| geneid | 2132 |
|---|---|
| ensemblid | ENSG00000151348.16 |
| hgncid | 3513 |
| symbol | EXT2 |
| name | exostosin glycosyltransferase 2 |
| refseq_nuc | NM_207122.2 |
| refseq_prot | NP_997005.1 |
| ensembl_nuc | ENST00000533608.7 |
| ensembl_prot | ENSP00000431173.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 44095678 |
| end | 44251962 |
| strand | + |
| ver | v1.2 |
| region | chr11:44095678-44251962 |
| region5000 | chr11:44090678-44256962 |
| regionname0 | EXT2_chr11_44095678_44251962 |
| regionname5000 | EXT2_chr11_44090678_44256962 |
| 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 | 718 | 323 | 72 | 46 | 161 | 10 | 32 | 123 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0002 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0003 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0004 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0005 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0006 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| 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 | 2157 | 256 | 57 | 43 | 116 | 10 | 28 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0002 | 0/0 | 2157 | 44 | 0 | 1 | 41 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0003 | 0/0 | 2157 | 8 | 6 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0004 | 0/0 | 2157 | 6 | 3 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0005 | 0/0 | 2157 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0006 | 0/0 | 2157 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0007 | 0/0 | 2157 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0008 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0009 | 0/0 | 2157 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0010 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0011 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0012 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0013 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| c0014 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| 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 | 7880 | 60 | 5 | 10 | 35 | 1 | 9 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0002 | 0/1 | 7881 | 45 | 5 | 9 | 21 | 2 | 7 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0003 | 0/0 | 7880 | 37 | 19 | 4 | 11 | 0 | 3 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0004 | 0/0 | 7877 | 25 | 0 | 0 | 23 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0005 | 0/0 | 7882 | 22 | 5 | 5 | 9 | 2 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0006 | 0/0 | 7881 | 16 | 0 | 0 | 14 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0007 | 1/0 | 7881 | 14 | 9 | 2 | 0 | 2 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0008 | 0/0 | 7877 | 12 | 0 | 0 | 12 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0009 | 0/0 | 7880 | 12 | 0 | 0 | 12 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0010 | 0/0 | 7880 | 5 | 5 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0011 | 0/0 | 7880 | 5 | 0 | 3 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0012 | 0/0 | 7882 | 4 | 1 | 2 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0013 | 0/0 | 7881 | 4 | 1 | 2 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0014 | 0/0 | 7882 | 4 | 3 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0015 | 0/0 | 7877 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0016 | 0/0 | 7882 | 3 | 1 | 0 | 1 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0017 | 0/0 | 7878 | 3 | 0 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0018 | 0/0 | 7880 | 3 | 2 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0019 | 0/0 | 7881 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0020 | 0/0 | 7879 | 2 | 1 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0021 | 0/0 | 7882 | 2 | 0 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0022 | 0/0 | 7881 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0023 | 0/0 | 7880 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0024 | 0/0 | 7881 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0025 | 0/0 | 7882 | 2 | 0 | 1 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0026 | 0/0 | 7882 | 2 | 0 | 1 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0027 | 0/0 | 7879 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0028 | 0/0 | 7880 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0029 | 0/0 | 7882 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0030 | 0/0 | 7882 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0031 | 0/0 | 7877 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0032 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0033 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0034 | 0/0 | 7878 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0035 | 0/0 | 7877 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0036 | 0/0 | 7881 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0037 | 0/0 | 7880 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0038 | 0/0 | 7881 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0039 | 0/0 | 7882 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0040 | 0/0 | 7882 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0041 | 0/0 | 7881 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0042 | 0/0 | 7880 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0043 | 0/0 | 7880 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0044 | 0/0 | 7881 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0045 | 0/0 | 7881 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0046 | 0/0 | 7867 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0047 | 0/0 | 7880 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0048 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0049 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0050 | 0/0 | 7880 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0051 | 0/0 | 7880 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0052 | 0/0 | 7880 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0053 | 0/0 | 7881 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0054 | 0/0 | 7881 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0055 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0056 | 0/0 | 7882 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0057 | 0/0 | 7882 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0058 | 0/0 | 7881 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0059 | 0/0 | 7881 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0060 | 0/0 | 7882 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0061 | 0/0 | 7878 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0062 | 0/0 | 7881 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| t0063 | 0/0 | 7880 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| 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 | 2157 | 256 | 57 | 43 | 116 | 10 | 28 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002 | 0/0 | 2157 | 44 | 0 | 1 | 41 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0003 | 0/0 | 2157 | 8 | 6 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0004 | 0/0 | 2157 | 6 | 3 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0007 | 0/0 | 2157 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0008 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0009 | 0/0 | 2157 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0013 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0014 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0002c0005 | 0/0 | 2157 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0003c0006 | 0/0 | 2157 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0004c0010 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0005c0012 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0006c0011 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10036 | 57 | 5 | 10 | 33 | 1 | 8 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0002 | 0/1 | 10037 | 33 | 4 | 8 | 11 | 2 | 7 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0003 | 0/0 | 10036 | 28 | 12 | 2 | 11 | 0 | 3 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0004 | 0/0 | 10033 | 2 | 0 | 0 | 1 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0005 | 0/0 | 10038 | 19 | 2 | 5 | 9 | 2 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0006 | 0/0 | 10037 | 16 | 0 | 0 | 14 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0007 | 1/0 | 10037 | 12 | 7 | 2 | 0 | 2 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0008 | 0/0 | 10033 | 10 | 0 | 0 | 10 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0009 | 0/0 | 10036 | 12 | 0 | 0 | 12 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0010 | 0/0 | 10036 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0011 | 0/0 | 10036 | 5 | 0 | 3 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0012 | 0/0 | 10038 | 4 | 1 | 2 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0013 | 0/0 | 10037 | 4 | 1 | 2 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0014 | 0/0 | 10038 | 4 | 3 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0015 | 0/0 | 10033 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0018 | 0/0 | 10036 | 3 | 2 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0020 | 0/0 | 10035 | 2 | 1 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0021 | 0/0 | 10038 | 2 | 0 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0022 | 0/0 | 10037 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0023 | 0/0 | 10036 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0024 | 0/0 | 10037 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0025 | 0/0 | 10038 | 2 | 0 | 1 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0026 | 0/0 | 10038 | 2 | 0 | 1 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0028 | 0/0 | 10036 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0029 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0031 | 0/0 | 10033 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0032 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0033 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0034 | 0/0 | 10034 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0035 | 0/0 | 10033 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0037 | 0/0 | 10036 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0038 | 0/0 | 10037 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0039 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0042 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0043 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0044 | 0/0 | 10037 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0045 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0047 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0050 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0051 | 0/0 | 10036 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0052 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0053 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0054 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0057 | 0/0 | 10038 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0058 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0059 | 0/0 | 10037 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0001t0063 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0002 | 0/0 | 10037 | 11 | 0 | 1 | 10 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0004 | 0/0 | 10033 | 23 | 0 | 0 | 22 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0008 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0017 | 0/0 | 10034 | 3 | 0 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0036 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0041 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0046 | 0/0 | 10023 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0048 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0049 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0002t0055 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0003t0003 | 0/0 | 10036 | 8 | 6 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0004t0016 | 0/0 | 10038 | 3 | 1 | 0 | 1 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0004t0030 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0004t0040 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0004t0060 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0007t0005 | 0/0 | 10038 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0008t0001 | 0/0 | 10036 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0009t0027 | 0/0 | 10035 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0013t0001 | 0/0 | 10036 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0001c0014t0062 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0002c0005t0019 | 0/0 | 10037 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0002c0005t0061 | 0/0 | 10034 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0003c0006t0003 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0003c0006t0007 | 0/0 | 10037 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0003c0006t0056 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0004c0010t0010 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0005c0012t0002 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| a0006c0011t0008 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | copy fasta | chr11 | 44090678 | 44256962 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0007g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0009g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0010g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0011g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0012g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0013g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0014g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0014g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0015g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0018g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0018g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0018g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0020g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0021g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0021g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0022g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0022g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0023g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0023g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0024g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0025g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0026g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0026g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0028g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0028g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0029g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0031g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0032g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0033g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0034g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0035g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0037g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0038g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0039g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0042g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0043g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0044g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0045g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0047g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0050g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0051g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0052g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0053g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0054g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0057g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0058g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0059g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0001t0063g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0017g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0017g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0036g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0041g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0046g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0048g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0049g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0002t0055g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0016g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0030g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0040g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0004t0060g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0007t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0007t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0007t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0008t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0008t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0009t0027g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0009t0027g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0013t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0001c0014t0062g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0002c0005t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0002c0005t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0002c0005t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0002c0005t0061g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0003c0006t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0003c0006t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0003c0006t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0003c0006t0056g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0004c0010t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0005c0012t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| a0006c0011t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00099 | hp2 | a0001 | c0001 | t0057 | g0066 | EUR | GBR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0326 | EUR | FIN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0256 | EUR | FIN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00438 | hp2 | a0001 | c0008 | t0001 | g0159 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0276 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0056 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00621 | hp2 | a0001 | c0002 | t0048 | g0051 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00639 | hp2 | a0001 | c0001 | t0018 | g0314 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00673 | hp2 | a0001 | c0002 | t0049 | g0025 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00735 | hp1 | a0001 | c0001 | t0021 | g0060 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00738 | hp2 | a0001 | c0001 | t0025 | g0057 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG00741 | hp2 | a0001 | c0001 | t0021 | g0059 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01099 | hp2 | a0001 | c0001 | t0037 | g0164 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0272 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0179 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0325 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01168 | hp2 | a0001 | c0001 | t0012 | g0083 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0065 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0242 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0286 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0080 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01346 | hp1 | a0001 | c0001 | t0026 | g0016 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01361 | hp1 | a0001 | c0001 | t0044 | g0208 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0261 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0017 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0082 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0063 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0329 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0265 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01891 | hp2 | a0002 | c0005 | t0019 | g0238 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0324 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0105 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01993 | hp1 | a0001 | c0001 | t0011 | g0106 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0028 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02056 | hp1 | a0001 | c0002 | t0055 | g0014 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02056 | hp2 | a0001 | c0001 | t0011 | g0162 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02074 | hp1 | a0001 | c0002 | t0036 | g0050 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0035 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02083 | hp2 | a0001 | c0002 | t0004 | g0030 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02135 | hp2 | a0001 | c0008 | t0001 | g0161 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0312 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0185 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0315 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02258 | hp1 | a0003 | c0006 | t0003 | g0319 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0088 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0260 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0181 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02615 | hp2 | a0001 | c0001 | t0054 | g0259 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0180 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02622 | hp2 | a0001 | c0001 | t0063 | g0254 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0252 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0316 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02698 | hp2 | a0001 | c0001 | t0012 | g0004 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02738 | hp1 | a0001 | c0001 | t0051 | g0101 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0310 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0308 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02818 | hp2 | a0001 | c0007 | t0005 | g0147 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02886 | hp1 | a0001 | c0001 | t0039 | g0070 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02886 | hp2 | a0003 | c0006 | t0007 | g0318 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02896 | hp1 | a0001 | c0009 | t0027 | g0306 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02922 | hp1 | a0001 | c0001 | t0029 | g0331 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0262 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0267 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02970 | hp2 | a0001 | c0009 | t0027 | g0307 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02976 | hp1 | a0001 | c0004 | t0016 | g0177 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03017 | hp1 | a0001 | c0001 | t0038 | g0226 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03017 | hp2 | a0001 | c0004 | t0016 | g0172 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0330 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0311 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0268 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03139 | hp1 | a0001 | c0001 | t0053 | g0255 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03139 | hp2 | a0003 | c0006 | t0007 | g0317 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03195 | hp1 | a0001 | c0001 | t0058 | g0171 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0270 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0170 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03239 | hp1 | a0001 | c0001 | t0025 | g0058 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03453 | hp2 | a0002 | c0005 | t0019 | g0236 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03486 | hp1 | a0005 | c0012 | t0002 | g0203 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03486 | hp2 | a0001 | c0014 | t0062 | g0239 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03540 | hp1 | a0001 | c0001 | t0028 | g0253 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0184 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03579 | hp1 | a0003 | c0006 | t0056 | g0320 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03831 | hp1 | a0001 | c0002 | t0017 | g0031 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0166 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0038 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04115 | hp2 | a0001 | c0001 | t0059 | g0128 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0009 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04199 | hp2 | a0001 | c0013 | t0001 | g0085 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04204 | hp2 | a0001 | c0001 | t0035 | g0248 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18522 | hp1 | a0002 | c0005 | t0019 | g0240 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0241 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0047 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18906 | hp2 | a0001 | c0007 | t0005 | g0194 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18942 | hp2 | a0001 | c0002 | t0041 | g0024 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0246 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18945 | hp2 | a0001 | c0001 | t0009 | g0279 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18949 | hp1 | a0001 | c0002 | t0017 | g0029 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18953 | hp1 | a0001 | c0001 | t0023 | g0257 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0290 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0052 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18971 | hp1 | a0006 | c0011 | t0008 | g0250 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18972 | hp1 | a0001 | c0001 | t0008 | g0245 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18973 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18973 | hp2 | a0001 | c0001 | t0024 | g0140 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18977 | hp2 | a0001 | c0001 | t0050 | g0093 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18981 | hp1 | a0001 | c0004 | t0016 | g0173 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0263 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18982 | hp2 | a0001 | c0001 | t0052 | g0143 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18984 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18986 | hp1 | a0001 | c0004 | t0040 | g0174 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18986 | hp2 | a0001 | c0001 | t0034 | g0230 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18987 | hp2 | a0001 | c0002 | t0017 | g0048 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0283 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18992 | hp2 | a0001 | c0001 | t0008 | g0249 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18993 | hp1 | a0001 | c0002 | t0046 | g0054 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA18999 | hp2 | a0001 | c0001 | t0033 | g0216 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0285 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19004 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0278 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19057 | hp1 | a0001 | c0001 | t0043 | g0284 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19070 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0244 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0273 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19075 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19077 | hp1 | a0001 | c0001 | t0009 | g0288 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19081 | hp1 | a0001 | c0001 | t0042 | g0264 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19082 | hp1 | a0001 | c0001 | t0013 | g0072 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19083 | hp1 | a0001 | c0001 | t0032 | g0231 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19083 | hp2 | a0001 | c0001 | t0045 | g0302 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19084 | hp2 | a0001 | c0001 | t0023 | g0258 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19088 | hp1 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19088 | hp2 | a0001 | c0001 | t0024 | g0141 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA19090 | hp2 | a0001 | c0002 | t0008 | g0053 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0322 | AFR | ASW | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ASW | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20752 | hp1 | a0001 | c0001 | t0031 | g0287 | EUR | TSI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0218 | EUR | TSI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0327 | SAS | GIH | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG01123 | hp2 | a0001 | c0001 | t0012 | g0006 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02559 | hp1 | a0002 | c0005 | t0061 | g0237 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03471 | hp1 | a0001 | c0001 | t0047 | g0313 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG06807 | hp1 | a0001 | c0003 | t0003 | g0269 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| HG06807 | hp2 | a0001 | c0004 | t0060 | g0289 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20300 | hp1 | a0001 | c0007 | t0005 | g0183 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA20300 | hp2 | a0004 | c0010 | t0010 | g0309 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0323 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| NA21309 | hp2 | a0001 | c0004 | t0030 | g0062 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0201 | REF | REF | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0221 | REF | REF | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44107836
|
A | G | 1 | a0003 | 4 | HG02258.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.124A>G | p.Met42Val | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 329/10037 | 124/2157 | 42/718 | chr11 | 44107836 | ||
| chr11:44108124
|
T | G | 1 | a0004 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.412T>G | p.Ser138Ala | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 617/10037 | 412/2157 | 138/718 | chr11 | 44108124 | ||
| chr11:44124877
|
G | A | 1 | a0006 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.832G>A | p.Glu278Lys | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/14 | 1037/10037 | 832/2157 | 278/718 | chr11 | 44124877 | ||
| chr11:44130075
|
G | T | 1 | a0002 | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1110G>T | p.Met370Ile | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/14 | 1315/10037 | 1110/2157 | 370/718 | chr11 | 44130075 | ||
| chr11:44206916
|
A | T | 1 | a0005 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1619A>T | p.Asp540Val | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/14 | 1824/10037 | 1619/2157 | 540/718 | chr11 | 44206916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44107740
|
C | A | 1 | a0001c0002 | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
synonymous_variant | LOW | c.28C>A | p.Arg10Arg | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 233/10037 | 28/2157 | 10/718 | chr11 | 44107740 | ||
| chr11:44107976
|
C | T | 3 | a0001c0009a0001c0014a0002c0005 | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.264C>T | p.His88His | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 469/10037 | 264/2157 | 88/718 | chr11 | 44107976 | ||
| chr11:44124963
|
C | T | 1 | a0001c0009 | 2 | HG02896.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.918C>T | p.Phe306Phe | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/14 | 1123/10037 | 918/2157 | 306/718 | chr11 | 44124963 | ||
| chr11:44126875
|
T | C | 1 | a0001c0004 | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
synonymous_variant | LOW | c.999T>C | p.Asp333Asp | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/14 | 1204/10037 | 999/2157 | 333/718 | chr11 | 44126875 | ||
| chr11:44126893
|
T | C | 1 | a0001c0007 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1017T>C | p.Cys339Cys | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/14 | 1222/10037 | 1017/2157 | 339/718 | chr11 | 44126893 | ||
| chr11:44197840
|
C | T | 1 | a0001c0013 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1317C>T | p.Ser439Ser | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/14 | 1522/10037 | 1317/2157 | 439/718 | chr11 | 44197840 | ||
| chr11:44206938
|
C | T | 1 | a0001c0008 | 2 | HG00438.hp2 HG02135.hp2 |
synonymous_variant | LOW | c.1641C>T | p.Asp547Asp | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/14 | 1846/10037 | 1641/2157 | 547/718 | chr11 | 44206938 | ||
| chr11:44232451
|
G | A | 1 | a0001c0003 | 8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.1761G>A | p.Thr587Thr | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/14 | 1966/10037 | 1761/2157 | 587/718 | chr11 | 44232451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44095686
|
C | G | 6 | a0001c0001t0028a0001c0001t0063a0001c0009t0027others(3): Show | 10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-197C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 12027 | chr11 | 44095686 | |||||
| chr11:44095731
|
C | G | 1 | a0001c0004t0060 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-152C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 11982 | chr11 | 44095731 | |||||
| chr11:44095735
|
G | A | 1 | a0001c0001t0029 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 11978 | chr11 | 44095735 | |||||
| chr11:44095822
|
C | G | 1 | a0001c0001t0059 | 1 | HG04115.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | chr11 | 44095822 | ||||||
| chr11:44244297
|
T | C | 1 | a0001c0004t0030 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 10 | chr11 | 44244297 | |||||
| chr11:44244343
|
G | A | 9 | a0001c0001t0008a0001c0001t0031a0001c0001t0032others(6): Show | 18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 56 | chr11 | 44244343 | |||||
| chr11:44244388
|
G | C | 1 | a0001c0001t0037 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 101 | chr11 | 44244388 | |||||
| chr11:44244759
|
C | T | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*472C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 472 | chr11 | 44244759 | |||||
| chr11:44245082
|
C | A | 1 | a0001c0009t0027 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*795C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 795 | chr11 | 44245082 | |||||
| chr11:44245158
|
G | A | 1 | a0001c0001t0038 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 871 | chr11 | 44245158 | |||||
| chr11:44245456
|
C | A | 1 | a0001c0001t0039 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1169 | chr11 | 44245456 | |||||
| chr11:44245484
|
G | A | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1197 | chr11 | 44245484 | |||||
| chr11:44245506
|
G | A | 8 | a0001c0001t0008a0001c0001t0031a0001c0001t0032others(5): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1219G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1219 | chr11 | 44245506 | |||||
| chr11:44245549
|
T | G | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1262T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1262 | chr11 | 44245549 | |||||
| chr11:44245760
|
C | G | 1 | a0001c0001t0011 | 5 | HG01978.hp2 HG01993.hp1 HG02056.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1473C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1473 | chr11 | 44245760 | |||||
| chr11:44245786
|
T | G | 9 | a0001c0001t0002a0001c0001t0012a0001c0001t0021others(6): Show | 55 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1499T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1499 | chr11 | 44245786 | |||||
| chr11:44246011
|
T | G | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1724T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1724 | chr11 | 44246011 | |||||
| chr11:44246079
|
G | A | 1 | a0001c0001t0022 | 2 | HG01884.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1792G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1792 | chr11 | 44246079 | |||||
| chr11:44246107
|
A | G | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(49): Show | 244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1820A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1820 | chr11 | 44246107 | |||||
| chr11:44246254
|
T | G | 1 | a0001c0001t0047 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1967T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1967 | chr11 | 44246254 | |||||
| chr11:44246278
|
T | C | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1991 | chr11 | 44246278 | |||||
| chr11:44246322
|
G | A | 1 | a0001c0002t0048 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2035 | chr11 | 44246322 | |||||
| chr11:44246511
|
G | A | 1 | a0001c0001t0042 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2224G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2224 | chr11 | 44246511 | |||||
| chr11:44246729
|
A | C | 1 | a0002c0005t0019 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2442A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2442 | chr11 | 44246729 | |||||
| chr11:44246750
|
T | A | 1 | a0001c0002t0049 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2463 | chr11 | 44246750 | |||||
| chr11:44246764
|
A | G | 12 | a0001c0001t0008a0001c0001t0018a0001c0001t0028others(9): Show | 24 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2477A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2477 | chr11 | 44246764 | |||||
| chr11:44246805
|
GGTCAGGA others(6): Show |
G | 1 | a0001c0002t0046 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2522_*2534delAGGA others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2522 | INFO_REALIGN_3_PRIME | chr11 | 44246805 | ||||
| chr11:44246948
|
C | T | 1 | a0001c0001t0035 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2661C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2661 | chr11 | 44246948 | |||||
| chr11:44246965
|
C | T | 1 | a0002c0005t0061 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2678C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2678 | chr11 | 44246965 | |||||
| chr11:44247154
|
C | A | 1 | a0001c0001t0050 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2867C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2867 | chr11 | 44247154 | |||||
| chr11:44247243
|
C | CT | 33 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(30): Show | 131 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*2976dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2977 | INFO_REALIGN_3_PRIME | chr11 | 44247243 | ||||
| chr11:44247243
|
C | CTT | 8 | a0001c0001t0005a0001c0001t0012a0001c0001t0029others(5): Show | 33 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2975_*2976dupTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2977 | INFO_REALIGN_3_PRIME | chr11 | 44247243 | ||||
| chr11:44247300
|
GCAA | G | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*3017_*3019delCAA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3017 | INFO_REALIGN_3_PRIME | chr11 | 44247300 | ||||
| chr11:44247441
|
A | AG | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 301 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*3157dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3158 | INFO_REALIGN_3_PRIME | chr11 | 44247441 | ||||
| chr11:44247471
|
C | G | 1 | a0001c0001t0052 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3184C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3184 | chr11 | 44247471 | |||||
| chr11:44247482
|
C | T | 2 | a0001c0001t0063a0002c0005t0061 | 2 | HG02559.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3195C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3195 | chr11 | 44247482 | |||||
| chr11:44247501
|
C | T | 6 | a0001c0001t0014a0001c0001t0021a0001c0001t0022others(3): Show | 13 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3214C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3214 | chr11 | 44247501 | |||||
| chr11:44247528
|
G | A | 1 | a0001c0001t0051 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3241G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3241 | chr11 | 44247528 | |||||
| chr11:44247716
|
G | A | 1 | a0001c0001t0044 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3429G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3429 | chr11 | 44247716 | |||||
| chr11:44247851
|
G | A | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*3564G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3564 | chr11 | 44247851 | |||||
| chr11:44247869
|
T | C | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3582T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3582 | chr11 | 44247869 | |||||
| chr11:44247930
|
T | C | 2 | a0001c0001t0053a0001c0014t0062 | 2 | HG03139.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3643 | chr11 | 44247930 | |||||
| chr11:44247946
|
T | C | 1 | a0001c0001t0031 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3659T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3659 | chr11 | 44247946 | |||||
| chr11:44247946
|
T | G | 1 | a0001c0001t0024 | 2 | NA18973.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3659T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3659 | chr11 | 44247946 | |||||
| chr11:44247991
|
G | A | 1 | a0001c0001t0043 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3704G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3704 | chr11 | 44247991 | |||||
| chr11:44248512
|
C | G | 1 | a0001c0001t0018 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4225C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4225 | chr11 | 44248512 | |||||
| chr11:44248964
|
G | GT | 9 | a0001c0001t0014a0001c0001t0021a0001c0001t0025others(6): Show | 17 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4684dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4685 | INFO_REALIGN_3_PRIME | chr11 | 44248964 | ||||
| chr11:44248964
|
GT | G | 9 | a0001c0001t0008a0001c0001t0031a0001c0001t0032others(6): Show | 18 | HG02559.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4684delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4684 | INFO_REALIGN_3_PRIME | chr11 | 44248964 | ||||
| chr11:44248968
|
TTTTG | T | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4701_*4704delGTTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4701 | INFO_REALIGN_3_PRIME | chr11 | 44248968 | ||||
| chr11:44248972
|
G | T | 3 | a0001c0001t0014a0001c0001t0021a0003c0006t0056 | 7 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4685G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4685 | chr11 | 44248972 | |||||
| chr11:44249051
|
T | C | 1 | a0001c0009t0027 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4764T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4764 | chr11 | 44249051 | |||||
| chr11:44249070
|
C | T | 1 | a0001c0001t0047 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4783C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4783 | chr11 | 44249070 | |||||
| chr11:44249093
|
C | T | 1 | a0001c0001t0026 | 2 | HG01346.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4806C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4806 | chr11 | 44249093 | |||||
| chr11:44249125
|
T | A | 1 | a0001c0001t0058 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4838T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4838 | chr11 | 44249125 | |||||
| chr11:44249329
|
CAGTT | C | 6 | a0001c0001t0004a0001c0002t0004a0001c0002t0017others(3): Show | 31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5043_*5046delAGTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5043 | chr11 | 44249329 | |||||
| chr11:44249413
|
A | G | 6 | a0001c0001t0004a0001c0002t0004a0001c0002t0017others(3): Show | 31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5126A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5126 | chr11 | 44249413 | |||||
| chr11:44249443
|
G | T | 1 | a0001c0001t0033 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5156 | chr11 | 44249443 | |||||
| chr11:44249451
|
A | C | 1 | a0001c0009t0027 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5164A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5164 | chr11 | 44249451 | |||||
| chr11:44249611
|
T | C | 1 | a0001c0001t0057 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5324T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5324 | chr11 | 44249611 | |||||
| chr11:44249623
|
T | G | 1 | a0001c0004t0060 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5336 | chr11 | 44249623 | |||||
| chr11:44250024
|
T | C | 1 | a0001c0009t0027 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5737T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5737 | chr11 | 44250024 | |||||
| chr11:44250115
|
A | G | 1 | a0001c0001t0032 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5828A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5828 | chr11 | 44250115 | |||||
| chr11:44250116
|
G | C | 1 | a0001c0001t0032 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5829 | chr11 | 44250116 | |||||
| chr11:44250523
|
C | T | 10 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(7): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6236C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6236 | chr11 | 44250523 | |||||
| chr11:44250529
|
A | G | 1 | a0001c0001t0053 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6242A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6242 | chr11 | 44250529 | |||||
| chr11:44250600
|
C | A | 1 | a0001c0002t0055 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6313C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6313 | chr11 | 44250600 | |||||
| chr11:44250724
|
G | A | 1 | a0001c0001t0029 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6437G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6437 | chr11 | 44250724 | |||||
| chr11:44250823
|
T | G | 1 | a0001c0001t0050 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6536T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6536 | chr11 | 44250823 | |||||
| chr11:44250972
|
A | G | 10 | a0001c0001t0002a0001c0001t0012a0001c0001t0021others(7): Show | 56 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*6685A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6685 | chr11 | 44250972 | |||||
| chr11:44251194
|
T | TC | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 296 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*6908dupC | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6909 | INFO_REALIGN_3_PRIME | chr11 | 44251194 | ||||
| chr11:44251408
|
G | A | 1 | a0003c0006t0056 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7121G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7121 | chr11 | 44251408 | |||||
| chr11:44251411
|
T | C | 1 | a0001c0001t0054 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7124T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7124 | chr11 | 44251411 | |||||
| chr11:44251516
|
G | A | 1 | a0001c0009t0027 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7229G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7229 | chr11 | 44251516 | |||||
| chr11:44251593
|
A | G | 1 | a0001c0001t0023 | 2 | NA18953.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7306A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7306 | chr11 | 44251593 | |||||
| chr11:44251874
|
C | T | 7 | a0001c0001t0014a0001c0001t0025a0001c0001t0026others(4): Show | 14 | HG00738.hp2 HG01109.hp2 HG01346.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7587C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7587 | chr11 | 44251874 | |||||
| chr11:44251892
|
A | G | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 291 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*7605A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7605 | chr11 | 44251892 | |||||
| chr11:44251935
|
T | C | 1 | a0001c0001t0047 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7648T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7648 | chr11 | 44251935 | |||||
| chr11:44251936
|
G | A | 5 | a0001c0001t0009a0001c0001t0023a0001c0001t0042others(2): Show | 17 | HG00544.hp2 HG02523.hp2 NA18945.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7649G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7649 | chr11 | 44251936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44095859
|
G | T | 15 | a0001c0001t0001g0328a0001c0001t0004g0327a0001c0001t0007g0321others(12): Show | 15 | HG00323.hp1 HG01168.hp1 HG01884.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-31+7G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095859 | ||||||
| chr11:44095874
|
G | A | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-31+22G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095874 | ||||||
| chr11:44095894
|
A | G | 270 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-31+42A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095894 | ||||||
| chr11:44095958
|
C | T | 7 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(4): Show | 7 | HG02723.hp1 HG03017.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+106C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095958 | ||||||
| chr11:44096217
|
C | T | 1 | a0001c0002t0002g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-31+365C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096217 | ||||||
| chr11:44096326
|
G | A | 3 | a0001c0001t0012g0004a0001c0001t0012g0005a0001c0001t0012g0006 | 3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-31+474G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096326 | ||||||
| chr11:44096348
|
T | G | 261 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-31+496T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096348 | ||||||
| chr11:44096365
|
TCGGGGGC others(39): Show |
T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-31+543_-31+588del others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44096365 | |||||
| chr11:44096509
|
G | A | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+657G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096509 | ||||||
| chr11:44096817
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+965G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096817 | ||||||
| chr11:44097086
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG04184.hp2 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+1234G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097086 | ||||||
| chr11:44097104
|
G | A | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+1252G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097104 | ||||||
| chr11:44097131
|
T | C | 6 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(3): Show | 6 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+1279T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097131 | ||||||
| chr11:44097201
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31+1349A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097201 | ||||||
| chr11:44097213
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-31+1361A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097213 | ||||||
| chr11:44097301
|
T | C | 10 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+1449T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097301 | ||||||
| chr11:44097380
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-31+1528A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097380 | ||||||
| chr11:44097443
|
A | G | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-31+1591A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097443 | ||||||
| chr11:44097515
|
C | T | 10 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+1663C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097515 | ||||||
| chr11:44097517
|
C | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+1665C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097517 | ||||||
| chr11:44097528
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-31+1676G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097528 | ||||||
| chr11:44097578
|
C | T | 15 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(12): Show | 15 | HG02027.hp2 HG02135.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+1726C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097578 | ||||||
| chr11:44097761
|
AAAAT | A | 16 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(13): Show | 16 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+1945_-31+1948d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097761 | |||||
| chr11:44097761
|
AAAATAAA others(1): Show |
A | 148 | a0001c0001t0001g0156a0001c0001t0001g0195a0001c0001t0001g0275others(145): Show | 149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-31+1941_-31+1948d others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097761 | |||||
| chr11:44097762
|
AAATAAAT | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(119): Show | 123 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-31+1913_-31+1919d others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097762 | |||||
| chr11:44097763
|
AATAAATA others(3): Show |
A | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+1913_-31+1922d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097763 | |||||
| chr11:44097764
|
ATAAATAA others(2): Show |
A | 12 | a0001c0001t0003g0301a0001c0001t0008g0002a0001c0001t0008g0243others(9): Show | 13 | HG02896.hp2 HG04204.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+1913_-31+1921d others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097764 | ||||||
| chr11:44097773
|
T | A | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-31+1921T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097773 | ||||||
| chr11:44097777
|
T | A | 150 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(147): Show | 152 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-31+1925T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097777 | ||||||
| chr11:44097781
|
T | A | 19 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0087others(16): Show | 20 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+1929T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097781 | ||||||
| chr11:44097957
|
G | A | 1 | a0001c0001t0011g0088 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-31+2105G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097957 | ||||||
| chr11:44098220
|
C | T | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-31+2368C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098220 | ||||||
| chr11:44098221
|
G | A | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+2369G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098221 | ||||||
| chr11:44098254
|
G | A | 1 | a0001c0001t0006g0089 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-31+2402G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098254 | ||||||
| chr11:44098477
|
G | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+2625G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098477 | ||||||
| chr11:44098626
|
C | G | 10 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+2774C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098626 | ||||||
| chr11:44098694
|
C | CA | 35 | a0001c0001t0001g0008a0001c0001t0001g0328a0001c0001t0002g0209others(32): Show | 36 | HG00323.hp1 HG01099.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-31+2860dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44098694 | |||||
| chr11:44098694
|
CA | C | 39 | a0001c0001t0001g0275a0001c0001t0003g0266a0001c0001t0003g0274others(36): Show | 40 | HG00544.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-31+2860delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44098694 | |||||
| chr11:44098699
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+2847A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098699 | ||||||
| chr11:44099063
|
G | A | 54 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-31+3211G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099063 | ||||||
| chr11:44099074
|
T | G | 51 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-31+3222T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099074 | ||||||
| chr11:44099141
|
G | A | 1 | a0001c0001t0006g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-31+3289G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099141 | ||||||
| chr11:44099176
|
G | GT | 7 | a0001c0001t0002g0233a0001c0001t0006g0154a0001c0001t0006g0155others(4): Show | 7 | HG00597.hp2 HG03834.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+3333dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44099176 | |||||
| chr11:44099177
|
T | G | 9 | a0001c0001t0001g0091a0001c0001t0021g0059a0001c0001t0021g0060others(6): Show | 9 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+3325T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099177 | ||||||
| chr11:44099256
|
G | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+3404G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099256 | ||||||
| chr11:44099451
|
C | T | 51 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-31+3599C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099451 | ||||||
| chr11:44099518
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(113): Show | 117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-31+3666C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099518 | ||||||
| chr11:44099890
|
C | A | 2 | a0001c0001t0023g0257a0001c0001t0023g0258 | 2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-31+4038C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099890 | ||||||
| chr11:44099957
|
G | A | 2 | a0001c0001t0053g0255a0001c0001t0054g0259 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-31+4105G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099957 | ||||||
| chr11:44099963
|
A | G | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+4111A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099963 | ||||||
| chr11:44100152
|
A | G | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-31+4300A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100152 | ||||||
| chr11:44100186
|
A | T | 80 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(77): Show | 80 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-31+4334A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100186 | ||||||
| chr11:44100525
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-31+4673G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100525 | ||||||
| chr11:44100533
|
G | T | 170 | a0001c0001t0001g0275a0001c0001t0001g0328a0001c0001t0002g0251others(167): Show | 172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.-31+4681G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100533 | ||||||
| chr11:44101005
|
C | T | 29 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(26): Show | 29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-31+5153C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101005 | ||||||
| chr11:44101070
|
A | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-31+5218A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101070 | ||||||
| chr11:44101129
|
T | G | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+5277T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101129 | ||||||
| chr11:44101151
|
G | C | 1 | a0001c0002t0004g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-31+5299G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101151 | ||||||
| chr11:44101277
|
G | A | 48 | a0001c0001t0001g0275a0001c0001t0003g0266a0001c0001t0003g0274others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-31+5425G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101277 | ||||||
| chr11:44101300
|
C | T | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-31+5448C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101300 | ||||||
| chr11:44101442
|
A | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+5590A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101442 | ||||||
| chr11:44101446
|
A | G | 6 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(3): Show | 6 | HG02559.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5594A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101446 | ||||||
| chr11:44101534
|
G | A | 2 | a0001c0001t0003g0299a0001c0001t0003g0301 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+5682G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101534 | ||||||
| chr11:44101694
|
G | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31+5842G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101694 | ||||||
| chr11:44101936
|
A | G | 1 | a0001c0001t0022g0330 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-30-5747A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101936 | ||||||
| chr11:44101944
|
T | TA | 114 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(111): Show | 116 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-30-5718dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | |||||
| chr11:44101944
|
T | TAA | 19 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 19 | HG00621.hp1 HG00735.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30-5719_-30-5718d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | |||||
| chr11:44101944
|
TA | T | 97 | a0001c0001t0001g0232a0001c0001t0003g0298a0001c0001t0003g0301others(94): Show | 97 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-30-5718delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | |||||
| chr11:44101953
|
A | G | 79 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(76): Show | 79 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30-5730A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101953 | ||||||
| chr11:44101954
|
A | G | 1 | a0001c0002t0002g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-30-5729A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101954 | ||||||
| chr11:44101961
|
A | G | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-30-5722A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101961 | ||||||
| chr11:44102029
|
C | T | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-30-5654C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102029 | ||||||
| chr11:44102065
|
T | C | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-5618T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102065 | ||||||
| chr11:44102100
|
C | T | 1 | a0001c0001t0006g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-30-5583C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102100 | ||||||
| chr11:44102174
|
T | C | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-30-5509T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102174 | ||||||
| chr11:44102413
|
G | T | 1 | a0001c0007t0005g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30-5270G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102413 | ||||||
| chr11:44102534
|
C | CT | 12 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(9): Show | 12 | HG00597.hp1 HG01361.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-5128dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | |||||
| chr11:44102534
|
CT | C | 93 | a0001c0001t0001g0091a0001c0001t0001g0157a0001c0001t0001g0275others(90): Show | 95 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-30-5128delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | |||||
| chr11:44102534
|
CTT | C | 89 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(86): Show | 89 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-30-5129_-30-5128d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | |||||
| chr11:44102537
|
T | C | 1 | a0001c0001t0008g0002 | 2 | NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-30-5146T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102537 | ||||||
| chr11:44102565
|
C | T | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-5118C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102565 | ||||||
| chr11:44102616
|
C | G | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-5067C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102616 | ||||||
| chr11:44102628
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-30-5055A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102628 | ||||||
| chr11:44102768
|
T | C | 84 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-30-4915T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102768 | ||||||
| chr11:44103177
|
G | A | 4 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-4506G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103177 | ||||||
| chr11:44103319
|
G | T | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-4364G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103319 | ||||||
| chr11:44103442
|
A | G | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-4241A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103442 | ||||||
| chr11:44103799
|
G | A | 48 | a0001c0001t0001g0275a0001c0001t0003g0266a0001c0001t0003g0274others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30-3884G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103799 | ||||||
| chr11:44103990
|
C | T | 171 | a0001c0001t0001g0275a0001c0001t0001g0328a0001c0001t0002g0251others(168): Show | 173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-30-3693C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103990 | ||||||
| chr11:44104147
|
G | A | 2 | a0001c0001t0026g0016a0001c0001t0026g0082 | 2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-30-3536G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104147 | ||||||
| chr11:44104690
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-30-2993C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104690 | ||||||
| chr11:44104780
|
T | C | 76 | a0001c0001t0001g0275a0001c0001t0001g0328a0001c0001t0003g0266others(73): Show | 77 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-30-2903T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104780 | ||||||
| chr11:44104836
|
G | A | 1 | a0001c0002t0004g0020 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-30-2847G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104836 | ||||||
| chr11:44104955
|
G | A | 1 | a0001c0001t0010g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-2728G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104955 | ||||||
| chr11:44105229
|
A | G | 1 | a0001c0004t0040g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-30-2454A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105229 | ||||||
| chr11:44105262
|
G | A | 4 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(1): Show | 4 | HG02723.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-2421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105262 | ||||||
| chr11:44105334
|
C | T | 80 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(77): Show | 80 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-30-2349C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105334 | ||||||
| chr11:44105438
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0051g0101 | 3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-30-2245T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105438 | ||||||
| chr11:44105555
|
G | C | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-2128G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105555 | ||||||
| chr11:44105743
|
G | C | 1 | a0001c0001t0002g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-1940G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105743 | ||||||
| chr11:44105760
|
T | C | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-1923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105760 | ||||||
| chr11:44106011
|
C | T | 1 | a0001c0001t0058g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30-1672C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106011 | ||||||
| chr11:44106273
|
A | G | 64 | a0001c0001t0001g0275a0001c0001t0001g0328a0001c0001t0003g0266others(61): Show | 65 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-30-1410A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106273 | ||||||
| chr11:44106369
|
T | A | 1 | a0001c0001t0011g0088 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-30-1314T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106369 | ||||||
| chr11:44106425
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-30-1258T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106425 | ||||||
| chr11:44106495
|
T | A | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 96 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-30-1188T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106495 | ||||||
| chr11:44106501
|
T | C | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-1182T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106501 | ||||||
| chr11:44106559
|
C | A | 1 | a0001c0001t0005g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-30-1124C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106559 | ||||||
| chr11:44106742
|
G | C | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-941G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106742 | ||||||
| chr11:44106777
|
A | C | 7 | a0001c0001t0001g0176a0001c0001t0010g0308a0001c0001t0014g0001others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-906A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106777 | ||||||
| chr11:44106793
|
C | G | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-890C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106793 | ||||||
| chr11:44107140
|
A | G | 48 | a0001c0001t0001g0275a0001c0001t0003g0266a0001c0001t0003g0274others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30-543A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107140 | ||||||
| chr11:44107245
|
G | A | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-438G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107245 | ||||||
| chr11:44107269
|
C | T | 1 | a0002c0005t0019g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-30-414C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107269 | ||||||
| chr11:44107536
|
A | T | 84 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-30-147A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107536 | ||||||
| chr11:44107603
|
A | C | 18 | a0001c0001t0006g0089a0001c0001t0006g0090a0001c0001t0006g0100others(15): Show | 18 | HG00423.hp2 HG02622.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-80A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107603 | ||||||
| chr11:44108380
|
G | C | 76 | a0001c0001t0001g0275a0001c0001t0001g0328a0001c0001t0003g0266others(73): Show | 77 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.536+132G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44108380 | ||||||
| chr11:44108429
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.536+181G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44108429 | ||||||
| chr11:44109096
|
T | G | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.537-98T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109096 | ||||||
| chr11:44109110
|
C | T | 1 | a0001c0001t0007g0326 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.537-84C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109110 | ||||||
| chr11:44109115
|
A | C | 48 | a0001c0001t0001g0275a0001c0001t0003g0266a0001c0001t0003g0274others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.537-79A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109115 | ||||||
| chr11:44109411
|
A | T | 2 | a0001c0001t0003g0299a0001c0001t0003g0301 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.626+128A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109411 | ||||||
| chr11:44109422
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.626+139C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109422 | ||||||
| chr11:44109545
|
C | G | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+262C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109545 | ||||||
| chr11:44109587
|
G | A | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+304G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109587 | ||||||
| chr11:44109623
|
G | A | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.626+340G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109623 | ||||||
| chr11:44109641
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.626+358T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109641 | ||||||
| chr11:44109674
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.626+391G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109674 | ||||||
| chr11:44109804
|
C | T | 220 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(217): Show | 222 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.626+521C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109804 | ||||||
| chr11:44109869
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.626+586A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109869 | ||||||
| chr11:44110014
|
G | C | 1 | a0001c0003t0003g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.626+731G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110014 | ||||||
| chr11:44110016
|
C | T | 1 | a0001c0002t0008g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.626+733C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110016 | ||||||
| chr11:44110017
|
G | A | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+734G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110017 | ||||||
| chr11:44110030
|
G | A | 2 | a0001c0001t0011g0105a0001c0001t0011g0106 | 2 | HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.626+747G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110030 | ||||||
| chr11:44110440
|
G | A | 1 | a0001c0004t0030g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+1157G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110440 | ||||||
| chr11:44110476
|
G | A | 4 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+1193G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110476 | ||||||
| chr11:44110779
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.626+1496C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110779 | ||||||
| chr11:44111083
|
G | A | 7 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(4): Show | 7 | NA18949.hp2 NA18980.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+1800G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111083 | ||||||
| chr11:44111330
|
C | T | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.626+2047C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111330 | ||||||
| chr11:44111354
|
CCT | C | 4 | a0001c0001t0005g0076a0001c0001t0005g0077a0001c0001t0005g0078others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+2074_626+2075d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr11 | 44111354 | |||||
| chr11:44111551
|
C | T | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.626+2268C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111551 | ||||||
| chr11:44111773
|
C | T | 1 | a0001c0001t0035g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.627-2412C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111773 | ||||||
| chr11:44111936
|
A | G | 3 | a0001c0001t0005g0061a0001c0001t0005g0075a0001c0002t0004g0052 | 3 | NA18968.hp2 NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.627-2249A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111936 | ||||||
| chr11:44112033
|
G | A | 45 | a0001c0001t0003g0291a0001c0002t0002g0019a0001c0002t0002g0021others(42): Show | 45 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.627-2152G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112033 | ||||||
| chr11:44112133
|
C | T | 196 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.627-2052C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112133 | ||||||
| chr11:44112166
|
G | A | 2 | a0001c0007t0005g0183a0001c0007t0005g0194 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.627-2019G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112166 | ||||||
| chr11:44112166
|
G | C | 1 | a0003c0006t0003g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.627-2019G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112166 | ||||||
| chr11:44112322
|
G | A | 16 | a0001c0001t0001g0328a0001c0001t0004g0327a0001c0001t0007g0169others(13): Show | 16 | HG00323.hp1 HG01168.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.627-1863G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112322 | ||||||
| chr11:44112591
|
G | A | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.627-1594G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112591 | ||||||
| chr11:44112749
|
C | T | 31 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(28): Show | 31 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.627-1436C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112749 | ||||||
| chr11:44112889
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.627-1296C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112889 | ||||||
| chr11:44113057
|
C | T | 45 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(42): Show | 45 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.627-1128C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113057 | ||||||
| chr11:44113227
|
A | G | 7 | a0001c0009t0027g0306a0001c0009t0027g0307a0001c0014t0062g0239others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-958A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113227 | ||||||
| chr11:44113366
|
G | A | 21 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(18): Show | 21 | HG00099.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.627-819G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113366 | ||||||
| chr11:44113439
|
T | G | 1 | a0001c0001t0018g0314 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.627-746T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113439 | ||||||
| chr11:44113663
|
G | A | 1 | a0001c0004t0040g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.627-522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113663 | ||||||
| chr11:44113869
|
G | A | 5 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(2): Show | 5 | NA18943.hp1 NA18947.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-316G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113869 | ||||||
| chr11:44113875
|
G | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.627-310G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113875 | ||||||
| chr11:44113885
|
A | T | 1 | a0001c0001t0003g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-300A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113885 | ||||||
| chr11:44113962
|
G | C | 1 | a0001c0014t0062g0239 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.627-223G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113962 | ||||||
| chr11:44113998
|
T | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.627-187T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113998 | ||||||
| chr11:44114117
|
C | T | 1 | a0001c0007t0005g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.627-68C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44114117 | ||||||
| chr11:44114444
|
C | T | 4 | a0001c0001t0012g0004a0001c0001t0012g0005a0001c0001t0012g0006others(1): Show | 4 | HG01123.hp2 HG01168.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+143C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114444 | ||||||
| chr11:44114510
|
A | C | 1 | a0001c0002t0002g0015 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.743+209A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114510 | ||||||
| chr11:44114574
|
A | G | 1 | a0001c0001t0038g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.743+273A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114574 | ||||||
| chr11:44114657
|
C | T | 1 | a0001c0001t0006g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.743+356C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114657 | ||||||
| chr11:44114692
|
C | T | 1 | a0001c0001t0007g0325 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.743+391C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114692 | ||||||
| chr11:44114788
|
T | TA | 46 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(43): Show | 46 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.743+488dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44114788 | |||||
| chr11:44114808
|
A | G | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.743+507A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114808 | ||||||
| chr11:44115036
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG00639.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.743+735G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115036 | ||||||
| chr11:44115088
|
C | G | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.743+787C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115088 | ||||||
| chr11:44115095
|
G | A | 1 | a0001c0003t0003g0262 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.743+794G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115095 | ||||||
| chr11:44115185
|
C | T | 54 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0003g0192others(51): Show | 55 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.743+884C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115185 | ||||||
| chr11:44115410
|
T | A | 7 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(4): Show | 7 | HG01993.hp2 NA18942.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+1109T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115410 | ||||||
| chr11:44115456
|
A | G | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+1155A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115456 | ||||||
| chr11:44115486
|
A | G | 16 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.743+1185A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115486 | ||||||
| chr11:44115670
|
C | A | 271 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.743+1369C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115670 | ||||||
| chr11:44115693
|
T | G | 52 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(49): Show | 52 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.743+1392T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115693 | ||||||
| chr11:44115872
|
G | A | 1 | a0001c0001t0028g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.743+1571G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115872 | ||||||
| chr11:44116067
|
C | T | 2 | a0001c0001t0053g0255a0001c0001t0054g0259 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.743+1766C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116067 | ||||||
| chr11:44116219
|
C | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.743+1918C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116219 | ||||||
| chr11:44116818
|
A | G | 1 | a0001c0001t0002g0109 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.743+2517A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116818 | ||||||
| chr11:44116899
|
G | A | 14 | a0001c0001t0001g0328a0001c0001t0004g0327a0001c0001t0007g0169others(11): Show | 14 | HG00323.hp1 HG01168.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.743+2598G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116899 | ||||||
| chr11:44116969
|
C | CT | 7 | a0001c0001t0001g0010a0001c0001t0002g0197a0001c0001t0026g0016others(4): Show | 7 | HG01081.hp2 HG01346.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+2685dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44116969 | |||||
| chr11:44116969
|
CT | C | 13 | a0001c0001t0003g0292a0001c0001t0005g0017a0001c0001t0008g0002others(10): Show | 14 | HG01515.hp2 HG01993.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+2685delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44116969 | |||||
| chr11:44117126
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.743+2825C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117126 | ||||||
| chr11:44117152
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.743+2851A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117152 | ||||||
| chr11:44117451
|
C | A | 195 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0001g0328others(192): Show | 198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.743+3150C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117451 | ||||||
| chr11:44117511
|
C | A | 5 | a0001c0001t0005g0063a0001c0001t0005g0064a0001c0001t0005g0067others(2): Show | 5 | HG00099.hp2 HG01192.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+3210C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117511 | ||||||
| chr11:44117557
|
T | C | 1 | a0001c0002t0049g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.743+3256T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117557 | ||||||
| chr11:44117653
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.743+3352C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117653 | ||||||
| chr11:44117733
|
A | C | 11 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(8): Show | 12 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+3432A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117733 | ||||||
| chr11:44117809
|
T | A | 29 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(26): Show | 29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.743+3508T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117809 | ||||||
| chr11:44117908
|
C | A | 1 | a0001c0001t0007g0326 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.743+3607C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117908 | ||||||
| chr11:44118121
|
G | A | 1 | a0001c0001t0005g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.743+3820G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118121 | ||||||
| chr11:44118123
|
A | G | 1 | a0001c0001t0005g0067 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.743+3822A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118123 | ||||||
| chr11:44118339
|
A | G | 1 | a0001c0004t0030g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.743+4038A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118339 | ||||||
| chr11:44118587
|
C | G | 10 | a0001c0001t0005g0061a0001c0001t0005g0071a0001c0001t0005g0073others(7): Show | 10 | HG00609.hp1 NA18747.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4286C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118587 | ||||||
| chr11:44118743
|
G | A | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.743+4442G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118743 | ||||||
| chr11:44118837
|
G | A | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4536G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118837 | ||||||
| chr11:44118841
|
G | A | 12 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(9): Show | 13 | HG01109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.743+4540G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118841 | ||||||
| chr11:44118844
|
A | G | 33 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(30): Show | 33 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.743+4543A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118844 | ||||||
| chr11:44118907
|
A | G | 10 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.743+4606A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118907 | ||||||
| chr11:44119122
|
A | ATT | 6 | a0001c0001t0001g0124a0001c0001t0001g0152a0001c0001t0006g0139others(3): Show | 6 | HG00673.hp1 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+4823_743+4824d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119122 | |||||
| chr11:44119124
|
T | A | 1 | a0001c0002t0008g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.743+4823T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | ||||||
| chr11:44119124
|
T | TA | 3 | a0001c0001t0002g0213a0001c0002t0004g0026a0001c0007t0005g0183 | 3 | HG02165.hp1 NA18966.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.743+4823_743+4824i others(3): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | ||||||
| chr11:44119124
|
T | TATATATA others(6): Show |
1 | a0001c0001t0009g0288 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(15): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | ||||||
| chr11:44119124
|
T | TATATATA others(10): Show |
1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(19): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | ||||||
| chr11:44119124
|
T | TCATATAT others(3): Show |
1 | a0001c0001t0053g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | ||||||
| chr11:44119124
|
T | TTA | 3 | a0001c0001t0007g0324a0003c0006t0007g0317a0003c0006t0007g0318 | 3 | HG01978.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.743+4868_743+4869d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTATA | 4 | a0001c0001t0004g0327a0001c0001t0007g0175a0001c0001t0007g0323others(1): Show | 4 | HG02258.hp1 HG02723.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4866_743+4869d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTATATA | 3 | a0001c0001t0001g0328a0001c0001t0003g0191a0001c0007t0005g0194 | 3 | NA18906.hp2 NA19001.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743+4864_743+4869d others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0058g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.743+4860_743+4869d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0007g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.743+4858_743+4869d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+4832_743+4833i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTA | 11 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0125others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+4824_743+4825i others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATA | 3 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00609.hp2 HG02165.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(3): Show |
1 | a0001c0001t0001g0157 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(5): Show |
2 | a0001c0001t0001g0165a0001c0001t0024g0140 | 2 | NA18950.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(7): Show |
1 | a0001c0001t0018g0316 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(9): Show |
2 | a0001c0001t0018g0314a0001c0001t0024g0141 | 2 | HG00639.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(11): Show |
1 | a0001c0001t0006g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(19): Show |
1 | a0001c0001t0002g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.743+4824_743+4825i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(21): Show |
2 | a0002c0005t0019g0236a0002c0005t0019g0240 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(30): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
T | TTTTATAT others(17): Show |
1 | a0002c0005t0019g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTA | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(19): Show | 22 | HG00423.hp2 HG01123.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.743+4868_743+4869d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATA | T | 14 | a0001c0001t0001g0110a0001c0001t0003g0182a0001c0001t0003g0186others(11): Show | 14 | HG02257.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+4866_743+4869d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(5): Show |
T | 3 | a0001c0001t0014g0179a0001c0014t0062g0239a0002c0005t0061g0237 | 3 | HG01109.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.743+4858_743+4869d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(7): Show |
T | 6 | a0001c0001t0007g0256a0001c0001t0010g0308a0001c0001t0014g0001others(3): Show | 7 | HG00323.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+4856_743+4869d others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(9): Show |
T | 6 | a0001c0001t0010g0310a0001c0001t0020g0241a0001c0001t0020g0242others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+4854_743+4869d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(11): Show |
T | 2 | a0001c0001t0010g0311a0001c0001t0010g0312 | 2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.743+4852_743+4869d others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(13): Show |
T | 4 | a0001c0001t0002g0215a0001c0001t0028g0252a0001c0001t0028g0253others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4850_743+4869d others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119124
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0043g0284 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.743+4844_743+4869d others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | |||||
| chr11:44119126
|
A | T | 80 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0091others(77): Show | 81 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.743+4825A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119126 | ||||||
| chr11:44119128
|
A | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.743+4827A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119128 | ||||||
| chr11:44119130
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0052g0143 | 2 | NA18982.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.743+4829A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119130 | ||||||
| chr11:44119136
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.743+4835A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119136 | ||||||
| chr11:44119137
|
T | TATAATAT others(32): Show |
1 | a0001c0001t0002g0214 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.743+4839_743+4840i others(41): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | |||||
| chr11:44119137
|
T | TATATATA others(7): Show |
1 | a0001c0002t0002g0015 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.743+4849_743+4850i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | |||||
| chr11:44119137
|
T | TATATATA others(13): Show |
2 | a0001c0001t0002g0202a0005c0012t0002g0203 | 2 | HG01515.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.743+4855_743+4856i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | |||||
| chr11:44119137
|
T | TATATATA others(19): Show |
1 | a0001c0001t0002g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.743+4861_743+4862i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | |||||
| chr11:44119138
|
A | T | 2 | a0001c0014t0062g0239a0002c0005t0061g0237 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.743+4837A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119138 | ||||||
| chr11:44119139
|
T | TATATATA others(9): Show |
1 | a0001c0001t0002g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.743+4853_743+4854i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | |||||
| chr11:44119139
|
T | TATATATA others(11): Show |
5 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+4855_743+4856i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | |||||
| chr11:44119139
|
T | TATATATA others(15): Show |
2 | a0001c0001t0008g0234a0001c0001t0034g0230 | 2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.743+4859_743+4860i others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | |||||
| chr11:44119139
|
T | TATATATA others(17): Show |
5 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0008g0217others(2): Show | 5 | NA18999.hp2 NA19004.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+4861_743+4862i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | |||||
| chr11:44119139
|
T | TATATATA others(25): Show |
1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.743+4865_743+4866i others(34): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | |||||
| chr11:44119140
|
A | T | 1 | a0001c0001t0014g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.743+4839A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119140 | ||||||
| chr11:44119143
|
T | C | 2 | a0001c0001t0002g0251a0001c0001t0031g0287 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.743+4842T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119143 | ||||||
| chr11:44119145
|
T | C | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4844T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119145 | ||||||
| chr11:44119151
|
T | C | 34 | a0001c0001t0002g0251a0001c0001t0003g0227a0001c0001t0005g0017others(31): Show | 34 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.743+4850T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119151 | ||||||
| chr11:44119153
|
T | C | 10 | a0001c0001t0005g0074a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+4852T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119153 | ||||||
| chr11:44119153
|
TATATATA others(11): Show |
T | 32 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(29): Show | 32 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.743+4854_743+4871d others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119153 | |||||
| chr11:44119153
|
TATATATA others(17): Show |
T | 2 | a0001c0001t0002g0251a0001c0001t0031g0287 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.743+4854_743+4877d others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119153 | |||||
| chr11:44119155
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0005g0074 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.743+4856_743+4871d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119155 | |||||
| chr11:44119155
|
TATATATA others(15): Show |
T | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4856_743+4877d others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119155 | |||||
| chr11:44119163
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0006g0160a0001c0008t0001g0159 | 2 | HG00438.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.743+4866_743+4875d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119163 | |||||
| chr11:44119167
|
T | C | 8 | a0001c0001t0007g0256a0001c0001t0042g0264a0001c0001t0043g0284others(5): Show | 8 | HG00323.hp2 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4866T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119167 | ||||||
| chr11:44119169
|
T | C | 36 | a0001c0001t0001g0176a0001c0001t0002g0196a0001c0001t0002g0197others(33): Show | 36 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.743+4868T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | ||||||
| chr11:44119169
|
T | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 33 | HG00423.hp2 HG01123.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.743+4868T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | ||||||
| chr11:44119169
|
T | TATACATA others(81): Show |
1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(90): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATACA others(29): Show |
4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | NA18947.hp1 NA18971.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(38): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(1): Show |
6 | a0001c0001t0003g0207a0001c0003t0003g0261a0001c0003t0003g0267others(3): Show | 6 | HG01496.hp1 HG02970.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(3): Show |
1 | a0001c0002t0046g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(31): Show |
1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(31): Show |
3 | a0001c0001t0002g0222a0001c0001t0002g0225a0001c0001t0002g0233 | 3 | HG01167.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(3): Show |
5 | a0001c0001t0003g0192a0001c0001t0003g0299a0001c0001t0003g0301others(2): Show | 5 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(5): Show |
1 | a0001c0002t0004g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(33): Show |
1 | a0001c0001t0002g0087 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(42): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(5): Show |
4 | a0001c0001t0003g0292a0001c0001t0003g0293a0001c0001t0003g0298others(1): Show | 4 | HG01361.hp1 NA18984.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(7): Show |
2 | a0001c0002t0002g0055a0001c0002t0017g0031 | 2 | HG03831.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(9): Show |
2 | a0001c0002t0004g0052a0001c0002t0055g0014 | 2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(35): Show |
1 | a0001c0001t0002g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(37): Show |
1 | a0001c0001t0002g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(7): Show |
8 | a0001c0001t0002g0210a0001c0001t0003g0294a0001c0001t0003g0295others(5): Show | 8 | HG01109.hp1 HG02027.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(9): Show |
4 | a0001c0001t0004g0271a0001c0002t0002g0021a0001c0002t0002g0081others(1): Show | 4 | NA18981.hp2 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(37): Show |
2 | a0001c0001t0002g0209a0001c0001t0002g0212 | 2 | HG00639.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(9): Show |
2 | a0001c0001t0003g0305a0001c0001t0038g0226 | 2 | HG03017.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(11): Show |
13 | a0001c0001t0001g0275a0001c0001t0003g0274a0001c0001t0009g0263others(10): Show | 13 | HG00438.hp1 HG01175.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(13): Show |
1 | a0001c0002t0004g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(11): Show |
4 | a0001c0001t0003g0291a0001c0001t0003g0304a0001c0001t0013g0300others(1): Show | 4 | HG03209.hp1 NA18979.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(13): Show |
9 | a0001c0001t0005g0277a0001c0001t0009g0276a0001c0001t0023g0258others(6): Show | 9 | HG00544.hp2 HG01258.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(15): Show |
9 | a0001c0001t0005g0280a0001c0001t0009g0260a0001c0001t0009g0278others(6): Show | 9 | HG00597.hp2 HG01256.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(17): Show |
1 | a0001c0002t0004g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(17): Show |
7 | a0001c0001t0009g0003a0001c0001t0009g0283a0001c0002t0002g0019others(4): Show | 8 | HG00673.hp2 HG01993.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(19): Show |
1 | a0001c0001t0007g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(19): Show |
3 | a0001c0001t0003g0282a0001c0002t0002g0168a0001c0002t0004g0047 | 3 | HG04115.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(21): Show |
4 | a0001c0001t0005g0286a0001c0002t0004g0049a0001c0002t0017g0048others(1): Show | 4 | HG01255.hp2 NA18942.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(30): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(23): Show |
1 | a0001c0002t0036g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(32): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(25): Show |
1 | a0001c0002t0048g0051 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(34): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATATA others(35): Show |
1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TATATTCA others(31): Show |
1 | a0001c0001t0002g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | |||||
| chr11:44119169
|
T | TGTATATA others(11): Show |
1 | a0001c0001t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.743+4868_743+4869i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | ||||||
| chr11:44119171
|
C | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0086others(46): Show | 49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4870C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119171 | ||||||
| chr11:44119173
|
C | T | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4872C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119173 | ||||||
| chr11:44119174
|
A | G | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.743+4873A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119174 | ||||||
| chr11:44119175
|
T | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0086others(46): Show | 49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4874T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119175 | ||||||
| chr11:44119175
|
TAC | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 46 | HG00423.hp2 HG01109.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.743+4892_743+4893d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119175 | |||||
| chr11:44119177
|
C | CAT | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4877_743+4878i others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119177 | |||||
| chr11:44119177
|
C | G | 3 | a0001c0001t0006g0160a0001c0008t0001g0159a0001c0008t0001g0161 | 3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4876C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119177 | ||||||
| chr11:44119177
|
C | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0086others(46): Show | 49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4876C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119177 | ||||||
| chr11:44119183
|
C | T | 3 | a0001c0001t0006g0160a0001c0008t0001g0159a0001c0008t0001g0161 | 3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4882C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119183 | ||||||
| chr11:44119191
|
C | G | 56 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0003g0192others(53): Show | 57 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.743+4890C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119191 | ||||||
| chr11:44119192
|
A | T | 3 | a0001c0001t0006g0160a0001c0008t0001g0159a0001c0008t0001g0161 | 3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4891A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119192 | ||||||
| chr11:44119235
|
C | T | 1 | a0001c0001t0039g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.743+4934C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119235 | ||||||
| chr11:44119337
|
G | A | 10 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(7): Show | 11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.743+5036G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119337 | ||||||
| chr11:44119345
|
A | C | 1 | a0001c0001t0053g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.743+5044A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119345 | ||||||
| chr11:44119504
|
T | G | 2 | a0001c0001t0023g0257a0001c0001t0023g0258 | 2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.743+5203T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119504 | ||||||
| chr11:44119559
|
G | A | 1 | a0001c0001t0005g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.744-5230G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119559 | ||||||
| chr11:44119627
|
T | C | 1 | a0001c0001t0013g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744-5162T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119627 | ||||||
| chr11:44119683
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.744-5106C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119683 | ||||||
| chr11:44119690
|
T | C | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-5099T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119690 | ||||||
| chr11:44119749
|
C | A | 2 | a0001c0014t0062g0239a0002c0005t0061g0237 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-5040C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119749 | ||||||
| chr11:44119827
|
G | A | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.744-4962G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119827 | ||||||
| chr11:44119854
|
C | T | 11 | a0001c0001t0002g0251a0001c0001t0008g0002a0001c0001t0008g0243others(8): Show | 12 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-4935C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119854 | ||||||
| chr11:44120300
|
G | A | 29 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(26): Show | 29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.744-4489G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120300 | ||||||
| chr11:44120509
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.744-4280G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120509 | ||||||
| chr11:44120559
|
C | T | 2 | a0001c0001t0003g0295a0001c0001t0003g0298 | 2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.744-4230C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120559 | ||||||
| chr11:44120776
|
C | T | 3 | a0001c0001t0005g0277a0001c0001t0005g0280a0001c0001t0005g0286 | 3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.744-4013C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120776 | ||||||
| chr11:44120912
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.744-3877C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120912 | ||||||
| chr11:44121045
|
G | C | 10 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254others(7): Show | 10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.744-3744G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121045 | ||||||
| chr11:44121100
|
T | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.744-3689T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121100 | ||||||
| chr11:44121146
|
T | C | 1 | a0001c0001t0050g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.744-3643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121146 | ||||||
| chr11:44121167
|
A | C | 44 | a0001c0001t0005g0061a0001c0001t0013g0300a0001c0002t0002g0019others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.744-3622A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121167 | ||||||
| chr11:44121187
|
T | C | 7 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.744-3602T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121187 | ||||||
| chr11:44121227
|
G | A | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.744-3562G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121227 | ||||||
| chr11:44121384
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.744-3405T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121384 | ||||||
| chr11:44121480
|
C | T | 6 | a0001c0001t0010g0311a0001c0001t0010g0312a0001c0001t0015g0129others(3): Show | 6 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-3309C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121480 | ||||||
| chr11:44121497
|
G | A | 1 | a0001c0001t0009g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.744-3292G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121497 | ||||||
| chr11:44121548
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.744-3241T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121548 | ||||||
| chr11:44121951
|
C | T | 8 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-2838C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121951 | ||||||
| chr11:44122056
|
G | C | 1 | a0003c0006t0007g0317 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744-2733G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122056 | ||||||
| chr11:44122349
|
GT | G | 3 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312 | 3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.744-2437delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44122349 | |||||
| chr11:44122425
|
G | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(106): Show | 110 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.744-2364G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122425 | ||||||
| chr11:44122509
|
A | G | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.744-2280A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122509 | ||||||
| chr11:44122566
|
A | G | 2 | a0001c0001t0003g0299a0001c0001t0003g0301 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.744-2223A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122566 | ||||||
| chr11:44122670
|
C | T | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.744-2119C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122670 | ||||||
| chr11:44122695
|
T | G | 1 | a0001c0001t0008g0243 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.744-2094T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122695 | ||||||
| chr11:44122927
|
G | A | 3 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.744-1862G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122927 | ||||||
| chr11:44123093
|
G | A | 210 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.744-1696G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123093 | ||||||
| chr11:44123148
|
G | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-1641G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123148 | ||||||
| chr11:44123228
|
C | T | 8 | a0001c0002t0004g0027a0001c0002t0004g0035a0001c0002t0004g0036others(5): Show | 8 | HG00621.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-1561C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123228 | ||||||
| chr11:44123343
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.744-1446C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123343 | ||||||
| chr11:44123484
|
C | T | 1 | a0001c0001t0014g0001 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.744-1305C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123484 | ||||||
| chr11:44123500
|
C | A | 1 | a0001c0002t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.744-1289C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123500 | ||||||
| chr11:44123773
|
TCTCTGTC others(150): Show |
T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-852_744-696del | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44123773 | |||||
| chr11:44124444
|
T | TAC | 42 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(39): Show | 42 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.744-307_744-306dup others(2): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
T | TACAC | 15 | a0001c0001t0001g0010a0001c0001t0002g0209a0001c0001t0002g0223others(12): Show | 15 | HG01261.hp2 HG01346.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.744-309_744-306dup others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
T | TACACAC | 35 | a0001c0001t0005g0061a0001c0001t0005g0063a0001c0001t0005g0064others(32): Show | 36 | HG00099.hp2 HG00609.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.744-311_744-306dup others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
T | TACACACA others(1): Show |
5 | a0001c0001t0002g0222a0001c0001t0021g0059a0001c0001t0021g0060others(2): Show | 5 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-313_744-306dup others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
T | TACACACA others(3): Show |
11 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-315_744-306dup others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
T | TACACACA others(5): Show |
1 | a0001c0001t0013g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744-317_744-306dup others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
TAC | T | 167 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0086others(164): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.744-307_744-306del others(2): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
TACAC | T | 9 | a0001c0001t0001g0094a0001c0001t0006g0134a0001c0001t0006g0154others(6): Show | 9 | HG00621.hp1 HG02486.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-309_744-306del others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124444
|
TACACAC | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 13 | HG00639.hp2 HG02257.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.744-311_744-306del others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | |||||
| chr11:44124459
|
A | G | 3 | a0001c0001t0053g0255a0001c0001t0054g0259a0001c0014t0062g0239 | 3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-330A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124459 | ||||||
| chr11:44124620
|
TATA | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-165_744-163del others(3): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124620 | |||||
| chr11:44124706
|
C | CG | 12 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(9): Show | 12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-83_744-82insG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124706 | ||||||
| chr11:44124707
|
A | G | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.744-82A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124707 | ||||||
| chr11:44124707
|
A | T | 12 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(9): Show | 12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-82A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124707 | ||||||
| chr11:44124744
|
C | T | 2 | a0001c0004t0016g0172a0001c0004t0016g0173 | 2 | HG03017.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.744-45C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124744 | ||||||
| chr11:44125007
|
C | T | 8 | a0001c0003t0003g0261a0001c0003t0003g0262a0001c0003t0003g0265others(5): Show | 8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+23C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125007 | ||||||
| chr11:44125020
|
G | T | 8 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+36G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125020 | ||||||
| chr11:44125081
|
A | G | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.939+97A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125081 | ||||||
| chr11:44125300
|
C | G | 43 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.939+316C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125300 | ||||||
| chr11:44125421
|
T | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0201others(1): Show | 4 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+437T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125421 | ||||||
| chr11:44125451
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.939+467T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125451 | ||||||
| chr11:44125513
|
A | G | 47 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(44): Show | 47 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.939+529A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125513 | ||||||
| chr11:44125680
|
A | AT | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(96): Show | 100 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.939+709dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 44125680 | |||||
| chr11:44125879
|
A | G | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.939+895A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125879 | ||||||
| chr11:44126112
|
T | C | 328 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.940-704T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126112 | ||||||
| chr11:44126367
|
C | T | 2 | a0001c0001t0008g0246a0001c0001t0008g0247 | 2 | NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.940-449C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126367 | ||||||
| chr11:44126487
|
A | C | 1 | a0001c0002t0004g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.940-329A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126487 | ||||||
| chr11:44126628
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.940-188A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126628 | ||||||
| chr11:44126737
|
A | C | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.940-79A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126737 | ||||||
| chr11:44127015
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1079+60T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127015 | ||||||
| chr11:44127323
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1079+368G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127323 | ||||||
| chr11:44127368
|
G | A | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1079+413G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127368 | ||||||
| chr11:44127779
|
A | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1079+824A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127779 | ||||||
| chr11:44127790
|
A | AGAG | 61 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1079+835_1079+836i others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127790 | ||||||
| chr11:44127791
|
C | T | 61 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1079+836C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127791 | ||||||
| chr11:44127796
|
C | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1079+841C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127796 | ||||||
| chr11:44128050
|
T | A | 1 | a0001c0001t0003g0266 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1079+1095T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128050 | ||||||
| chr11:44128295
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1079+1340C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128295 | ||||||
| chr11:44128547
|
C | G | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080-1498C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128547 | ||||||
| chr11:44128954
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1080-1091G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128954 | ||||||
| chr11:44128980
|
A | T | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1080-1065A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128980 | ||||||
| chr11:44128981
|
G | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080-1064G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128981 | ||||||
| chr11:44129022
|
C | T | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.1080-1023C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129022 | ||||||
| chr11:44129185
|
C | T | 152 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0003g0178others(149): Show | 154 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1080-860C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129185 | ||||||
| chr11:44129369
|
T | C | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1080-676T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129369 | ||||||
| chr11:44129431
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1080-614G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129431 | ||||||
| chr11:44129465
|
C | T | 3 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312 | 3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-580C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129465 | ||||||
| chr11:44129466
|
T | C | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1080-579T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129466 | ||||||
| chr11:44129531
|
T | G | 1 | a0001c0001t0002g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1080-514T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129531 | ||||||
| chr11:44129674
|
C | T | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(310): Show | 316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1080-371C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129674 | ||||||
| chr11:44129907
|
T | C | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.1080-138T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129907 | ||||||
| chr11:44129912
|
CT | C | 7 | a0001c0002t0004g0026a0001c0002t0004g0032a0001c0002t0004g0043others(4): Show | 7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-131delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 44129912 | |||||
| chr11:44129930
|
G | T | 82 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1080-115G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129930 | ||||||
| chr11:44130027
|
T | A | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(97): Show | 101 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1080-18T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44130027 | ||||||
| chr11:44130309
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0124 | 2 | HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1173+171G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130309 | ||||||
| chr11:44130365
|
G | A | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+227G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130365 | ||||||
| chr11:44130379
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1173+241C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130379 | ||||||
| chr11:44130512
|
T | G | 26 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(23): Show | 26 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1173+374T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130512 | ||||||
| chr11:44130555
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1173+417T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130555 | ||||||
| chr11:44130559
|
G | A | 3 | a0001c0001t0053g0255a0001c0001t0054g0259a0001c0014t0062g0239 | 3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130559 | ||||||
| chr11:44131106
|
G | A | 1 | a0001c0001t0013g0300 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1173+968G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131106 | ||||||
| chr11:44131146
|
CTT | C | 3 | a0001c0001t0009g0276a0001c0001t0009g0278a0001c0001t0042g0264 | 3 | HG00544.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1173+1009_1173+101 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131146 | ||||||
| chr11:44131456
|
C | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+1318C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131456 | ||||||
| chr11:44131499
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+1361T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131499 | ||||||
| chr11:44131908
|
T | G | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1173+1770T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131908 | ||||||
| chr11:44131938
|
A | T | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+1800A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131938 | ||||||
| chr11:44131983
|
G | A | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1173+1845G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131983 | ||||||
| chr11:44132179
|
A | G | 50 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(47): Show | 50 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1173+2041A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132179 | ||||||
| chr11:44132508
|
C | T | 3 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312 | 3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1173+2370C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132508 | ||||||
| chr11:44132682
|
C | T | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+2544C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132682 | ||||||
| chr11:44132879
|
C | T | 4 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0139others(1): Show | 4 | NA18942.hp1 NA18966.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+2741C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132879 | ||||||
| chr11:44132908
|
C | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+2770C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132908 | ||||||
| chr11:44133276
|
A | C | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1173+3138A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133276 | ||||||
| chr11:44133733
|
G | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1173+3595G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133733 | ||||||
| chr11:44133744
|
A | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+3606A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133744 | ||||||
| chr11:44133845
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1173+3707A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133845 | ||||||
| chr11:44133885
|
C | T | 44 | a0001c0001t0004g0327a0001c0002t0002g0019a0001c0002t0002g0021others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1173+3747C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133885 | ||||||
| chr11:44133886
|
G | A | 1 | a0001c0001t0014g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173+3748G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133886 | ||||||
| chr11:44133904
|
A | G | 1 | a0001c0001t0007g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1173+3766A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133904 | ||||||
| chr11:44134049
|
C | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+3911C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134049 | ||||||
| chr11:44134053
|
G | T | 1 | a0001c0001t0008g0249 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1173+3915G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134053 | ||||||
| chr11:44134059
|
G | T | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1173+3921G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134059 | ||||||
| chr11:44134075
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+3937G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134075 | ||||||
| chr11:44134101
|
C | T | 140 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0002g0087others(137): Show | 142 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1173+3963C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134101 | ||||||
| chr11:44134275
|
G | T | 9 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+4137G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134275 | ||||||
| chr11:44134317
|
AT | A | 9 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+4180delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134317 | ||||||
| chr11:44134395
|
C | T | 52 | a0001c0001t0001g0176a0001c0001t0001g0275a0001c0001t0003g0192others(49): Show | 53 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1173+4257C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134395 | ||||||
| chr11:44134479
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+4341T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134479 | ||||||
| chr11:44134987
|
G | A | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+4849G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134987 | ||||||
| chr11:44135149
|
G | A | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+5011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135149 | ||||||
| chr11:44135206
|
G | A | 2 | a0001c0001t0002g0204a0001c0001t0002g0206 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1173+5068G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135206 | ||||||
| chr11:44135390
|
C | CT | 7 | a0001c0001t0003g0178a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG01243.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+5271dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | |||||
| chr11:44135390
|
C | CTT | 10 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(7): Show | 10 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+5270_1173+527 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | |||||
| chr11:44135390
|
CT | C | 269 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1173+5271delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | |||||
| chr11:44135392
|
T | TC | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+5254_1173+525 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135392 | ||||||
| chr11:44135474
|
C | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+5336C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135474 | ||||||
| chr11:44135478
|
G | C | 1 | a0001c0001t0007g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1173+5340G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135478 | ||||||
| chr11:44135501
|
C | T | 1 | a0002c0005t0019g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+5363C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135501 | ||||||
| chr11:44135579
|
A | G | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+5441A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135579 | ||||||
| chr11:44135805
|
G | A | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.1173+5667G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135805 | ||||||
| chr11:44135955
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1173+5817T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135955 | ||||||
| chr11:44136050
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1173+5912A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136050 | ||||||
| chr11:44136240
|
C | A | 1 | a0001c0001t0007g0321 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1173+6102C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136240 | ||||||
| chr11:44136519
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1173+6381C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136519 | ||||||
| chr11:44136603
|
C | G | 35 | a0001c0001t0003g0227a0001c0001t0005g0017a0001c0001t0005g0061others(32): Show | 36 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1173+6465C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136603 | ||||||
| chr11:44136653
|
A | G | 1 | a0001c0002t0017g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1173+6515A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136653 | ||||||
| chr11:44136888
|
A | G | 83 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1173+6750A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136888 | ||||||
| chr11:44137000
|
A | G | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+6862A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137000 | ||||||
| chr11:44137017
|
A | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+6879A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137017 | ||||||
| chr11:44137188
|
T | A | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+7050T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137188 | ||||||
| chr11:44137453
|
G | A | 4 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(1): Show | 4 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+7315G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137453 | ||||||
| chr11:44137581
|
G | C | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+7443G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137581 | ||||||
| chr11:44137644
|
C | T | 1 | a0001c0001t0009g0288 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1173+7506C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137644 | ||||||
| chr11:44137776
|
G | T | 3 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312 | 3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1173+7638G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137776 | ||||||
| chr11:44138284
|
A | G | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1173+8146A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138284 | ||||||
| chr11:44138558
|
A | T | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+8420A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138558 | ||||||
| chr11:44138770
|
G | A | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+8632G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138770 | ||||||
| chr11:44139120
|
C | CT | 96 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0176others(93): Show | 98 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1173+8995dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139120 | |||||
| chr11:44139120
|
C | CTT | 45 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(42): Show | 45 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1173+8994_1173+899 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139120 | |||||
| chr11:44139135
|
C | T | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+8997C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139135 | ||||||
| chr11:44139198
|
CT | C | 6 | a0001c0002t0002g0021a0001c0002t0004g0013a0002c0005t0019g0236others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+9073delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139198 | |||||
| chr11:44139352
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1173+9214C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139352 | ||||||
| chr11:44139402
|
G | A | 6 | a0001c0001t0002g0219a0001c0001t0008g0217a0001c0001t0008g0234others(3): Show | 6 | NA18986.hp2 NA18999.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+9264G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139402 | ||||||
| chr11:44139734
|
C | T | 2 | a0001c0002t0002g0021a0001c0002t0041g0024 | 2 | NA18942.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1173+9596C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139734 | ||||||
| chr11:44140315
|
C | T | 4 | a0001c0002t0004g0020a0001c0002t0004g0028a0001c0002t0004g0034others(1): Show | 4 | HG02027.hp1 NA18990.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10177C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140315 | ||||||
| chr11:44140751
|
T | G | 54 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(51): Show | 54 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1173+10613T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140751 | ||||||
| chr11:44140797
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1173+10659A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140797 | ||||||
| chr11:44140833
|
A | C | 4 | a0001c0001t0011g0088a0001c0001t0011g0105a0001c0001t0011g0106others(1): Show | 4 | HG01978.hp2 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10695A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140833 | ||||||
| chr11:44140936
|
TTATAGTA others(15): Show |
T | 1 | a0001c0001t0023g0258 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1173+10804_1173+10 others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44140936 | |||||
| chr11:44141023
|
C | T | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+10885C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141023 | ||||||
| chr11:44141079
|
T | C | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+10941T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141079 | ||||||
| chr11:44141189
|
C | T | 7 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11051C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141189 | ||||||
| chr11:44141289
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1173+11151T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141289 | ||||||
| chr11:44141307
|
A | G | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+11169A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141307 | ||||||
| chr11:44141323
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+11185A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141323 | ||||||
| chr11:44141390
|
GA | G | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+11253delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141390 | ||||||
| chr11:44141454
|
A | C | 12 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 13 | HG02896.hp1 HG02970.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+11316A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141454 | ||||||
| chr11:44141535
|
A | G | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+11397A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141535 | ||||||
| chr11:44141668
|
C | T | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+11530C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141668 | ||||||
| chr11:44141671
|
A | G | 1 | a0001c0001t0006g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1173+11533A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141671 | ||||||
| chr11:44141704
|
C | T | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+11566C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141704 | ||||||
| chr11:44141721
|
G | A | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+11583G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141721 | ||||||
| chr11:44141839
|
C | A | 1 | a0001c0001t0035g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1173+11701C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141839 | ||||||
| chr11:44141896
|
A | G | 4 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0022g0329others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+11758A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141896 | ||||||
| chr11:44141988
|
G | A | 1 | a0001c0001t0003g0178 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1173+11850G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141988 | ||||||
| chr11:44142156
|
A | C | 1 | a0001c0001t0003g0291 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1173+12018A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142156 | ||||||
| chr11:44142267
|
T | C | 5 | a0001c0001t0021g0059a0001c0001t0021g0060a0001c0001t0025g0058others(2): Show | 5 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+12129T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142267 | ||||||
| chr11:44142278
|
C | T | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+12140C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142278 | ||||||
| chr11:44142287
|
T | C | 183 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1173+12149T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142287 | ||||||
| chr11:44142347
|
T | G | 1 | a0001c0001t0009g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1173+12209T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142347 | ||||||
| chr11:44142352
|
A | G | 34 | a0001c0001t0003g0207a0001c0001t0003g0266a0001c0001t0003g0274others(31): Show | 35 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1173+12214A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142352 | ||||||
| chr11:44142482
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1173+12344T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142482 | ||||||
| chr11:44142873
|
C | T | 1 | a0001c0001t0008g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1173+12735C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142873 | ||||||
| chr11:44143013
|
G | A | 1 | a0001c0001t0013g0300 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1173+12875G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143013 | ||||||
| chr11:44143050
|
C | T | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+12912C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143050 | ||||||
| chr11:44143078
|
A | T | 1 | a0001c0002t0036g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1173+12940A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143078 | ||||||
| chr11:44143088
|
A | G | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+12950A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143088 | ||||||
| chr11:44143350
|
T | C | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1173+13212T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143350 | ||||||
| chr11:44143363
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+13225G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143363 | ||||||
| chr11:44143589
|
A | G | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1173+13451A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143589 | ||||||
| chr11:44143815
|
G | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+13677G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143815 | ||||||
| chr11:44143945
|
A | T | 56 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(53): Show | 56 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1173+13807A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143945 | ||||||
| chr11:44144056
|
G | A | 1 | a0001c0002t0004g0046 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1173+13918G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144056 | ||||||
| chr11:44144142
|
C | T | 1 | a0001c0001t0009g0290 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173+14004C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144142 | ||||||
| chr11:44144144
|
C | T | 1 | a0001c0001t0009g0290 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173+14006C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144144 | ||||||
| chr11:44144644
|
C | T | 2 | a0001c0001t0006g0134a0001c0001t0006g0154 | 2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1173+14506C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144644 | ||||||
| chr11:44144892
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1173+14754A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144892 | ||||||
| chr11:44144982
|
A | G | 1 | a0001c0001t0059g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1173+14844A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144982 | ||||||
| chr11:44145278
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1173+15140C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145278 | ||||||
| chr11:44145285
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+15147T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145285 | ||||||
| chr11:44145352
|
A | C | 1 | a0001c0001t0052g0143 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1173+15214A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145352 | ||||||
| chr11:44145447
|
A | G | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1173+15309A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145447 | ||||||
| chr11:44145717
|
G | A | 4 | a0001c0001t0004g0271a0001c0001t0009g0003a0001c0001t0009g0260others(1): Show | 5 | HG02523.hp2 NA18973.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+15579G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145717 | ||||||
| chr11:44145744
|
A | C | 1 | a0001c0001t0002g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1173+15606A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145744 | ||||||
| chr11:44145802
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+15664T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145802 | ||||||
| chr11:44145904
|
T | C | 15 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(12): Show | 15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+15766T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145904 | ||||||
| chr11:44145993
|
A | C | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+15855A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145993 | ||||||
| chr11:44146446
|
C | T | 182 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(179): Show | 184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1173+16308C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146446 | ||||||
| chr11:44146524
|
G | C | 1 | a0001c0001t0007g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1173+16386G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146524 | ||||||
| chr11:44146553
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1173+16415G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146553 | ||||||
| chr11:44146649
|
C | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1173+16511C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146649 | ||||||
| chr11:44146857
|
T | A | 3 | a0001c0001t0005g0277a0001c0001t0005g0280a0001c0001t0005g0286 | 3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1173+16719T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146857 | ||||||
| chr11:44147108
|
T | G | 3 | a0001c0001t0015g0181a0001c0001t0015g0184a0001c0001t0015g0185 | 3 | HG02257.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+16970T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147108 | ||||||
| chr11:44147259
|
A | G | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+17121A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147259 | ||||||
| chr11:44147449
|
C | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+17311C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147449 | ||||||
| chr11:44147498
|
A | G | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1173+17360A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147498 | ||||||
| chr11:44147562
|
TTTG | T | 52 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(49): Show | 53 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1173+17436_1173+17 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147562 | |||||
| chr11:44147646
|
C | T | 13 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+17508C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147646 | ||||||
| chr11:44147706
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0148a0001c0001t0001g0163others(1): Show | 4 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+17568G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147706 | ||||||
| chr11:44147726
|
A | C | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+17588A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147726 | ||||||
| chr11:44147727
|
AT | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1173+17602delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147727 | |||||
| chr11:44147775
|
C | CTTTT | 166 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1173+17649_1173+17 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | |||||
| chr11:44147775
|
C | CTTTTT | 110 | a0001c0001t0001g0158a0001c0001t0001g0165a0001c0001t0001g0176others(107): Show | 112 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1173+17648_1173+17 others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | |||||
| chr11:44147775
|
C | CTTTTTT | 16 | a0001c0001t0002g0108a0001c0001t0002g0219a0001c0001t0002g0225others(13): Show | 16 | HG01243.hp2 HG02135.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1173+17647_1173+17 others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | |||||
| chr11:44147775
|
C | CTTTTTTT | 15 | a0001c0001t0003g0193a0001c0001t0018g0314a0001c0001t0018g0315others(12): Show | 15 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+17646_1173+17 others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | |||||
| chr11:44147883
|
A | G | 3 | a0001c0001t0005g0068a0001c0001t0005g0069a0001c0001t0039g0070 | 3 | HG02280.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1173+17745A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147883 | ||||||
| chr11:44148112
|
G | A | 12 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 13 | HG02896.hp1 HG02970.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+17974G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148112 | ||||||
| chr11:44148191
|
A | G | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1173+18053A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148191 | ||||||
| chr11:44148192
|
G | C | 1 | a0001c0014t0062g0239 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1173+18054G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148192 | ||||||
| chr11:44148239
|
T | C | 299 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(296): Show | 302 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.1173+18101T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148239 | ||||||
| chr11:44148248
|
C | A | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+18110C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148248 | ||||||
| chr11:44148286
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1173+18148A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148286 | ||||||
| chr11:44148372
|
G | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+18234G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148372 | ||||||
| chr11:44148465
|
G | A | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173+18327G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148465 | ||||||
| chr11:44148647
|
G | A | 9 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+18509G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148647 | ||||||
| chr11:44148709
|
G | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+18571G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148709 | ||||||
| chr11:44148803
|
A | G | 2 | a0001c0001t0012g0005a0001c0001t0012g0006 | 2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1173+18665A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148803 | ||||||
| chr11:44149116
|
C | G | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+18978C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149116 | ||||||
| chr11:44149254
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1173+19116C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149254 | ||||||
| chr11:44149395
|
A | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1173+19257A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149395 | ||||||
| chr11:44149459
|
G | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+19321G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149459 | ||||||
| chr11:44149505
|
T | C | 1 | a0001c0001t0006g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1173+19367T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149505 | ||||||
| chr11:44149599
|
T | C | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1173+19461T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149599 | ||||||
| chr11:44149610
|
A | G | 2 | a0001c0001t0009g0285a0001c0001t0043g0284 | 2 | NA19000.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1173+19472A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149610 | ||||||
| chr11:44149754
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1173+19616T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149754 | ||||||
| chr11:44149774
|
C | T | 16 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(13): Show | 17 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1173+19636C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149774 | ||||||
| chr11:44149799
|
A | G | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+19661A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149799 | ||||||
| chr11:44149906
|
T | C | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(100): Show | 104 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1173+19768T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149906 | ||||||
| chr11:44150149
|
G | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+20011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150149 | ||||||
| chr11:44150274
|
T | A | 44 | a0001c0001t0004g0327a0001c0002t0002g0019a0001c0002t0002g0021others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1173+20136T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150274 | ||||||
| chr11:44150281
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1173+20143T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150281 | ||||||
| chr11:44150302
|
CT | C | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1173+20173delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44150302 | |||||
| chr11:44150396
|
T | C | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+20258T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150396 | ||||||
| chr11:44150455
|
G | A | 1 | a0001c0001t0032g0231 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1173+20317G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150455 | ||||||
| chr11:44150613
|
A | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1173+20475A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150613 | ||||||
| chr11:44150662
|
C | T | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+20524C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150662 | ||||||
| chr11:44150861
|
G | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+20723G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150861 | ||||||
| chr11:44150996
|
G | A | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1174-20615G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150996 | ||||||
| chr11:44151065
|
T | G | 2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1174-20546T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151065 | ||||||
| chr11:44151266
|
A | T | 1 | a0001c0001t0005g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1174-20345A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151266 | ||||||
| chr11:44151291
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-20320C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151291 | ||||||
| chr11:44151453
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-20158G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151453 | ||||||
| chr11:44151476
|
T | C | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-20135T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151476 | ||||||
| chr11:44151506
|
C | T | 253 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1174-20105C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151506 | ||||||
| chr11:44151767
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1174-19844G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151767 | ||||||
| chr11:44152128
|
T | A | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1174-19483T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152128 | ||||||
| chr11:44152167
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1174-19444A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152167 | ||||||
| chr11:44152343
|
G | GGTT | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-19246_1174-19 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44152343 | |||||
| chr11:44152511
|
C | T | 1 | a0001c0001t0006g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1174-19100C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152511 | ||||||
| chr11:44152512
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-19099G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152512 | ||||||
| chr11:44152527
|
T | C | 183 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1174-19084T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152527 | ||||||
| chr11:44152531
|
A | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1174-19080A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152531 | ||||||
| chr11:44152597
|
C | T | 183 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1174-19014C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152597 | ||||||
| chr11:44152602
|
C | T | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-19009C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152602 | ||||||
| chr11:44152627
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(114): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1174-18984G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152627 | ||||||
| chr11:44152834
|
A | G | 61 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1174-18777A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152834 | ||||||
| chr11:44152862
|
G | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-18749G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152862 | ||||||
| chr11:44152910
|
A | G | 2 | a0001c0002t0004g0033a0001c0002t0004g0038 | 2 | HG00438.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1174-18701A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152910 | ||||||
| chr11:44152954
|
T | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-18657T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152954 | ||||||
| chr11:44153052
|
A | G | 183 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1174-18559A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153052 | ||||||
| chr11:44153084
|
G | A | 46 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(43): Show | 46 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1174-18527G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153084 | ||||||
| chr11:44153115
|
G | A | 15 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(12): Show | 15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-18496G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153115 | ||||||
| chr11:44153131
|
T | C | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-18480T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153131 | ||||||
| chr11:44153493
|
A | G | 1 | a0001c0001t0011g0088 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1174-18118A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153493 | ||||||
| chr11:44153873
|
T | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-17738T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153873 | ||||||
| chr11:44153925
|
T | G | 61 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1174-17686T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153925 | ||||||
| chr11:44153938
|
T | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-17673T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153938 | ||||||
| chr11:44153965
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-17646A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153965 | ||||||
| chr11:44154073
|
G | T | 1 | a0001c0001t0022g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1174-17538G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154073 | ||||||
| chr11:44154145
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1174-17466G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154145 | ||||||
| chr11:44154207
|
C | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1174-17404C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154207 | ||||||
| chr11:44154392
|
A | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1174-17219A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154392 | ||||||
| chr11:44154495
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-17116C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154495 | ||||||
| chr11:44154593
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-17018T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154593 | ||||||
| chr11:44154787
|
T | A | 1 | a0001c0001t0005g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1174-16824T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154787 | ||||||
| chr11:44154851
|
T | G | 61 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1174-16760T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154851 | ||||||
| chr11:44155263
|
T | G | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1174-16348T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155263 | ||||||
| chr11:44155504
|
A | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1174-16107A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155504 | ||||||
| chr11:44155785
|
G | A | 137 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(134): Show | 139 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1174-15826G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155785 | ||||||
| chr11:44155821
|
A | G | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1174-15790A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155821 | ||||||
| chr11:44155883
|
G | A | 2 | a0001c0002t0002g0039a0001c0002t0002g0040 | 2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1174-15728G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155883 | ||||||
| chr11:44155886
|
T | C | 1 | a0001c0002t0002g0015 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1174-15725T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155886 | ||||||
| chr11:44156197
|
G | C | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-15414G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156197 | ||||||
| chr11:44156505
|
T | C | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-15106T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156505 | ||||||
| chr11:44156644
|
A | G | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1174-14967A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156644 | ||||||
| chr11:44156777
|
G | A | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-14834G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156777 | ||||||
| chr11:44156868
|
A | T | 1 | a0001c0001t0003g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1174-14743A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156868 | ||||||
| chr11:44156875
|
C | T | 1 | a0001c0001t0003g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1174-14736C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156875 | ||||||
| chr11:44156940
|
G | C | 2 | a0001c0002t0004g0034a0001c0002t0004g0046 | 2 | NA19066.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1174-14671G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156940 | ||||||
| chr11:44156963
|
C | G | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1174-14648C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156963 | ||||||
| chr11:44157074
|
C | T | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-14537C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157074 | ||||||
| chr11:44157086
|
G | A | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-14525G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157086 | ||||||
| chr11:44157316
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1174-14295C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157316 | ||||||
| chr11:44157417
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1174-14194C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157417 | ||||||
| chr11:44157556
|
C | T | 1 | a0001c0001t0012g0004 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1174-14055C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157556 | ||||||
| chr11:44157602
|
C | A | 1 | a0001c0001t0002g0202 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1174-14009C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157602 | ||||||
| chr11:44158172
|
G | A | 1 | a0001c0002t0004g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1174-13439G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158172 | ||||||
| chr11:44158185
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-13426T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158185 | ||||||
| chr11:44158212
|
A | T | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-13399A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158212 | ||||||
| chr11:44158431
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-13180G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158431 | ||||||
| chr11:44158547
|
AATTT | A | 12 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(9): Show | 12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1174-13062_1174-13 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44158547 | |||||
| chr11:44158726
|
A | G | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1174-12885A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158726 | ||||||
| chr11:44158775
|
G | A | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-12836G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158775 | ||||||
| chr11:44158822
|
C | G | 1 | a0001c0001t0018g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1174-12789C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158822 | ||||||
| chr11:44158877
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1174-12734T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158877 | ||||||
| chr11:44159004
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1174-12607T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159004 | ||||||
| chr11:44159118
|
G | A | 45 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(42): Show | 45 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-12493G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159118 | ||||||
| chr11:44159121
|
CT | C | 62 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0002g0087others(59): Show | 63 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1174-12477delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44159121 | |||||
| chr11:44159151
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-12460T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159151 | ||||||
| chr11:44159180
|
G | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0094 | 2 | HG00621.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1174-12431G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159180 | ||||||
| chr11:44159188
|
T | C | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-12423T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159188 | ||||||
| chr11:44159346
|
CT | C | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-12256delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44159346 | |||||
| chr11:44159478
|
A | G | 150 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(147): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1174-12133A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159478 | ||||||
| chr11:44159719
|
G | A | 1 | a0001c0001t0006g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1174-11892G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159719 | ||||||
| chr11:44159771
|
G | C | 44 | a0001c0001t0004g0327a0001c0002t0002g0019a0001c0002t0002g0021others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1174-11840G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159771 | ||||||
| chr11:44160141
|
G | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1174-11470G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160141 | ||||||
| chr11:44160202
|
G | A | 1 | a0001c0004t0030g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-11409G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160202 | ||||||
| chr11:44160467
|
A | G | 145 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(142): Show | 147 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1174-11144A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160467 | ||||||
| chr11:44160830
|
A | G | 1 | a0001c0002t0002g0015 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1174-10781A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160830 | ||||||
| chr11:44160870
|
C | T | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-10741C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160870 | ||||||
| chr11:44160933
|
T | A | 146 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(143): Show | 148 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1174-10678T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160933 | ||||||
| chr11:44161108
|
A | C | 54 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(51): Show | 54 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1174-10503A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161108 | ||||||
| chr11:44161177
|
A | G | 2 | a0001c0001t0002g0218a0001c0001t0002g0220 | 2 | HG03654.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1174-10434A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161177 | ||||||
| chr11:44161433
|
G | A | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-10178G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161433 | ||||||
| chr11:44161620
|
C | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-9991C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161620 | ||||||
| chr11:44161759
|
G | A | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-9852G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161759 | ||||||
| chr11:44161993
|
A | T | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9618A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161993 | ||||||
| chr11:44162059
|
C | T | 1 | a0001c0001t0013g0300 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174-9552C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162059 | ||||||
| chr11:44162140
|
G | C | 12 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(9): Show | 12 | HG02027.hp2 HG02135.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-9471G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162140 | ||||||
| chr11:44162402
|
T | C | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1174-9209T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162402 | ||||||
| chr11:44162575
|
C | CA | 13 | a0001c0001t0001g0132a0001c0001t0002g0222a0001c0001t0003g0192others(10): Show | 13 | HG00597.hp2 HG01167.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1174-9015dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44162575 | |||||
| chr11:44162575
|
CA | C | 11 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0008g0002others(8): Show | 12 | HG03491.hp1 HG03492.hp1 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-9015delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44162575 | |||||
| chr11:44162609
|
T | C | 1 | a0001c0002t0002g0041 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1174-9002T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162609 | ||||||
| chr11:44162794
|
A | G | 58 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(55): Show | 58 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1174-8817A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162794 | ||||||
| chr11:44162896
|
C | T | 1 | a0001c0001t0007g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1174-8715C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162896 | ||||||
| chr11:44162897
|
G | A | 1 | a0001c0004t0040g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1174-8714G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162897 | ||||||
| chr11:44162979
|
G | C | 58 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(55): Show | 58 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1174-8632G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162979 | ||||||
| chr11:44163224
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1174-8387C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163224 | ||||||
| chr11:44163312
|
G | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-8299G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163312 | ||||||
| chr11:44163528
|
C | A | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1174-8083C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163528 | ||||||
| chr11:44163690
|
A | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-7921A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163690 | ||||||
| chr11:44163726
|
G | A | 1 | a0001c0001t0005g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1174-7885G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163726 | ||||||
| chr11:44163754
|
G | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-7857G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163754 | ||||||
| chr11:44163977
|
C | T | 1 | a0001c0004t0030g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-7634C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163977 | ||||||
| chr11:44163999
|
G | A | 1 | a0001c0001t0014g0001 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1174-7612G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163999 | ||||||
| chr11:44164238
|
A | G | 51 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(48): Show | 52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1174-7373A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164238 | ||||||
| chr11:44164284
|
T | G | 1 | a0001c0001t0011g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1174-7327T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164284 | ||||||
| chr11:44164291
|
T | C | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-7320T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164291 | ||||||
| chr11:44164301
|
C | G | 51 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(48): Show | 51 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1174-7310C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164301 | ||||||
| chr11:44164366
|
T | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1174-7245T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164366 | ||||||
| chr11:44164467
|
C | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-7144C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164467 | ||||||
| chr11:44164781
|
C | T | 2 | a0001c0001t0007g0321a0001c0001t0007g0322 | 2 | HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174-6830C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164781 | ||||||
| chr11:44164876
|
C | CT | 10 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0148others(7): Show | 10 | HG01261.hp1 HG01361.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-6715dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44164876 | |||||
| chr11:44164876
|
CT | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0157a0001c0001t0001g0165others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-6715delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44164876 | |||||
| chr11:44165068
|
C | T | 1 | a0001c0001t0039g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1174-6543C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165068 | ||||||
| chr11:44165089
|
G | A | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165089 | ||||||
| chr11:44165120
|
C | T | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-6491C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165120 | ||||||
| chr11:44165129
|
C | T | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6482C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165129 | ||||||
| chr11:44165183
|
T | C | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6428T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165183 | ||||||
| chr11:44165283
|
G | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-6328G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165283 | ||||||
| chr11:44165311
|
T | A | 2 | a0001c0008t0001g0159a0001c0008t0001g0161 | 2 | HG00438.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1174-6300T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165311 | ||||||
| chr11:44165315
|
T | G | 3 | a0001c0001t0003g0192a0001c0001t0003g0299a0001c0001t0003g0301 | 3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-6296T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165315 | ||||||
| chr11:44165335
|
A | G | 10 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(7): Show | 10 | HG01993.hp2 HG02074.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-6276A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165335 | ||||||
| chr11:44165352
|
G | T | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-6259G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165352 | ||||||
| chr11:44165361
|
T | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0111others(2): Show | 5 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6250T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165361 | ||||||
| chr11:44165364
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-6247T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165364 | ||||||
| chr11:44165596
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1174-6015C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165596 | ||||||
| chr11:44165721
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174-5890A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165721 | ||||||
| chr11:44165815
|
A | G | 1 | a0003c0006t0056g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-5796A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165815 | ||||||
| chr11:44165852
|
T | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-5759T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165852 | ||||||
| chr11:44165947
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0167 | 2 | NA18987.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1174-5664T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165947 | ||||||
| chr11:44166179
|
C | T | 1 | a0001c0007t0005g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-5432C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166179 | ||||||
| chr11:44166788
|
T | G | 46 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(43): Show | 46 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1174-4823T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166788 | ||||||
| chr11:44166847
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1174-4764T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166847 | ||||||
| chr11:44166854
|
G | A | 2 | a0001c0001t0003g0266a0001c0001t0003g0282 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1174-4757G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166854 | ||||||
| chr11:44166922
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-4689C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166922 | ||||||
| chr11:44166979
|
C | G | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-4632C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166979 | ||||||
| chr11:44167115
|
C | T | 4 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0013g0065others(1): Show | 4 | HG00099.hp2 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-4496C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167115 | ||||||
| chr11:44167151
|
T | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-4460T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167151 | ||||||
| chr11:44167241
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1174-4370C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167241 | ||||||
| chr11:44167402
|
C | T | 3 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312 | 3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1174-4209C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167402 | ||||||
| chr11:44167845
|
G | C | 1 | a0001c0001t0008g0002 | 2 | NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1174-3766G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167845 | ||||||
| chr11:44167915
|
T | C | 4 | a0001c0001t0009g0263a0001c0001t0009g0273a0001c0001t0009g0279others(1): Show | 4 | NA18945.hp2 NA18982.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-3696T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167915 | ||||||
| chr11:44167973
|
CCCCCGA | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-3633_1174-362 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44167973 | |||||
| chr11:44168024
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1174-3587A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168024 | ||||||
| chr11:44168119
|
G | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1174-3492G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168119 | ||||||
| chr11:44168185
|
A | G | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1174-3426A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168185 | ||||||
| chr11:44168214
|
GT | G | 186 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(183): Show | 188 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1174-3394delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44168214 | |||||
| chr11:44168361
|
A | G | 15 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(12): Show | 15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-3250A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168361 | ||||||
| chr11:44168682
|
G | A | 8 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(5): Show | 8 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2929G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168682 | ||||||
| chr11:44168813
|
A | G | 4 | a0001c0001t0012g0004a0001c0001t0012g0005a0001c0001t0012g0006others(1): Show | 4 | HG01123.hp2 HG01168.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-2798A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168813 | ||||||
| chr11:44168865
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1174-2746A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168865 | ||||||
| chr11:44168867
|
G | A | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1174-2744G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168867 | ||||||
| chr11:44168908
|
C | T | 3 | a0001c0001t0003g0192a0001c0001t0003g0299a0001c0001t0003g0301 | 3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-2703C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168908 | ||||||
| chr11:44169081
|
G | A | 1 | a0001c0001t0007g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1174-2530G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169081 | ||||||
| chr11:44169174
|
C | T | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-2437C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169174 | ||||||
| chr11:44169175
|
G | A | 1 | a0001c0002t0049g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1174-2436G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169175 | ||||||
| chr11:44169345
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1174-2266T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169345 | ||||||
| chr11:44169366
|
C | T | 1 | a0001c0001t0006g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1174-2245C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169366 | ||||||
| chr11:44169453
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0005g0228 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1174-2158C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169453 | ||||||
| chr11:44169674
|
G | A | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-1937G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169674 | ||||||
| chr11:44169762
|
T | C | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1174-1849T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169762 | ||||||
| chr11:44169829
|
A | AG | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1174-1782_1174-178 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169829 | ||||||
| chr11:44169904
|
G | A | 19 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(16): Show | 20 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1174-1707G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169904 | ||||||
| chr11:44170047
|
A | C | 1 | a0001c0001t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1174-1564A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170047 | ||||||
| chr11:44170150
|
C | T | 44 | a0001c0001t0004g0327a0001c0002t0002g0019a0001c0002t0002g0021others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1174-1461C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170150 | ||||||
| chr11:44170166
|
C | T | 1 | a0005c0012t0002g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1174-1445C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170166 | ||||||
| chr11:44170167
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0167 | 2 | NA18987.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1174-1444G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170167 | ||||||
| chr11:44170357
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1174-1254T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170357 | ||||||
| chr11:44170363
|
A | G | 1 | a0001c0001t0010g0311 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1174-1248A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170363 | ||||||
| chr11:44170665
|
G | A | 8 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(5): Show | 8 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-946G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170665 | ||||||
| chr11:44170701
|
A | C | 3 | a0001c0001t0005g0063a0001c0001t0026g0016a0001c0001t0026g0082 | 3 | HG01346.hp1 HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1174-910A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170701 | ||||||
| chr11:44170703
|
C | CAT | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1174-905_1174-904d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170703 | |||||
| chr11:44170769
|
G | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-842G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170769 | ||||||
| chr11:44170794
|
T | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-817T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170794 | ||||||
| chr11:44170810
|
TCA | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0195a0001c0001t0007g0324others(2): Show | 5 | HG00741.hp2 HG01168.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-755_1174-754d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACA | T | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(89): Show | 92 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1174-757_1174-754d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACA | T | 18 | a0001c0001t0002g0149a0001c0001t0002g0209a0001c0001t0005g0063others(15): Show | 19 | HG00735.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1174-759_1174-754d others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACAC others(1): Show |
T | 16 | a0001c0001t0002g0199a0001c0001t0002g0204a0001c0001t0002g0214others(13): Show | 16 | HG00099.hp2 HG00741.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-761_1174-754d others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACAC others(3): Show |
T | 78 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(75): Show | 79 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1174-763_1174-754d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACAC others(5): Show |
T | 94 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(91): Show | 95 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1174-765_1174-754d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACAC others(9): Show |
T | 5 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-769_1174-754d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170810
|
TCACACAC others(19): Show |
T | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-779_1174-754d others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | |||||
| chr11:44170837
|
C | G | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-774C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170837 | ||||||
| chr11:44170837
|
C | T | 4 | a0001c0001t0013g0080a0001c0007t0005g0147a0001c0007t0005g0183others(1): Show | 4 | HG01261.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-774C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170837 | ||||||
| chr11:44170847
|
C | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1174-764C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170847 | ||||||
| chr11:44170848
|
ACACACAC others(2): Show |
A | 3 | a0001c0001t0008g0245a0001c0001t0012g0005a0001c0002t0004g0056 | 3 | HG00597.hp2 HG02615.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1174-760_1174-752d others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170848 | |||||
| chr11:44171025
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-586C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171025 | ||||||
| chr11:44171157
|
G | A | 185 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(182): Show | 187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1174-454G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171157 | ||||||
| chr11:44171254
|
A | G | 15 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(12): Show | 15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-357A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171254 | ||||||
| chr11:44171303
|
A | G | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1174-308A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171303 | ||||||
| chr11:44171341
|
C | A | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1174-270C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171341 | ||||||
| chr11:44171494
|
TCC | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-115_1174-114d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44171494 | |||||
| chr11:44171593
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1174-18G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171593 | ||||||
| chr11:44171868
|
T | C | 6 | a0001c0001t0005g0063a0001c0001t0021g0059a0001c0001t0021g0060others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+126T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44171868 | ||||||
| chr11:44171996
|
G | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0111others(2): Show | 5 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+254G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44171996 | ||||||
| chr11:44172131
|
T | A | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1305+389T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172131 | ||||||
| chr11:44172433
|
C | T | 2 | a0001c0002t0004g0030a0001c0002t0017g0029 | 2 | HG02083.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1305+691C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172433 | ||||||
| chr11:44172535
|
C | G | 2 | a0001c0001t0009g0279a0001c0001t0009g0283 | 2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1305+793C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172535 | ||||||
| chr11:44172564
|
T | A | 1 | a0001c0001t0007g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1305+822T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172564 | ||||||
| chr11:44172583
|
C | CT | 7 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+858dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44172583 | |||||
| chr11:44172583
|
CT | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.1305+858delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44172583 | |||||
| chr11:44172592
|
T | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+850T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172592 | ||||||
| chr11:44172605
|
T | C | 1 | a0001c0002t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1305+863T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172605 | ||||||
| chr11:44172793
|
C | T | 1 | a0001c0001t0006g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1305+1051C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172793 | ||||||
| chr11:44172862
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1305+1120T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172862 | ||||||
| chr11:44172875
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1305+1133C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172875 | ||||||
| chr11:44173077
|
C | T | 13 | a0001c0001t0010g0310a0001c0001t0010g0311a0001c0001t0010g0312others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1305+1335C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173077 | ||||||
| chr11:44173134
|
A | G | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(106): Show | 110 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1305+1392A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173134 | ||||||
| chr11:44173158
|
A | T | 189 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(186): Show | 191 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1305+1416A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173158 | ||||||
| chr11:44173293
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1305+1551A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173293 | ||||||
| chr11:44173332
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+1590G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173332 | ||||||
| chr11:44173359
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+1617A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173359 | ||||||
| chr11:44173518
|
A | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+1776A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173518 | ||||||
| chr11:44173563
|
C | CT | 11 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(8): Show | 12 | HG02647.hp2 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+1844dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44173563 | |||||
| chr11:44173563
|
CT | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1305+1844delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44173563 | |||||
| chr11:44173566
|
T | TC | 6 | a0001c0001t0005g0063a0001c0001t0013g0300a0001c0001t0026g0016others(3): Show | 6 | HG01346.hp1 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+1824_1305+182 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173566 | ||||||
| chr11:44173567
|
T | C | 188 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(185): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1305+1825T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173567 | ||||||
| chr11:44173568
|
T | C | 4 | a0001c0001t0002g0197a0001c0001t0005g0075a0001c0001t0038g0226others(1): Show | 4 | HG01081.hp2 HG03017.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+1826T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173568 | ||||||
| chr11:44173569
|
T | C | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1305+1827T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173569 | ||||||
| chr11:44173571
|
T | C | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+1829T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173571 | ||||||
| chr11:44173599
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+1857C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173599 | ||||||
| chr11:44173729
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1305+1987C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173729 | ||||||
| chr11:44173741
|
T | A | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1305+1999T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173741 | ||||||
| chr11:44173758
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2016C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173758 | ||||||
| chr11:44173809
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0005g0228 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1305+2067C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173809 | ||||||
| chr11:44173908
|
T | C | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+2166T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173908 | ||||||
| chr11:44173930
|
G | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1305+2188G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173930 | ||||||
| chr11:44174025
|
A | G | 41 | a0001c0001t0001g0176a0001c0001t0005g0017a0001c0001t0005g0061others(38): Show | 42 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1305+2283A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174025 | ||||||
| chr11:44174097
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1305+2355A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174097 | ||||||
| chr11:44174152
|
A | G | 1 | a0001c0001t0052g0143 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1305+2410A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174152 | ||||||
| chr11:44174174
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1305+2432C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174174 | ||||||
| chr11:44174336
|
C | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2594C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174336 | ||||||
| chr11:44174366
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+2624T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174366 | ||||||
| chr11:44174410
|
T | TTA | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+2684_1305+268 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44174410 | |||||
| chr11:44174414
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+2672A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174414 | ||||||
| chr11:44174476
|
G | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+2734G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174476 | ||||||
| chr11:44174494
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | NA18966.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1305+2752A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174494 | ||||||
| chr11:44174556
|
G | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0127others(2): Show | 5 | HG00597.hp1 HG00673.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+2814G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174556 | ||||||
| chr11:44174568
|
C | A | 9 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1305+2826C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174568 | ||||||
| chr11:44174569
|
T | C | 189 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(186): Show | 191 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1305+2827T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174569 | ||||||
| chr11:44174605
|
C | A | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1305+2863C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174605 | ||||||
| chr11:44174707
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2965C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174707 | ||||||
| chr11:44174899
|
A | G | 3 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1305+3157A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174899 | ||||||
| chr11:44175262
|
C | T | 5 | a0001c0001t0010g0308a0001c0001t0014g0179a0001c0009t0027g0306others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+3520C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175262 | ||||||
| chr11:44175361
|
C | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+3619C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175361 | ||||||
| chr11:44175376
|
C | CT | 16 | a0001c0001t0001g0095a0001c0001t0001g0275a0001c0001t0002g0199others(13): Show | 16 | HG00741.hp1 HG01256.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1305+3642dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44175376 | |||||
| chr11:44175554
|
T | G | 1 | a0001c0002t0002g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1305+3812T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175554 | ||||||
| chr11:44176922
|
T | TA | 120 | a0001c0001t0001g0092a0001c0001t0001g0176a0001c0001t0002g0087others(117): Show | 121 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1305+5197dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | |||||
| chr11:44176922
|
T | TAA | 11 | a0001c0001t0002g0109a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG00639.hp1 HG01099.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+5196_1305+519 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | |||||
| chr11:44176922
|
TA | T | 29 | a0001c0001t0003g0189a0001c0001t0007g0325a0001c0001t0008g0002others(26): Show | 30 | HG01109.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+5197delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | |||||
| chr11:44177025
|
A | C | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+5283A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177025 | ||||||
| chr11:44177124
|
T | C | 2 | a0001c0001t0021g0059a0001c0001t0021g0060 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1305+5382T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177124 | ||||||
| chr11:44177196
|
G | A | 1 | a0001c0002t0036g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1305+5454G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177196 | ||||||
| chr11:44177312
|
T | G | 1 | a0001c0001t0007g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1305+5570T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177312 | ||||||
| chr11:44177414
|
G | A | 271 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.1305+5672G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177414 | ||||||
| chr11:44177449
|
C | G | 184 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(181): Show | 186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1305+5707C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177449 | ||||||
| chr11:44177526
|
G | A | 7 | a0001c0001t0009g0263a0001c0001t0009g0273a0001c0001t0009g0276others(4): Show | 7 | HG00544.hp2 NA18945.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+5784G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177526 | ||||||
| chr11:44177722
|
G | GT | 183 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1305+5988dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44177722 | |||||
| chr11:44177722
|
GT | G | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+5988delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44177722 | |||||
| chr11:44177730
|
T | C | 1 | a0001c0001t0024g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1305+5988T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177730 | ||||||
| chr11:44177836
|
C | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+6094C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177836 | ||||||
| chr11:44178349
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1305+6607G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178349 | ||||||
| chr11:44178419
|
G | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+6677G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178419 | ||||||
| chr11:44178445
|
G | T | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1305+6703G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178445 | ||||||
| chr11:44178615
|
G | A | 1 | a0001c0001t0006g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1305+6873G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178615 | ||||||
| chr11:44178744
|
C | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+7002C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178744 | ||||||
| chr11:44178800
|
TA | T | 191 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(188): Show | 194 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1305+7070delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44178800 | |||||
| chr11:44178800
|
TAA | T | 12 | a0001c0001t0002g0199a0001c0001t0022g0329a0001c0001t0042g0264others(9): Show | 12 | HG00741.hp1 HG01109.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+7069_1305+707 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44178800 | |||||
| chr11:44178801
|
A | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+7059A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178801 | ||||||
| chr11:44179018
|
A | G | 1 | a0001c0001t0012g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1305+7276A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179018 | ||||||
| chr11:44179105
|
C | G | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+7363C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179105 | ||||||
| chr11:44179169
|
G | C | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+7427G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179169 | ||||||
| chr11:44179296
|
G | A | 1 | a0001c0001t0014g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1305+7554G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179296 | ||||||
| chr11:44179542
|
A | G | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1305+7800A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179542 | ||||||
| chr11:44179590
|
T | C | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1305+7848T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179590 | ||||||
| chr11:44179596
|
T | C | 1 | a0001c0001t0007g0256 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1305+7854T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179596 | ||||||
| chr11:44179680
|
A | G | 1 | a0001c0001t0026g0016 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1305+7938A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179680 | ||||||
| chr11:44179807
|
G | A | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+8065G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179807 | ||||||
| chr11:44180275
|
C | T | 1 | a0001c0001t0021g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+8533C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180275 | ||||||
| chr11:44180439
|
A | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+8697A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180439 | ||||||
| chr11:44180748
|
T | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+9006T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180748 | ||||||
| chr11:44180830
|
G | A | 1 | a0001c0001t0009g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1305+9088G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180830 | ||||||
| chr11:44180867
|
C | T | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9125C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180867 | ||||||
| chr11:44180877
|
G | A | 1 | a0001c0001t0035g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1305+9135G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180877 | ||||||
| chr11:44180944
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9202T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180944 | ||||||
| chr11:44181032
|
C | T | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9290C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181032 | ||||||
| chr11:44181049
|
C | T | 55 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(52): Show | 56 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.1305+9307C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181049 | ||||||
| chr11:44181057
|
C | T | 186 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(183): Show | 188 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1305+9315C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181057 | ||||||
| chr11:44181100
|
CA | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+9371delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44181100 | |||||
| chr11:44181146
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9404T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181146 | ||||||
| chr11:44181186
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+9444T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181186 | ||||||
| chr11:44181348
|
G | A | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1305+9606G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181348 | ||||||
| chr11:44181461
|
G | C | 51 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(48): Show | 52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1305+9719G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181461 | ||||||
| chr11:44181501
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+9759C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181501 | ||||||
| chr11:44181533
|
C | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1305+9791C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181533 | ||||||
| chr11:44181547
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1305+9805G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181547 | ||||||
| chr11:44181639
|
G | T | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9897G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181639 | ||||||
| chr11:44181663
|
A | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+9921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181663 | ||||||
| chr11:44181789
|
A | G | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+10047A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181789 | ||||||
| chr11:44181797
|
T | C | 1 | a0001c0001t0059g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1305+10055T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181797 | ||||||
| chr11:44182357
|
C | A | 3 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0045g0302 | 3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1305+10615C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182357 | ||||||
| chr11:44182469
|
A | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+10727A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182469 | ||||||
| chr11:44182516
|
G | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+10774G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182516 | ||||||
| chr11:44182609
|
G | A | 184 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(181): Show | 186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1305+10867G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182609 | ||||||
| chr11:44182763
|
G | A | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+11021G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182763 | ||||||
| chr11:44182973
|
A | C | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1305+11231A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182973 | ||||||
| chr11:44183122
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1305+11380A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183122 | ||||||
| chr11:44183161
|
A | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1305+11419A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183161 | ||||||
| chr11:44183663
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1305+11921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183663 | ||||||
| chr11:44183782
|
T | A | 1 | a0001c0001t0012g0004 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1305+12040T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183782 | ||||||
| chr11:44183802
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0044g0208 | 2 | HG01361.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1305+12060G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183802 | ||||||
| chr11:44183945
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1305+12203T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183945 | ||||||
| chr11:44184082
|
G | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+12340G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184082 | ||||||
| chr11:44184252
|
G | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1305+12510G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184252 | ||||||
| chr11:44184295
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1305+12553C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184295 | ||||||
| chr11:44184296
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1305+12554G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184296 | ||||||
| chr11:44184392
|
G | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+12650G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184392 | ||||||
| chr11:44184553
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+12811C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184553 | ||||||
| chr11:44184623
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1305+12881C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184623 | ||||||
| chr11:44184758
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1305+13016T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184758 | ||||||
| chr11:44184796
|
A | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-13033A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184796 | ||||||
| chr11:44185610
|
T | C | 1 | a0001c0001t0005g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1306-12219T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185610 | ||||||
| chr11:44185671
|
C | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-12158C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185671 | ||||||
| chr11:44185745
|
A | T | 41 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(38): Show | 41 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1306-12084A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185745 | ||||||
| chr11:44185746
|
T | C | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-12083T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185746 | ||||||
| chr11:44185906
|
T | C | 39 | a0001c0001t0001g0176a0001c0001t0005g0017a0001c0001t0005g0061others(36): Show | 40 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306-11923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185906 | ||||||
| chr11:44185958
|
A | C | 1 | a0001c0001t0053g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1306-11871A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185958 | ||||||
| chr11:44185992
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-11837A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185992 | ||||||
| chr11:44186313
|
C | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-11516C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186313 | ||||||
| chr11:44186357
|
A | G | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1306-11472A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186357 | ||||||
| chr11:44186673
|
T | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-11156T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186673 | ||||||
| chr11:44186790
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-11039C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186790 | ||||||
| chr11:44186836
|
A | G | 1 | a0001c0001t0043g0284 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1306-10993A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186836 | ||||||
| chr11:44186887
|
T | C | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1306-10942T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186887 | ||||||
| chr11:44186982
|
T | TTTCC | 53 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(50): Show | 53 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1306-10786_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
T | TTTCCTTC others(1): Show |
48 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0111others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-10790_1306-10 others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
T | TTTCCTTC others(5): Show |
7 | a0001c0001t0006g0138a0001c0001t0018g0314a0001c0001t0028g0252others(4): Show | 7 | HG00639.hp2 HG01109.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306-10794_1306-10 others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
T | TTTCCTTC others(9): Show |
4 | a0001c0001t0006g0160a0001c0003t0003g0262a0001c0003t0003g0267others(1): Show | 4 | HG00438.hp2 HG00544.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-10798_1306-10 others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
T | TTTCCTTC others(13): Show |
1 | a0001c0001t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1306-10802_1306-10 others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
TTTCC | T | 50 | a0001c0001t0002g0196a0001c0001t0002g0201a0001c0001t0002g0202others(47): Show | 50 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1306-10786_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
TTTCCTTC others(1): Show |
T | 72 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(69): Show | 72 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.1306-10790_1306-10 others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
TTTCCTTC others(5): Show |
T | 21 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0200others(18): Show | 22 | HG00738.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1306-10794_1306-10 others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186982
|
TTTCCTTC others(9): Show |
T | 1 | a0001c0002t0004g0028 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1306-10798_1306-10 others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | |||||
| chr11:44186984
|
T | TCCTC | 5 | a0001c0001t0010g0308a0001c0001t0010g0312a0002c0005t0019g0238others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-10842_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186984 | |||||
| chr11:44186988
|
T | C | 4 | a0001c0001t0010g0310a0001c0001t0010g0311a0002c0005t0019g0236others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-10841T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186988 | ||||||
| chr11:44187015
|
T | C | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1306-10814T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187015 | ||||||
| chr11:44187047
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10782C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187047 | ||||||
| chr11:44187051
|
T | TTCCCTCC others(8): Show |
1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10770_1306-10 others(21): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44187051 | |||||
| chr11:44187139
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1306-10690G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187139 | ||||||
| chr11:44187185
|
G | T | 1 | a0001c0001t0013g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1306-10644G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187185 | ||||||
| chr11:44187208
|
A | T | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-10621A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187208 | ||||||
| chr11:44187296
|
GCCT | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1306-10529_1306-10 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44187296 | |||||
| chr11:44187344
|
A | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-10485A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187344 | ||||||
| chr11:44187449
|
T | C | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1306-10380T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187449 | ||||||
| chr11:44187477
|
A | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-10352A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187477 | ||||||
| chr11:44187521
|
T | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-10308T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187521 | ||||||
| chr11:44187552
|
T | C | 1 | a0001c0001t0002g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1306-10277T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187552 | ||||||
| chr11:44187588
|
T | C | 1 | a0001c0001t0003g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1306-10241T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187588 | ||||||
| chr11:44187593
|
A | G | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1306-10236A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187593 | ||||||
| chr11:44187607
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10222T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187607 | ||||||
| chr11:44187651
|
G | A | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-10178G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187651 | ||||||
| chr11:44187755
|
G | A | 9 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(6): Show | 9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-10074G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187755 | ||||||
| chr11:44187913
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1306-9916A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187913 | ||||||
| chr11:44188057
|
G | T | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-9772G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188057 | ||||||
| chr11:44188203
|
G | A | 44 | a0001c0001t0004g0327a0001c0002t0002g0019a0001c0002t0002g0021others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1306-9626G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188203 | ||||||
| chr11:44188213
|
A | G | 1 | a0001c0004t0016g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1306-9616A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188213 | ||||||
| chr11:44188220
|
C | T | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1306-9609C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188220 | ||||||
| chr11:44188275
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1306-9554C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188275 | ||||||
| chr11:44188301
|
G | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-9528G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188301 | ||||||
| chr11:44188396
|
G | C | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1306-9433G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188396 | ||||||
| chr11:44188708
|
T | G | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-9121T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188708 | ||||||
| chr11:44189060
|
C | T | 3 | a0001c0001t0005g0068a0001c0001t0005g0069a0001c0001t0039g0070 | 3 | HG02280.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1306-8769C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189060 | ||||||
| chr11:44189089
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1306-8740C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189089 | ||||||
| chr11:44189089
|
C | T | 185 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(182): Show | 187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1306-8740C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189089 | ||||||
| chr11:44189260
|
TAA | T | 3 | a0001c0001t0008g0002a0001c0001t0008g0244a0001c0001t0008g0245 | 4 | NA18962.hp2 NA18972.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-8568_1306-856 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189260 | ||||||
| chr11:44189466
|
G | A | 3 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0040g0174 | 3 | HG03017.hp2 NA18981.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1306-8363G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189466 | ||||||
| chr11:44189514
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-8315C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189514 | ||||||
| chr11:44189643
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-8186G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189643 | ||||||
| chr11:44189714
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1306-8115A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189714 | ||||||
| chr11:44189778
|
A | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1306-8051A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189778 | ||||||
| chr11:44190658
|
G | T | 1 | a0001c0002t0004g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1306-7171G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190658 | ||||||
| chr11:44190763
|
G | A | 8 | a0001c0003t0003g0261a0001c0003t0003g0262a0001c0003t0003g0265others(5): Show | 8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306-7066G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190763 | ||||||
| chr11:44190785
|
C | G | 1 | a0003c0006t0056g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1306-7044C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190785 | ||||||
| chr11:44190815
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1306-7014G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190815 | ||||||
| chr11:44191208
|
G | C | 1 | a0001c0001t0050g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1306-6621G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191208 | ||||||
| chr11:44191446
|
T | C | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-6383T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191446 | ||||||
| chr11:44191667
|
G | T | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1306-6162G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191667 | ||||||
| chr11:44192155
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-5674C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192155 | ||||||
| chr11:44192185
|
C | T | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-5644C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192185 | ||||||
| chr11:44192641
|
G | A | 1 | a0001c0001t0022g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306-5188G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192641 | ||||||
| chr11:44192857
|
T | C | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1306-4972T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192857 | ||||||
| chr11:44192858
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1306-4971A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192858 | ||||||
| chr11:44192931
|
A | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0191 | 2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1306-4898A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192931 | ||||||
| chr11:44192963
|
G | A | 2 | a0001c0001t0006g0134a0001c0001t0006g0154 | 2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1306-4866G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192963 | ||||||
| chr11:44193040
|
G | C | 1 | a0006c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1306-4789G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193040 | ||||||
| chr11:44193114
|
T | C | 3 | a0001c0001t0007g0324a0001c0001t0007g0325a0001c0001t0007g0326 | 3 | HG00323.hp1 HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1306-4715T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193114 | ||||||
| chr11:44193369
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1306-4460G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193369 | ||||||
| chr11:44193375
|
A | G | 1 | a0001c0001t0025g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1306-4454A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193375 | ||||||
| chr11:44193411
|
A | C | 1 | a0001c0001t0007g0321 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1306-4418A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193411 | ||||||
| chr11:44193605
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-4224A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193605 | ||||||
| chr11:44193868
|
T | C | 328 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1306-3961T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193868 | ||||||
| chr11:44193999
|
T | C | 283 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1306-3830T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193999 | ||||||
| chr11:44194036
|
G | A | 2 | a0001c0001t0002g0201a0001c0001t0002g0202 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1306-3793G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194036 | ||||||
| chr11:44194110
|
G | T | 2 | a0001c0001t0003g0295a0001c0001t0003g0298 | 2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1306-3719G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194110 | ||||||
| chr11:44194150
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1306-3679G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194150 | ||||||
| chr11:44194285
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0028g0253 | 2 | HG02080.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1306-3544G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194285 | ||||||
| chr11:44194301
|
A | G | 1 | a0001c0001t0005g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1306-3528A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194301 | ||||||
| chr11:44194593
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1306-3236C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194593 | ||||||
| chr11:44194628
|
T | C | 9 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-3201T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194628 | ||||||
| chr11:44194784
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-3045C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194784 | ||||||
| chr11:44195055
|
A | G | 4 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0022g0329others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-2774A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195055 | ||||||
| chr11:44195157
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1306-2672G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195157 | ||||||
| chr11:44195244
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1306-2585T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195244 | ||||||
| chr11:44195423
|
ACT | A | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1306-2403_1306-240 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44195423 | |||||
| chr11:44195432
|
C | CA | 8 | a0001c0001t0003g0292a0001c0004t0016g0172a0001c0004t0016g0173others(5): Show | 8 | HG02976.hp1 HG03017.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306-2386dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44195432 | |||||
| chr11:44195460
|
C | T | 2 | a0001c0001t0012g0005a0001c0001t0012g0006 | 2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1306-2369C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195460 | ||||||
| chr11:44195584
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1306-2245A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195584 | ||||||
| chr11:44195630
|
C | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-2199C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195630 | ||||||
| chr11:44195758
|
C | T | 2 | a0001c0001t0005g0073a0001c0001t0013g0072 | 2 | NA18969.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1306-2071C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195758 | ||||||
| chr11:44195798
|
T | C | 3 | a0001c0001t0053g0255a0001c0001t0054g0259a0001c0014t0062g0239 | 3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1306-2031T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195798 | ||||||
| chr11:44195859
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1306-1970C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195859 | ||||||
| chr11:44195947
|
C | A | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1306-1882C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195947 | ||||||
| chr11:44196242
|
A | T | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-1587A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196242 | ||||||
| chr11:44196389
|
G | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-1440G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196389 | ||||||
| chr11:44196599
|
A | AG | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-1228dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44196599 | |||||
| chr11:44196662
|
G | A | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-1167G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196662 | ||||||
| chr11:44197097
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1306-732C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197097 | ||||||
| chr11:44197186
|
T | C | 3 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1306-643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197186 | ||||||
| chr11:44197284
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1306-545G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197284 | ||||||
| chr11:44197736
|
C | T | 186 | a0001c0001t0001g0011a0001c0001t0001g0176a0001c0001t0002g0087others(183): Show | 188 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1306-93C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197736 | ||||||
| chr11:44198155
|
G | A | 4 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+137G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198155 | ||||||
| chr11:44198383
|
C | CA | 15 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(12): Show | 16 | HG02615.hp2 HG02818.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.1495+377dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44198383 | |||||
| chr11:44198743
|
T | C | 1 | a0001c0002t0049g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1495+725T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198743 | ||||||
| chr11:44198823
|
T | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+805T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198823 | ||||||
| chr11:44198885
|
C | A | 9 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1495+867C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198885 | ||||||
| chr11:44199313
|
AAAG | A | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+1299_1495+130 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44199313 | |||||
| chr11:44199477
|
T | A | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+1459T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199477 | ||||||
| chr11:44199540
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495+1522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199540 | ||||||
| chr11:44199691
|
G | C | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1495+1673G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199691 | ||||||
| chr11:44199725
|
A | AT | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(112): Show | 116 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495+1716dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44199725 | |||||
| chr11:44199989
|
A | T | 10 | a0001c0001t0008g0002a0001c0001t0008g0243a0001c0001t0008g0244others(7): Show | 11 | HG00544.hp2 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495+1971A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199989 | ||||||
| chr11:44200088
|
C | G | 9 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495+2070C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200088 | ||||||
| chr11:44200151
|
T | TA | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+2147dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44200151 | |||||
| chr11:44200152
|
A | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1495+2134A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200152 | ||||||
| chr11:44200195
|
C | G | 1 | a0001c0002t0008g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1495+2177C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200195 | ||||||
| chr11:44200666
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1495+2648C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200666 | ||||||
| chr11:44200709
|
G | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+2691G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200709 | ||||||
| chr11:44200709
|
G | T | 1 | a0001c0001t0013g0300 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1495+2691G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200709 | ||||||
| chr11:44200726
|
T | A | 1 | a0001c0001t0009g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1495+2708T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200726 | ||||||
| chr11:44200805
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1495+2787A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200805 | ||||||
| chr11:44200866
|
A | C | 4 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0022g0329others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+2848A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200866 | ||||||
| chr11:44200912
|
G | C | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+2894G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200912 | ||||||
| chr11:44201048
|
A | T | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1495+3030A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201048 | ||||||
| chr11:44201204
|
A | G | 1 | a0006c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1495+3186A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201204 | ||||||
| chr11:44201240
|
GAC | G | 4 | a0001c0001t0005g0071a0001c0001t0005g0073a0001c0001t0013g0072others(1): Show | 4 | NA18747.hp1 NA18969.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+3226_1495+322 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44201240 | |||||
| chr11:44201273
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+3255C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201273 | ||||||
| chr11:44201572
|
T | C | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1495+3554T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201572 | ||||||
| chr11:44201608
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495+3590A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201608 | ||||||
| chr11:44202004
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1495+3986A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202004 | ||||||
| chr11:44202072
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1495+4054G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202072 | ||||||
| chr11:44202072
|
G | C | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1495+4054G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202072 | ||||||
| chr11:44202206
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1495+4188C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202206 | ||||||
| chr11:44202286
|
T | G | 17 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(14): Show | 17 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1495+4268T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202286 | ||||||
| chr11:44202306
|
T | C | 1 | a0001c0001t0037g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1495+4288T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202306 | ||||||
| chr11:44202537
|
G | A | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1496-4256G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202537 | ||||||
| chr11:44202604
|
T | G | 1 | a0001c0001t0010g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1496-4189T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202604 | ||||||
| chr11:44202622
|
G | T | 1 | a0001c0001t0013g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1496-4171G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202622 | ||||||
| chr11:44203210
|
G | C | 179 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(176): Show | 181 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1496-3583G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203210 | ||||||
| chr11:44203267
|
C | T | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-3526C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203267 | ||||||
| chr11:44203433
|
A | G | 2 | a0001c0001t0022g0329a0001c0001t0022g0330 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1496-3360A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203433 | ||||||
| chr11:44203722
|
C | T | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1496-3071C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203722 | ||||||
| chr11:44203725
|
G | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-3068G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203725 | ||||||
| chr11:44203751
|
CAGGCACT others(9): Show |
C | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1496-3039_1496-302 others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44203751 | |||||
| chr11:44203773
|
T | TAAA | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(85): Show | 88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1496-3016_1496-301 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44203773 | |||||
| chr11:44203781
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0097others(2): Show | 5 | HG00735.hp2 HG01175.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496-3012G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203781 | ||||||
| chr11:44203810
|
C | T | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(85): Show | 88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1496-2983C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203810 | ||||||
| chr11:44203944
|
G | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-2849G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203944 | ||||||
| chr11:44204033
|
T | G | 41 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(38): Show | 41 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1496-2760T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204033 | ||||||
| chr11:44204104
|
A | C | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1496-2689A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204104 | ||||||
| chr11:44204485
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1496-2308C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204485 | ||||||
| chr11:44204499
|
G | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0201others(1): Show | 4 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1496-2294G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204499 | ||||||
| chr11:44204551
|
G | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0051g0101 | 3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1496-2242G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204551 | ||||||
| chr11:44204633
|
C | T | 193 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(190): Show | 195 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1496-2160C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204633 | ||||||
| chr11:44204676
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1496-2117C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204676 | ||||||
| chr11:44205235
|
A | G | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1496-1558A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205235 | ||||||
| chr11:44205299
|
G | T | 2 | a0001c0001t0003g0295a0001c0001t0003g0298 | 2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1496-1494G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205299 | ||||||
| chr11:44205359
|
A | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1496-1434A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205359 | ||||||
| chr11:44205533
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1496-1260A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205533 | ||||||
| chr11:44205640
|
A | G | 18 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(15): Show | 18 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1496-1153A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205640 | ||||||
| chr11:44205726
|
G | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1496-1067G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205726 | ||||||
| chr11:44205825
|
T | A | 1 | a0001c0001t0058g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1496-968T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205825 | ||||||
| chr11:44205850
|
T | A | 2 | a0001c0001t0003g0295a0001c0001t0003g0298 | 2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1496-943T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205850 | ||||||
| chr11:44206052
|
AAATCCCA others(3): Show |
A | 17 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(14): Show | 17 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1496-737_1496-728d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44206052 | |||||
| chr11:44206250
|
C | T | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-543C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206250 | ||||||
| chr11:44206260
|
C | A | 10 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(7): Show | 10 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-533C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206260 | ||||||
| chr11:44206263
|
C | T | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-530C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206263 | ||||||
| chr11:44206413
|
A | G | 2 | a0001c0001t0002g0205a0005c0012t0002g0203 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1496-380A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206413 | ||||||
| chr11:44206429
|
T | C | 2 | a0001c0002t0017g0031a0001c0002t0048g0051 | 2 | HG00621.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1496-364T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206429 | ||||||
| chr11:44206564
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1496-229T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206564 | ||||||
| chr11:44206572
|
GTGTATAT others(4): Show |
G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-209_1496-199d others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44206572 | |||||
| chr11:44206598
|
C | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1496-195C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206598 | ||||||
| chr11:44206684
|
G | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1496-109G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206684 | ||||||
| chr11:44206687
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1496-106G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206687 | ||||||
| chr11:44206718
|
G | A | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496-75G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206718 | ||||||
| chr11:44207287
|
A | G | 1 | a0001c0001t0053g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+328A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207287 | ||||||
| chr11:44207297
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1662+338C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207297 | ||||||
| chr11:44207426
|
T | C | 5 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0218others(2): Show | 5 | HG00639.hp1 HG01099.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+467T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207426 | ||||||
| chr11:44207538
|
A | T | 1 | a0001c0001t0011g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1662+579A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207538 | ||||||
| chr11:44207575
|
C | T | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+616C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207575 | ||||||
| chr11:44207600
|
G | A | 1 | a0001c0001t0028g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1662+641G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207600 | ||||||
| chr11:44207808
|
T | C | 7 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(4): Show | 7 | HG02559.hp1 HG02976.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+849T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207808 | ||||||
| chr11:44207863
|
C | G | 1 | a0006c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1662+904C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207863 | ||||||
| chr11:44208098
|
C | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+1139C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208098 | ||||||
| chr11:44208198
|
A | AT | 47 | a0001c0001t0004g0271a0001c0001t0004g0327a0001c0001t0028g0252others(44): Show | 47 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1662+1252dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44208198 | |||||
| chr11:44208312
|
G | A | 192 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(189): Show | 194 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1662+1353G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208312 | ||||||
| chr11:44208313
|
A | G | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+1354A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208313 | ||||||
| chr11:44208354
|
C | T | 48 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(45): Show | 49 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1662+1395C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208354 | ||||||
| chr11:44208551
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1662+1592A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208551 | ||||||
| chr11:44208680
|
C | T | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1662+1721C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208680 | ||||||
| chr11:44208752
|
T | C | 196 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(193): Show | 198 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.1662+1793T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208752 | ||||||
| chr11:44208765
|
G | C | 1 | a0001c0001t0037g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1662+1806G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208765 | ||||||
| chr11:44208825
|
G | A | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1662+1866G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208825 | ||||||
| chr11:44208825
|
G | T | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+1866G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208825 | ||||||
| chr11:44209034
|
A | G | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1662+2075A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209034 | ||||||
| chr11:44209104
|
A | G | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1662+2145A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209104 | ||||||
| chr11:44209166
|
C | T | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+2207C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209166 | ||||||
| chr11:44209209
|
G | A | 1 | a0006c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1662+2250G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209209 | ||||||
| chr11:44209285
|
A | G | 51 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(48): Show | 52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+2326A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209285 | ||||||
| chr11:44209327
|
G | A | 1 | a0001c0004t0016g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1662+2368G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209327 | ||||||
| chr11:44209448
|
A | G | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+2489A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209448 | ||||||
| chr11:44209493
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0086 | 3 | HG02258.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+2534A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209493 | ||||||
| chr11:44209730
|
C | T | 5 | a0001c0002t0004g0030a0001c0002t0004g0047a0001c0002t0004g0049others(2): Show | 5 | HG00673.hp2 HG02083.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+2771C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209730 | ||||||
| chr11:44209802
|
C | T | 25 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(22): Show | 25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1662+2843C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209802 | ||||||
| chr11:44209966
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+3007A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209966 | ||||||
| chr11:44209993
|
G | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+3034G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209993 | ||||||
| chr11:44210048
|
G | A | 1 | a0001c0001t0007g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1662+3089G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210048 | ||||||
| chr11:44210183
|
A | T | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1662+3224A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210183 | ||||||
| chr11:44210191
|
G | A | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+3232G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210191 | ||||||
| chr11:44210377
|
G | A | 1 | a0001c0001t0008g0246 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1662+3418G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210377 | ||||||
| chr11:44210569
|
G | C | 7 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+3610G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210569 | ||||||
| chr11:44210647
|
A | C | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1662+3688A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210647 | ||||||
| chr11:44210829
|
A | G | 1 | a0001c0001t0010g0311 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1662+3870A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210829 | ||||||
| chr11:44210885
|
T | C | 202 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(199): Show | 204 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1662+3926T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210885 | ||||||
| chr11:44210894
|
G | T | 1 | a0003c0006t0056g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1662+3935G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210894 | ||||||
| chr11:44210900
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1662+3941A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210900 | ||||||
| chr11:44211481
|
G | A | 5 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(2): Show | 5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+4522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211481 | ||||||
| chr11:44211570
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | NA18962.hp1 NA18980.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1662+4611G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211570 | ||||||
| chr11:44211633
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1662+4674A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211633 | ||||||
| chr11:44211756
|
G | C | 4 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0022g0329others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+4797G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211756 | ||||||
| chr11:44211845
|
T | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+4886T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211845 | ||||||
| chr11:44212055
|
T | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+5096T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212055 | ||||||
| chr11:44212154
|
A | G | 328 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1662+5195A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212154 | ||||||
| chr11:44212169
|
C | A | 3 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1662+5210C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212169 | ||||||
| chr11:44212260
|
G | A | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+5301G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212260 | ||||||
| chr11:44212263
|
C | T | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+5304C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212263 | ||||||
| chr11:44212298
|
TATAA | T | 76 | a0001c0001t0003g0193a0001c0001t0004g0271a0001c0001t0004g0327others(73): Show | 76 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1662+5387_1662+539 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | |||||
| chr11:44212298
|
TATAAATA others(1): Show |
T | 146 | a0001c0001t0001g0116a0001c0001t0001g0176a0001c0001t0002g0087others(143): Show | 149 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1662+5383_1662+539 others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | |||||
| chr11:44212298
|
TATAAATA others(5): Show |
T | 5 | a0001c0001t0002g0233a0001c0001t0006g0009a0001c0001t0018g0314others(2): Show | 5 | HG00639.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+5379_1662+539 others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | |||||
| chr11:44212298
|
TATAAATA others(9): Show |
T | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1662+5375_1662+539 others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | |||||
| chr11:44212298
|
TATAAATA others(13): Show |
T | 6 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0201others(3): Show | 6 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+5371_1662+539 others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | |||||
| chr11:44212300
|
T | A | 6 | a0001c0001t0007g0256a0001c0001t0009g0273a0001c0004t0040g0174others(3): Show | 6 | HG00323.hp2 HG01891.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+5341T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212300 | ||||||
| chr11:44212302
|
A | C | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1662+5343A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212302 | ||||||
| chr11:44212304
|
T | A | 63 | a0001c0001t0003g0193a0001c0001t0004g0271a0001c0001t0004g0327others(60): Show | 63 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1662+5345T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212304 | ||||||
| chr11:44212306
|
AAT | A | 3 | a0001c0001t0003g0305a0001c0009t0027g0306a0001c0009t0027g0307 | 3 | HG02896.hp1 HG02970.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1662+5349_1662+535 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212306 | |||||
| chr11:44212308
|
T | A | 128 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(125): Show | 130 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1662+5349T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212308 | ||||||
| chr11:44212312
|
T | A | 3 | a0001c0001t0002g0233a0001c0001t0018g0314a0001c0002t0002g0015 | 3 | HG00639.hp2 HG03834.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1662+5353T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212312 | ||||||
| chr11:44212316
|
T | A | 3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0251 | 3 | HG00639.hp1 HG01099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1662+5357T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212316 | ||||||
| chr11:44212320
|
T | A | 5 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0201others(2): Show | 5 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+5361T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212320 | ||||||
| chr11:44212407
|
C | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+5448C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212407 | ||||||
| chr11:44212414
|
A | T | 1 | a0001c0001t0003g0282 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1662+5455A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212414 | ||||||
| chr11:44212418
|
T | C | 98 | a0001c0001t0001g0176a0001c0001t0003g0192a0001c0001t0003g0207others(95): Show | 100 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1662+5459T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212418 | ||||||
| chr11:44212497
|
G | A | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+5538G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212497 | ||||||
| chr11:44212660
|
T | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+5701T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212660 | ||||||
| chr11:44212803
|
A | C | 5 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0127others(2): Show | 5 | HG00597.hp1 HG00673.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+5844A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212803 | ||||||
| chr11:44212849
|
G | A | 1 | a0001c0002t0004g0034 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1662+5890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212849 | ||||||
| chr11:44213024
|
G | T | 2 | a0001c0004t0016g0172a0001c0004t0016g0173 | 2 | HG03017.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1662+6065G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213024 | ||||||
| chr11:44213179
|
T | G | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1662+6220T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213179 | ||||||
| chr11:44213451
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+6492A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213451 | ||||||
| chr11:44213469
|
A | G | 1 | a0001c0001t0014g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1662+6510A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213469 | ||||||
| chr11:44213605
|
C | T | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+6646C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213605 | ||||||
| chr11:44213703
|
C | T | 192 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(189): Show | 194 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1662+6744C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213703 | ||||||
| chr11:44213766
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1662+6807T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213766 | ||||||
| chr11:44214042
|
T | C | 1 | a0001c0001t0008g0249 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1662+7083T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214042 | ||||||
| chr11:44214106
|
T | TTTC | 5 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+7165_1662+716 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214106 | |||||
| chr11:44214106
|
TTTC | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1662+7165_1662+716 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214106 | |||||
| chr11:44214150
|
G | C | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+7191G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214150 | ||||||
| chr11:44214153
|
G | A | 35 | a0001c0001t0001g0176a0001c0001t0005g0017a0001c0001t0005g0061others(32): Show | 36 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1662+7194G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214153 | ||||||
| chr11:44214164
|
A | AGTGT | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+7208_1662+720 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214164 | |||||
| chr11:44214176
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+7217C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214176 | ||||||
| chr11:44214177
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+7218A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214177 | ||||||
| chr11:44214300
|
G | C | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+7341G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214300 | ||||||
| chr11:44214305
|
G | C | 1 | a0001c0001t0001g0328 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1662+7346G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214305 | ||||||
| chr11:44214327
|
C | G | 4 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0022g0329others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+7368C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214327 | ||||||
| chr11:44214372
|
C | G | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1662+7413C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214372 | ||||||
| chr11:44214486
|
C | T | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1662+7527C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214486 | ||||||
| chr11:44214751
|
C | CT | 20 | a0001c0001t0002g0206a0001c0001t0008g0002a0001c0001t0008g0217others(17): Show | 21 | HG02074.hp1 HG02280.hp1 HG02976.hp1 others(18): Show |
intron_variant | MODIFIER | c.1662+7807dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214751 | |||||
| chr11:44214928
|
C | CG | 17 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(14): Show | 18 | HG02027.hp1 HG02074.hp1 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.1662+7975dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214928 | |||||
| chr11:44214929
|
G | A | 2 | a0001c0001t0026g0016a0001c0001t0026g0082 | 2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1662+7970G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214929 | ||||||
| chr11:44215102
|
T | G | 62 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0130others(59): Show | 63 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1662+8143T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215102 | ||||||
| chr11:44215442
|
A | G | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+8483A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215442 | ||||||
| chr11:44215694
|
C | T | 1 | a0001c0001t0003g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+8735C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215694 | ||||||
| chr11:44215716
|
AAATTC | A | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+8759_1662+876 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215716 | |||||
| chr11:44215865
|
A | AT | 11 | a0001c0001t0003g0178a0001c0001t0007g0323a0001c0001t0015g0129others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1662+8928dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | |||||
| chr11:44215865
|
AT | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1662+8928delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | |||||
| chr11:44215865
|
ATTT | A | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+8926_1662+892 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | |||||
| chr11:44215865
|
ATTTTTTT others(2): Show |
A | 50 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(47): Show | 51 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1662+8920_1662+892 others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | |||||
| chr11:44215871
|
T | G | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+8912T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215871 | ||||||
| chr11:44215917
|
C | T | 43 | a0001c0001t0004g0271a0001c0001t0004g0327a0001c0002t0002g0019others(40): Show | 43 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1662+8958C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215917 | ||||||
| chr11:44215963
|
G | A | 135 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(132): Show | 136 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.1662+9004G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215963 | ||||||
| chr11:44215969
|
C | T | 2 | a0001c0001t0003g0295a0001c0001t0003g0298 | 2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1662+9010C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215969 | ||||||
| chr11:44215970
|
G | A | 32 | a0001c0001t0003g0207a0001c0001t0003g0266a0001c0001t0003g0274others(29): Show | 33 | HG00544.hp2 HG01109.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1662+9011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215970 | ||||||
| chr11:44215985
|
T | C | 1 | a0001c0001t0003g0291 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1662+9026T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215985 | ||||||
| chr11:44216127
|
C | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1662+9168C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216127 | ||||||
| chr11:44216130
|
T | C | 107 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 108 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1662+9171T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216130 | ||||||
| chr11:44216490
|
A | G | 1 | a0001c0001t0004g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1662+9531A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216490 | ||||||
| chr11:44216539
|
C | T | 1 | a0001c0001t0032g0231 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1662+9580C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216539 | ||||||
| chr11:44216628
|
C | T | 139 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(136): Show | 140 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.1662+9669C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216628 | ||||||
| chr11:44216672
|
T | C | 2 | a0001c0001t0053g0255a0001c0014t0062g0239 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+9713T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216672 | ||||||
| chr11:44217175
|
A | G | 1 | a0001c0001t0042g0264 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1662+10216A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217175 | ||||||
| chr11:44217683
|
AT | A | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+10734delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44217683 | |||||
| chr11:44217769
|
T | A | 2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1662+10810T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217769 | ||||||
| chr11:44217923
|
A | T | 2 | a0001c0001t0009g0285a0001c0001t0043g0284 | 2 | NA19000.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1662+10964A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217923 | ||||||
| chr11:44218051
|
C | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0055 | 2 | NA18954.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1662+11092C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218051 | ||||||
| chr11:44218350
|
G | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1662+11391G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218350 | ||||||
| chr11:44218423
|
C | T | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+11464C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218423 | ||||||
| chr11:44218431
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1662+11472C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218431 | ||||||
| chr11:44218731
|
T | TTTTA | 60 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(57): Show | 61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11772_1662+11 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218731 | ||||||
| chr11:44218732
|
A | C | 60 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(57): Show | 61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11773A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218732 | ||||||
| chr11:44218733
|
A | T | 60 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(57): Show | 61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11774A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218733 | ||||||
| chr11:44218749
|
A | G | 11 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(8): Show | 11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+11790A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218749 | ||||||
| chr11:44218793
|
C | CT | 265 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.1662+11856dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | |||||
| chr11:44218793
|
C | CTT | 26 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0132others(23): Show | 26 | HG00673.hp1 HG00741.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1662+11855_1662+11 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | |||||
| chr11:44218793
|
C | CTTT | 18 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(15): Show | 19 | HG01978.hp2 HG02300.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1662+11854_1662+11 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | |||||
| chr11:44218834
|
G | T | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+11875G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218834 | ||||||
| chr11:44219096
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1662+12137C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219096 | ||||||
| chr11:44219164
|
T | C | 1 | a0001c0001t0007g0256 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1662+12205T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219164 | ||||||
| chr11:44219215
|
C | T | 11 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(8): Show | 11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12256C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219215 | ||||||
| chr11:44219229
|
C | T | 1 | a0001c0002t0004g0028 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1662+12270C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219229 | ||||||
| chr11:44219286
|
G | A | 2 | a0001c0001t0009g0279a0001c0001t0009g0283 | 2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1662+12327G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219286 | ||||||
| chr11:44219351
|
TA | T | 17 | a0001c0001t0001g0099a0001c0001t0010g0308a0001c0001t0010g0310others(14): Show | 17 | HG00639.hp2 HG01243.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1662+12405delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44219351 | |||||
| chr11:44219406
|
C | T | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+12447C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219406 | ||||||
| chr11:44219527
|
A | G | 11 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(8): Show | 11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12568A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219527 | ||||||
| chr11:44219620
|
T | C | 11 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(8): Show | 11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12661T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219620 | ||||||
| chr11:44219776
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-12577C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219776 | ||||||
| chr11:44219881
|
A | T | 2 | a0001c0001t0008g0244a0001c0001t0008g0245 | 2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1663-12472A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219881 | ||||||
| chr11:44220236
|
C | T | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-12117C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220236 | ||||||
| chr11:44220345
|
G | A | 2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1663-12008G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220345 | ||||||
| chr11:44220359
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1663-11994G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220359 | ||||||
| chr11:44220694
|
G | T | 8 | a0001c0001t0004g0271a0001c0002t0004g0027a0001c0002t0004g0035others(5): Show | 8 | HG00621.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-11659G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220694 | ||||||
| chr11:44221011
|
T | G | 28 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(25): Show | 28 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.1663-11342T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221011 | ||||||
| chr11:44221063
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1663-11290G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221063 | ||||||
| chr11:44221169
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-11184G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221169 | ||||||
| chr11:44221261
|
C | T | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-11092C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221261 | ||||||
| chr11:44221315
|
G | A | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-11038G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221315 | ||||||
| chr11:44221339
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1663-11014G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221339 | ||||||
| chr11:44221660
|
C | G | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-10693C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221660 | ||||||
| chr11:44221951
|
C | G | 3 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0045g0302 | 3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1663-10402C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221951 | ||||||
| chr11:44222001
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1663-10352A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222001 | ||||||
| chr11:44222273
|
C | T | 1 | a0001c0007t0005g0147 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1663-10080C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222273 | ||||||
| chr11:44222753
|
T | A | 1 | a0001c0001t0002g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1663-9600T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222753 | ||||||
| chr11:44222779
|
A | T | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-9574A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222779 | ||||||
| chr11:44223127
|
A | G | 139 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(136): Show | 140 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.1663-9226A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223127 | ||||||
| chr11:44223292
|
A | G | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-9061A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223292 | ||||||
| chr11:44223520
|
A | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1663-8833A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223520 | ||||||
| chr11:44223641
|
A | C | 138 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(135): Show | 139 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1663-8712A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223641 | ||||||
| chr11:44223641
|
A | G | 1 | a0001c0004t0030g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1663-8712A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223641 | ||||||
| chr11:44223642
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-8711G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223642 | ||||||
| chr11:44223651
|
C | CT | 7 | a0001c0001t0001g0144a0001c0001t0003g0295a0001c0001t0006g0166others(4): Show | 7 | HG02572.hp2 HG03831.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-8686dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44223651 | |||||
| chr11:44223672
|
C | T | 25 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(22): Show | 25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-8681C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223672 | ||||||
| chr11:44223689
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0044g0208 | 2 | HG01361.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1663-8664G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223689 | ||||||
| chr11:44223865
|
A | G | 3 | a0001c0001t0012g0004a0001c0001t0012g0005a0001c0001t0012g0006 | 3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1663-8488A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223865 | ||||||
| chr11:44223898
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0007g0321 | 2 | HG02155.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1663-8455G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223898 | ||||||
| chr11:44223930
|
A | C | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.1663-8423A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223930 | ||||||
| chr11:44224193
|
T | G | 1 | a0001c0001t0037g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-8160T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224193 | ||||||
| chr11:44224243
|
G | A | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1663-8110G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224243 | ||||||
| chr11:44224360
|
A | G | 1 | a0001c0001t0037g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-7993A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224360 | ||||||
| chr11:44224412
|
A | T | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1663-7941A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224412 | ||||||
| chr11:44224450
|
A | G | 6 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-7903A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224450 | ||||||
| chr11:44224620
|
G | A | 10 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(7): Show | 10 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-7733G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224620 | ||||||
| chr11:44224760
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1663-7593G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224760 | ||||||
| chr11:44224761
|
A | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0151 | 2 | NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1663-7592A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224761 | ||||||
| chr11:44224941
|
T | G | 1 | a0001c0001t0026g0082 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1663-7412T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224941 | ||||||
| chr11:44224949
|
A | G | 60 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(57): Show | 61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1663-7404A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224949 | ||||||
| chr11:44225003
|
C | T | 2 | a0001c0001t0021g0059a0001c0001t0021g0060 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1663-7350C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225003 | ||||||
| chr11:44225154
|
A | G | 1 | a0001c0001t0007g0324 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1663-7199A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225154 | ||||||
| chr11:44225180
|
C | A | 47 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(44): Show | 48 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1663-7173C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225180 | ||||||
| chr11:44225185
|
C | T | 1 | a0001c0001t0004g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1663-7168C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225185 | ||||||
| chr11:44225370
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1663-6983T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225370 | ||||||
| chr11:44225380
|
T | C | 6 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(3): Show | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-6973T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225380 | ||||||
| chr11:44225423
|
C | G | 1 | a0001c0001t0054g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-6930C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225423 | ||||||
| chr11:44225437
|
A | G | 1 | a0001c0002t0004g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1663-6916A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225437 | ||||||
| chr11:44225585
|
C | T | 1 | a0001c0001t0003g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1663-6768C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225585 | ||||||
| chr11:44225769
|
G | A | 1 | a0001c0004t0040g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1663-6584G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225769 | ||||||
| chr11:44225827
|
C | T | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-6526C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225827 | ||||||
| chr11:44225861
|
G | T | 1 | a0001c0001t0058g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-6492G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225861 | ||||||
| chr11:44225909
|
C | A | 1 | a0001c0001t0006g0089 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1663-6444C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225909 | ||||||
| chr11:44226254
|
G | A | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-6099G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226254 | ||||||
| chr11:44226392
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-5961A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226392 | ||||||
| chr11:44226420
|
T | C | 1 | a0001c0001t0012g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-5933T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226420 | ||||||
| chr11:44226665
|
G | A | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1663-5688G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226665 | ||||||
| chr11:44226777
|
T | C | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1663-5576T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226777 | ||||||
| chr11:44226931
|
A | G | 3 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0045g0302 | 3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1663-5422A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226931 | ||||||
| chr11:44227010
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-5343C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227010 | ||||||
| chr11:44227034
|
C | G | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-5319C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227034 | ||||||
| chr11:44227072
|
C | T | 2 | a0001c0008t0001g0159a0001c0008t0001g0161 | 2 | HG00438.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1663-5281C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227072 | ||||||
| chr11:44227178
|
G | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1663-5175G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227178 | ||||||
| chr11:44227276
|
G | C | 202 | a0001c0001t0001g0176a0001c0001t0002g0087a0001c0001t0002g0107others(199): Show | 204 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1663-5077G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227276 | ||||||
| chr11:44227314
|
A | G | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-5039A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227314 | ||||||
| chr11:44227387
|
C | G | 15 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(12): Show | 16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-4966C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227387 | ||||||
| chr11:44227432
|
A | G | 9 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316others(6): Show | 9 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-4921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227432 | ||||||
| chr11:44227434
|
C | T | 25 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(22): Show | 26 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1663-4919C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227434 | ||||||
| chr11:44227572
|
A | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-4781A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227572 | ||||||
| chr11:44227641
|
A | T | 1 | a0001c0002t0004g0028 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1663-4712A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227641 | ||||||
| chr11:44227683
|
G | C | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-4670G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227683 | ||||||
| chr11:44227775
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-4578G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227775 | ||||||
| chr11:44227794
|
G | A | 7 | a0001c0002t0004g0026a0001c0002t0004g0032a0001c0002t0004g0043others(4): Show | 7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-4559G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227794 | ||||||
| chr11:44228024
|
C | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1663-4329C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228024 | ||||||
| chr11:44228447
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-3906C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228447 | ||||||
| chr11:44228448
|
G | A | 1 | a0001c0002t0004g0028 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1663-3905G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228448 | ||||||
| chr11:44228519
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0233 | 2 | HG03491.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1663-3834C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228519 | ||||||
| chr11:44228541
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1663-3812C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228541 | ||||||
| chr11:44228731
|
T | C | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.1663-3622T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228731 | ||||||
| chr11:44228788
|
G | A | 1 | a0001c0001t0003g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1663-3565G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228788 | ||||||
| chr11:44228841
|
A | C | 1 | a0001c0001t0037g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-3512A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228841 | ||||||
| chr11:44228855
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-3498T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228855 | ||||||
| chr11:44228936
|
G | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1663-3417G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228936 | ||||||
| chr11:44228954
|
CAAAGT | C | 37 | a0001c0001t0001g0176a0001c0001t0005g0017a0001c0001t0005g0063others(34): Show | 38 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1663-3395_1663-339 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44228954 | |||||
| chr11:44229070
|
G | A | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-3283G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229070 | ||||||
| chr11:44229093
|
G | A | 2 | a0001c0001t0001g0275a0001c0013t0001g0085 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1663-3260G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229093 | ||||||
| chr11:44229345
|
C | T | 57 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(54): Show | 58 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1663-3008C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229345 | ||||||
| chr11:44229391
|
T | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-2962T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229391 | ||||||
| chr11:44229559
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1663-2794G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229559 | ||||||
| chr11:44229827
|
G | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1663-2526G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229827 | ||||||
| chr11:44229986
|
A | G | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-2367A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229986 | ||||||
| chr11:44230221
|
G | A | 7 | a0001c0002t0004g0026a0001c0002t0004g0032a0001c0002t0004g0043others(4): Show | 7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-2132G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230221 | ||||||
| chr11:44230286
|
A | G | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-2067A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230286 | ||||||
| chr11:44230953
|
A | G | 42 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(39): Show | 42 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1663-1400A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230953 | ||||||
| chr11:44230982
|
G | A | 1 | a0001c0001t0012g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-1371G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230982 | ||||||
| chr11:44231138
|
C | G | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1663-1215C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231138 | ||||||
| chr11:44231167
|
G | T | 47 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(44): Show | 48 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1663-1186G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231167 | ||||||
| chr11:44231253
|
C | T | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-1100C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231253 | ||||||
| chr11:44231296
|
G | A | 1 | a0001c0001t0012g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-1057G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231296 | ||||||
| chr11:44231408
|
G | A | 25 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(22): Show | 25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-945G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231408 | ||||||
| chr11:44231430
|
T | C | 2 | a0001c0002t0004g0034a0001c0002t0004g0046 | 2 | NA19066.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1663-923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231430 | ||||||
| chr11:44231505
|
A | G | 2 | a0001c0001t0021g0059a0001c0001t0021g0060 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1663-848A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231505 | ||||||
| chr11:44231787
|
A | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-566A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231787 | ||||||
| chr11:44231853
|
G | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-500G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231853 | ||||||
| chr11:44231917
|
C | CT | 17 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(14): Show | 18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-428dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44231917 | |||||
| chr11:44231925
|
T | A | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-428T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231925 | ||||||
| chr11:44231926
|
A | T | 17 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(14): Show | 18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-427A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231926 | ||||||
| chr11:44232038
|
G | A | 1 | a0001c0001t0003g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1663-315G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44232038 | ||||||
| chr11:44232097
|
C | A | 17 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(14): Show | 18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-256C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44232097 | ||||||
| chr11:44232663
|
C | T | 1 | a0001c0001t0021g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1806+167C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232663 | ||||||
| chr11:44232756
|
C | T | 1 | a0001c0001t0025g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1806+260C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232756 | ||||||
| chr11:44232790
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1806+294G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232790 | ||||||
| chr11:44232843
|
A | G | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1806+347A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232843 | ||||||
| chr11:44232915
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1806+419T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232915 | ||||||
| chr11:44232936
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1806+440A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232936 | ||||||
| chr11:44233019
|
A | T | 3 | a0001c0001t0020g0241a0001c0001t0020g0242a0002c0005t0061g0237 | 3 | HG01243.hp1 HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1806+523A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233019 | ||||||
| chr11:44233203
|
C | T | 9 | a0001c0001t0009g0003a0001c0001t0009g0260a0001c0001t0009g0285others(6): Show | 10 | HG02523.hp2 NA18953.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+707C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233203 | ||||||
| chr11:44233225
|
T | A | 1 | a0001c0008t0001g0161 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1806+729T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233225 | ||||||
| chr11:44233323
|
G | C | 2 | a0001c0001t0012g0005a0001c0001t0012g0006 | 2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1807-792G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233323 | ||||||
| chr11:44233324
|
A | G | 9 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(6): Show | 9 | HG01891.hp2 HG02976.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-791A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233324 | ||||||
| chr11:44233428
|
C | G | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1807-687C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233428 | ||||||
| chr11:44233430
|
C | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1807-685C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233430 | ||||||
| chr11:44233450
|
G | A | 1 | a0001c0004t0060g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1807-665G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233450 | ||||||
| chr11:44233530
|
G | C | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1807-585G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233530 | ||||||
| chr11:44233548
|
G | C | 9 | a0001c0004t0016g0172a0001c0004t0016g0173a0001c0004t0016g0177others(6): Show | 9 | HG01891.hp2 HG02976.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-567G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233548 | ||||||
| chr11:44233587
|
A | T | 3 | a0002c0005t0019g0236a0002c0005t0019g0238a0002c0005t0019g0240 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1807-528A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233587 | ||||||
| chr11:44233671
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1807-444T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233671 | ||||||
| chr11:44233675
|
T | C | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1807-440T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233675 | ||||||
| chr11:44233933
|
C | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1807-182C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233933 | ||||||
| chr11:44234034
|
C | G | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-81C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234034 | ||||||
| chr11:44234064
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1807-51T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234064 | ||||||
| chr11:44234086
|
A | G | 1 | a0001c0001t0031g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1807-29A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234086 | ||||||
| chr11:44234395
|
T | C | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1935+152T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44234395 | ||||||
| chr11:44234599
|
G | GT | 292 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(289): Show | 294 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.1935+366dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44234599 | |||||
| chr11:44234740
|
G | C | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1935+497G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44234740 | ||||||
| chr11:44235059
|
T | A | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1935+816T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235059 | ||||||
| chr11:44235214
|
C | G | 1 | a0001c0001t0018g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1935+971C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235214 | ||||||
| chr11:44235225
|
C | CT | 67 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0124others(64): Show | 68 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1935+1007dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | |||||
| chr11:44235225
|
C | CTT | 82 | a0001c0001t0001g0104a0001c0001t0002g0087a0001c0001t0002g0107others(79): Show | 82 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1935+1006_1935+100 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | |||||
| chr11:44235225
|
C | CTTT | 35 | a0001c0001t0001g0103a0001c0001t0002g0108a0001c0001t0002g0149others(32): Show | 35 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1935+1005_1935+100 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | |||||
| chr11:44235225
|
CT | C | 12 | a0001c0001t0001g0095a0001c0001t0007g0169a0001c0001t0007g0170others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1935+1007delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | |||||
| chr11:44235250
|
T | TTTG | 22 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(19): Show | 23 | HG00544.hp2 HG01099.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | ||||||
| chr11:44235250
|
T | TTTTG | 22 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0190others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | ||||||
| chr11:44235250
|
T | TTTTTG | 7 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0188others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | ||||||
| chr11:44235303
|
C | T | 46 | a0001c0001t0003g0192a0001c0001t0003g0207a0001c0001t0003g0227others(43): Show | 47 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1936-990C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235303 | ||||||
| chr11:44235390
|
C | T | 138 | a0001c0001t0002g0087a0001c0001t0002g0107a0001c0001t0002g0108others(135): Show | 139 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1936-903C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235390 | ||||||
| chr11:44235398
|
T | C | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1936-895T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235398 | ||||||
| chr11:44235403
|
G | A | 1 | a0001c0001t0003g0305 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1936-890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235403 | ||||||
| chr11:44235421
|
A | G | 5 | a0001c0002t0004g0032a0001c0002t0004g0044a0001c0002t0004g0045others(2): Show | 5 | HG00597.hp2 NA18984.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-872A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235421 | ||||||
| chr11:44235463
|
C | A | 1 | a0006c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1936-830C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235463 | ||||||
| chr11:44235610
|
T | A | 3 | a0001c0001t0005g0277a0001c0001t0005g0280a0001c0001t0005g0286 | 3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1936-683T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235610 | ||||||
| chr11:44235872
|
G | A | 1 | a0001c0001t0023g0257 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1936-421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235872 | ||||||
| chr11:44235906
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1936-387G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235906 | ||||||
| chr11:44235979
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1936-314A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235979 | ||||||
| chr11:44236119
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1936-174G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236119 | ||||||
| chr11:44236158
|
G | GGT | 3 | a0001c0001t0005g0061a0001c0001t0005g0075a0001c0001t0047g0313 | 3 | HG03471.hp1 NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1936-117_1936-116d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44236158 | |||||
| chr11:44236158
|
GGT | G | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1936-117_1936-116d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44236158 | |||||
| chr11:44236180
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1936-113C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236180 | ||||||
| chr11:44236227
|
G | C | 18 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(15): Show | 19 | HG01243.hp1 HG04204.hp2 NA18522.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936-66G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236227 | ||||||
| chr11:44236252
|
T | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1936-41T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236252 | ||||||
| chr11:44236825
|
G | A | 1 | a0001c0001t0053g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2018+450G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44236825 | ||||||
| chr11:44236985
|
G | A | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+610G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44236985 | ||||||
| chr11:44237027
|
A | G | 1 | a0001c0001t0006g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2018+652A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237027 | ||||||
| chr11:44237174
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2018+799G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237174 | ||||||
| chr11:44237227
|
A | G | 1 | a0001c0002t0004g0037 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2018+852A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237227 | ||||||
| chr11:44237277
|
T | TTG | 3 | a0001c0001t0007g0324a0001c0001t0007g0325a0001c0001t0007g0326 | 3 | HG00323.hp1 HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2018+913_2018+914d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237277 | |||||
| chr11:44237287
|
G | C | 1 | a0001c0001t0003g0294 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2018+912G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237287 | ||||||
| chr11:44237439
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+1064T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237439 | ||||||
| chr11:44237739
|
A | G | 3 | a0001c0001t0018g0314a0001c0001t0018g0315a0001c0001t0018g0316 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2018+1364A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237739 | ||||||
| chr11:44237858
|
G | A | 1 | a0001c0002t0004g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2018+1483G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237858 | ||||||
| chr11:44237902
|
T | TA | 50 | a0001c0001t0002g0108a0001c0001t0002g0196a0001c0001t0002g0197others(47): Show | 50 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2018+1555dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237902 | |||||
| chr11:44237902
|
TA | T | 58 | a0001c0001t0002g0210a0001c0001t0002g0233a0001c0001t0003g0192others(55): Show | 60 | HG00544.hp2 HG00639.hp2 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.2018+1555delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237902 | |||||
| chr11:44237919
|
A | AC | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2018+1544_2018+154 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237919 | ||||||
| chr11:44237920
|
A | C | 1 | a0001c0002t0004g0047 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2018+1545A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237920 | ||||||
| chr11:44237942
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0151 | 2 | NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2018+1567A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237942 | ||||||
| chr11:44238053
|
C | T | 56 | a0001c0001t0003g0178a0001c0001t0003g0182a0001c0001t0003g0186others(53): Show | 57 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2018+1678C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238053 | ||||||
| chr11:44238275
|
T | G | 1 | a0001c0001t0007g0326 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2018+1900T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238275 | ||||||
| chr11:44238592
|
A | G | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+2217A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238592 | ||||||
| chr11:44238606
|
G | A | 7 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(4): Show | 7 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018+2231G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238606 | ||||||
| chr11:44238707
|
T | C | 2 | a0001c0001t0005g0068a0001c0001t0005g0069 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2018+2332T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238707 | ||||||
| chr11:44238884
|
A | G | 328 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.2018+2509A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238884 | ||||||
| chr11:44238899
|
A | G | 1 | a0001c0009t0027g0307 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2018+2524A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238899 | ||||||
| chr11:44239003
|
G | A | 2 | a0001c0001t0002g0205a0005c0012t0002g0203 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2018+2628G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239003 | ||||||
| chr11:44239092
|
A | C | 1 | a0001c0001t0029g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2018+2717A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239092 | ||||||
| chr11:44239235
|
T | A | 1 | a0001c0001t0039g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2018+2860T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239235 | ||||||
| chr11:44239254
|
G | A | 35 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(32): Show | 36 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2018+2879G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239254 | ||||||
| chr11:44239298
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2018+2923C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239298 | ||||||
| chr11:44239393
|
C | CT | 279 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.2018+3036dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239393 | |||||
| chr11:44239393
|
C | CTT | 13 | a0001c0001t0001g0195a0001c0001t0001g0275a0001c0001t0002g0107others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2018+3035_2018+303 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239393 | |||||
| chr11:44239427
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2018+3052T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239427 | ||||||
| chr11:44239517
|
C | T | 1 | a0001c0001t0005g0073 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2018+3142C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239517 | ||||||
| chr11:44239633
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2018+3258C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239633 | ||||||
| chr11:44239642
|
C | T | 1 | a0001c0001t0047g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2018+3267C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239642 | ||||||
| chr11:44239689
|
C | CT | 30 | a0001c0001t0001g0008a0001c0001t0001g0097a0001c0001t0001g0122others(27): Show | 30 | HG00597.hp1 HG00639.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.2018+3340dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | |||||
| chr11:44239689
|
CT | C | 80 | a0001c0001t0001g0121a0001c0001t0002g0107a0001c0001t0002g0108others(77): Show | 80 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.2018+3340delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | |||||
| chr11:44239689
|
CTT | C | 11 | a0001c0001t0020g0241a0001c0001t0020g0242a0001c0001t0029g0331others(8): Show | 11 | HG01243.hp1 HG01993.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2018+3339_2018+334 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | |||||
| chr11:44239689
|
CTTTTTTT others(4): Show |
C | 41 | a0001c0001t0005g0017a0001c0001t0005g0061a0001c0001t0005g0063others(38): Show | 42 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2018+3330_2018+334 others(15): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | |||||
| chr11:44239820
|
A | T | 17 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(14): Show | 18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.2018+3445A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239820 | ||||||
| chr11:44239906
|
C | T | 3 | a0001c0007t0005g0147a0001c0007t0005g0183a0001c0007t0005g0194 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2018+3531C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239906 | ||||||
| chr11:44240019
|
A | G | 2 | a0001c0001t0009g0279a0001c0001t0009g0283 | 2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2018+3644A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240019 | ||||||
| chr11:44240020
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2018+3645T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240020 | ||||||
| chr11:44240305
|
G | A | 1 | a0001c0001t0042g0264 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2019-3844G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240305 | ||||||
| chr11:44240878
|
C | G | 4 | a0001c0001t0015g0129a0001c0001t0015g0181a0001c0001t0015g0184others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019-3271C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240878 | ||||||
| chr11:44240879
|
T | C | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2019-3270T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240879 | ||||||
| chr11:44241131
|
A | G | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.2019-3018A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241131 | ||||||
| chr11:44241249
|
G | A | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-2900G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241249 | ||||||
| chr11:44241259
|
G | A | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.2019-2890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241259 | ||||||
| chr11:44241326
|
A | C | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-2823A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241326 | ||||||
| chr11:44241687
|
A | G | 31 | a0001c0001t0004g0271a0001c0001t0004g0327a0001c0002t0004g0013others(28): Show | 31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2019-2462A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241687 | ||||||
| chr11:44242055
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2019-2094G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242055 | ||||||
| chr11:44242149
|
G | A | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0175others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-2000G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242149 | ||||||
| chr11:44242237
|
T | C | 1 | a0001c0002t0036g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2019-1912T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242237 | ||||||
| chr11:44242298
|
C | T | 3 | a0001c0001t0028g0252a0001c0001t0028g0253a0001c0001t0063g0254 | 3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2019-1851C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242298 | ||||||
| chr11:44242349
|
A | C | 3 | a0001c0001t0012g0004a0001c0001t0012g0005a0001c0001t0012g0006 | 3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2019-1800A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242349 | ||||||
| chr11:44242782
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2019-1367T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242782 | ||||||
| chr11:44242948
|
A | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2019-1201A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242948 | ||||||
| chr11:44243045
|
A | C | 26 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(23): Show | 27 | HG00639.hp2 HG01243.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2019-1104A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243045 | ||||||
| chr11:44243097
|
A | G | 16 | a0001c0001t0008g0002a0001c0001t0008g0217a0001c0001t0008g0234others(13): Show | 17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-1052A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243097 | ||||||
| chr11:44243158
|
G | A | 5 | a0001c0001t0010g0308a0001c0001t0010g0310a0001c0001t0010g0311others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-991G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243158 | ||||||
| chr11:44243238
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-911T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243238 | ||||||
| chr11:44243349
|
A | G | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.2019-800A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243349 | ||||||
| chr11:44243412
|
A | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-737A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243412 | ||||||
| chr11:44243498
|
T | G | 1 | a0004c0010t0010g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2019-651T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243498 | ||||||
| chr11:44243562
|
T | C | 328 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.2019-587T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243562 | ||||||
| chr11:44243618
|
C | CT | 19 | a0001c0001t0001g0086a0001c0001t0001g0152a0001c0001t0003g0295others(16): Show | 19 | HG00735.hp1 HG01099.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2019-506dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | |||||
| chr11:44243618
|
C | CTT | 18 | a0001c0001t0001g0131a0001c0001t0008g0002a0001c0001t0008g0217others(15): Show | 19 | HG00609.hp2 HG02074.hp1 HG04204.hp2 others(16): Show |
intron_variant | MODIFIER | c.2019-507_2019-506d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | |||||
| chr11:44243618
|
CT | C | 77 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0232others(74): Show | 77 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.2019-506delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | |||||
| chr11:44244065
|
T | C | 2 | a0001c0009t0027g0306a0001c0009t0027g0307 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-84T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44244065 | ||||||
| chr11:44244135
|
T | C | 1 | a0002c0005t0061g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2019-14T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44244135 |