 | ||||||
| chr6:70274929
|
A | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG00323.hp1 HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.976-157T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70274929 | ||||||
| chr6:70274945
|
G | T | 43 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(40): Show | 47 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.976-173C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70274945 | ||||||
| chr6:70275077
|
A | G | 3 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293 | 3 | HG02155.hp2 NA19003.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.976-305T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275077 | ||||||
| chr6:70275391
|
T | C | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-619A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275391 | ||||||
| chr6:70275424
|
TAAGTATA others(12): Show |
T | 42 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(39): Show | 46 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.976-671_976-653del others(19): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275424 | ||||||
| chr6:70275451
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.976-679G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275451 | ||||||
| chr6:70275515
|
G | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.976-743C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275515 | ||||||
| chr6:70275703
|
C | T | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.976-931G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275703 | ||||||
| chr6:70275725
|
G | T | 2 | a0002c0004t0011g0330a0008c0023t0012g0329 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.976-953C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275725 | ||||||
| chr6:70275813
|
C | T | 1 | a0009c0020t0003g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.976-1041G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275813 | ||||||
| chr6:70275974
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.976-1202T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70275974 | ||||||
| chr6:70276130
|
G | C | 2 | a0003c0003t0010g0241a0003c0003t0010g0250 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.976-1358C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276130 | ||||||
| chr6:70276153
|
G | A | 2 | a0002c0002t0001g0269a0007c0014t0002g0270 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.976-1381C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276153 | ||||||
| chr6:70276158
|
A | G | 3 | a0005c0005t0001g0150a0005c0005t0001g0151a0005c0005t0001g0189 | 3 | HG01243.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.976-1386T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276158 | ||||||
| chr6:70276203
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.976-1431G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276203 | ||||||
| chr6:70276235
|
G | C | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.976-1463C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276235 | ||||||
| chr6:70276342
|
T | A | 2 | a0002c0004t0011g0330a0008c0023t0012g0329 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.976-1570A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276342 | ||||||
| chr6:70276646
|
G | A | 173 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(170): Show | 180 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(177): Show |
intron_variant | MODIFIER | c.976-1874C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276646 | ||||||
| chr6:70276661
|
A | G | 2 | a0007c0014t0001g0065a0007c0014t0001g0066 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.976-1889T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276661 | ||||||
| chr6:70276738
|
A | G | 1 | a0004c0007t0001g0018 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.976-1966T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70276738 | ||||||
| chr6:70277148
|
T | C | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.976-2376A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277148 | ||||||
| chr6:70277343
|
C | CA | 8 | a0002c0004t0001g0240a0002c0004t0003g0286a0002c0004t0004g0212others(5): Show | 8 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.976-2572dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277343 | ||||||
| chr6:70277497
|
G | T | 215 | a0001c0001t0002g0019a0001c0001t0002g0318a0001c0001t0002g0327others(212): Show | 222 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.976-2725C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277497 | ||||||
| chr6:70277520
|
T | A | 1 | a0007c0014t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.976-2748A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277520 | ||||||
| chr6:70277531
|
A | G | 2 | a0002c0002t0001g0044a0002c0002t0001g0186 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.976-2759T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277531 | ||||||
| chr6:70277539
|
A | C | 61 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(58): Show | 64 | HG00609.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.976-2767T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277539 | ||||||
| chr6:70277591
|
T | G | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-2819A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277591 | ||||||
| chr6:70277911
|
A | C | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+2901T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277911 | ||||||
| chr6:70277945
|
G | A | 1 | a0002c0004t0004g0254 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.975+2867C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277945 | ||||||
| chr6:70277977
|
C | G | 1 | a0001c0001t0003g0310 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.975+2835G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70277977 | ||||||
| chr6:70278000
|
T | C | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+2812A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278000 | ||||||
| chr6:70278003
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.975+2809G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278003 | ||||||
| chr6:70278273
|
G | A | 109 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0025others(106): Show | 112 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.975+2539C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278273 | ||||||
| chr6:70278355
|
A | G | 6 | a0006c0011t0003g0278a0006c0011t0004g0007a0006c0011t0004g0275others(3): Show | 7 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.975+2457T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278355 | ||||||
| chr6:70278358
|
T | C | 2 | a0001c0012t0001g0131a0001c0012t0001g0180 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.975+2454A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278358 | ||||||
| chr6:70278424
|
A | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.975+2388T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278424 | ||||||
| chr6:70278516
|
G | A | 175 | a0001c0001t0006g0342a0002c0002t0001g0005a0002c0002t0001g0008others(172): Show | 182 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(179): Show |
intron_variant | MODIFIER | c.975+2296C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278516 | ||||||
| chr6:70278886
|
C | A | 1 | a0001c0001t0002g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.975+1926G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278886 | ||||||
| chr6:70278945
|
G | T | 2 | a0004c0007t0001g0028a0004c0007t0001g0308 | 2 | NA18949.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.975+1867C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278945 | ||||||
| chr6:70278961
|
C | T | 175 | a0001c0001t0006g0342a0002c0002t0001g0005a0002c0002t0001g0008others(172): Show | 182 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(179): Show |
intron_variant | MODIFIER | c.975+1851G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278961 | ||||||
| chr6:70278982
|
A | G | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1830T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278982 | ||||||
| chr6:70278983
|
T | C | 52 | a0002c0004t0002g0086a0002c0004t0003g0286a0002c0004t0004g0212others(49): Show | 56 | HG00741.hp1 HG01069.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.975+1829A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70278983 | ||||||
| chr6:70279006
|
C | A | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1806G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279006 | ||||||
| chr6:70279029
|
C | T | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.975+1783G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279029 | ||||||
| chr6:70279164
|
A | G | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975+1648T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279164 | ||||||
| chr6:70279183
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.975+1629C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279183 | ||||||
| chr6:70279209
|
A | C | 49 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0004t0011g0330others(46): Show | 53 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.975+1603T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279209 | ||||||
| chr6:70279246
|
C | T | 42 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(39): Show | 46 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.975+1566G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279246 | ||||||
| chr6:70279277
|
T | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG01175.hp2 HG01257.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+1535A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279277 | ||||||
| chr6:70279323
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0129a0008c0015t0003g0002 | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+1489G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279323 | ||||||
| chr6:70279352
|
T | TTTAGATA others(1): Show |
3 | a0005c0005t0002g0248a0005c0005t0003g0247a0005c0005t0006g0345 | 3 | HG02293.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.975+1459_975+1460i others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279352 | ||||||
| chr6:70279353
|
A | T | 3 | a0005c0005t0002g0248a0005c0005t0003g0247a0005c0005t0006g0345 | 3 | HG02293.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.975+1459T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279353 | ||||||
| chr6:70279354
|
A | T | 3 | a0005c0005t0002g0248a0005c0005t0003g0247a0005c0005t0006g0345 | 3 | HG02293.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.975+1458T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279354 | ||||||
| chr6:70279372
|
C | T | 24 | a0001c0001t0003g0040a0001c0001t0003g0079a0001c0001t0003g0089others(21): Show | 25 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+1440G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279372 | ||||||
| chr6:70279378
|
G | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975+1434C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279378 | ||||||
| chr6:70279468
|
C | T | 4 | a0001c0001t0002g0318a0001c0012t0001g0233a0004c0009t0001g0325others(1): Show | 4 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1344G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279468 | ||||||
| chr6:70279534
|
G | A | 42 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(39): Show | 46 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.975+1278C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279534 | ||||||
| chr6:70279603
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0035others(77): Show | 83 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.975+1209C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279603 | ||||||
| chr6:70279648
|
C | CA | 25 | a0001c0001t0002g0098a0001c0001t0002g0124a0001c0001t0002g0125others(22): Show | 26 | HG00642.hp1 HG01192.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.975+1163dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(1): Show |
56 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0048others(53): Show | 57 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.975+1156_975+1163d others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(2): Show |
37 | a0002c0002t0001g0008a0002c0002t0001g0044a0002c0002t0001g0045others(34): Show | 39 | HG00099.hp2 HG01361.hp2 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.975+1155_975+1163d others(11): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(3): Show |
10 | a0002c0002t0001g0030a0002c0002t0001g0261a0002c0002t0001g0297others(7): Show | 10 | HG01106.hp2 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+1154_975+1163d others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(4): Show |
2 | a0002c0002t0001g0058a0002c0022t0001g0281 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.975+1153_975+1163d others(13): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(8): Show |
1 | a0002c0004t0008g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.975+1149_975+1163d others(17): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(19): Show |
1 | a0002c0004t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.975+1163_975+1164i others(28): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(21): Show |
1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.975+1163_975+1164i others(30): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
C | CAAAAAAA others(25): Show |
1 | a0003c0003t0008g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.975+1163_975+1164i others(34): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
CAAAA | C | 39 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(36): Show | 41 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.975+1160_975+1163d others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279648
|
CAAAAA | C | 8 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(5): Show | 10 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.975+1159_975+1163d others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279648 | ||||||
| chr6:70279669
|
A | C | 4 | a0002c0004t0011g0330a0003c0003t0010g0241a0003c0003t0010g0250others(1): Show | 4 | HG02451.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1143T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279669 | ||||||
| chr6:70279670
|
A | AAAAAAAA others(5): Show |
1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975+1141_975+1142i others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279670 | ||||||
| chr6:70279670
|
A | C | 42 | a0002c0004t0002g0086a0002c0004t0004g0274a0002c0008t0002g0069others(39): Show | 46 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.975+1142T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279670 | ||||||
| chr6:70279730
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.975+1082T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70279730 | ||||||
| chr6:70280000
|
A | G | 175 | a0001c0001t0006g0342a0002c0002t0001g0005a0002c0002t0001g0008others(172): Show | 182 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(179): Show |
intron_variant | MODIFIER | c.975+812T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280000 | ||||||
| chr6:70280005
|
G | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975+807C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280005 | ||||||
| chr6:70280068
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.975+744C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280068 | ||||||
| chr6:70280274
|
C | G | 23 | a0002c0004t0001g0105a0002c0004t0002g0049a0002c0004t0002g0050others(20): Show | 23 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.975+538G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280274 | ||||||
| chr6:70280614
|
T | C | 1 | a0002c0018t0006g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.975+198A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280614 | ||||||
| chr6:70280658
|
C | G | 1 | a0012c0025t0001g0282 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.975+154G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280658 | ||||||
| chr6:70280679
|
G | C | 4 | a0002c0008t0005g0332a0002c0008t0005g0333a0002c0008t0005g0334others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+133C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280679 | ||||||
| chr6:70280680
|
A | T | 47 | a0002c0002t0001g0030a0002c0002t0001g0044a0002c0002t0001g0045others(44): Show | 47 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.975+132T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280680 | ||||||
| chr6:70280732
|
T | TC | 32 | a0001c0001t0003g0040a0001c0001t0003g0089a0001c0001t0003g0117others(29): Show | 33 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.975+79dupG | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280732 | ||||||
| chr6:70280760
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.975+52C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280760 | ||||||
| chr6:70280767
|
C | T | 46 | a0002c0002t0001g0030a0002c0002t0001g0044a0002c0002t0001g0045others(43): Show | 46 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.975+45G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 10/37 | chr6 | 70280767 | ||||||
| chr6:70280967
|
G | A | 2 | a0003c0003t0001g0226a0003c0003t0001g0232 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.912+37C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 9/37 | chr6 | 70280967 | ||||||
| chr6:70281062
|
G | C | 25 | a0001c0001t0002g0019a0001c0001t0002g0148a0001c0001t0003g0012others(22): Show | 25 | HG00438.hp1 HG00738.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.877-23C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281062 | ||||||
| chr6:70281300
|
G | GA | 9 | a0001c0001t0003g0194a0001c0019t0006g0344a0002c0004t0003g0286others(6): Show | 9 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.876+89dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281300 | ||||||
| chr6:70281300
|
G | GAA | 12 | a0001c0001t0006g0342a0002c0008t0005g0009a0002c0008t0005g0332others(9): Show | 13 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.876+88_876+89dupTT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281300 | ||||||
| chr6:70281300
|
GA | G | 216 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0033others(213): Show | 225 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.876+89delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281300 | ||||||
| chr6:70281314
|
C | A | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0241 | 3 | HG02559.hp2 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.876+76G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281314 | ||||||
| chr6:70281377
|
G | A | 7 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(4): Show | 7 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+13C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281377 | ||||||
| chr6:70281384
|
A | G | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.876+6T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 8/37 | chr6 | 70281384 | ||||||
| chr6:70281486
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.802-22C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281486 | ||||||
| chr6:70281612
|
G | C | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.802-148C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281612 | ||||||
| chr6:70281723
|
C | T | 3 | a0003c0003t0001g0231a0003c0003t0001g0289a0003c0003t0001g0293 | 3 | HG02155.hp2 NA19003.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.802-259G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281723 | ||||||
| chr6:70281763
|
G | C | 1 | a0001c0001t0002g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802-299C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281763 | ||||||
| chr6:70281901
|
G | C | 1 | a0001c0001t0002g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802-437C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281901 | ||||||
| chr6:70281924
|
A | G | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.802-460T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281924 | ||||||
| chr6:70281927
|
C | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG00323.hp1 HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.802-463G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281927 | ||||||
| chr6:70281927
|
C | T | 263 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(260): Show | 274 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.802-463G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70281927 | ||||||
| chr6:70282036
|
T | C | 2 | a0002c0022t0001g0281a0003c0003t0008g0280 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.802-572A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282036 | ||||||
| chr6:70282117
|
A | G | 1 | a0001c0001t0002g0208 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.802-653T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282117 | ||||||
| chr6:70282179
|
G | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.802-715C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282179 | ||||||
| chr6:70282336
|
T | G | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.801+562A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282336 | ||||||
| chr6:70282432
|
T | A | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.801+466A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282432 | ||||||
| chr6:70282433
|
C | T | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.801+465G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282433 | ||||||
| chr6:70282484
|
C | T | 1 | a0005c0005t0001g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.801+414G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282484 | ||||||
| chr6:70282485
|
G | C | 197 | a0001c0001t0002g0001a0001c0001t0002g0019a0001c0001t0002g0033others(194): Show | 206 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.801+413C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282485 | ||||||
| chr6:70282508
|
G | A | 6 | a0004c0009t0001g0315a0004c0009t0001g0316a0004c0009t0001g0321others(3): Show | 6 | NA18965.hp1 NA18967.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+390C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282508 | ||||||
| chr6:70282574
|
G | A | 1 | a0002c0004t0004g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.801+324C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282574 | ||||||
| chr6:70282592
|
C | T | 4 | a0003c0003t0002g0047a0003c0003t0002g0052a0003c0003t0002g0053others(1): Show | 4 | HG01169.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+306G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282592 | ||||||
| chr6:70282623
|
T | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.801+275A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282623 | ||||||
| chr6:70282683
|
C | T | 1 | a0002c0002t0001g0298 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.801+215G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282683 | ||||||
| chr6:70282744
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.801+154A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 7/37 | chr6 | 70282744 | ||||||
| chr6:70283008
|
C | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.781-90G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283008 | ||||||
| chr6:70283136
|
G | A | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781-218C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283136 | ||||||
| chr6:70283357
|
C | T | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+380G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283357 | ||||||
| chr6:70283454
|
T | C | 2 | a0003c0003t0001g0226a0003c0003t0001g0232 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.780+283A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283454 | ||||||
| chr6:70283475
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.780+262C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283475 | ||||||
| chr6:70283554
|
C | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.780+183G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283554 | ||||||
| chr6:70283566
|
A | C | 28 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(25): Show | 30 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.780+171T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283566 | ||||||
| chr6:70283576
|
C | T | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.780+161G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 6/37 | chr6 | 70283576 | ||||||
| chr6:70283897
|
C | T | 1 | a0002c0002t0002g0214 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.697-77G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70283897 | ||||||
| chr6:70283903
|
A | T | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.697-83T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70283903 | ||||||
| chr6:70283945
|
C | T | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.697-125G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70283945 | ||||||
| chr6:70284232
|
C | T | 21 | a0001c0001t0003g0040a0001c0001t0003g0117a0001c0012t0001g0120others(18): Show | 23 | HG00741.hp1 HG00741.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.697-412G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284232 | ||||||
| chr6:70284254
|
G | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.697-434C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284254 | ||||||
| chr6:70284340
|
T | A | 1 | a0003c0006t0003g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.697-520A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284340 | ||||||
| chr6:70284415
|
C | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-595G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284415 | ||||||
| chr6:70284469
|
T | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-649A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284469 | ||||||
| chr6:70284486
|
G | T | 6 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-666C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284486 | ||||||
| chr6:70284695
|
C | T | 5 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-875G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284695 | ||||||
| chr6:70284726
|
C | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-906G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284726 | ||||||
| chr6:70284799
|
C | G | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-979G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70284799 | ||||||
| chr6:70285038
|
G | A | 5 | a0001c0001t0004g0257a0002c0002t0001g0201a0005c0005t0001g0022others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-1218C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285038 | ||||||
| chr6:70285085
|
A | C | 3 | a0002c0004t0002g0006a0002c0004t0002g0229a0002c0004t0002g0235 | 4 | NA18973.hp1 NA18983.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-1265T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285085 | ||||||
| chr6:70285162
|
G | C | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.697-1342C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285162 | ||||||
| chr6:70285213
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-1393C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285213 | ||||||
| chr6:70285266
|
T | C | 129 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(126): Show | 136 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.697-1446A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285266 | ||||||
| chr6:70285517
|
A | G | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-1697T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285517 | ||||||
| chr6:70285583
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0003g0310others(48): Show | 55 | HG00609.hp2 HG00733.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.697-1763G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285583 | ||||||
| chr6:70285587
|
T | C | 3 | a0001c0019t0006g0344a0002c0018t0006g0343a0003c0003t0010g0250 | 3 | HG02559.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.697-1767A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285587 | ||||||
| chr6:70285672
|
G | T | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.697-1852C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285672 | ||||||
| chr6:70285699
|
T | C | 1 | a0003c0003t0001g0289 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.697-1879A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285699 | ||||||
| chr6:70285738
|
A | G | 6 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0208others(3): Show | 6 | HG02080.hp1 HG02083.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-1918T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285738 | ||||||
| chr6:70285970
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-2150G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285970 | ||||||
| chr6:70285991
|
C | G | 7 | a0005c0005t0001g0133a0005c0005t0001g0150a0005c0005t0001g0151others(4): Show | 7 | HG00639.hp2 HG01109.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.697-2171G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285991 | ||||||
| chr6:70285991
|
C | T | 1 | a0003c0006t0003g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.697-2171G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285991 | ||||||
| chr6:70285992
|
G | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(126): Show | 136 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.697-2172C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70285992 | ||||||
| chr6:70286078
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.697-2258C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286078 | ||||||
| chr6:70286092
|
T | C | 11 | a0002c0004t0002g0049a0002c0004t0002g0050a0002c0004t0002g0051others(8): Show | 11 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.697-2272A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286092 | ||||||
| chr6:70286162
|
TA | T | 5 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-2343delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286162 | ||||||
| chr6:70286187
|
C | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-2367G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286187 | ||||||
| chr6:70286205
|
T | C | 4 | a0001c0001t0003g0039a0003c0006t0003g0038a0003c0006t0003g0078others(1): Show | 4 | HG02027.hp1 NA18962.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-2385A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286205 | ||||||
| chr6:70286512
|
T | G | 25 | a0001c0001t0003g0040a0001c0001t0003g0117a0001c0012t0001g0120others(22): Show | 27 | HG00741.hp1 HG00741.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.697-2692A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286512 | ||||||
| chr6:70286887
|
G | A | 288 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0019others(285): Show | 300 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.697-3067C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286887 | ||||||
| chr6:70286914
|
G | A | 1 | a0003c0010t0008g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.697-3094C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286914 | ||||||
| chr6:70286945
|
G | A | 6 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-3125C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286945 | ||||||
| chr6:70286979
|
C | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(71): Show | 79 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.697-3159G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70286979 | ||||||
| chr6:70287089
|
C | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(126): Show | 136 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.697-3269G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287089 | ||||||
| chr6:70287090
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.697-3270C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287090 | ||||||
| chr6:70287268
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(130): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.697-3448G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287268 | ||||||
| chr6:70287503
|
G | A | 2 | a0002c0008t0002g0069a0002c0008t0002g0091 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.697-3683C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287503 | ||||||
| chr6:70287556
|
A | G | 1 | a0002c0008t0002g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.697-3736T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287556 | ||||||
| chr6:70287633
|
TCTC | T | 129 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(126): Show | 136 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.697-3816_697-3814d others(5): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287633 | ||||||
| chr6:70287818
|
G | A | 1 | a0006c0011t0004g0122 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.697-3998C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70287818 | ||||||
| chr6:70288046
|
G | C | 1 | a0008c0023t0012g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.697-4226C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288046 | ||||||
| chr6:70288052
|
C | T | 1 | a0004c0009t0001g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.697-4232G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288052 | ||||||
| chr6:70288080
|
C | A | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.697-4260G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288080 | ||||||
| chr6:70288119
|
A | T | 5 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-4299T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288119 | ||||||
| chr6:70288125
|
A | G | 6 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-4305T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288125 | ||||||
| chr6:70288218
|
T | A | 5 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-4398A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288218 | ||||||
| chr6:70288400
|
C | T | 2 | a0003c0003t0007g0349a0003c0003t0007g0350 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.697-4580G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288400 | ||||||
| chr6:70288411
|
C | G | 1 | a0004c0007t0007g0331 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.697-4591G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288411 | ||||||
| chr6:70288436
|
A | G | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.697-4616T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288436 | ||||||
| chr6:70288590
|
A | G | 5 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-4770T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288590 | ||||||
| chr6:70288840
|
A | C | 2 | a0001c0001t0003g0157a0001c0001t0003g0190 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.697-5020T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288840 | ||||||
| chr6:70288860
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(134): Show | 144 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.697-5040T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288860 | ||||||
| chr6:70288952
|
G | A | 4 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-5132C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70288952 | ||||||
| chr6:70289020
|
A | T | 1 | a0004c0007t0001g0018 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.696+5147T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289020 | ||||||
| chr6:70289106
|
G | A | 3 | a0007c0014t0001g0065a0007c0014t0001g0066a0008c0023t0012g0329 | 3 | HG01884.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.696+5061C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289106 | ||||||
| chr6:70289120
|
A | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(130): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.696+5047T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289120 | ||||||
| chr6:70289428
|
C | T | 137 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(134): Show | 144 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.696+4739G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289428 | ||||||
| chr6:70289488
|
TG | T | 3 | a0002c0004t0002g0049a0002c0004t0002g0050a0002c0004t0002g0051 | 3 | HG00733.hp2 HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.696+4678delC | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289488 | ||||||
| chr6:70289514
|
G | A | 138 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(135): Show | 145 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.696+4653C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289514 | ||||||
| chr6:70289628
|
G | A | 157 | a0001c0001t0002g0001a0001c0001t0002g0019a0001c0001t0002g0033others(154): Show | 166 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.696+4539C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289628 | ||||||
| chr6:70289647
|
C | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(141): Show | 151 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.696+4520G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289647 | ||||||
| chr6:70289726
|
A | G | 11 | a0002c0002t0001g0025a0002c0002t0001g0216a0002c0002t0001g0218others(8): Show | 11 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.696+4441T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289726 | ||||||
| chr6:70289827
|
A | G | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.696+4340T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289827 | ||||||
| chr6:70289922
|
G | A | 1 | a0001c0001t0003g0140 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.696+4245C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70289922 | ||||||
| chr6:70290012
|
G | A | 1 | a0003c0010t0008g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.696+4155C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70290012 | ||||||
| chr6:70290093
|
G | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(134): Show | 144 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.696+4074C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70290093 | ||||||
| chr6:70290507
|
T | C | 138 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(135): Show | 145 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.696+3660A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70290507 | ||||||
| chr6:70290638
|
C | CTT | 197 | a0001c0001t0002g0001a0001c0001t0002g0019a0001c0001t0002g0033others(194): Show | 208 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.696+3527_696+3528d others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70290638 | ||||||
| chr6:70291111
|
C | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(130): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.696+3056G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291111 | ||||||
| chr6:70291170
|
G | A | 1 | a0003c0013t0003g0311 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.696+2997C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291170 | ||||||
| chr6:70291285
|
C | T | 1 | a0003c0003t0002g0127 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.696+2882G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291285 | ||||||
| chr6:70291329
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.696+2838G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291329 | ||||||
| chr6:70291666
|
C | T | 128 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(125): Show | 135 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.696+2501G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291666 | ||||||
| chr6:70291739
|
G | A | 4 | a0001c0001t0002g0126a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | NA18962.hp2 NA18985.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+2428C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70291739 | ||||||
| chr6:70292048
|
G | A | 5 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+2119C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292048 | ||||||
| chr6:70292068
|
T | C | 1 | a0002c0004t0002g0020 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.696+2099A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292068 | ||||||
| chr6:70292233
|
C | T | 132 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(129): Show | 138 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.696+1934G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292233 | ||||||
| chr6:70292293
|
G | A | 1 | a0003c0006t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.696+1874C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292293 | ||||||
| chr6:70292326
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.696+1841T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292326 | ||||||
| chr6:70292457
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.696+1710A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292457 | ||||||
| chr6:70292511
|
A | C | 1 | a0001c0001t0002g0134 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.696+1656T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292511 | ||||||
| chr6:70292769
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.696+1398T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292769 | ||||||
| chr6:70292806
|
G | C | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.696+1361C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292806 | ||||||
| chr6:70292917
|
C | T | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.696+1250G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292917 | ||||||
| chr6:70292927
|
A | G | 1 | a0002c0002t0001g0264 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.696+1240T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292927 | ||||||
| chr6:70292951
|
C | T | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.696+1216G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292951 | ||||||
| chr6:70292976
|
C | T | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+1191G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70292976 | ||||||
| chr6:70293066
|
A | G | 139 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(136): Show | 146 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.696+1101T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293066 | ||||||
| chr6:70293143
|
G | A | 2 | a0003c0003t0010g0250a0004c0009t0002g0237 | 2 | HG02135.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.696+1024C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293143 | ||||||
| chr6:70293222
|
C | T | 4 | a0002c0004t0004g0246a0005c0005t0002g0248a0005c0005t0003g0247others(1): Show | 4 | HG02293.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+945G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293222 | ||||||
| chr6:70293551
|
A | G | 1 | a0005c0005t0003g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.696+616T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293551 | ||||||
| chr6:70293628
|
C | T | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+539G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293628 | ||||||
| chr6:70293629
|
TTTCACA | T | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+532_696+537del others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293629 | ||||||
| chr6:70293631
|
T | TCA | 13 | a0001c0001t0003g0101a0001c0001t0003g0115a0001c0001t0003g0116others(10): Show | 13 | HG00673.hp1 HG01069.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.696+534_696+535dup others(2): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACA | 6 | a0002c0002t0001g0186a0002c0016t0004g0187a0003c0006t0003g0026others(3): Show | 6 | HG02293.hp1 HG02976.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+532_696+535dup others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACACA | 13 | a0001c0001t0003g0012a0002c0004t0002g0020a0003c0006t0003g0027others(10): Show | 13 | HG00438.hp1 HG00738.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.696+530_696+535dup others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACACAC others(1): Show |
5 | a0001c0001t0004g0257a0004c0007t0001g0021a0004c0007t0007g0348others(2): Show | 5 | HG02055.hp1 HG03139.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+528_696+535dup others(8): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACACAC others(3): Show |
2 | a0001c0001t0002g0019a0004c0007t0007g0331 | 2 | HG02258.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.696+526_696+535dup others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACACAC others(5): Show |
2 | a0005c0005t0001g0260a0006c0011t0004g0259 | 2 | HG02280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.696+524_696+535dup others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
T | TCACACAC others(7): Show |
1 | a0005c0005t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.696+522_696+535dup others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCA | T | 57 | a0001c0001t0002g0098a0001c0001t0002g0141a0001c0001t0002g0153others(54): Show | 58 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.696+534_696+535del others(2): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACA | T | 46 | a0001c0001t0002g0144a0001c0001t0002g0147a0001c0001t0002g0148others(43): Show | 47 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.696+532_696+535del others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACA | T | 40 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0068others(37): Show | 43 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.696+530_696+535del others(6): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACAC others(1): Show |
T | 49 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0003g0310others(46): Show | 53 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.696+528_696+535del others(8): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACAC others(3): Show |
T | 6 | a0002c0002t0001g0243a0002c0004t0002g0295a0003c0003t0001g0328others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+526_696+535del others(10): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACAC others(5): Show |
T | 5 | a0002c0002t0001g0288a0002c0004t0002g0294a0003c0003t0001g0289others(2): Show | 5 | HG02155.hp2 HG02602.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+524_696+535del others(12): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACAC others(7): Show |
T | 1 | a0015c0032t0013g0341 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.696+522_696+535del others(14): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293631
|
TCACACAC others(9): Show |
T | 1 | a0001c0001t0006g0342 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.696+520_696+535del others(16): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293631 | ||||||
| chr6:70293663
|
ACACACAC others(4): Show |
A | 1 | a0002c0002t0001g0230 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.696+493_696+503del others(11): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293663 | ||||||
| chr6:70293672
|
C | T | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+495G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293672 | ||||||
| chr6:70293694
|
A | T | 1 | a0001c0001t0002g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.696+473T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293694 | ||||||
| chr6:70293741
|
A | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.696+426T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293741 | ||||||
| chr6:70293953
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.696+214A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70293953 | ||||||
| chr6:70294035
|
C | T | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.696+132G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70294035 | ||||||
| chr6:70294141
|
G | T | 1 | a0002c0002t0001g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.696+26C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 5/37 | chr6 | 70294141 | ||||||
| chr6:70294629
|
TC | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(72): Show | 80 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.300-67delG | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70294629 | ||||||
| chr6:70294699
|
T | C | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.300-136A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70294699 | ||||||
| chr6:70294745
|
C | T | 1 | a0001c0012t0001g0132 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.300-182G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70294745 | ||||||
| chr6:70295089
|
A | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG00323.hp1 HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.300-526T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295089 | ||||||
| chr6:70295177
|
TA | T | 6 | a0001c0001t0002g0098a0001c0001t0003g0096a0001c0001t0003g0101others(3): Show | 6 | HG02040.hp2 HG02738.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-615delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295177 | ||||||
| chr6:70295228
|
G | A | 145 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(142): Show | 152 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.300-665C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295228 | ||||||
| chr6:70295281
|
C | CT | 134 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0095others(131): Show | 136 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.300-719dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295281 | ||||||
| chr6:70295281
|
C | CTT | 83 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0093others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.300-720_300-719dup others(2): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295281 | ||||||
| chr6:70295281
|
C | CTTT | 56 | a0001c0001t0002g0001a0001c0001t0002g0068a0001c0001t0002g0287others(53): Show | 60 | HG00609.hp2 HG00733.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.300-721_300-719dup others(3): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295281 | ||||||
| chr6:70295281
|
C | CTTTT | 6 | a0002c0002t0001g0288a0002c0002t0001g0290a0002c0002t0001g0291others(3): Show | 6 | HG02155.hp2 HG02559.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.300-722_300-719dup others(4): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295281 | ||||||
| chr6:70295320
|
T | C | 3 | a0001c0001t0002g0130a0001c0001t0003g0195a0004c0007t0001g0196 | 3 | HG00673.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.300-757A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295320 | ||||||
| chr6:70295364
|
G | A | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.300-801C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295364 | ||||||
| chr6:70295419
|
T | A | 1 | a0002c0004t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.300-856A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295419 | ||||||
| chr6:70295431
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.300-868G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295431 | ||||||
| chr6:70295438
|
C | A | 1 | a0003c0003t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-875G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295438 | ||||||
| chr6:70295450
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.300-887G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295450 | ||||||
| chr6:70295476
|
T | C | 145 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(142): Show | 152 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.300-913A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295476 | ||||||
| chr6:70295484
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.300-921G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295484 | ||||||
| chr6:70295492
|
C | G | 1 | a0003c0003t0001g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.300-929G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295492 | ||||||
| chr6:70295607
|
C | T | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.300-1044G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295607 | ||||||
| chr6:70295631
|
C | T | 22 | a0001c0001t0003g0040a0001c0001t0003g0117a0001c0012t0001g0120others(19): Show | 24 | HG00741.hp1 HG00741.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.300-1068G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295631 | ||||||
| chr6:70295685
|
C | A | 1 | a0001c0001t0002g0001 | 4 | NA18952.hp1 NA18981.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-1122G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70295685 | ||||||
| chr6:70296083
|
T | C | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.300-1520A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296083 | ||||||
| chr6:70296288
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.300-1725C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296288 | ||||||
| chr6:70296315
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.300-1752T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296315 | ||||||
| chr6:70296395
|
T | C | 138 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(135): Show | 145 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.300-1832A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296395 | ||||||
| chr6:70296443
|
A | G | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.300-1880T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296443 | ||||||
| chr6:70296450
|
G | T | 189 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0062others(186): Show | 194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.300-1887C>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296450 | ||||||
| chr6:70296519
|
C | T | 4 | a0002c0004t0004g0246a0005c0005t0002g0248a0005c0005t0003g0247others(1): Show | 4 | HG02293.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-1956G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296519 | ||||||
| chr6:70296672
|
T | C | 138 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(135): Show | 145 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.300-2109A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296672 | ||||||
| chr6:70296693
|
C | G | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.300-2130G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296693 | ||||||
| chr6:70296701
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300-2138A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296701 | ||||||
| chr6:70296763
|
T | C | 1 | a0001c0001t0002g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.300-2200A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296763 | ||||||
| chr6:70296907
|
C | G | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.300-2344G>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70296907 | ||||||
| chr6:70297015
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.300-2452C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297015 | ||||||
| chr6:70297041
|
A | G | 2 | a0002c0022t0001g0281a0003c0003t0008g0280 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.300-2478T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297041 | ||||||
| chr6:70297063
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.300-2500T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297063 | ||||||
| chr6:70297122
|
A | G | 5 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.300-2559T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297122 | ||||||
| chr6:70297213
|
T | C | 3 | a0003c0013t0003g0197a0003c0013t0003g0198a0003c0013t0003g0199 | 3 | NA18955.hp1 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.300-2650A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297213 | ||||||
| chr6:70297313
|
G | A | 5 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+2730C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297313 | ||||||
| chr6:70297408
|
G | A | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299+2635C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297408 | ||||||
| chr6:70297411
|
G | A | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299+2632C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297411 | ||||||
| chr6:70297562
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(131): Show | 140 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.299+2481C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297562 | ||||||
| chr6:70297576
|
T | C | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299+2467A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297576 | ||||||
| chr6:70297761
|
A | G | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299+2282T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297761 | ||||||
| chr6:70297796
|
G | A | 6 | a0002c0002t0001g0243a0002c0004t0002g0242a0003c0003t0001g0328others(3): Show | 6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+2247C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297796 | ||||||
| chr6:70297888
|
CA | C | 160 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(157): Show | 168 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.299+2154delT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70297888 | ||||||
| chr6:70298046
|
A | G | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+1997T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298046 | ||||||
| chr6:70298243
|
C | T | 191 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0062others(188): Show | 197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.299+1800G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298243 | ||||||
| chr6:70298296
|
C | T | 1 | a0002c0008t0002g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.299+1747G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298296 | ||||||
| chr6:70298297
|
A | G | 139 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(136): Show | 146 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.299+1746T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298297 | ||||||
| chr6:70298309
|
C | T | 140 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(137): Show | 146 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.299+1734G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298309 | ||||||
| chr6:70298474
|
C | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(71): Show | 79 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.299+1569G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298474 | ||||||
| chr6:70298491
|
C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0129 | 2 | NA18949.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.299+1552G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298491 | ||||||
| chr6:70298534
|
G | A | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299+1509C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298534 | ||||||
| chr6:70298636
|
G | A | 186 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0062others(183): Show | 191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.299+1407C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298636 | ||||||
| chr6:70298679
|
A | C | 1 | a0001c0001t0002g0068 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.299+1364T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298679 | ||||||
| chr6:70298787
|
C | T | 90 | a0001c0001t0002g0013a0001c0001t0002g0062a0001c0001t0002g0124others(87): Show | 91 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.299+1256G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298787 | ||||||
| chr6:70298788
|
G | A | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.299+1255C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298788 | ||||||
| chr6:70298824
|
A | G | 139 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(136): Show | 146 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.299+1219T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298824 | ||||||
| chr6:70298847
|
T | C | 1 | a0002c0002t0001g0245 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.299+1196A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298847 | ||||||
| chr6:70298894
|
T | G | 1 | a0001c0001t0003g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.299+1149A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298894 | ||||||
| chr6:70298948
|
C | T | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299+1095G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298948 | ||||||
| chr6:70298955
|
C | T | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299+1088G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70298955 | ||||||
| chr6:70299001
|
G | A | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.299+1042C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299001 | ||||||
| chr6:70299042
|
A | G | 88 | a0001c0001t0002g0013a0001c0001t0002g0062a0001c0001t0002g0124others(85): Show | 89 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.299+1001T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299042 | ||||||
| chr6:70299224
|
A | G | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.299+819T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299224 | ||||||
| chr6:70299420
|
G | C | 1 | a0005c0005t0001g0204 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.299+623C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299420 | ||||||
| chr6:70299466
|
A | G | 1 | a0003c0006t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299+577T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299466 | ||||||
| chr6:70299607
|
C | T | 124 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(121): Show | 130 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.299+436G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299607 | ||||||
| chr6:70299766
|
T | C | 2 | a0001c0001t0006g0342a0015c0032t0013g0341 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.299+277A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299766 | ||||||
| chr6:70299879
|
A | T | 4 | a0002c0004t0011g0330a0007c0014t0001g0065a0007c0014t0001g0066others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+164T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299879 | ||||||
| chr6:70299915
|
T | G | 1 | a0002c0008t0005g0334 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299+128A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70299915 | ||||||
| chr6:70300029
|
T | G | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299+14A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 4/37 | chr6 | 70300029 | ||||||
| chr6:70300248
|
T | TA | 8 | a0001c0019t0006g0344a0002c0004t0003g0286a0002c0004t0004g0212others(5): Show | 8 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+60dupT | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 3/37 | chr6 | 70300248 | ||||||
| chr6:70300398
|
A | G | 38 | a0002c0002t0001g0030a0002c0002t0001g0044a0002c0002t0001g0045others(35): Show | 38 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-12T>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300398 | ||||||
| chr6:70300468
|
T | G | 1 | a0002c0004t0011g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89-82A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300468 | ||||||
| chr6:70300578
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.89-192A>C | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300578 | ||||||
| chr6:70300632
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89-246G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300632 | ||||||
| chr6:70300689
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-303C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300689 | ||||||
| chr6:70300704
|
G | A | 4 | a0001c0001t0006g0342a0001c0019t0006g0344a0002c0018t0006g0343others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-318C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300704 | ||||||
| chr6:70300739
|
C | T | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.89-353G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300739 | ||||||
| chr6:70300845
|
T | A | 2 | a0001c0019t0006g0344a0002c0018t0006g0343 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.89-459A>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70300845 | ||||||
| chr6:70301001
|
G | A | 2 | a0002c0004t0002g0020a0004c0007t0001g0021 | 2 | NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.89-615C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301001 | ||||||
| chr6:70301047
|
C | T | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-661G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301047 | ||||||
| chr6:70301085
|
C | A | 1 | a0002c0002t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.89-699G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301085 | ||||||
| chr6:70301133
|
T | C | 4 | a0002c0004t0004g0246a0005c0005t0002g0248a0005c0005t0003g0247others(1): Show | 4 | HG02293.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-747A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301133 | ||||||
| chr6:70301471
|
G | A | 6 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0208others(3): Show | 6 | HG02080.hp1 HG02083.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+530C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301471 | ||||||
| chr6:70301545
|
C | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88+456G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301545 | ||||||
| chr6:70301806
|
C | T | 6 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+195G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301806 | ||||||
| chr6:70301850
|
A | T | 95 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(92): Show | 100 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.88+151T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301850 | ||||||
| chr6:70301851
|
C | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(92): Show | 100 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.88+150G>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301851 | ||||||
| chr6:70301893
|
G | A | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 28 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+108C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301893 | ||||||
| chr6:70301966
|
G | A | 1 | a0004c0009t0001g0211 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.88+35C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 2/37 | chr6 | 70301966 | ||||||
| chr6:70302128
|
C | T | 169 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0062others(166): Show | 173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.15-54G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302128 | ||||||
| chr6:70302155
|
CCTAATTA | C | 26 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(23): Show | 28 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.15-88_15-82delTAAT others(3): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302155 | ||||||
| chr6:70302204
|
C | CT | 37 | a0001c0001t0002g0019a0001c0001t0002g0033a0001c0001t0002g0035others(34): Show | 37 | HG00323.hp2 HG00408.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.15-131dupA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302204 | ||||||
| chr6:70302204
|
CT | C | 10 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(7): Show | 12 | HG01069.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.15-131delA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302204 | ||||||
| chr6:70302204
|
CTT | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0129a0001c0001t0002g0130others(87): Show | 92 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.15-132_15-131delAA | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302204 | ||||||
| chr6:70302204
|
CTTTTTTT others(2): Show |
C | 88 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(85): Show | 93 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.15-139_15-131delAA others(7): Show |
COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302204 | ||||||
| chr6:70302208
|
T | C | 6 | a0002c0004t0003g0286a0002c0004t0004g0212a0002c0004t0004g0254others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-134A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302208 | ||||||
| chr6:70302218
|
T | C | 88 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(85): Show | 93 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.15-144A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302218 | ||||||
| chr6:70302233
|
G | A | 1 | a0013c0026t0001g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15-159C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302233 | ||||||
| chr6:70302273
|
G | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0287a0001c0001t0002g0318others(83): Show | 91 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.15-199C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302273 | ||||||
| chr6:70302280
|
G | C | 1 | a0008c0015t0003g0002 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.15-206C>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302280 | ||||||
| chr6:70302355
|
A | T | 1 | a0002c0002t0001g0025 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.15-281T>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302355 | ||||||
| chr6:70302390
|
A | C | 23 | a0001c0001t0002g0019a0001c0001t0003g0012a0001c0001t0004g0257others(20): Show | 23 | HG00323.hp2 HG00438.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.15-316T>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302390 | ||||||
| chr6:70302460
|
G | A | 1 | a0003c0003t0010g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15-386C>T | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302460 | ||||||
| chr6:70302688
|
C | T | 1 | a0004c0007t0007g0331 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+223G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302688 | ||||||
| chr6:70302778
|
C | T | 3 | a0004c0007t0006g0346a0004c0007t0006g0347a0008c0015t0003g0002 | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+133G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302778 | ||||||
| chr6:70302779
|
C | T | 5 | a0001c0001t0002g0013a0001c0001t0003g0251a0002c0004t0004g0254others(2): Show | 5 | HG01070.hp1 HG01433.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+132G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302779 | ||||||
| chr6:70302872
|
T | C | 86 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0287others(83): Show | 90 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.14+39A>G | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302872 | ||||||
| chr6:70302881
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.14+30G>A | COL9A1 | ENSG00000112280.18 | transcript | ENST00000357250.11 | protein_coding | 1/37 | chr6 | 70302881 |