Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1123 |
|---|---|
| ensemblid | ENSG00000128656.15 |
| hgncid | 1943 |
| symbol | CHN1 |
| name | chimerin 1 |
| refseq_nuc | NM_001822.7 |
| refseq_prot | NP_001813.1 |
| ensembl_nuc | ENST00000409900.9 |
| ensembl_prot | ENSP00000386741.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 174798809 |
| end | 175005381 |
| strand | - |
| ver | v1.2 |
| region | chr2:174798809-175005381 |
| region5000 | chr2:174793809-175010381 |
| regionname0 | CHN1_chr2_174798809_175005381 |
| regionname5000 | CHN1_chr2_174793809_175010381 |
| 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 | 459 | 275 | 84 | 30 | 122 | 10 | 27 | 96 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0002 | 0/0 | 459 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| 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 | 1380 | 275 | 84 | 30 | 122 | 10 | 27 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| c0002 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1777 | 174 | 46 | 22 | 81 | 8 | 15 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0002 | 0/0 | 1773 | 31 | 10 | 4 | 11 | 1 | 5 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0003 | 0/0 | 1777 | 23 | 0 | 1 | 22 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0004 | 0/0 | 1777 | 14 | 14 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0005 | 0/0 | 1777 | 12 | 0 | 1 | 6 | 1 | 4 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0006 | 0/0 | 1777 | 9 | 9 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0007 | 0/0 | 1777 | 3 | 0 | 1 | 0 | 0 | 2 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0008 | 0/0 | 1777 | 2 | 0 | 1 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0009 | 0/0 | 1777 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0010 | 0/0 | 1777 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0011 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0012 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0013 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0014 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0015 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| t0016 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| 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 | 1380 | 275 | 84 | 30 | 122 | 10 | 27 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0002c0002 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3156 | 173 | 46 | 22 | 81 | 8 | 14 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0002 | 0/0 | 3152 | 31 | 10 | 4 | 11 | 1 | 5 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0003 | 0/0 | 3156 | 23 | 0 | 1 | 22 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0004 | 0/0 | 3156 | 14 | 14 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0005 | 0/0 | 3156 | 12 | 0 | 1 | 6 | 1 | 4 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0006 | 0/0 | 3156 | 9 | 9 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0007 | 0/0 | 3156 | 3 | 0 | 1 | 0 | 0 | 2 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0008 | 0/0 | 3156 | 2 | 0 | 1 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0009 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0010 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0011 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0012 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0013 | 0/0 | 3152 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0014 | 0/0 | 3152 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0015 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0001c0001t0016 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| a0002c0002t0001 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | copy fasta | chr2 | 174793809 | 175010381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0014g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0101 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CDX | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CDX | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0261 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PEL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0030 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0035 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0267 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0068 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0125 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0029 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | BEB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0142 | SAS | BEB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0212 | SAS | BEB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18959 | hp1 | a0001 | c0001 | t0014 | g0260 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | LWK | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | YRI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0180 | EUR | TSI | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | GIH | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | GIH | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0121 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | USA | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0087 | REF | REF | CHN1_chr2_174793809_175010381 | CHN1 | chr2 | 174793809 | 175010381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174915140
|
C | T | 1 | a0002 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.178G>A | p.Asp60Asn | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/13 | 647/3156 | 178/1380 | 60/459 | chr2 | 174915140 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174798861
|
G | A | 1 | a0001c0001t0007 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 1255 | chr2 | 174798861 | |||||
| chr2:174798929
|
C | G | 1 | a0001c0001t0012 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 1187 | chr2 | 174798929 | |||||
| chr2:174798950
|
A | G | 1 | a0001c0001t0015 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1166T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 1166 | chr2 | 174798950 | |||||
| chr2:174798977
|
T | G | 1 | a0001c0001t0005 | 12 | HG00423.hp2 HG01433.hp2 HG02071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1139A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 1139 | chr2 | 174798977 | |||||
| chr2:174799149
|
C | A | 3 | a0001c0001t0006a0001c0001t0007a0001c0001t0008 | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*967G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 967 | chr2 | 174799149 | |||||
| chr2:174799378
|
AAAGT | A | 3 | a0001c0001t0002a0001c0001t0013a0001c0001t0014 | 33 | HG00639.hp2 HG00673.hp2 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*734_*737delACTT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 734 | chr2 | 174799378 | |||||
| chr2:174799439
|
C | T | 1 | a0001c0001t0008 | 2 | HG02300.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 677 | chr2 | 174799439 | |||||
| chr2:174799473
|
T | A | 1 | a0001c0001t0013 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*643A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 643 | chr2 | 174799473 | |||||
| chr2:174799886
|
T | C | 1 | a0001c0001t0016 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 230 | chr2 | 174799886 | |||||
| chr2:174800088
|
A | G | 1 | a0001c0001t0011 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 13/13 | 28 | chr2 | 174800088 | |||||
| chr2:175004980
|
C | T | 1 | a0001c0001t0003 | 23 | HG00558.hp2 HG01258.hp1 HG02015.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-68G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/13 | 68 | chr2 | 175004980 | |||||
| chr2:175005026
|
G | A | 1 | a0001c0001t0014 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/13 | 114 | chr2 | 175005026 | |||||
| chr2:175005128
|
A | G | 1 | a0001c0001t0010 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/13 | 216 | chr2 | 175005128 | |||||
| chr2:175005200
|
A | C | 1 | a0001c0001t0009 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-288T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/13 | 288 | chr2 | 175005200 | |||||
| chr2:175005345
|
G | A | 3 | a0001c0001t0004a0001c0001t0015a0001c0001t0016 | 16 | HG02257.hp1 HG02257.hp2 HG02486.hp2 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-433C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/13 | chr2 | 175005345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174800305
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209-18T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174800305 | ||||||
| chr2:174800487
|
A | G | 155 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1209-200T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174800487 | ||||||
| chr2:174800741
|
A | AATGGCT | 154 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0044others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1209-455_1209-454i others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174800741 | ||||||
| chr2:174800939
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-652A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174800939 | ||||||
| chr2:174801286
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1208+421G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174801286 | ||||||
| chr2:174801339
|
C | CTTGCAAG | 108 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0094others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1208+361_1208+367d others(9): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174801339 | ||||||
| chr2:174801578
|
A | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0051others(22): Show | 25 | HG00438.hp2 HG02027.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1208+129T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174801578 | ||||||
| chr2:174801591
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1208+116G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 12/12 | chr2 | 174801591 | ||||||
| chr2:174801928
|
G | A | 175 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1103-116C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174801928 | ||||||
| chr2:174801990
|
T | G | 4 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0015others(1): Show | 4 | NA18959.hp2 NA18966.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-178A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174801990 | ||||||
| chr2:174802137
|
C | T | 61 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1103-325G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174802137 | ||||||
| chr2:174802567
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0051others(1): Show | 4 | HG02451.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103-755A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174802567 | ||||||
| chr2:174802907
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1103-1095C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174802907 | ||||||
| chr2:174802965
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1103-1153C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174802965 | ||||||
| chr2:174803081
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1103-1269C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803081 | ||||||
| chr2:174803140
|
C | T | 1 | a0001c0001t0004g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1103-1328G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803140 | ||||||
| chr2:174803188
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-1376A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803188 | ||||||
| chr2:174803618
|
G | A | 62 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1103-1806C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803618 | ||||||
| chr2:174803650
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1103-1838C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803650 | ||||||
| chr2:174803711
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1103-1899A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803711 | ||||||
| chr2:174803760
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1103-1948G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174803760 | ||||||
| chr2:174804018
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1103-2206A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804018 | ||||||
| chr2:174804180
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA19081.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1103-2368A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804180 | ||||||
| chr2:174804255
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1103-2443C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804255 | ||||||
| chr2:174804581
|
A | AG | 5 | a0001c0001t0001g0066a0001c0001t0001g0080a0001c0001t0001g0190others(2): Show | 5 | HG00735.hp1 HG01175.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-2770dupC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804581 | ||||||
| chr2:174804621
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1103-2809C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804621 | ||||||
| chr2:174804726
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-2914C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804726 | ||||||
| chr2:174804885
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1103-3073A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804885 | ||||||
| chr2:174804951
|
C | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-3139G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804951 | ||||||
| chr2:174804952
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103-3140T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174804952 | ||||||
| chr2:174805084
|
A | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103-3272T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805084 | ||||||
| chr2:174805102
|
C | G | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1103-3290G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805102 | ||||||
| chr2:174805172
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1103-3360T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805172 | ||||||
| chr2:174805190
|
A | G | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1103-3378T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805190 | ||||||
| chr2:174805675
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1102+3230G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805675 | ||||||
| chr2:174805832
|
TCTC | T | 97 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1102+3070_1102+307 others(7): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174805832 | ||||||
| chr2:174806099
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1102+2806T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806099 | ||||||
| chr2:174806185
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1102+2720C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806185 | ||||||
| chr2:174806436
|
A | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1102+2469T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806436 | ||||||
| chr2:174806460
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1102+2445C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806460 | ||||||
| chr2:174806625
|
G | T | 8 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102+2280C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806625 | ||||||
| chr2:174806712
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1102+2193G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806712 | ||||||
| chr2:174806758
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1102+2147G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806758 | ||||||
| chr2:174806868
|
A | C | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102+2037T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174806868 | ||||||
| chr2:174807101
|
A | G | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1102+1804T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807101 | ||||||
| chr2:174807151
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1102+1754G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807151 | ||||||
| chr2:174807446
|
C | CTG | 27 | a0001c0001t0001g0105a0001c0001t0001g0122a0001c0001t0001g0126others(24): Show | 27 | HG00423.hp2 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1102+1457_1102+145 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTG | 11 | a0001c0001t0001g0079a0001c0001t0001g0133a0001c0001t0001g0136others(8): Show | 11 | HG00140.hp1 HG01175.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1102+1455_1102+145 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTG | 13 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG00280.hp1 HG03017.hp2 HG03486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1102+1453_1102+145 others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(1): Show |
16 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0106others(13): Show | 16 | HG02027.hp1 HG02040.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1102+1451_1102+145 others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(3): Show |
9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(6): Show | 9 | HG00438.hp2 HG01496.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102+1449_1102+145 others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0086a0001c0001t0001g0153a0001c0001t0001g0192others(2): Show | 5 | HG01192.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+1447_1102+145 others(16): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(7): Show |
5 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0164others(2): Show | 5 | HG03654.hp1 NA18968.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+1445_1102+145 others(18): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG00735.hp1 HG01070.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1102+1443_1102+145 others(20): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(11): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0139 | 2 | NA18948.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1102+1441_1102+145 others(22): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | CTGTGTGT others(19): Show |
1 | a0001c0001t0005g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1102+1433_1102+145 others(30): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1102+1459G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTG | C | 22 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0108others(19): Show | 22 | HG00558.hp2 HG01168.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1102+1457_1102+145 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTG | C | 20 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0163others(17): Show | 20 | HG00609.hp2 HG00673.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1102+1455_1102+145 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTG | C | 15 | a0001c0001t0001g0095a0001c0001t0001g0147a0001c0001t0001g0181others(12): Show | 15 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1102+1453_1102+145 others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(1): Show |
C | 23 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0051others(20): Show | 23 | HG00738.hp1 HG01255.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102+1451_1102+145 others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(3): Show |
C | 13 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0130others(10): Show | 13 | HG00639.hp1 HG01081.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1102+1449_1102+145 others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(5): Show |
C | 18 | a0001c0001t0001g0047a0001c0001t0001g0094a0001c0001t0001g0096others(15): Show | 18 | HG01069.hp1 HG01070.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1102+1447_1102+145 others(16): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(7): Show |
C | 13 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0172others(10): Show | 13 | HG00140.hp2 HG00423.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+1445_1102+145 others(18): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(9): Show |
C | 5 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0217others(2): Show | 5 | HG00099.hp2 HG00673.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+1443_1102+145 others(20): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(11): Show |
C | 18 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(15): Show | 18 | HG00438.hp1 HG00735.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1102+1441_1102+145 others(22): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(13): Show |
C | 4 | a0001c0001t0006g0031a0001c0001t0006g0034a0001c0001t0011g0054others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102+1439_1102+145 others(24): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(15): Show |
C | 2 | a0001c0001t0001g0065a0001c0001t0001g0233 | 2 | HG02055.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1102+1437_1102+145 others(26): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(17): Show |
C | 3 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0006g0027 | 3 | HG03516.hp2 HG03654.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1102+1435_1102+145 others(28): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807446
|
CTGTGTGT others(25): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1102+1427_1102+145 others(36): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807446 | ||||||
| chr2:174807663
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1102+1242G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807663 | ||||||
| chr2:174807710
|
G | T | 1 | a0001c0001t0003g0005 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1102+1195C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807710 | ||||||
| chr2:174807736
|
A | G | 272 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1102+1169T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807736 | ||||||
| chr2:174807769
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1102+1136T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174807769 | ||||||
| chr2:174808034
|
A | G | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1102+871T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808034 | ||||||
| chr2:174808162
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1102+743A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808162 | ||||||
| chr2:174808203
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102+702A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808203 | ||||||
| chr2:174808273
|
T | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1102+632A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808273 | ||||||
| chr2:174808312
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1102+593A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808312 | ||||||
| chr2:174808429
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1102+476C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808429 | ||||||
| chr2:174808747
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1102+158C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808747 | ||||||
| chr2:174808849
|
G | C | 1 | a0001c0001t0005g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1102+56C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 11/12 | chr2 | 174808849 | ||||||
| chr2:174809092
|
C | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-50G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809092 | ||||||
| chr2:174809142
|
C | T | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-100G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809142 | ||||||
| chr2:174809735
|
T | A | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.965-693A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809735 | ||||||
| chr2:174809749
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.965-707G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809749 | ||||||
| chr2:174809801
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.965-759C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809801 | ||||||
| chr2:174809841
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0053others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-799T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809841 | ||||||
| chr2:174809865
|
ACTGTAC | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-829_965-824del others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809865 | ||||||
| chr2:174809872
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.965-830G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809872 | ||||||
| chr2:174809896
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.965-854G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174809896 | ||||||
| chr2:174810291
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.964+1220G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810291 | ||||||
| chr2:174810364
|
A | G | 15 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(12): Show | 15 | HG01361.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.964+1147T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810364 | ||||||
| chr2:174810428
|
C | G | 51 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(48): Show | 51 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.964+1083G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810428 | ||||||
| chr2:174810460
|
G | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+1051C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810460 | ||||||
| chr2:174810611
|
C | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+900G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810611 | ||||||
| chr2:174810667
|
A | T | 11 | a0001c0001t0002g0043a0001c0001t0002g0069a0001c0001t0002g0075others(8): Show | 11 | HG00673.hp2 HG02083.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+844T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810667 | ||||||
| chr2:174810676
|
A | T | 254 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.964+835T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810676 | ||||||
| chr2:174810746
|
T | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(21): Show | 24 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+765A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810746 | ||||||
| chr2:174810948
|
A | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+563T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174810948 | ||||||
| chr2:174811127
|
C | G | 29 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(26): Show | 29 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.964+384G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174811127 | ||||||
| chr2:174811388
|
T | A | 16 | a0001c0001t0001g0152a0001c0001t0006g0027a0001c0001t0006g0031others(13): Show | 16 | HG01361.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.964+123A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174811388 | ||||||
| chr2:174811471
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+40A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 10/12 | chr2 | 174811471 | ||||||
| chr2:174811656
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.887-68A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174811656 | ||||||
| chr2:174811851
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.887-263G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174811851 | ||||||
| chr2:174811892
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.887-304A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174811892 | ||||||
| chr2:174811956
|
TTA | T | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.886+351_886+352del others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174811956 | ||||||
| chr2:174811983
|
T | C | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.886+326A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174811983 | ||||||
| chr2:174812294
|
C | T | 64 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.886+15G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 9/12 | chr2 | 174812294 | ||||||
| chr2:174812695
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.713-213G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812695 | ||||||
| chr2:174812768
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.713-286T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812768 | ||||||
| chr2:174812796
|
A | T | 274 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.713-314T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812796 | ||||||
| chr2:174812836
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-354A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812836 | ||||||
| chr2:174812864
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.713-382A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812864 | ||||||
| chr2:174812913
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-431C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812913 | ||||||
| chr2:174812969
|
A | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-487T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174812969 | ||||||
| chr2:174813130
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-648A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813130 | ||||||
| chr2:174813179
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.713-697T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813179 | ||||||
| chr2:174813677
|
A | T | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.713-1195T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813677 | ||||||
| chr2:174813708
|
T | C | 1 | a0001c0001t0003g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.713-1226A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813708 | ||||||
| chr2:174813808
|
A | G | 3 | a0001c0001t0006g0038a0001c0001t0006g0040a0001c0001t0006g0041 | 3 | HG02258.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.713-1326T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813808 | ||||||
| chr2:174813924
|
G | A | 8 | a0001c0001t0002g0099a0001c0001t0002g0107a0001c0001t0002g0111others(5): Show | 8 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-1442C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174813924 | ||||||
| chr2:174814431
|
C | T | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-1949G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174814431 | ||||||
| chr2:174814485
|
TTTATATC | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.713-2010_713-2004d others(9): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174814485 | ||||||
| chr2:174814501
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.713-2019G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174814501 | ||||||
| chr2:174814742
|
A | T | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.713-2260T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174814742 | ||||||
| chr2:174815084
|
T | A | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.713-2602A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815084 | ||||||
| chr2:174815225
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.713-2743T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815225 | ||||||
| chr2:174815235
|
G | A | 2 | a0001c0001t0004g0266a0001c0001t0016g0267 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.713-2753C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815235 | ||||||
| chr2:174815280
|
T | A | 158 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.713-2798A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815280 | ||||||
| chr2:174815403
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713-2921T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815403 | ||||||
| chr2:174815580
|
G | T | 150 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.713-3098C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815580 | ||||||
| chr2:174815589
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0002g0118a0001c0001t0002g0182others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.713-3108dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815589 | ||||||
| chr2:174815589
|
CT | C | 43 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(40): Show | 43 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.713-3108delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815589 | ||||||
| chr2:174815700
|
C | T | 144 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.713-3218G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815700 | ||||||
| chr2:174815783
|
T | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(21): Show | 24 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.713-3301A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815783 | ||||||
| chr2:174815800
|
G | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-3318C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815800 | ||||||
| chr2:174815863
|
A | C | 1 | a0001c0001t0002g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.713-3381T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815863 | ||||||
| chr2:174815936
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-3454A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174815936 | ||||||
| chr2:174816013
|
G | C | 100 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.713-3531C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816013 | ||||||
| chr2:174816138
|
C | CA | 99 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.713-3657dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816138 | ||||||
| chr2:174816177
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-3695G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816177 | ||||||
| chr2:174816210
|
C | T | 99 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.713-3728G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816210 | ||||||
| chr2:174816249
|
C | T | 2 | a0001c0001t0004g0262a0001c0001t0004g0263 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.713-3767G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816249 | ||||||
| chr2:174816372
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0228 | 2 | HG00639.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.713-3890C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816372 | ||||||
| chr2:174816441
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-3959C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816441 | ||||||
| chr2:174816497
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.713-4015A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816497 | ||||||
| chr2:174816716
|
A | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-4234T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816716 | ||||||
| chr2:174816778
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.713-4296G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816778 | ||||||
| chr2:174816810
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.713-4328G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174816810 | ||||||
| chr2:174817178
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-4696G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817178 | ||||||
| chr2:174817275
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.713-4793A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817275 | ||||||
| chr2:174817287
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.713-4805G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817287 | ||||||
| chr2:174817430
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.713-4948G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817430 | ||||||
| chr2:174817456
|
A | T | 1 | a0001c0001t0002g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.713-4974T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817456 | ||||||
| chr2:174817464
|
AT | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0123a0001c0001t0001g0127others(8): Show | 11 | HG00609.hp2 HG01517.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.713-4983delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817464 | ||||||
| chr2:174817627
|
G | A | 154 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.713-5145C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817627 | ||||||
| chr2:174817638
|
C | CT | 10 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0181others(7): Show | 10 | HG02257.hp1 HG02559.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-5157dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817638 | ||||||
| chr2:174817638
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.713-5156G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817638 | ||||||
| chr2:174817648
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.713-5166A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817648 | ||||||
| chr2:174817660
|
C | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.713-5178G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817660 | ||||||
| chr2:174817858
|
C | T | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.713-5376G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817858 | ||||||
| chr2:174817883
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.713-5401G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817883 | ||||||
| chr2:174817932
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-5450G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817932 | ||||||
| chr2:174817936
|
C | T | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.713-5454G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174817936 | ||||||
| chr2:174818198
|
T | C | 4 | a0001c0001t0001g0105a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18951.hp1 NA18978.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-5716A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818198 | ||||||
| chr2:174818233
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-5751C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818233 | ||||||
| chr2:174818528
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.712+5906T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818528 | ||||||
| chr2:174818607
|
ATTTTTAT others(21): Show |
A | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.712+5799_712+5826d others(30): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818607 | ||||||
| chr2:174818723
|
A | G | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.712+5711T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818723 | ||||||
| chr2:174818775
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+5659A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818775 | ||||||
| chr2:174818878
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+5556A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818878 | ||||||
| chr2:174818898
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.712+5536A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818898 | ||||||
| chr2:174818918
|
CTTTATG | C | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.712+5510_712+5515d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174818918 | ||||||
| chr2:174819015
|
GT | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+5418delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819015 | ||||||
| chr2:174819016
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.712+5418A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819016 | ||||||
| chr2:174819119
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+5315A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819119 | ||||||
| chr2:174819207
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.712+5227G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819207 | ||||||
| chr2:174819351
|
T | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.712+5083A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819351 | ||||||
| chr2:174819414
|
A | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+5020T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819414 | ||||||
| chr2:174819432
|
A | T | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.712+5002T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819432 | ||||||
| chr2:174819511
|
A | C | 1 | a0001c0001t0001g0200 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.712+4923T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819511 | ||||||
| chr2:174819667
|
TA | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0004g0273others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.712+4766delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819667 | ||||||
| chr2:174819693
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.712+4741A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819693 | ||||||
| chr2:174819753
|
T | C | 31 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(28): Show | 31 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.712+4681A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819753 | ||||||
| chr2:174819762
|
T | C | 31 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(28): Show | 31 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.712+4672A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819762 | ||||||
| chr2:174819934
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.712+4500C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819934 | ||||||
| chr2:174819973
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0173 | 3 | HG02027.hp1 NA18943.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.712+4461C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174819973 | ||||||
| chr2:174820096
|
C | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+4338G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174820096 | ||||||
| chr2:174820378
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.712+4056C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174820378 | ||||||
| chr2:174820701
|
G | A | 13 | a0001c0001t0006g0031a0001c0001t0006g0034a0001c0001t0006g0038others(10): Show | 13 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.712+3733C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174820701 | ||||||
| chr2:174821281
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.712+3153T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174821281 | ||||||
| chr2:174822028
|
A | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+2406T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822028 | ||||||
| chr2:174822191
|
C | G | 1 | a0002c0002t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.712+2243G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822191 | ||||||
| chr2:174822414
|
C | T | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.712+2020G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822414 | ||||||
| chr2:174822525
|
T | C | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.712+1909A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822525 | ||||||
| chr2:174822709
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0247 | 2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.712+1725G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822709 | ||||||
| chr2:174822718
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.712+1716A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822718 | ||||||
| chr2:174822765
|
C | G | 5 | a0001c0001t0002g0117a0001c0001t0002g0160a0001c0001t0002g0161others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+1669G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822765 | ||||||
| chr2:174822865
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+1569C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822865 | ||||||
| chr2:174822977
|
C | T | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.712+1457G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174822977 | ||||||
| chr2:174823318
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.712+1116T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823318 | ||||||
| chr2:174823379
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.712+1055A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823379 | ||||||
| chr2:174823435
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.712+999C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823435 | ||||||
| chr2:174823446
|
G | C | 1 | a0001c0001t0003g0011 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.712+988C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823446 | ||||||
| chr2:174823479
|
T | A | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712+955A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823479 | ||||||
| chr2:174823523
|
T | C | 155 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.712+911A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823523 | ||||||
| chr2:174823539
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.712+895A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823539 | ||||||
| chr2:174823619
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0136a0001c0001t0001g0158 | 3 | NA18944.hp2 NA18995.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.712+815G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823619 | ||||||
| chr2:174823649
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+785A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823649 | ||||||
| chr2:174823664
|
G | GA | 8 | a0001c0001t0001g0046a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+769dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823664 | ||||||
| chr2:174823664
|
GA | G | 17 | a0001c0001t0001g0148a0001c0001t0002g0082a0001c0001t0003g0024others(14): Show | 17 | HG01168.hp1 HG01361.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.712+769delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823664 | ||||||
| chr2:174823980
|
C | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.712+454G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174823980 | ||||||
| chr2:174824147
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712+287C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174824147 | ||||||
| chr2:174824314
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.712+120A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 8/12 | chr2 | 174824314 | ||||||
| chr2:174824521
|
G | GA | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.628-4dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824521 | ||||||
| chr2:174824614
|
C | CTA | 3 | a0001c0001t0001g0126a0001c0001t0011g0054a0001c0001t0013g0121 | 3 | HG02015.hp1 HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.628-98_628-97dupTA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824614 | ||||||
| chr2:174824614
|
C | CTATA | 97 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.628-100_628-97dupT others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824614 | ||||||
| chr2:174824614
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0255 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.628-106_628-97dupT others(9): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824614 | ||||||
| chr2:174824614
|
CTA | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-98_628-97delTA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824614 | ||||||
| chr2:174824680
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-162C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824680 | ||||||
| chr2:174824757
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-239G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824757 | ||||||
| chr2:174824761
|
C | T | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-243G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824761 | ||||||
| chr2:174824927
|
C | T | 1 | a0001c0001t0005g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.628-409G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174824927 | ||||||
| chr2:174825087
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.628-569G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825087 | ||||||
| chr2:174825314
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-796A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825314 | ||||||
| chr2:174825495
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-977G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825495 | ||||||
| chr2:174825496
|
C | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-978G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825496 | ||||||
| chr2:174825581
|
A | C | 100 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.628-1063T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825581 | ||||||
| chr2:174825692
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.628-1174G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825692 | ||||||
| chr2:174825700
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-1182T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825700 | ||||||
| chr2:174825875
|
C | T | 1 | a0001c0001t0004g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.628-1357G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174825875 | ||||||
| chr2:174826501
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0172 | 3 | HG02572.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.628-1983C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826501 | ||||||
| chr2:174826535
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.628-2017C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826535 | ||||||
| chr2:174826549
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2031A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826549 | ||||||
| chr2:174826624
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628-2106C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826624 | ||||||
| chr2:174826646
|
T | C | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.628-2128A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826646 | ||||||
| chr2:174826868
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.628-2350T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826868 | ||||||
| chr2:174826931
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-2413C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826931 | ||||||
| chr2:174826936
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.628-2418C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174826936 | ||||||
| chr2:174827127
|
G | A | 4 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2609C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827127 | ||||||
| chr2:174827159
|
T | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0225others(1): Show | 4 | HG01168.hp2 HG03654.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-2641A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827159 | ||||||
| chr2:174827217
|
T | C | 156 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.628-2699A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827217 | ||||||
| chr2:174827687
|
C | T | 3 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264 | 3 | HG02886.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628-3169G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827687 | ||||||
| chr2:174827750
|
A | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-3232T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827750 | ||||||
| chr2:174827767
|
C | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0144a0001c0001t0005g0176 | 3 | HG02683.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.628-3249G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827767 | ||||||
| chr2:174827811
|
T | C | 18 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.628-3293A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174827811 | ||||||
| chr2:174828187
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-3669C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174828187 | ||||||
| chr2:174828276
|
G | C | 6 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(3): Show | 6 | NA18943.hp1 NA18965.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-3758C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174828276 | ||||||
| chr2:174828712
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0128a0001c0001t0001g0133 | 3 | NA18956.hp1 NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.628-4194A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174828712 | ||||||
| chr2:174829007
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.628-4489A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829007 | ||||||
| chr2:174829276
|
T | C | 15 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 15 | HG00423.hp2 HG00438.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.628-4758A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829276 | ||||||
| chr2:174829345
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.628-4827C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829345 | ||||||
| chr2:174829636
|
T | C | 38 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(35): Show | 38 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.628-5118A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829636 | ||||||
| chr2:174829647
|
C | T | 60 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.628-5129G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829647 | ||||||
| chr2:174829721
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.628-5203T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829721 | ||||||
| chr2:174829799
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-5281C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829799 | ||||||
| chr2:174829968
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-5450A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829968 | ||||||
| chr2:174829999
|
G | A | 3 | a0001c0001t0007g0030a0001c0001t0007g0033a0001c0001t0007g0035 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.628-5481C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174829999 | ||||||
| chr2:174830002
|
C | T | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.628-5484G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830002 | ||||||
| chr2:174830101
|
C | T | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.628-5583G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830101 | ||||||
| chr2:174830232
|
C | CA | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.628-5715dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830232 | ||||||
| chr2:174830328
|
A | C | 3 | a0001c0001t0007g0030a0001c0001t0007g0033a0001c0001t0007g0035 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.628-5810T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830328 | ||||||
| chr2:174830509
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.628-5991G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830509 | ||||||
| chr2:174830971
|
G | T | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-6453C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830971 | ||||||
| chr2:174830983
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00609.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.628-6465A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174830983 | ||||||
| chr2:174831148
|
T | C | 1 | a0001c0001t0013g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.628-6630A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174831148 | ||||||
| chr2:174831193
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-6675T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174831193 | ||||||
| chr2:174831562
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.628-7044A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174831562 | ||||||
| chr2:174831894
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.628-7376T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174831894 | ||||||
| chr2:174831997
|
C | A | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.628-7479G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174831997 | ||||||
| chr2:174832045
|
C | A | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.628-7527G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174832045 | ||||||
| chr2:174832067
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-7549A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174832067 | ||||||
| chr2:174832402
|
G | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-7884C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174832402 | ||||||
| chr2:174833262
|
A | G | 12 | a0001c0001t0005g0068a0001c0001t0005g0089a0001c0001t0005g0090others(9): Show | 12 | HG00423.hp2 HG01433.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-8744T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833262 | ||||||
| chr2:174833328
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.628-8810A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833328 | ||||||
| chr2:174833417
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-8899G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833417 | ||||||
| chr2:174833620
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628-9102T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833620 | ||||||
| chr2:174833687
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.628-9169A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833687 | ||||||
| chr2:174833795
|
C | CT | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-9278dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833795 | ||||||
| chr2:174833795
|
CT | C | 254 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.628-9278delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833795 | ||||||
| chr2:174833918
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.628-9400G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174833918 | ||||||
| chr2:174834145
|
G | T | 39 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(36): Show | 39 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.628-9627C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174834145 | ||||||
| chr2:174834233
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628-9715G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174834233 | ||||||
| chr2:174834239
|
G | T | 60 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.628-9721C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174834239 | ||||||
| chr2:174834320
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628-9802T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174834320 | ||||||
| chr2:174834616
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628-10098A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174834616 | ||||||
| chr2:174835069
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-10551A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835069 | ||||||
| chr2:174835161
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.628-10643A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835161 | ||||||
| chr2:174835247
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-10729C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835247 | ||||||
| chr2:174835316
|
T | G | 1 | a0001c0001t0004g0273 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.628-10798A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835316 | ||||||
| chr2:174835573
|
AT | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0126others(2): Show | 5 | HG02015.hp1 HG02895.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-11056delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835573 | ||||||
| chr2:174835594
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.628-11076G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835594 | ||||||
| chr2:174835718
|
C | T | 1 | a0001c0001t0005g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.627+11162G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835718 | ||||||
| chr2:174835845
|
A | AT | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+11034dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835845 | ||||||
| chr2:174835872
|
C | T | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.627+11008G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835872 | ||||||
| chr2:174835915
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.627+10965T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174835915 | ||||||
| chr2:174836002
|
G | A | 1 | a0001c0001t0005g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.627+10878C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836002 | ||||||
| chr2:174836319
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.627+10561A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836319 | ||||||
| chr2:174836395
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627+10485A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836395 | ||||||
| chr2:174836439
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+10441G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836439 | ||||||
| chr2:174836656
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.627+10224T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836656 | ||||||
| chr2:174836969
|
C | G | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+9911G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174836969 | ||||||
| chr2:174837225
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+9655G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174837225 | ||||||
| chr2:174837227
|
C | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+9653G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174837227 | ||||||
| chr2:174837409
|
C | T | 14 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 14 | HG00423.hp2 HG00438.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+9471G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174837409 | ||||||
| chr2:174837595
|
G | A | 39 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(36): Show | 39 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.627+9285C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174837595 | ||||||
| chr2:174837864
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.627+9016G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174837864 | ||||||
| chr2:174838037
|
C | T | 1 | a0001c0001t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.627+8843G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838037 | ||||||
| chr2:174838048
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.627+8832C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838048 | ||||||
| chr2:174838251
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG01891.hp2 HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.627+8629C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838251 | ||||||
| chr2:174838281
|
C | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0136 | 2 | NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.627+8599G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838281 | ||||||
| chr2:174838282
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0136 | 2 | NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.627+8598T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838282 | ||||||
| chr2:174838283
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0136 | 2 | NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.627+8597T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838283 | ||||||
| chr2:174838294
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0136 | 2 | NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.627+8586A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838294 | ||||||
| chr2:174838647
|
C | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+8233G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838647 | ||||||
| chr2:174838661
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.627+8219G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838661 | ||||||
| chr2:174838699
|
T | G | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.627+8181A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838699 | ||||||
| chr2:174838813
|
A | G | 154 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.627+8067T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838813 | ||||||
| chr2:174838878
|
T | G | 154 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.627+8002A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838878 | ||||||
| chr2:174838954
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.627+7926A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838954 | ||||||
| chr2:174838992
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.627+7888G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838992 | ||||||
| chr2:174838996
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627+7884C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174838996 | ||||||
| chr2:174839016
|
T | TA | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+7863dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839016 | ||||||
| chr2:174839016
|
TA | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0181a0001c0001t0001g0208others(4): Show | 7 | HG01496.hp2 HG01517.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+7863delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839016 | ||||||
| chr2:174839185
|
A | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627+7695T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839185 | ||||||
| chr2:174839236
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+7644A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839236 | ||||||
| chr2:174839242
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+7638A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839242 | ||||||
| chr2:174839254
|
G | A | 61 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.627+7626C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839254 | ||||||
| chr2:174839284
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+7596A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839284 | ||||||
| chr2:174839604
|
A | AT | 23 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0154others(20): Show | 23 | HG00558.hp1 HG01361.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.627+7275dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839604 | ||||||
| chr2:174839957
|
A | AC | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.627+6922_627+6923i others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839957 | ||||||
| chr2:174839958
|
A | C | 11 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0184others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+6922T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839958 | ||||||
| chr2:174839997
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0136 | 2 | NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.627+6883C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174839997 | ||||||
| chr2:174840109
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.627+6771A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840109 | ||||||
| chr2:174840161
|
C | CT | 89 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0096others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.627+6718dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840161 | ||||||
| chr2:174840161
|
C | CTT | 18 | a0001c0001t0001g0097a0001c0001t0001g0120a0001c0001t0001g0200others(15): Show | 18 | HG01361.hp2 HG02055.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.627+6717_627+6718d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840161 | ||||||
| chr2:174840161
|
CT | C | 16 | a0001c0001t0001g0067a0001c0001t0001g0147a0001c0001t0001g0168others(13): Show | 16 | HG00280.hp2 HG00558.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.627+6718delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840161 | ||||||
| chr2:174840161
|
CTT | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(25): Show | 28 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.627+6717_627+6718d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840161 | ||||||
| chr2:174840161
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+6709_627+6718d others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840161 | ||||||
| chr2:174840293
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+6587A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840293 | ||||||
| chr2:174840379
|
T | C | 275 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.627+6501A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840379 | ||||||
| chr2:174840465
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.627+6415G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840465 | ||||||
| chr2:174840479
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.627+6401T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840479 | ||||||
| chr2:174840588
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.627+6292A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840588 | ||||||
| chr2:174840717
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.627+6163G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840717 | ||||||
| chr2:174840897
|
T | C | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.627+5983A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840897 | ||||||
| chr2:174840949
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+5931C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174840949 | ||||||
| chr2:174841034
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+5846G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841034 | ||||||
| chr2:174841072
|
T | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+5808A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841072 | ||||||
| chr2:174841220
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.627+5660G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841220 | ||||||
| chr2:174841301
|
C | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+5579G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841301 | ||||||
| chr2:174841438
|
A | G | 4 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+5442T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841438 | ||||||
| chr2:174841492
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+5388A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841492 | ||||||
| chr2:174841532
|
C | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.627+5348G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841532 | ||||||
| chr2:174841643
|
T | G | 1 | a0001c0001t0003g0021 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.627+5237A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841643 | ||||||
| chr2:174841804
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0011g0054 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.627+5076C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841804 | ||||||
| chr2:174841914
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.627+4966A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174841914 | ||||||
| chr2:174842001
|
C | T | 98 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.627+4879G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842001 | ||||||
| chr2:174842173
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+4707A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842173 | ||||||
| chr2:174842351
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+4529A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842351 | ||||||
| chr2:174842373
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0011g0054 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.627+4507A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842373 | ||||||
| chr2:174842549
|
AATT | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.627+4328_627+4330d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842549 | ||||||
| chr2:174842817
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.627+4063A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174842817 | ||||||
| chr2:174843089
|
C | T | 90 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.627+3791G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843089 | ||||||
| chr2:174843228
|
A | ATTAT | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+3648_627+3651d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843228 | ||||||
| chr2:174843438
|
C | T | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.627+3442G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843438 | ||||||
| chr2:174843576
|
C | G | 138 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0044others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.627+3304G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843576 | ||||||
| chr2:174843699
|
GA | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.627+3180delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843699 | ||||||
| chr2:174843721
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.627+3159C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843721 | ||||||
| chr2:174843729
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.627+3151A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843729 | ||||||
| chr2:174843764
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0011g0054 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.627+3116T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843764 | ||||||
| chr2:174843830
|
T | TAATAAGC others(335): Show |
1 | a0001c0001t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.627+3049_627+3050i others(344): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843830 | ||||||
| chr2:174843974
|
C | CTG | 96 | a0001c0001t0001g0028a0001c0001t0001g0094a0001c0001t0001g0095others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.627+2904_627+2905d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843974 | ||||||
| chr2:174843974
|
C | CTGTG | 7 | a0001c0001t0001g0036a0001c0001t0001g0204a0001c0001t0001g0228others(4): Show | 7 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+2902_627+2905d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174843974 | ||||||
| chr2:174844165
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.627+2715A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844165 | ||||||
| chr2:174844199
|
G | GA | 6 | a0001c0001t0004g0263a0001c0001t0005g0068a0001c0001t0005g0089others(3): Show | 6 | HG00423.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+2680dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844199 | ||||||
| chr2:174844199
|
GAA | G | 98 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.627+2679_627+2680d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844199 | ||||||
| chr2:174844561
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.627+2319G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844561 | ||||||
| chr2:174844589
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.627+2291T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844589 | ||||||
| chr2:174844649
|
C | T | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(1): Show | 4 | HG01069.hp1 HG01070.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2231G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844649 | ||||||
| chr2:174844840
|
T | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.627+2040A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844840 | ||||||
| chr2:174844919
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+1961T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174844919 | ||||||
| chr2:174845106
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.627+1774G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845106 | ||||||
| chr2:174845329
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+1551C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845329 | ||||||
| chr2:174845470
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.627+1410G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845470 | ||||||
| chr2:174845513
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.627+1367A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845513 | ||||||
| chr2:174845692
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.627+1188T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845692 | ||||||
| chr2:174845703
|
T | C | 1 | a0001c0001t0003g0004 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.627+1177A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845703 | ||||||
| chr2:174845780
|
G | GT | 3 | a0001c0001t0001g0139a0001c0001t0001g0159a0001c0001t0001g0220 | 3 | HG02129.hp2 NA18948.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.627+1099dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845780 | ||||||
| chr2:174845781
|
T | TG | 37 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0102others(34): Show | 37 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.627+1098dupC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845781 | ||||||
| chr2:174845781
|
TG | T | 125 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0044others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.627+1098delC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845781 | ||||||
| chr2:174845785
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.627+1095C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845785 | ||||||
| chr2:174845791
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.627+1089C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845791 | ||||||
| chr2:174845861
|
A | C | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.627+1019T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845861 | ||||||
| chr2:174845900
|
CTGAATAA others(4): Show |
C | 1 | a0001c0001t0001g0165 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.627+969_627+979del others(11): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174845900 | ||||||
| chr2:174846062
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627+818A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174846062 | ||||||
| chr2:174846088
|
T | G | 1 | a0001c0001t0004g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.627+792A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 7/12 | chr2 | 174846088 | ||||||
| chr2:174847097
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.550-140C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847097 | ||||||
| chr2:174847214
|
C | T | 120 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0042others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.550-257G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847214 | ||||||
| chr2:174847395
|
AAAAG | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG03209.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.550-442_550-439del others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847395 | ||||||
| chr2:174847437
|
CTCTT | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0254 | 3 | HG02559.hp1 NA19081.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.550-484_550-481del others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847437 | ||||||
| chr2:174847582
|
A | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-625T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847582 | ||||||
| chr2:174847773
|
C | CA | 44 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0088others(41): Show | 44 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.550-817dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAA | 6 | a0001c0001t0001g0051a0001c0001t0001g0146a0001c0001t0001g0156others(3): Show | 6 | HG02486.hp1 HG02698.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-818_550-817dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0053others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-824_550-817dup others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0006g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.550-827_550-817dup others(11): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0006g0027a0001c0001t0006g0049 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.550-829_550-817dup others(13): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0006g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.550-831_550-817dup others(15): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.550-834_550-817dup others(18): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.550-835_550-817dup others(19): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0006g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.550-836_550-817dup others(20): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0008g0032 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.550-837_550-817dup others(21): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0184a0001c0001t0008g0029 | 2 | HG03209.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.550-838_550-817dup others(22): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0006g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.550-839_550-817dup others(23): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0006g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.550-842_550-817dup others(26): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.550-817_550-816ins others(30): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.550-817_550-816ins others(34): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
CAAA | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0195a0001c0001t0001g0206others(9): Show | 12 | HG01255.hp2 HG02258.hp2 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-819_550-817del others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
CAAAA | C | 89 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0055others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.550-820_550-817del others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
CAAAAA | C | 9 | a0001c0001t0001g0211a0001c0001t0004g0262a0001c0001t0004g0263others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-821_550-817del others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847773
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.550-831_550-817del others(15): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847773 | ||||||
| chr2:174847959
|
T | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1002A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174847959 | ||||||
| chr2:174848039
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.550-1082A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848039 | ||||||
| chr2:174848217
|
A | C | 1 | a0001c0001t0010g0002 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.550-1260T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848217 | ||||||
| chr2:174848396
|
ATACC | A | 91 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.550-1443_550-1440d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848396 | ||||||
| chr2:174848629
|
G | A | 5 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0007g0030others(2): Show | 5 | HG01361.hp2 HG02698.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1672C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848629 | ||||||
| chr2:174848700
|
C | T | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.550-1743G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848700 | ||||||
| chr2:174848751
|
C | A | 2 | a0001c0001t0003g0006a0001c0001t0003g0024 | 2 | NA18987.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.550-1794G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174848751 | ||||||
| chr2:174849260
|
G | A | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.550-2303C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174849260 | ||||||
| chr2:174849746
|
C | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0163 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.550-2789G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174849746 | ||||||
| chr2:174849884
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.550-2927T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174849884 | ||||||
| chr2:174850066
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-3109C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174850066 | ||||||
| chr2:174850393
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.550-3436A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174850393 | ||||||
| chr2:174850424
|
T | C | 1 | a0001c0001t0003g0010 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.550-3467A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174850424 | ||||||
| chr2:174850802
|
G | T | 1 | a0001c0001t0014g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.550-3845C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174850802 | ||||||
| chr2:174851049
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.550-4092T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851049 | ||||||
| chr2:174851212
|
T | C | 28 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(25): Show | 28 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.550-4255A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851212 | ||||||
| chr2:174851381
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550-4424A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851381 | ||||||
| chr2:174851415
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550-4458C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851415 | ||||||
| chr2:174851454
|
A | AT | 4 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0002g0182others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-4498dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851454 | ||||||
| chr2:174851461
|
T | C | 1 | a0001c0001t0006g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.550-4504A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851461 | ||||||
| chr2:174851655
|
C | T | 110 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.550-4698G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851655 | ||||||
| chr2:174851798
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.550-4841C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851798 | ||||||
| chr2:174851942
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.550-4985A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174851942 | ||||||
| chr2:174852083
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.550-5126G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852083 | ||||||
| chr2:174852120
|
TA | T | 93 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.550-5164delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852120 | ||||||
| chr2:174852303
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-5346C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852303 | ||||||
| chr2:174852375
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.550-5418C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852375 | ||||||
| chr2:174852411
|
T | C | 19 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0055others(16): Show | 19 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.550-5454A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852411 | ||||||
| chr2:174852538
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.550-5581G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852538 | ||||||
| chr2:174852589
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550-5632G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852589 | ||||||
| chr2:174852642
|
A | G | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.550-5685T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852642 | ||||||
| chr2:174852748
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-5791T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174852748 | ||||||
| chr2:174853055
|
C | T | 119 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.550-6098G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853055 | ||||||
| chr2:174853112
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0122 | 2 | NA19000.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.550-6155C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853112 | ||||||
| chr2:174853326
|
TGACA | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.550-6373_550-6370d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853326 | ||||||
| chr2:174853489
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.550-6532T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853489 | ||||||
| chr2:174853749
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.550-6792A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853749 | ||||||
| chr2:174853774
|
A | T | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275 | 3 | HG02630.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.550-6817T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853774 | ||||||
| chr2:174853857
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.550-6900A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174853857 | ||||||
| chr2:174854319
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-7362T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174854319 | ||||||
| chr2:174855262
|
G | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-8305C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174855262 | ||||||
| chr2:174855272
|
C | T | 2 | a0001c0001t0005g0100a0001c0001t0005g0101 | 2 | HG02071.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.550-8315G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174855272 | ||||||
| chr2:174855750
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.550-8793C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174855750 | ||||||
| chr2:174855784
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0219 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.550-8827T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174855784 | ||||||
| chr2:174856174
|
G | A | 1 | a0001c0001t0008g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.550-9217C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856174 | ||||||
| chr2:174856199
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.550-9242C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856199 | ||||||
| chr2:174856503
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.550-9546A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856503 | ||||||
| chr2:174856604
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0225others(1): Show | 4 | HG01168.hp2 HG03654.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-9647A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856604 | ||||||
| chr2:174856627
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.550-9670A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856627 | ||||||
| chr2:174856645
|
T | C | 2 | a0001c0001t0002g0075a0001c0001t0002g0077 | 2 | NA18979.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.550-9688A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856645 | ||||||
| chr2:174856686
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.550-9729C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174856686 | ||||||
| chr2:174857390
|
A | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-10433T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174857390 | ||||||
| chr2:174857456
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.550-10499C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174857456 | ||||||
| chr2:174857641
|
A | C | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.550-10684T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174857641 | ||||||
| chr2:174857672
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.550-10715A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174857672 | ||||||
| chr2:174858194
|
C | T | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-11237G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858194 | ||||||
| chr2:174858416
|
G | A | 26 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(23): Show | 26 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.550-11459C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858416 | ||||||
| chr2:174858434
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA19081.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.550-11477C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858434 | ||||||
| chr2:174858677
|
A | C | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.550-11720T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858677 | ||||||
| chr2:174858764
|
C | G | 111 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.550-11807G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858764 | ||||||
| chr2:174858979
|
T | TAC | 18 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0092others(15): Show | 18 | HG00558.hp1 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.550-12024_550-1202 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACAC | 3 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0002g0118 | 3 | HG02451.hp1 NA18995.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.550-12026_550-1202 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACAC | 5 | a0001c0001t0001g0044a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01496.hp2 HG03017.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-12028_550-1202 others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0094others(3): Show | 6 | HG03540.hp2 HG03579.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-12030_550-1202 others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(3): Show |
92 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.550-12032_550-1202 others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0098a0001c0001t0001g0205a0001c0001t0001g0223others(5): Show | 8 | HG01168.hp2 HG02735.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-12034_550-1202 others(16): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(7): Show |
14 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0066others(11): Show | 14 | HG01361.hp2 HG02300.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.550-12036_550-1202 others(18): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(9): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.550-12038_550-1202 others(20): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.550-12040_550-1202 others(22): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(13): Show |
1 | a0001c0001t0001g0259 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.550-12042_550-1202 others(24): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-12044_550-1202 others(26): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174858979
|
T | TACACACA others(17): Show |
1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.550-12046_550-1202 others(28): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174858979 | ||||||
| chr2:174859343
|
T | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.550-12386A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859343 | ||||||
| chr2:174859374
|
G | A | 134 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0046others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.550-12417C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859374 | ||||||
| chr2:174859621
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.550-12664A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859621 | ||||||
| chr2:174859803
|
G | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0147 | 2 | HG00280.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.550-12846C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859803 | ||||||
| chr2:174859831
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.550-12874T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859831 | ||||||
| chr2:174859866
|
T | C | 18 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0181others(15): Show | 18 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.550-12909A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859866 | ||||||
| chr2:174859883
|
G | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.550-12926C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174859883 | ||||||
| chr2:174860090
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.550-13133A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860090 | ||||||
| chr2:174860179
|
T | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-13222A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860179 | ||||||
| chr2:174860310
|
C | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.550-13353G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860310 | ||||||
| chr2:174860333
|
A | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.550-13376T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860333 | ||||||
| chr2:174860397
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-13440A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860397 | ||||||
| chr2:174860399
|
A | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-13442T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860399 | ||||||
| chr2:174860472
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.550-13515A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860472 | ||||||
| chr2:174860626
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.550-13669A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860626 | ||||||
| chr2:174860699
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.550-13742A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860699 | ||||||
| chr2:174860711
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.550-13754C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174860711 | ||||||
| chr2:174861039
|
A | T | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.550-14082T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861039 | ||||||
| chr2:174861054
|
A | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.550-14097T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861054 | ||||||
| chr2:174861119
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.550-14162C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861119 | ||||||
| chr2:174861353
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.550-14396T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861353 | ||||||
| chr2:174861406
|
T | C | 1 | a0001c0001t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.550-14449A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861406 | ||||||
| chr2:174861447
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550-14490G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861447 | ||||||
| chr2:174861481
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-14524C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861481 | ||||||
| chr2:174861691
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550-14734C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174861691 | ||||||
| chr2:174862373
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(3): Show | 6 | HG01361.hp2 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-15416C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174862373 | ||||||
| chr2:174862393
|
C | T | 8 | a0001c0001t0002g0043a0001c0001t0002g0075a0001c0001t0002g0076others(5): Show | 8 | HG00673.hp2 HG02083.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-15436G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174862393 | ||||||
| chr2:174862426
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.549+15414C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174862426 | ||||||
| chr2:174862482
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0243 | 2 | NA19006.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.549+15358C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174862482 | ||||||
| chr2:174862851
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.549+14989A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174862851 | ||||||
| chr2:174863241
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.549+14599A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174863241 | ||||||
| chr2:174863275
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.549+14565A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174863275 | ||||||
| chr2:174863619
|
C | A | 1 | a0001c0001t0005g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.549+14221G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174863619 | ||||||
| chr2:174863972
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.549+13868A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174863972 | ||||||
| chr2:174864024
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.549+13816A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864024 | ||||||
| chr2:174864025
|
A | G | 17 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0001t0001g0170others(14): Show | 17 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.549+13815T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864025 | ||||||
| chr2:174864107
|
G | C | 1 | a0001c0001t0013g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.549+13733C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864107 | ||||||
| chr2:174864216
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.549+13624C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864216 | ||||||
| chr2:174864392
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.549+13448T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864392 | ||||||
| chr2:174864541
|
T | C | 15 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.549+13299A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864541 | ||||||
| chr2:174864642
|
G | A | 3 | a0001c0001t0002g0110a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG02109.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.549+13198C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864642 | ||||||
| chr2:174864648
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.549+13192T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864648 | ||||||
| chr2:174864720
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.549+13120A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864720 | ||||||
| chr2:174864930
|
T | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.549+12910A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174864930 | ||||||
| chr2:174865329
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.549+12511A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174865329 | ||||||
| chr2:174865566
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.549+12274G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174865566 | ||||||
| chr2:174865652
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.549+12188T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174865652 | ||||||
| chr2:174865678
|
T | C | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.549+12162A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174865678 | ||||||
| chr2:174865912
|
A | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0140a0001c0001t0001g0147 | 3 | HG00280.hp2 NA18942.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.549+11928T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174865912 | ||||||
| chr2:174866039
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.549+11801T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866039 | ||||||
| chr2:174866254
|
A | G | 18 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0181others(15): Show | 18 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.549+11586T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866254 | ||||||
| chr2:174866261
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.549+11579A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866261 | ||||||
| chr2:174866355
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.549+11485T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866355 | ||||||
| chr2:174866432
|
T | A | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275 | 3 | HG02630.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.549+11408A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866432 | ||||||
| chr2:174866620
|
G | T | 3 | a0001c0001t0001g0042a0001c0001t0002g0182a0001c0001t0011g0054 | 3 | HG02622.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.549+11220C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866620 | ||||||
| chr2:174866865
|
A | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.549+10975T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866865 | ||||||
| chr2:174866873
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.549+10967C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174866873 | ||||||
| chr2:174867060
|
AT | A | 135 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.549+10779delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867060 | ||||||
| chr2:174867078
|
A | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0004g0276 | 3 | HG01891.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.549+10762T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867078 | ||||||
| chr2:174867274
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.549+10566C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867274 | ||||||
| chr2:174867378
|
C | CA | 11 | a0001c0001t0001g0065a0001c0001t0001g0149a0001c0001t0001g0169others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.549+10461dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867378 | ||||||
| chr2:174867634
|
T | C | 96 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0001g0094others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.549+10206A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867634 | ||||||
| chr2:174867854
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.549+9986A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867854 | ||||||
| chr2:174867897
|
T | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+9943A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174867897 | ||||||
| chr2:174868115
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.549+9725C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174868115 | ||||||
| chr2:174868346
|
C | A | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.549+9494G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174868346 | ||||||
| chr2:174868551
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.549+9289A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174868551 | ||||||
| chr2:174868680
|
C | T | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+9160G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174868680 | ||||||
| chr2:174869134
|
C | T | 1 | a0001c0001t0005g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.549+8706G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869134 | ||||||
| chr2:174869389
|
A | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+8451T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869389 | ||||||
| chr2:174869505
|
G | GGA | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+8334_549+8335i others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869505 | ||||||
| chr2:174869506
|
T | C | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+8334A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869506 | ||||||
| chr2:174869507
|
C | A | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+8333G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869507 | ||||||
| chr2:174869508
|
T | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+8332A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869508 | ||||||
| chr2:174869759
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.549+8081C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869759 | ||||||
| chr2:174869767
|
G | A | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.549+8073C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869767 | ||||||
| chr2:174869806
|
C | T | 2 | a0001c0001t0007g0033a0001c0001t0007g0035 | 2 | HG01361.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.549+8034G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869806 | ||||||
| chr2:174869815
|
T | A | 1 | a0001c0001t0010g0002 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.549+8025A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174869815 | ||||||
| chr2:174870301
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+7539A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870301 | ||||||
| chr2:174870346
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.549+7494G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870346 | ||||||
| chr2:174870525
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.549+7315T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870525 | ||||||
| chr2:174870689
|
T | C | 1 | a0001c0001t0005g0091 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.549+7151A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870689 | ||||||
| chr2:174870694
|
T | TAAGCTAC others(30): Show |
1 | a0001c0001t0001g0092 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.549+7109_549+7145d others(39): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870694 | ||||||
| chr2:174870791
|
A | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.549+7049T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174870791 | ||||||
| chr2:174871020
|
C | T | 1 | a0001c0001t0004g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.549+6820G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871020 | ||||||
| chr2:174871070
|
T | C | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+6770A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871070 | ||||||
| chr2:174871112
|
GGGA | G | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+6725_549+6727d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871112 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(313): Show |
1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.549+6635_549+6636i others(322): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(314): Show |
1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.549+6635_549+6636i others(323): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(313): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0219 | 2 | HG01069.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.549+6635_549+6636i others(322): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(314): Show |
6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG01070.hp1 HG02071.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(323): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(315): Show |
1 | a0001c0001t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.549+6635_549+6636i others(324): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(301): Show |
5 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(2): Show | 5 | NA18943.hp1 NA18965.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(310): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(313): Show |
4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0255others(1): Show | 4 | HG00639.hp1 HG02055.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(322): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(314): Show |
50 | a0001c0001t0001g0036a0001c0001t0001g0193a0001c0001t0001g0194others(47): Show | 50 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(323): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(315): Show |
19 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(16): Show | 19 | HG00099.hp2 HG00423.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(324): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(316): Show |
5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0224others(2): Show | 5 | HG00438.hp1 HG00673.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+6635_549+6636i others(325): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871204
|
T | TAAAGAGG others(314): Show |
1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.549+6635_549+6636i others(323): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871204 | ||||||
| chr2:174871234
|
G | A | 1 | a0001c0001t0006g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.549+6606C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871234 | ||||||
| chr2:174871240
|
T | G | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+6600A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871240 | ||||||
| chr2:174871282
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+6558A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871282 | ||||||
| chr2:174871753
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.549+6087A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871753 | ||||||
| chr2:174871930
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.549+5910A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871930 | ||||||
| chr2:174871934
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0144a0001c0001t0005g0176 | 3 | HG02683.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.549+5906C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174871934 | ||||||
| chr2:174872118
|
C | CA | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0225others(1): Show | 4 | HG01168.hp2 HG03654.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+5721dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872118 | ||||||
| chr2:174872118
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.549+5722G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872118 | ||||||
| chr2:174872135
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.549+5705A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872135 | ||||||
| chr2:174872616
|
T | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0181a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+5224A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872616 | ||||||
| chr2:174872688
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+5152G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872688 | ||||||
| chr2:174872764
|
T | G | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.549+5076A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872764 | ||||||
| chr2:174872947
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.549+4893T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872947 | ||||||
| chr2:174872977
|
A | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+4863T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174872977 | ||||||
| chr2:174873020
|
C | CT | 141 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.549+4819dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873020 | ||||||
| chr2:174873020
|
C | CTT | 10 | a0001c0001t0001g0046a0001c0001t0004g0262a0001c0001t0004g0263others(7): Show | 10 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.549+4818_549+4819d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873020 | ||||||
| chr2:174873179
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+4661A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873179 | ||||||
| chr2:174873251
|
C | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.549+4589G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873251 | ||||||
| chr2:174873252
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.549+4588A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873252 | ||||||
| chr2:174873311
|
C | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+4529G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873311 | ||||||
| chr2:174873330
|
T | C | 93 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.549+4510A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873330 | ||||||
| chr2:174873447
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+4393C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873447 | ||||||
| chr2:174873492
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.549+4348A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873492 | ||||||
| chr2:174873709
|
A | G | 4 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+4131T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873709 | ||||||
| chr2:174873738
|
A | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.549+4102T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873738 | ||||||
| chr2:174873739
|
G | A | 113 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.549+4101C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873739 | ||||||
| chr2:174873778
|
A | C | 1 | a0001c0001t0005g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.549+4062T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873778 | ||||||
| chr2:174873832
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+4008A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873832 | ||||||
| chr2:174873895
|
C | CA | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+3944dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174873895 | ||||||
| chr2:174874107
|
C | T | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.549+3733G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874107 | ||||||
| chr2:174874128
|
T | C | 143 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.549+3712A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874128 | ||||||
| chr2:174874736
|
A | C | 1 | a0001c0001t0003g0024 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.549+3104T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874736 | ||||||
| chr2:174874746
|
T | C | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+3094A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874746 | ||||||
| chr2:174874789
|
T | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.549+3051A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874789 | ||||||
| chr2:174874872
|
C | CT | 262 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.549+2967dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874872 | ||||||
| chr2:174874872
|
C | CTT | 7 | a0001c0001t0001g0028a0001c0001t0001g0067a0001c0001t0001g0092others(4): Show | 7 | HG02809.hp2 HG03041.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+2966_549+2967d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874872 | ||||||
| chr2:174874937
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.549+2903C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174874937 | ||||||
| chr2:174875034
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.549+2806G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875034 | ||||||
| chr2:174875189
|
A | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.549+2651T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875189 | ||||||
| chr2:174875301
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.549+2539T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875301 | ||||||
| chr2:174875515
|
T | C | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.549+2325A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875515 | ||||||
| chr2:174875591
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.549+2249G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875591 | ||||||
| chr2:174875691
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.549+2149T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174875691 | ||||||
| chr2:174876234
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.549+1606A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876234 | ||||||
| chr2:174876270
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.549+1570C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876270 | ||||||
| chr2:174876325
|
C | G | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.549+1515G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876325 | ||||||
| chr2:174876400
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.549+1440C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876400 | ||||||
| chr2:174876659
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.549+1181T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876659 | ||||||
| chr2:174876838
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+1002G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174876838 | ||||||
| chr2:174877714
|
A | C | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.549+126T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174877714 | ||||||
| chr2:174877804
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0004g0265others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+36G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174877804 | ||||||
| chr2:174877819
|
T | C | 6 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 6 | NA18959.hp2 NA18966.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+21A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 6/12 | chr2 | 174877819 | ||||||
| chr2:174878152
|
T | A | 1 | a0001c0001t0005g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.261-24A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878152 | ||||||
| chr2:174878186
|
T | TA | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-59_261-58insT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878186 | ||||||
| chr2:174878187
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-59C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878187 | ||||||
| chr2:174878187
|
G | GA | 5 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG01069.hp1 HG01070.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-60dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878187 | ||||||
| chr2:174878217
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-89G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878217 | ||||||
| chr2:174878410
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-282A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878410 | ||||||
| chr2:174878528
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.261-400T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878528 | ||||||
| chr2:174878774
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-646A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878774 | ||||||
| chr2:174878825
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA19081.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.261-697C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878825 | ||||||
| chr2:174878852
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.261-724C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174878852 | ||||||
| chr2:174879019
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261-891C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879019 | ||||||
| chr2:174879070
|
C | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-942G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879070 | ||||||
| chr2:174879183
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.261-1055T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879183 | ||||||
| chr2:174879329
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.261-1201G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879329 | ||||||
| chr2:174879330
|
G | T | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.261-1202C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879330 | ||||||
| chr2:174879365
|
A | G | 1 | a0001c0001t0006g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.261-1237T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879365 | ||||||
| chr2:174879387
|
C | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 15 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.261-1259G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879387 | ||||||
| chr2:174879860
|
T | C | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.261-1732A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879860 | ||||||
| chr2:174879917
|
G | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-1789C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174879917 | ||||||
| chr2:174880008
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.261-1880C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880008 | ||||||
| chr2:174880045
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.261-1917A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880045 | ||||||
| chr2:174880472
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-2344C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880472 | ||||||
| chr2:174880503
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-2375C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880503 | ||||||
| chr2:174880536
|
C | CA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.261-2409dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880536 | ||||||
| chr2:174880590
|
T | C | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.261-2462A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880590 | ||||||
| chr2:174880709
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.261-2581T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880709 | ||||||
| chr2:174880907
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.261-2779C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174880907 | ||||||
| chr2:174881046
|
C | CA | 39 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0046others(36): Show | 39 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.261-2919dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881046 | ||||||
| chr2:174881464
|
T | C | 90 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.261-3336A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881464 | ||||||
| chr2:174881500
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.261-3372C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881500 | ||||||
| chr2:174881586
|
C | A | 1 | a0001c0001t0007g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.261-3458G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881586 | ||||||
| chr2:174881642
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-3514A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881642 | ||||||
| chr2:174881769
|
C | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261-3641G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881769 | ||||||
| chr2:174881800
|
A | T | 1 | a0001c0001t0005g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261-3672T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174881800 | ||||||
| chr2:174882035
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.261-3907G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174882035 | ||||||
| chr2:174882050
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.261-3922A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174882050 | ||||||
| chr2:174882739
|
C | T | 61 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0079others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.261-4611G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174882739 | ||||||
| chr2:174883102
|
C | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.261-4974G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883102 | ||||||
| chr2:174883300
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.261-5172T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883300 | ||||||
| chr2:174883419
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00609.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.261-5291T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883419 | ||||||
| chr2:174883845
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-5717A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883845 | ||||||
| chr2:174883922
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.261-5794T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883922 | ||||||
| chr2:174883923
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.261-5795C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883923 | ||||||
| chr2:174883965
|
C | CT | 21 | a0001c0001t0001g0135a0001c0001t0001g0154a0001c0001t0001g0177others(18): Show | 21 | HG00738.hp1 HG01517.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.261-5838dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883965 | ||||||
| chr2:174883965
|
C | CTTT | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-5840_261-5838d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883965 | ||||||
| chr2:174883986
|
T | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.261-5858A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883986 | ||||||
| chr2:174883990
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.261-5862G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174883990 | ||||||
| chr2:174884058
|
C | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-5930G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884058 | ||||||
| chr2:174884118
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.261-5990C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884118 | ||||||
| chr2:174884167
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-6039A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884167 | ||||||
| chr2:174884207
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-6079C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884207 | ||||||
| chr2:174884218
|
A | G | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.261-6090T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884218 | ||||||
| chr2:174884453
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0009g0001 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.261-6325A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884453 | ||||||
| chr2:174884563
|
A | G | 1 | a0001c0001t0005g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.261-6435T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884563 | ||||||
| chr2:174884654
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.261-6526A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884654 | ||||||
| chr2:174884739
|
G | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.261-6611C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884739 | ||||||
| chr2:174884840
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-6712T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174884840 | ||||||
| chr2:174885025
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.261-6897A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885025 | ||||||
| chr2:174885038
|
A | T | 93 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.261-6910T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885038 | ||||||
| chr2:174885103
|
T | C | 3 | a0001c0001t0002g0072a0001c0001t0002g0099a0001c0001t0003g0004 | 3 | HG00558.hp2 HG01175.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.261-6975A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885103 | ||||||
| chr2:174885104
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.261-6976C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885104 | ||||||
| chr2:174885114
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.261-6986G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885114 | ||||||
| chr2:174885115
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.261-6987T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885115 | ||||||
| chr2:174885115
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-6987T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885115 | ||||||
| chr2:174885123
|
TA | T | 10 | a0001c0001t0001g0028a0001c0001t0004g0262a0001c0001t0004g0263others(7): Show | 10 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.261-6996delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885123 | ||||||
| chr2:174885144
|
A | G | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-7016T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885144 | ||||||
| chr2:174885148
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-7020C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885148 | ||||||
| chr2:174885231
|
C | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0163others(1): Show | 4 | HG00738.hp2 HG03239.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-7103G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885231 | ||||||
| chr2:174885291
|
A | T | 27 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0051others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.261-7163T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885291 | ||||||
| chr2:174885293
|
T | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0002g0110others(6): Show | 9 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-7165A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885293 | ||||||
| chr2:174885295
|
T | A | 6 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0002g0110others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-7167A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885295 | ||||||
| chr2:174885301
|
T | G | 9 | a0001c0001t0001g0036a0001c0001t0004g0262a0001c0001t0004g0263others(6): Show | 9 | HG02809.hp1 HG02886.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-7173A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885301 | ||||||
| chr2:174885303
|
T | G | 10 | a0001c0001t0001g0036a0001c0001t0004g0262a0001c0001t0004g0263others(7): Show | 10 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.261-7175A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885303 | ||||||
| chr2:174885305
|
G | T | 149 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0042others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.261-7177C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885305 | ||||||
| chr2:174885307
|
G | T | 23 | a0001c0001t0001g0028a0001c0001t0001g0086a0001c0001t0001g0119others(20): Show | 23 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.261-7179C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885307 | ||||||
| chr2:174885434
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.261-7306A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885434 | ||||||
| chr2:174885660
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18968.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.261-7532C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885660 | ||||||
| chr2:174885973
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.261-7845T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174885973 | ||||||
| chr2:174886141
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.261-8013C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886141 | ||||||
| chr2:174886202
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.261-8074G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886202 | ||||||
| chr2:174886349
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0132 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.261-8221T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886349 | ||||||
| chr2:174886456
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.261-8328G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886456 | ||||||
| chr2:174886778
|
A | C | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.261-8650T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886778 | ||||||
| chr2:174886956
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.261-8828G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174886956 | ||||||
| chr2:174887010
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.261-8882G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887010 | ||||||
| chr2:174887048
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.261-8920G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887048 | ||||||
| chr2:174887129
|
A | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-9001T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887129 | ||||||
| chr2:174887316
|
TAAC | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-9191_261-9189d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887316 | ||||||
| chr2:174887396
|
T | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.261-9268A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887396 | ||||||
| chr2:174887424
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261-9296A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887424 | ||||||
| chr2:174887448
|
T | C | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261-9320A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887448 | ||||||
| chr2:174887586
|
G | T | 1 | a0001c0001t0003g0016 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.261-9458C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887586 | ||||||
| chr2:174887671
|
G | A | 1 | a0002c0002t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.261-9543C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887671 | ||||||
| chr2:174887778
|
G | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-9650C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887778 | ||||||
| chr2:174887870
|
A | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-9742T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174887870 | ||||||
| chr2:174888424
|
G | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-10296C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174888424 | ||||||
| chr2:174888632
|
G | C | 1 | a0001c0001t0006g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.261-10504C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174888632 | ||||||
| chr2:174888739
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.261-10611C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174888739 | ||||||
| chr2:174888838
|
A | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0229a0001c0001t0001g0232others(3): Show | 6 | NA18951.hp2 NA18956.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-10710T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174888838 | ||||||
| chr2:174888848
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.261-10720G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174888848 | ||||||
| chr2:174889200
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.261-11072C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889200 | ||||||
| chr2:174889272
|
G | GT | 17 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.261-11145dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889272 | ||||||
| chr2:174889272
|
GT | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-11145delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889272 | ||||||
| chr2:174889539
|
A | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.261-11411T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889539 | ||||||
| chr2:174889881
|
A | ATG | 14 | a0001c0001t0001g0028a0001c0001t0001g0146a0001c0001t0001g0255others(11): Show | 14 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.261-11755_261-1175 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889881 | ||||||
| chr2:174889881
|
ATG | A | 3 | a0001c0001t0001g0179a0001c0001t0005g0068a0001c0001t0008g0032 | 3 | HG02300.hp2 HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261-11755_261-1175 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889881 | ||||||
| chr2:174889905
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.261-11777C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889905 | ||||||
| chr2:174889906
|
C | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261-11778G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889906 | ||||||
| chr2:174889977
|
AC | A | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-11850delG | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174889977 | ||||||
| chr2:174890552
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.261-12424A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174890552 | ||||||
| chr2:174890849
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.261-12721T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174890849 | ||||||
| chr2:174890882
|
C | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-12754G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174890882 | ||||||
| chr2:174890980
|
CA | C | 131 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0046others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.261-12853delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174890980 | ||||||
| chr2:174891089
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.261-12961G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891089 | ||||||
| chr2:174891140
|
C | CA | 18 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0165others(15): Show | 18 | HG00609.hp1 HG01175.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-13013dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891140 | ||||||
| chr2:174891140
|
CA | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0169others(19): Show | 22 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.261-13013delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891140 | ||||||
| chr2:174891140
|
CAAAAAAA | C | 18 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(15): Show | 18 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-13019_261-1301 others(11): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891140 | ||||||
| chr2:174891160
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261-13032T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891160 | ||||||
| chr2:174891294
|
G | A | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.261-13166C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891294 | ||||||
| chr2:174891311
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.261-13183G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891311 | ||||||
| chr2:174891369
|
A | C | 1 | a0001c0001t0003g0005 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.261-13241T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891369 | ||||||
| chr2:174891528
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.261-13400G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891528 | ||||||
| chr2:174891765
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.261-13637A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891765 | ||||||
| chr2:174891785
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.261-13657T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174891785 | ||||||
| chr2:174892021
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.261-13893T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892021 | ||||||
| chr2:174892022
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.261-13894G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892022 | ||||||
| chr2:174892201
|
C | G | 1 | a0001c0001t0003g0022 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.261-14073G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892201 | ||||||
| chr2:174892316
|
A | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0227others(1): Show | 4 | HG00639.hp1 HG03490.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-14188T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892316 | ||||||
| chr2:174892339
|
T | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(14): Show | 17 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.261-14211A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892339 | ||||||
| chr2:174892384
|
C | G | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261-14256G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892384 | ||||||
| chr2:174892817
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.261-14689A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892817 | ||||||
| chr2:174892944
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.261-14816G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174892944 | ||||||
| chr2:174893394
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-15266G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174893394 | ||||||
| chr2:174893675
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.261-15547G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174893675 | ||||||
| chr2:174893683
|
G | C | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.261-15555C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174893683 | ||||||
| chr2:174893793
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0004g0265others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-15665T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174893793 | ||||||
| chr2:174893920
|
T | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0144a0001c0001t0005g0176 | 3 | HG02683.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.261-15792A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174893920 | ||||||
| chr2:174894114
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.261-15986T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894114 | ||||||
| chr2:174894134
|
ACTT | A | 91 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.261-16009_261-1600 others(7): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894134 | ||||||
| chr2:174894532
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.261-16404G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894532 | ||||||
| chr2:174894594
|
AT | A | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.261-16467delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894594 | ||||||
| chr2:174894687
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00280.hp1 HG01192.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-16559A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894687 | ||||||
| chr2:174894787
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0126a0001c0001t0001g0139others(4): Show | 7 | HG00609.hp2 HG02015.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-16659C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174894787 | ||||||
| chr2:174895028
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.261-16900A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895028 | ||||||
| chr2:174895043
|
ACG | A | 29 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(26): Show | 29 | HG01361.hp2 HG02257.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.261-16917_261-1691 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895043 | ||||||
| chr2:174895045
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261-16917C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895045 | ||||||
| chr2:174895047
|
G | GCA | 5 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0207others(2): Show | 5 | HG02559.hp2 HG04115.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-16920_261-1691 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895047 | ||||||
| chr2:174895047
|
GCGCA | G | 17 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.261-16923_261-1692 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895047 | ||||||
| chr2:174895048
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.261-16920G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895048 | ||||||
| chr2:174895049
|
G | A | 104 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.261-16921C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895049 | ||||||
| chr2:174895049
|
G | GCA | 3 | a0001c0001t0001g0181a0001c0001t0002g0138a0001c0001t0002g0182 | 3 | HG02622.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.261-16923_261-1692 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895049 | ||||||
| chr2:174895186
|
A | ATG | 3 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0122 | 3 | NA18970.hp1 NA19000.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.261-17060_261-1705 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895186 | ||||||
| chr2:174895186
|
ATG | A | 13 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.261-17060_261-1705 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895186 | ||||||
| chr2:174895196
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0015 | 2 | NA18966.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.261-17068C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895196 | ||||||
| chr2:174895196
|
G | GTA | 89 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0001g0063others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.261-17069_261-1706 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895196 | ||||||
| chr2:174895196
|
G | GTATA | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02040.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-17069_261-1706 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895196 | ||||||
| chr2:174895198
|
G | A | 122 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.261-17070C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895198 | ||||||
| chr2:174895198
|
G | GTA | 3 | a0001c0001t0001g0181a0001c0001t0002g0182a0001c0001t0002g0189 | 3 | HG02622.hp1 HG02735.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.261-17072_261-1707 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895198 | ||||||
| chr2:174895200
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.261-17072T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895200 | ||||||
| chr2:174895213
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0102others(2): Show | 5 | HG02280.hp1 HG02698.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-17085A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895213 | ||||||
| chr2:174895213
|
T | TAC | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01070.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-17087_261-1708 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895213 | ||||||
| chr2:174895213
|
TAC | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG00140.hp1 HG01361.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-17087_261-1708 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895213 | ||||||
| chr2:174895213
|
TACAC | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-17089_261-1708 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895213 | ||||||
| chr2:174895215
|
C | T | 126 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0046others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.261-17087G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895215 | ||||||
| chr2:174895217
|
C | T | 24 | a0001c0001t0001g0046a0001c0001t0001g0066a0001c0001t0001g0169others(21): Show | 24 | HG00558.hp2 HG01496.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.261-17089G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895217 | ||||||
| chr2:174895219
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.261-17091G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895219 | ||||||
| chr2:174895225
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.261-17097G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895225 | ||||||
| chr2:174895324
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.261-17196G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895324 | ||||||
| chr2:174895465
|
G | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-17337C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895465 | ||||||
| chr2:174895616
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.261-17488A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895616 | ||||||
| chr2:174895629
|
A | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.261-17501T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895629 | ||||||
| chr2:174895715
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-17587A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174895715 | ||||||
| chr2:174896020
|
G | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(14): Show | 17 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.261-17892C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896020 | ||||||
| chr2:174896120
|
T | TA | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.261-17993dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896120 | ||||||
| chr2:174896169
|
C | A | 1 | a0001c0001t0004g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.261-18041G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896169 | ||||||
| chr2:174896233
|
G | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(14): Show | 17 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.261-18105C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896233 | ||||||
| chr2:174896651
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+18407G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896651 | ||||||
| chr2:174896725
|
T | C | 1 | a0001c0001t0010g0002 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.260+18333A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896725 | ||||||
| chr2:174896895
|
C | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+18163G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174896895 | ||||||
| chr2:174897112
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.260+17946A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897112 | ||||||
| chr2:174897394
|
A | G | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+17664T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897394 | ||||||
| chr2:174897423
|
T | TTG | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+17633_260+1763 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897423 | ||||||
| chr2:174897431
|
G | GTT | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+17626_260+1762 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897431 | ||||||
| chr2:174897515
|
TA | T | 145 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.260+17542delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897515 | ||||||
| chr2:174897678
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.260+17380G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897678 | ||||||
| chr2:174897690
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260+17368A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897690 | ||||||
| chr2:174897894
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.260+17164A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174897894 | ||||||
| chr2:174898325
|
G | A | 1 | a0001c0001t0006g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.260+16733C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898325 | ||||||
| chr2:174898344
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+16714C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898344 | ||||||
| chr2:174898438
|
G | GA | 137 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0044others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.260+16619dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898438 | ||||||
| chr2:174898438
|
GA | G | 10 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+16619delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898438 | ||||||
| chr2:174898560
|
C | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+16498G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898560 | ||||||
| chr2:174898583
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0213 | 2 | NA18942.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.260+16475C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898583 | ||||||
| chr2:174898653
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.260+16405G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898653 | ||||||
| chr2:174898870
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.260+16188A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174898870 | ||||||
| chr2:174899086
|
C | T | 90 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.260+15972G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899086 | ||||||
| chr2:174899203
|
G | GT | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.260+15854_260+1585 others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899203 | ||||||
| chr2:174899228
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0002g0069 | 2 | NA18994.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.260+15830G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899228 | ||||||
| chr2:174899237
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.260+15821A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899237 | ||||||
| chr2:174899268
|
T | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | NA18947.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.260+15790A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899268 | ||||||
| chr2:174899821
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.260+15237A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899821 | ||||||
| chr2:174899905
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.260+15153A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174899905 | ||||||
| chr2:174900532
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.260+14526C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900532 | ||||||
| chr2:174900672
|
A | G | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.260+14386T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900672 | ||||||
| chr2:174900723
|
T | C | 15 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251others(12): Show | 15 | HG00423.hp2 HG00609.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.260+14335A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900723 | ||||||
| chr2:174900793
|
G | A | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.260+14265C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900793 | ||||||
| chr2:174900819
|
G | C | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+14239C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900819 | ||||||
| chr2:174900904
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.260+14154T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174900904 | ||||||
| chr2:174901345
|
A | T | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.260+13713T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901345 | ||||||
| chr2:174901368
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.260+13690G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901368 | ||||||
| chr2:174901620
|
T | C | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.260+13438A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901620 | ||||||
| chr2:174901657
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+13401A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901657 | ||||||
| chr2:174901856
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.260+13202T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901856 | ||||||
| chr2:174901902
|
C | T | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.260+13156G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174901902 | ||||||
| chr2:174902032
|
C | T | 1 | a0001c0001t0004g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.260+13026G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902032 | ||||||
| chr2:174902169
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02071.hp1 NA18947.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+12889A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902169 | ||||||
| chr2:174902206
|
T | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0144a0001c0001t0005g0176 | 3 | HG02683.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.260+12852A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902206 | ||||||
| chr2:174902224
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.260+12834A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902224 | ||||||
| chr2:174902398
|
C | T | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.260+12660G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902398 | ||||||
| chr2:174902712
|
A | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+12346T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902712 | ||||||
| chr2:174902713
|
C | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+12345G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902713 | ||||||
| chr2:174902714
|
A | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260+12344T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902714 | ||||||
| chr2:174902847
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260+12211A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902847 | ||||||
| chr2:174902892
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+12166T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174902892 | ||||||
| chr2:174903042
|
T | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+12016A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174903042 | ||||||
| chr2:174903561
|
A | C | 1 | a0001c0001t0005g0090 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.260+11497T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174903561 | ||||||
| chr2:174903593
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0132 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.260+11465A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174903593 | ||||||
| chr2:174903658
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.260+11400G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174903658 | ||||||
| chr2:174903757
|
G | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(14): Show | 17 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.260+11301C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174903757 | ||||||
| chr2:174904079
|
A | T | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.260+10979T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904079 | ||||||
| chr2:174904081
|
G | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+10977C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904081 | ||||||
| chr2:174904120
|
G | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+10938C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904120 | ||||||
| chr2:174904121
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.260+10937C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904121 | ||||||
| chr2:174904179
|
C | T | 4 | a0001c0001t0005g0068a0001c0001t0005g0089a0001c0001t0005g0090others(1): Show | 4 | HG00423.hp2 HG03017.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+10879G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904179 | ||||||
| chr2:174904235
|
G | A | 1 | a0001c0001t0005g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.260+10823C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904235 | ||||||
| chr2:174904285
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.260+10773T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904285 | ||||||
| chr2:174904503
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.260+10555G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904503 | ||||||
| chr2:174904860
|
G | A | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.260+10198C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904860 | ||||||
| chr2:174904918
|
T | C | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275 | 3 | HG02630.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.260+10140A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904918 | ||||||
| chr2:174904929
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260+10129C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174904929 | ||||||
| chr2:174905054
|
T | G | 135 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.260+10004A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905054 | ||||||
| chr2:174905480
|
T | A | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.260+9578A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905480 | ||||||
| chr2:174905525
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.260+9533C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905525 | ||||||
| chr2:174905531
|
T | C | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+9527A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905531 | ||||||
| chr2:174905554
|
G | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.260+9504C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905554 | ||||||
| chr2:174905565
|
A | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.260+9493T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905565 | ||||||
| chr2:174905567
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.260+9491A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905567 | ||||||
| chr2:174905683
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.260+9375C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905683 | ||||||
| chr2:174905685
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.260+9373G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905685 | ||||||
| chr2:174905780
|
G | A | 1 | a0001c0001t0004g0265 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.260+9278C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905780 | ||||||
| chr2:174905800
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.260+9258A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905800 | ||||||
| chr2:174905804
|
C | A | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.260+9254G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905804 | ||||||
| chr2:174905928
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260+9130A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905928 | ||||||
| chr2:174905961
|
A | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0257others(14): Show | 17 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.260+9097T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174905961 | ||||||
| chr2:174906090
|
C | T | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.260+8968G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906090 | ||||||
| chr2:174906091
|
G | A | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.260+8967C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906091 | ||||||
| chr2:174906137
|
CAT | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0004g0265others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+8919_260+8920d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906137 | ||||||
| chr2:174906142
|
G | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0004g0265others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+8916C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906142 | ||||||
| chr2:174906155
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260+8903G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906155 | ||||||
| chr2:174906321
|
C | T | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.260+8737G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906321 | ||||||
| chr2:174906486
|
T | G | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.260+8572A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906486 | ||||||
| chr2:174906664
|
G | GA | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.260+8393dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906664 | ||||||
| chr2:174906708
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.260+8350A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906708 | ||||||
| chr2:174906729
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.260+8329A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906729 | ||||||
| chr2:174906879
|
C | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+8179G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906879 | ||||||
| chr2:174906941
|
G | A | 1 | a0001c0001t0008g0032 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.260+8117C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174906941 | ||||||
| chr2:174907004
|
C | T | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+8054G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907004 | ||||||
| chr2:174907190
|
C | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+7868G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907190 | ||||||
| chr2:174907499
|
T | A | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.260+7559A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907499 | ||||||
| chr2:174907613
|
G | GT | 6 | a0001c0001t0001g0128a0001c0001t0001g0218a0001c0001t0002g0137others(3): Show | 6 | HG00140.hp2 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+7444dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907613 | ||||||
| chr2:174907663
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+7395T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907663 | ||||||
| chr2:174907802
|
A | G | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.260+7256T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907802 | ||||||
| chr2:174907828
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0132 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.260+7230T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174907828 | ||||||
| chr2:174908553
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.260+6505G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174908553 | ||||||
| chr2:174908890
|
C | A | 5 | a0001c0001t0001g0108a0001c0001t0002g0069a0001c0001t0002g0082others(2): Show | 5 | HG02155.hp1 NA18612.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+6168G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174908890 | ||||||
| chr2:174909066
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0002g0182 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.260+5992A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909066 | ||||||
| chr2:174909087
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.260+5971A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909087 | ||||||
| chr2:174909248
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.260+5810C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909248 | ||||||
| chr2:174909419
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260+5639T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909419 | ||||||
| chr2:174909443
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260+5615C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909443 | ||||||
| chr2:174909444
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260+5614A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909444 | ||||||
| chr2:174909610
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.260+5448T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909610 | ||||||
| chr2:174909697
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.260+5361T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909697 | ||||||
| chr2:174909900
|
G | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+5158C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909900 | ||||||
| chr2:174909975
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.260+5083C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174909975 | ||||||
| chr2:174910022
|
C | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+5036G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910022 | ||||||
| chr2:174910098
|
T | C | 1 | a0001c0001t0006g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.260+4960A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910098 | ||||||
| chr2:174910137
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+4921A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910137 | ||||||
| chr2:174910418
|
T | C | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+4640A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910418 | ||||||
| chr2:174910606
|
T | C | 154 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.260+4452A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910606 | ||||||
| chr2:174910675
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+4383A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910675 | ||||||
| chr2:174910757
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.260+4301C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910757 | ||||||
| chr2:174910847
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0016g0267 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.260+4211G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910847 | ||||||
| chr2:174910895
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0002g0069a0001c0001t0002g0082others(2): Show | 5 | HG02155.hp1 NA18612.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+4163C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910895 | ||||||
| chr2:174910899
|
C | CA | 18 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 18 | HG00423.hp2 HG00438.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.260+4158dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174910899
|
CA | C | 26 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(23): Show | 26 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.260+4158delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174910899
|
CAA | C | 101 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0066others(98): Show | 101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.260+4157_260+4158d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174910899
|
CAAA | C | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+4156_260+4158d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174910899
|
CAAAAAAA others(2): Show |
C | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.260+4150_260+4158d others(11): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174910899
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.260+4144_260+4158d others(17): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174910899 | ||||||
| chr2:174911040
|
T | C | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.260+4018A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911040 | ||||||
| chr2:174911085
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.260+3973C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911085 | ||||||
| chr2:174911434
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.260+3624T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911434 | ||||||
| chr2:174911557
|
A | AG | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(1): Show | 4 | HG01069.hp1 HG01070.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+3500dupC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911557 | ||||||
| chr2:174911628
|
G | A | 1 | a0001c0001t0005g0091 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.260+3430C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911628 | ||||||
| chr2:174911655
|
A | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.260+3403T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911655 | ||||||
| chr2:174911698
|
A | G | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.260+3360T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911698 | ||||||
| chr2:174911804
|
C | T | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.260+3254G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911804 | ||||||
| chr2:174911927
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.260+3131C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174911927 | ||||||
| chr2:174912100
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260+2958C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912100 | ||||||
| chr2:174912202
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+2856T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912202 | ||||||
| chr2:174912536
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+2522G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912536 | ||||||
| chr2:174912691
|
A | G | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+2367T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912691 | ||||||
| chr2:174912696
|
G | A | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.260+2362C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912696 | ||||||
| chr2:174912921
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+2137G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174912921 | ||||||
| chr2:174913638
|
A | C | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.260+1420T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174913638 | ||||||
| chr2:174913691
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.260+1367A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174913691 | ||||||
| chr2:174913789
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.260+1269T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174913789 | ||||||
| chr2:174914246
|
A | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+812T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914246 | ||||||
| chr2:174914286
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+772C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914286 | ||||||
| chr2:174914399
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.260+659C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914399 | ||||||
| chr2:174914476
|
C | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+582G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914476 | ||||||
| chr2:174914626
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0221a0001c0001t0001g0224 | 3 | HG00423.hp1 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.260+432G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914626 | ||||||
| chr2:174914842
|
C | CA | 38 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(35): Show | 38 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.260+215dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914842 | ||||||
| chr2:174914842
|
C | CAA | 107 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.260+214_260+215dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914842 | ||||||
| chr2:174914898
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.260+160G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 5/12 | chr2 | 174914898 | ||||||
| chr2:174915514
|
G | GA | 136 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.147-344dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174915514 | ||||||
| chr2:174915780
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.147-609T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174915780 | ||||||
| chr2:174915868
|
AAAGCCAC others(13): Show |
A | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02071.hp1 NA18947.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-717_147-698del others(20): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174915868 | ||||||
| chr2:174915875
|
C | T | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.147-704G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174915875 | ||||||
| chr2:174916081
|
C | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.147-910G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916081 | ||||||
| chr2:174916322
|
G | A | 89 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-1151C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916322 | ||||||
| chr2:174916356
|
T | C | 1 | a0001c0001t0005g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.147-1185A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916356 | ||||||
| chr2:174916405
|
C | T | 89 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-1234G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916405 | ||||||
| chr2:174916428
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-1257C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916428 | ||||||
| chr2:174916590
|
G | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-1419C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916590 | ||||||
| chr2:174916695
|
G | T | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-1524C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916695 | ||||||
| chr2:174916703
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.147-1532T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916703 | ||||||
| chr2:174916740
|
G | A | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.147-1569C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916740 | ||||||
| chr2:174916929
|
C | T | 1 | a0001c0001t0005g0180 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.146+1605G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916929 | ||||||
| chr2:174916935
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.146+1599A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174916935 | ||||||
| chr2:174917026
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.146+1508G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174917026 | ||||||
| chr2:174917037
|
C | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.146+1497G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174917037 | ||||||
| chr2:174917064
|
T | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.146+1470A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174917064 | ||||||
| chr2:174917146
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.146+1388A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174917146 | ||||||
| chr2:174917988
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.146+546G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174917988 | ||||||
| chr2:174918174
|
A | G | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+360T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 4/12 | chr2 | 174918174 | ||||||
| chr2:174918622
|
A | C | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.115-57T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918622 | ||||||
| chr2:174918791
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-226T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918791 | ||||||
| chr2:174918809
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-244A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918809 | ||||||
| chr2:174918868
|
CA | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-304delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918868 | ||||||
| chr2:174918877
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-312A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918877 | ||||||
| chr2:174918964
|
A | T | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-399T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174918964 | ||||||
| chr2:174919290
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0135 | 3 | NA18991.hp1 NA19006.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.115-725C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919290 | ||||||
| chr2:174919293
|
G | C | 8 | a0001c0001t0001g0120a0001c0001t0002g0099a0001c0001t0002g0107others(5): Show | 8 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-728C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919293 | ||||||
| chr2:174919387
|
G | A | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.115-822C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919387 | ||||||
| chr2:174919420
|
T | TACAA | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-856_115-855ins others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919420 | ||||||
| chr2:174919421
|
G | A | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-856C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919421 | ||||||
| chr2:174919422
|
T | A | 148 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-857A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919422 | ||||||
| chr2:174919450
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.115-885G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919450 | ||||||
| chr2:174919970
|
C | T | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.115-1405G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174919970 | ||||||
| chr2:174920099
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115-1534C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174920099 | ||||||
| chr2:174920158
|
T | C | 92 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.115-1593A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174920158 | ||||||
| chr2:174920451
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.115-1886A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174920451 | ||||||
| chr2:174921106
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.115-2541A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921106 | ||||||
| chr2:174921205
|
T | C | 8 | a0001c0001t0002g0043a0001c0001t0002g0075a0001c0001t0002g0076others(5): Show | 8 | HG00673.hp2 HG02083.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-2640A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921205 | ||||||
| chr2:174921219
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-2654A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921219 | ||||||
| chr2:174921294
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.115-2729A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921294 | ||||||
| chr2:174921352
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-2787G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921352 | ||||||
| chr2:174921391
|
C | G | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-2826G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921391 | ||||||
| chr2:174921412
|
G | T | 1 | a0001c0001t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.115-2847C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921412 | ||||||
| chr2:174921684
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.115-3119A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921684 | ||||||
| chr2:174921783
|
C | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA19081.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.115-3218G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921783 | ||||||
| chr2:174921862
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.115-3297G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174921862 | ||||||
| chr2:174922341
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.115-3776A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174922341 | ||||||
| chr2:174922360
|
A | G | 1 | a0001c0001t0014g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.115-3795T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174922360 | ||||||
| chr2:174922447
|
T | C | 5 | a0001c0001t0002g0099a0001c0001t0002g0117a0001c0001t0002g0160others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-3882A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174922447 | ||||||
| chr2:174922722
|
A | AT | 3 | a0001c0001t0007g0030a0001c0001t0007g0033a0001c0001t0007g0035 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.115-4158dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174922722 | ||||||
| chr2:174923113
|
A | G | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-4548T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923113 | ||||||
| chr2:174923164
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115-4599C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923164 | ||||||
| chr2:174923203
|
T | C | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.115-4638A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923203 | ||||||
| chr2:174923265
|
T | C | 9 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02615.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-4700A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923265 | ||||||
| chr2:174923330
|
C | T | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.115-4765G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923330 | ||||||
| chr2:174923341
|
C | T | 36 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0046others(33): Show | 36 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.115-4776G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923341 | ||||||
| chr2:174923530
|
TCA | T | 4 | a0001c0001t0004g0266a0001c0001t0004g0269a0001c0001t0004g0272others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-4967_115-4966d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923530 | ||||||
| chr2:174923534
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.115-4969C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923534 | ||||||
| chr2:174923726
|
C | G | 1 | a0001c0001t0004g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.115-5161G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923726 | ||||||
| chr2:174923926
|
C | T | 131 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.115-5361G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174923926 | ||||||
| chr2:174924046
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-5481G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174924046 | ||||||
| chr2:174924213
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.115-5648A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174924213 | ||||||
| chr2:174924250
|
G | C | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.115-5685C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174924250 | ||||||
| chr2:174924747
|
T | C | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275 | 3 | HG02630.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.115-6182A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174924747 | ||||||
| chr2:174924945
|
T | C | 91 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.115-6380A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174924945 | ||||||
| chr2:174925118
|
C | A | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115-6553G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925118 | ||||||
| chr2:174925327
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115-6762T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925327 | ||||||
| chr2:174925586
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.115-7021C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925586 | ||||||
| chr2:174925669
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-7104A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925669 | ||||||
| chr2:174925717
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115-7152A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925717 | ||||||
| chr2:174925772
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.115-7207G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925772 | ||||||
| chr2:174925974
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-7409A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174925974 | ||||||
| chr2:174926226
|
C | G | 4 | a0001c0001t0001g0105a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18951.hp1 NA18978.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-7661G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174926226 | ||||||
| chr2:174926231
|
T | C | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-7666A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174926231 | ||||||
| chr2:174926374
|
TTTTAAAT others(6): Show |
T | 2 | a0001c0001t0001g0214a0001c0001t0001g0219 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.115-7822_115-7810d others(15): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174926374 | ||||||
| chr2:174926563
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-7998G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174926563 | ||||||
| chr2:174927047
|
T | C | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.115-8482A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927047 | ||||||
| chr2:174927197
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-8632A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927197 | ||||||
| chr2:174927521
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0053 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.115-8956T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927521 | ||||||
| chr2:174927777
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.115-9212A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927777 | ||||||
| chr2:174927787
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.115-9222A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927787 | ||||||
| chr2:174927855
|
T | G | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-9290A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174927855 | ||||||
| chr2:174928011
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.115-9446A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174928011 | ||||||
| chr2:174928226
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.115-9661C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174928226 | ||||||
| chr2:174929444
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-10879C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174929444 | ||||||
| chr2:174929470
|
C | T | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.115-10905G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174929470 | ||||||
| chr2:174929577
|
C | CA | 40 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-11013dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174929577 | ||||||
| chr2:174929603
|
G | T | 81 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.115-11038C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174929603 | ||||||
| chr2:174929609
|
C | A | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.115-11044G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174929609 | ||||||
| chr2:174930274
|
A | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00609.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.115-11709T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930274 | ||||||
| chr2:174930305
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-11740C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930305 | ||||||
| chr2:174930439
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.115-11874G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930439 | ||||||
| chr2:174930445
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.115-11880C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930445 | ||||||
| chr2:174930704
|
G | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-12139C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930704 | ||||||
| chr2:174930768
|
A | AT | 6 | a0001c0001t0001g0197a0001c0001t0002g0117a0001c0001t0002g0160others(3): Show | 6 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-12204dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930768 | ||||||
| chr2:174930852
|
C | T | 37 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(34): Show | 37 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.115-12287G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930852 | ||||||
| chr2:174930923
|
C | T | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-12358G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930923 | ||||||
| chr2:174930924
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.115-12359C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930924 | ||||||
| chr2:174930959
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.115-12394T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930959 | ||||||
| chr2:174930999
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.115-12434T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174930999 | ||||||
| chr2:174931106
|
A | G | 1 | a0001c0001t0006g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115-12541T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931106 | ||||||
| chr2:174931133
|
CA | C | 139 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.115-12569delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931133 | ||||||
| chr2:174931133
|
CAA | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-12570_115-1256 others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931133 | ||||||
| chr2:174931526
|
A | T | 150 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.115-12961T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931526 | ||||||
| chr2:174931557
|
A | G | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-12992T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931557 | ||||||
| chr2:174931707
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.115-13142T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931707 | ||||||
| chr2:174931739
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0136a0001c0001t0001g0158 | 3 | NA18944.hp2 NA18995.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.114+13149A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931739 | ||||||
| chr2:174931784
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114+13104A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931784 | ||||||
| chr2:174931974
|
A | G | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+12914T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931974 | ||||||
| chr2:174931982
|
C | T | 145 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.114+12906G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174931982 | ||||||
| chr2:174932047
|
T | C | 10 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(7): Show | 10 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+12841A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932047 | ||||||
| chr2:174932401
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+12487G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932401 | ||||||
| chr2:174932456
|
C | G | 156 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.114+12432G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932456 | ||||||
| chr2:174932520
|
T | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0002g0110others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+12368A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932520 | ||||||
| chr2:174932751
|
C | CCTCT | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+12133_114+1213 others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932751 | ||||||
| chr2:174932934
|
G | A | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.114+11954C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174932934 | ||||||
| chr2:174933159
|
T | C | 5 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(2): Show | 5 | NA18943.hp1 NA18965.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+11729A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933159 | ||||||
| chr2:174933229
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+11659T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933229 | ||||||
| chr2:174933299
|
G | A | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.114+11589C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933299 | ||||||
| chr2:174933302
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+11586C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933302 | ||||||
| chr2:174933318
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.114+11570C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933318 | ||||||
| chr2:174933645
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+11243C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933645 | ||||||
| chr2:174933799
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00609.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.114+11089T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933799 | ||||||
| chr2:174933850
|
T | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+11038A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933850 | ||||||
| chr2:174933948
|
G | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0024 | 2 | NA18987.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.114+10940C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933948 | ||||||
| chr2:174933973
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+10915T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933973 | ||||||
| chr2:174933974
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+10914C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174933974 | ||||||
| chr2:174934079
|
A | C | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.114+10809T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174934079 | ||||||
| chr2:174934310
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+10578G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174934310 | ||||||
| chr2:174934839
|
T | C | 3 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275 | 3 | HG02630.hp2 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.114+10049A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174934839 | ||||||
| chr2:174934951
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+9937A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174934951 | ||||||
| chr2:174935148
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.114+9740A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935148 | ||||||
| chr2:174935162
|
G | A | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114+9726C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935162 | ||||||
| chr2:174935494
|
T | C | 37 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(34): Show | 37 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.114+9394A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935494 | ||||||
| chr2:174935735
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+9153C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935735 | ||||||
| chr2:174935953
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.114+8935T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935953 | ||||||
| chr2:174935965
|
A | G | 1 | a0001c0001t0006g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+8923T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935965 | ||||||
| chr2:174935966
|
CAT | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0012g0125 | 3 | HG02896.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.114+8920_114+8921d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174935966 | ||||||
| chr2:174936009
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+8879A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936009 | ||||||
| chr2:174936027
|
A | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+8861T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936027 | ||||||
| chr2:174936256
|
A | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0163others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+8632T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936256 | ||||||
| chr2:174936273
|
C | T | 1 | a0001c0001t0006g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114+8615G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936273 | ||||||
| chr2:174936285
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114+8603A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936285 | ||||||
| chr2:174936309
|
G | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0126a0001c0001t0001g0139others(6): Show | 9 | HG00609.hp2 HG02015.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+8579C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936309 | ||||||
| chr2:174936432
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.114+8456A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936432 | ||||||
| chr2:174936463
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0006g0027others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+8425T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936463 | ||||||
| chr2:174936628
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114+8260T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936628 | ||||||
| chr2:174936682
|
T | G | 1 | a0001c0001t0003g0003 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.114+8206A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936682 | ||||||
| chr2:174936888
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+8000T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174936888 | ||||||
| chr2:174937320
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.114+7568A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937320 | ||||||
| chr2:174937433
|
G | A | 7 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(4): Show | 7 | HG02257.hp1 NA18943.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+7455C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937433 | ||||||
| chr2:174937453
|
C | A | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.114+7435G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937453 | ||||||
| chr2:174937523
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.114+7365A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937523 | ||||||
| chr2:174937643
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+7245C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937643 | ||||||
| chr2:174937863
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.114+7025G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937863 | ||||||
| chr2:174937958
|
T | C | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114+6930A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174937958 | ||||||
| chr2:174938329
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+6559A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938329 | ||||||
| chr2:174938378
|
T | TA | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.114+6509dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938378 | ||||||
| chr2:174938518
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.114+6370A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938518 | ||||||
| chr2:174938553
|
G | A | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114+6335C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938553 | ||||||
| chr2:174938756
|
T | C | 1 | a0001c0001t0005g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.114+6132A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938756 | ||||||
| chr2:174938766
|
G | A | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.114+6122C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938766 | ||||||
| chr2:174938895
|
C | CA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+5992dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938895 | ||||||
| chr2:174938987
|
T | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+5901A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174938987 | ||||||
| chr2:174939116
|
G | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+5772C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939116 | ||||||
| chr2:174939222
|
G | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG01891.hp2 HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.114+5666C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939222 | ||||||
| chr2:174939334
|
T | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+5554A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939334 | ||||||
| chr2:174939426
|
T | A | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+5462A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939426 | ||||||
| chr2:174939585
|
T | C | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.114+5303A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939585 | ||||||
| chr2:174939614
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+5274G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939614 | ||||||
| chr2:174939643
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+5245G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939643 | ||||||
| chr2:174939713
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.114+5175A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939713 | ||||||
| chr2:174939760
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+5128C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939760 | ||||||
| chr2:174939798
|
TA | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+5089delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939798 | ||||||
| chr2:174939894
|
TC | T | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+4993delG | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939894 | ||||||
| chr2:174939946
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+4942C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939946 | ||||||
| chr2:174939972
|
CA | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+4915delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174939972 | ||||||
| chr2:174940016
|
C | CTTTTA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+4867_114+4871d others(7): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940016 | ||||||
| chr2:174940139
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.114+4749G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940139 | ||||||
| chr2:174940306
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0096 | 2 | NA18947.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.114+4582G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940306 | ||||||
| chr2:174940436
|
T | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0122 | 2 | NA19000.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.114+4452A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940436 | ||||||
| chr2:174940533
|
G | GT | 37 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(34): Show | 37 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.114+4354dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940533 | ||||||
| chr2:174940673
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+4215A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940673 | ||||||
| chr2:174940728
|
A | C | 1 | a0001c0001t0002g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.114+4160T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940728 | ||||||
| chr2:174940751
|
A | T | 1 | a0001c0001t0004g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114+4137T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940751 | ||||||
| chr2:174940813
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.114+4075A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940813 | ||||||
| chr2:174940856
|
T | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+4032A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174940856 | ||||||
| chr2:174941292
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.114+3596C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941292 | ||||||
| chr2:174941298
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+3590G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941298 | ||||||
| chr2:174941343
|
C | A | 4 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+3545G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941343 | ||||||
| chr2:174941618
|
CTT | C | 21 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0210others(18): Show | 21 | HG02040.hp1 HG02129.hp2 NA18942.hp2 others(18): Show |
intron_variant | MODIFIER | c.114+3268_114+3269d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941618 | ||||||
| chr2:174941650
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+3238G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941650 | ||||||
| chr2:174941661
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.114+3227G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941661 | ||||||
| chr2:174941780
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.114+3108C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941780 | ||||||
| chr2:174941789
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+3099A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941789 | ||||||
| chr2:174941851
|
T | C | 1 | a0001c0001t0004g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+3037A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941851 | ||||||
| chr2:174941935
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+2953C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941935 | ||||||
| chr2:174941979
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.114+2909T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941979 | ||||||
| chr2:174941987
|
C | T | 149 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.114+2901G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174941987 | ||||||
| chr2:174942091
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.114+2797A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942091 | ||||||
| chr2:174942149
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0016g0267 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.114+2739G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942149 | ||||||
| chr2:174942178
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.114+2710T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942178 | ||||||
| chr2:174942334
|
A | G | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+2554T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942334 | ||||||
| chr2:174942446
|
G | A | 1 | a0001c0001t0007g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.114+2442C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942446 | ||||||
| chr2:174942506
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+2382C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942506 | ||||||
| chr2:174942544
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+2344A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942544 | ||||||
| chr2:174942550
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0002g0069a0001c0001t0002g0082 | 3 | NA18612.hp2 NA18994.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.114+2338A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942550 | ||||||
| chr2:174942630
|
A | T | 1 | a0001c0001t0003g0009 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.114+2258T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942630 | ||||||
| chr2:174942659
|
C | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+2229G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942659 | ||||||
| chr2:174942782
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+2106C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942782 | ||||||
| chr2:174942785
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+2103G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942785 | ||||||
| chr2:174942787
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+2101G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942787 | ||||||
| chr2:174942790
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114+2098G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174942790 | ||||||
| chr2:174943046
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.114+1842A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943046 | ||||||
| chr2:174943078
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.114+1810T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943078 | ||||||
| chr2:174943111
|
CTTTTTT | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+1771_114+1776d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943111 | ||||||
| chr2:174943178
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.114+1710A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943178 | ||||||
| chr2:174943182
|
T | TTG | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 8 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+1704_114+1705d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943182 | ||||||
| chr2:174943182
|
TTG | T | 26 | a0001c0001t0001g0051a0001c0001t0001g0183a0001c0001t0001g0184others(23): Show | 26 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.114+1704_114+1705d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943182 | ||||||
| chr2:174943182
|
TTGTG | T | 23 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+1702_114+1705d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943182 | ||||||
| chr2:174943182
|
TTGTGTG | T | 93 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.114+1700_114+1705d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943182 | ||||||
| chr2:174943262
|
T | C | 15 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251others(12): Show | 15 | HG00423.hp2 HG00609.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+1626A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943262 | ||||||
| chr2:174943295
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+1593G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943295 | ||||||
| chr2:174943362
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG00738.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114+1526C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943362 | ||||||
| chr2:174943372
|
A | G | 21 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.114+1516T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943372 | ||||||
| chr2:174943505
|
A | G | 192 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(189): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.114+1383T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943505 | ||||||
| chr2:174943523
|
C | A | 131 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.114+1365G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943523 | ||||||
| chr2:174943704
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+1184A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174943704 | ||||||
| chr2:174944020
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+868A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174944020 | ||||||
| chr2:174944048
|
G | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+840C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174944048 | ||||||
| chr2:174944414
|
T | C | 3 | a0001c0001t0007g0030a0001c0001t0007g0033a0001c0001t0007g0035 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.114+474A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174944414 | ||||||
| chr2:174944649
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114+239G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174944649 | ||||||
| chr2:174944762
|
T | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.114+126A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 3/12 | chr2 | 174944762 | ||||||
| chr2:174944993
|
A | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-50T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174944993 | ||||||
| chr2:174945585
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-642T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945585 | ||||||
| chr2:174945784
|
G | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0074 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.59-841C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945784 | ||||||
| chr2:174945817
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0195 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-874G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945817 | ||||||
| chr2:174945867
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-924A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945867 | ||||||
| chr2:174945909
|
CTGTG | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0079a0001c0001t0003g0018 | 3 | HG01496.hp2 HG03490.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.59-970_59-967delCA others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945909 | ||||||
| chr2:174945925
|
G | GTATA | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-983_59-982insTA others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945925 | ||||||
| chr2:174945927
|
G | A | 44 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0046others(41): Show | 44 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.59-984C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945927 | ||||||
| chr2:174945927
|
G | GTA | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-985_59-984insTA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945927 | ||||||
| chr2:174945929
|
G | A | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.59-986C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945929 | ||||||
| chr2:174945931
|
G | A | 150 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.59-988C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945931 | ||||||
| chr2:174945942
|
T | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0015g0261 | 3 | HG00099.hp2 HG01433.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.59-999A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945942 | ||||||
| chr2:174945942
|
T | TAA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.59-1001_59-1000dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945942 | ||||||
| chr2:174945966
|
ATCTC | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.59-1027_59-1024del others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174945966 | ||||||
| chr2:174946303
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-1360A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946303 | ||||||
| chr2:174946344
|
C | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.59-1401G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946344 | ||||||
| chr2:174946479
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1536G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946479 | ||||||
| chr2:174946522
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-1579A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946522 | ||||||
| chr2:174946762
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.59-1819T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946762 | ||||||
| chr2:174946783
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.59-1840C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946783 | ||||||
| chr2:174946900
|
TA | T | 206 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0042others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.59-1958delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174946900 | ||||||
| chr2:174947089
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-2146A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947089 | ||||||
| chr2:174947321
|
T | C | 2 | a0001c0001t0007g0033a0001c0001t0007g0035 | 2 | HG01361.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.59-2378A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947321 | ||||||
| chr2:174947487
|
A | ATT | 14 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0006g0027others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-2546_59-2545dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947487 | ||||||
| chr2:174947487
|
AT | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-2545delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947487 | ||||||
| chr2:174947579
|
A | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.59-2636T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947579 | ||||||
| chr2:174947590
|
G | T | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-2647C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947590 | ||||||
| chr2:174947622
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-2679A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947622 | ||||||
| chr2:174947644
|
A | C | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-2701T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947644 | ||||||
| chr2:174947780
|
A | G | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-2837T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174947780 | ||||||
| chr2:174948050
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.59-3107T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948050 | ||||||
| chr2:174948213
|
AACTT | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3274_59-3271del others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948213 | ||||||
| chr2:174948298
|
A | G | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3355T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948298 | ||||||
| chr2:174948347
|
C | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-3404G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948347 | ||||||
| chr2:174948425
|
A | G | 1 | a0001c0001t0008g0032 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.59-3482T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948425 | ||||||
| chr2:174948929
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3235T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174948929 | ||||||
| chr2:174949200
|
CT | C | 152 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.58+2963delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174949200 | ||||||
| chr2:174949313
|
A | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58+2851T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174949313 | ||||||
| chr2:174949337
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.58+2827C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174949337 | ||||||
| chr2:174949483
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0009g0001 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.58+2681T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174949483 | ||||||
| chr2:174950131
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0009g0001 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.58+2033T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950131 | ||||||
| chr2:174950253
|
T | C | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+1911A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950253 | ||||||
| chr2:174950385
|
G | C | 87 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.58+1779C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950385 | ||||||
| chr2:174950456
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+1708C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950456 | ||||||
| chr2:174950598
|
T | C | 1 | a0001c0001t0005g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.58+1566A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950598 | ||||||
| chr2:174950714
|
T | C | 1 | a0001c0001t0005g0091 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.58+1450A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950714 | ||||||
| chr2:174950777
|
G | GT | 45 | a0001c0001t0001g0044a0001c0001t0001g0103a0001c0001t0001g0116others(42): Show | 45 | HG00438.hp2 HG01175.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.58+1386dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950777 | ||||||
| chr2:174950777
|
G | GTT | 7 | a0001c0001t0001g0028a0001c0001t0001g0171a0001c0001t0001g0257others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+1385_58+1386dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950777 | ||||||
| chr2:174950936
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.58+1228G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174950936 | ||||||
| chr2:174951212
|
G | A | 1 | a0001c0001t0003g0005 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.58+952C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951212 | ||||||
| chr2:174951365
|
T | G | 1 | a0001c0001t0003g0007 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.58+799A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951365 | ||||||
| chr2:174951510
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+654G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951510 | ||||||
| chr2:174951661
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.58+503A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951661 | ||||||
| chr2:174951701
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+463G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951701 | ||||||
| chr2:174951759
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58+405A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951759 | ||||||
| chr2:174951838
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+326G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951838 | ||||||
| chr2:174951867
|
A | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+297T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951867 | ||||||
| chr2:174951885
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.58+279G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951885 | ||||||
| chr2:174951924
|
T | C | 1 | a0001c0001t0014g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.58+240A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 2/12 | chr2 | 174951924 | ||||||
| chr2:174952285
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.20-83A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952285 | ||||||
| chr2:174952334
|
C | T | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-132G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952334 | ||||||
| chr2:174952344
|
T | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-142A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952344 | ||||||
| chr2:174952515
|
T | C | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-313A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952515 | ||||||
| chr2:174952647
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.20-445A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952647 | ||||||
| chr2:174952959
|
T | A | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-757A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952959 | ||||||
| chr2:174952961
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-759G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174952961 | ||||||
| chr2:174953057
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.20-855G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953057 | ||||||
| chr2:174953164
|
C | CA | 8 | a0001c0001t0001g0063a0001c0001t0001g0175a0001c0001t0001g0204others(5): Show | 8 | HG00423.hp1 HG00673.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-963dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953164 | ||||||
| chr2:174953240
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-1038A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953240 | ||||||
| chr2:174953296
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20-1094A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953296 | ||||||
| chr2:174953477
|
G | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-1275C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953477 | ||||||
| chr2:174953509
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-1307G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953509 | ||||||
| chr2:174953788
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.20-1586T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174953788 | ||||||
| chr2:174954171
|
A | C | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.20-1969T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954171 | ||||||
| chr2:174954190
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.20-1988C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954190 | ||||||
| chr2:174954229
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-2027A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954229 | ||||||
| chr2:174954495
|
A | G | 21 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(18): Show | 21 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-2293T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954495 | ||||||
| chr2:174954650
|
T | G | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-2448A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954650 | ||||||
| chr2:174954704
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.20-2502G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954704 | ||||||
| chr2:174954845
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-2643C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954845 | ||||||
| chr2:174954873
|
C | T | 10 | a0001c0001t0003g0007a0001c0001t0003g0010a0001c0001t0003g0011others(7): Show | 10 | HG01258.hp1 NA18943.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-2671G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954873 | ||||||
| chr2:174954903
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.20-2701T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954903 | ||||||
| chr2:174954992
|
T | A | 1 | a0001c0001t0006g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.20-2790A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174954992 | ||||||
| chr2:174955056
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.20-2854G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955056 | ||||||
| chr2:174955076
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-2874C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955076 | ||||||
| chr2:174955087
|
C | T | 2 | a0001c0001t0003g0004a0001c0001t0003g0014 | 2 | HG00558.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.20-2885G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955087 | ||||||
| chr2:174955103
|
A | C | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-2901T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955103 | ||||||
| chr2:174955106
|
G | T | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-2904C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955106 | ||||||
| chr2:174955109
|
C | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-2907G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955109 | ||||||
| chr2:174955112
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-2910A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955112 | ||||||
| chr2:174955117
|
C | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-2915G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955117 | ||||||
| chr2:174955120
|
T | C | 14 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0006g0027others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-2918A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955120 | ||||||
| chr2:174955122
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.20-2920C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955122 | ||||||
| chr2:174955136
|
C | G | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-2934G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955136 | ||||||
| chr2:174955154
|
CTA | C | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-2954_20-2953del others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955154 | ||||||
| chr2:174955184
|
C | CTA | 35 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0103others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.20-2984_20-2983dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955184 | ||||||
| chr2:174955184
|
C | CTATA | 51 | a0001c0001t0001g0026a0001c0001t0001g0092a0001c0001t0001g0093others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.20-2986_20-2983dup others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955184 | ||||||
| chr2:174955187
|
T | TATAG | 22 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-2986_20-2985ins others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955187 | ||||||
| chr2:174955194
|
A | C | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-2992T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955194 | ||||||
| chr2:174955196
|
A | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-2994T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955196 | ||||||
| chr2:174955196
|
ATATAATT others(16): Show |
A | 147 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.20-3017_20-2995del others(23): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955196 | ||||||
| chr2:174955198
|
ATAATTGA others(14): Show |
A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-3017_20-2997del others(21): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955198 | ||||||
| chr2:174955201
|
A | T | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-2999T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955201 | ||||||
| chr2:174955202
|
T | A | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-3000A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955202 | ||||||
| chr2:174955204
|
G | A | 1 | a0001c0001t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-3002C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955204 | ||||||
| chr2:174955219
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.20-3017G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955219 | ||||||
| chr2:174955230
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-3028A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955230 | ||||||
| chr2:174955400
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-3198C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955400 | ||||||
| chr2:174955624
|
A | T | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.20-3422T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955624 | ||||||
| chr2:174955811
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-3609C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955811 | ||||||
| chr2:174955876
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.20-3674A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174955876 | ||||||
| chr2:174956272
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.20-4070T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174956272 | ||||||
| chr2:174956771
|
CA | C | 120 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0055others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-4570delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174956771 | ||||||
| chr2:174956806
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-4604T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174956806 | ||||||
| chr2:174956880
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.20-4678T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174956880 | ||||||
| chr2:174956929
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-4727A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174956929 | ||||||
| chr2:174957195
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.20-4993C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957195 | ||||||
| chr2:174957349
|
G | A | 96 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.20-5147C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957349 | ||||||
| chr2:174957358
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.20-5156C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957358 | ||||||
| chr2:174957446
|
T | TGG | 87 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0048others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.20-5246_20-5245dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957446 | ||||||
| chr2:174957446
|
T | TGGG | 38 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0063others(35): Show | 38 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.20-5247_20-5245dup others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957446 | ||||||
| chr2:174957449
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.20-5247C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957449 | ||||||
| chr2:174957542
|
A | G | 15 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 15 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-5340T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957542 | ||||||
| chr2:174957588
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.20-5386T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957588 | ||||||
| chr2:174957666
|
A | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-5464T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957666 | ||||||
| chr2:174957825
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-5623T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957825 | ||||||
| chr2:174957852
|
A | G | 1 | a0001c0001t0005g0180 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.20-5650T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957852 | ||||||
| chr2:174957957
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.20-5755G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957957 | ||||||
| chr2:174957964
|
G | A | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-5762C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957964 | ||||||
| chr2:174957995
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.20-5793C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174957995 | ||||||
| chr2:174958109
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-5907C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174958109 | ||||||
| chr2:174958194
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.20-5992C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174958194 | ||||||
| chr2:174958613
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.20-6411A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174958613 | ||||||
| chr2:174958622
|
T | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-6420A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174958622 | ||||||
| chr2:174959065
|
C | A | 14 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0006g0027others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-6863G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959065 | ||||||
| chr2:174959196
|
C | T | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-6994G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959196 | ||||||
| chr2:174959201
|
T | C | 1 | a0001c0001t0005g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.20-6999A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959201 | ||||||
| chr2:174959304
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.20-7102A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959304 | ||||||
| chr2:174959438
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.20-7236C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959438 | ||||||
| chr2:174959525
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20-7323G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959525 | ||||||
| chr2:174959737
|
G | T | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-7535C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959737 | ||||||
| chr2:174959820
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.20-7618A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959820 | ||||||
| chr2:174959848
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0132 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.20-7646G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959848 | ||||||
| chr2:174959961
|
A | C | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-7759T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174959961 | ||||||
| chr2:174960002
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.20-7800A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960002 | ||||||
| chr2:174960200
|
A | G | 7 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0002g0110others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-7998T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960200 | ||||||
| chr2:174960256
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.20-8054T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960256 | ||||||
| chr2:174960498
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-8296C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960498 | ||||||
| chr2:174960679
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.20-8477T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960679 | ||||||
| chr2:174960795
|
C | G | 5 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(2): Show | 5 | NA18943.hp1 NA18965.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-8593G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960795 | ||||||
| chr2:174960808
|
C | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(7): Show | 10 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-8606G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174960808 | ||||||
| chr2:174961021
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0034others(9): Show | 12 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-8819T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961021 | ||||||
| chr2:174961115
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0147 | 2 | HG00280.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.20-8913G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961115 | ||||||
| chr2:174961122
|
A | AAGGAAGG others(22): Show |
96 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.20-8949_20-8921dup others(29): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961122 | ||||||
| chr2:174961215
|
A | AAGGG | 8 | a0001c0001t0001g0152a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-9017_20-9014dup others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961215 | ||||||
| chr2:174961232
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.20-9030T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961232 | ||||||
| chr2:174961242
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG00609.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.20-9040C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961242 | ||||||
| chr2:174961523
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-9321C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961523 | ||||||
| chr2:174961538
|
G | C | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.20-9336C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961538 | ||||||
| chr2:174961543
|
A | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.20-9341T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961543 | ||||||
| chr2:174961559
|
C | A | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.20-9357G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961559 | ||||||
| chr2:174961583
|
C | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.20-9381G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961583 | ||||||
| chr2:174961661
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.20-9459T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174961661 | ||||||
| chr2:174962013
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0213a0001c0001t0001g0245 | 3 | NA18942.hp2 NA18967.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.20-9811C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962013 | ||||||
| chr2:174962051
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.20-9849G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962051 | ||||||
| chr2:174962156
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-9954C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962156 | ||||||
| chr2:174962157
|
C | T | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-9955G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962157 | ||||||
| chr2:174962200
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-9998C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962200 | ||||||
| chr2:174962256
|
G | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-10054C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962256 | ||||||
| chr2:174962323
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-10121T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962323 | ||||||
| chr2:174962425
|
G | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00438.hp1 HG02083.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-10223C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962425 | ||||||
| chr2:174962663
|
C | CG | 16 | a0001c0001t0001g0056a0001c0001t0001g0062a0001c0001t0001g0080others(13): Show | 16 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.20-10462dupC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962663 | ||||||
| chr2:174962663
|
C | CGGG | 16 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0001g0065others(13): Show | 16 | HG00423.hp2 HG01175.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.20-10464_20-10462d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962663 | ||||||
| chr2:174962663
|
CG | C | 32 | a0001c0001t0001g0059a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 32 | HG00639.hp2 HG01192.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-10462delC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962663 | ||||||
| chr2:174962663
|
CGG | C | 22 | a0001c0001t0001g0045a0001c0001t0001g0088a0001c0001t0001g0105others(19): Show | 22 | HG00438.hp2 HG01175.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.20-10463_20-10462d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962663 | ||||||
| chr2:174962663
|
CGGGGGGG others(4): Show |
C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-10472_20-10462d others(13): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962663 | ||||||
| chr2:174962668
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.20-10466C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962668 | ||||||
| chr2:174962670
|
G | GT | 32 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0203others(29): Show | 32 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-10469_20-10468i others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962670 | ||||||
| chr2:174962671
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.20-10469C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962671 | ||||||
| chr2:174962671
|
G | GT | 8 | a0001c0001t0001g0169a0001c0001t0004g0262a0001c0001t0004g0263others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-10470_20-10469i others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962671 | ||||||
| chr2:174962671
|
G | T | 49 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(46): Show | 49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.20-10469C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962671 | ||||||
| chr2:174962672
|
G | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0236others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-10470C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962672 | ||||||
| chr2:174962673
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-10471C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962673 | ||||||
| chr2:174962674
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.20-10472C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962674 | ||||||
| chr2:174962674
|
G | T | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | NA18979.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.20-10472C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962674 | ||||||
| chr2:174962677
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-10475C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962677 | ||||||
| chr2:174962682
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-10480C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962682 | ||||||
| chr2:174962721
|
C | T | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-10519G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962721 | ||||||
| chr2:174962747
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-10545A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962747 | ||||||
| chr2:174962754
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.20-10552T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962754 | ||||||
| chr2:174962813
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-10611C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962813 | ||||||
| chr2:174962830
|
A | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.20-10628T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962830 | ||||||
| chr2:174962898
|
A | C | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.20-10696T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174962898 | ||||||
| chr2:174963044
|
C | T | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-10842G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963044 | ||||||
| chr2:174963415
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.20-11213G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963415 | ||||||
| chr2:174963527
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.20-11325A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963527 | ||||||
| chr2:174963578
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-11376T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963578 | ||||||
| chr2:174963657
|
C | T | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-11455G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963657 | ||||||
| chr2:174963666
|
C | T | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.20-11464G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963666 | ||||||
| chr2:174963726
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.20-11524A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963726 | ||||||
| chr2:174963751
|
A | G | 1 | a0001c0001t0011g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.20-11549T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963751 | ||||||
| chr2:174963934
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-11732C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174963934 | ||||||
| chr2:174964196
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20-11994T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964196 | ||||||
| chr2:174964250
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.20-12048C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964250 | ||||||
| chr2:174964283
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.20-12081C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964283 | ||||||
| chr2:174964484
|
C | T | 1 | a0001c0001t0006g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.20-12282G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964484 | ||||||
| chr2:174964830
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.20-12628A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964830 | ||||||
| chr2:174964865
|
C | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-12663G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174964865 | ||||||
| chr2:174965142
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.20-12940G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174965142 | ||||||
| chr2:174965808
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20-13606C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174965808 | ||||||
| chr2:174966426
|
G | A | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.20-14224C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966426 | ||||||
| chr2:174966437
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-14235A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966437 | ||||||
| chr2:174966545
|
G | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.20-14343C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966545 | ||||||
| chr2:174966854
|
G | C | 2 | a0001c0001t0004g0266a0001c0001t0016g0267 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.20-14652C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966854 | ||||||
| chr2:174966881
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.20-14679T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966881 | ||||||
| chr2:174966931
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.20-14729T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174966931 | ||||||
| chr2:174967052
|
G | A | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.20-14850C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967052 | ||||||
| chr2:174967119
|
G | A | 16 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0002g0160others(13): Show | 16 | HG00639.hp2 HG01255.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.20-14917C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967119 | ||||||
| chr2:174967305
|
C | G | 275 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.20-15103G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967305 | ||||||
| chr2:174967318
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20-15116A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967318 | ||||||
| chr2:174967368
|
A | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-15166T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967368 | ||||||
| chr2:174967441
|
T | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.20-15239A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967441 | ||||||
| chr2:174967501
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20-15299A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967501 | ||||||
| chr2:174967513
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.20-15311T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967513 | ||||||
| chr2:174967532
|
A | G | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-15330T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967532 | ||||||
| chr2:174967539
|
A | G | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-15337T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967539 | ||||||
| chr2:174967803
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-15601G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967803 | ||||||
| chr2:174967876
|
G | GTAGCACT others(12): Show |
1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.20-15693_20-15675d others(21): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967876 | ||||||
| chr2:174967918
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0248others(1): Show | 4 | NA18968.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-15716G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174967918 | ||||||
| chr2:174968006
|
A | AATG | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-15807_20-15805d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968006 | ||||||
| chr2:174968104
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-15902A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968104 | ||||||
| chr2:174968158
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-15956C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968158 | ||||||
| chr2:174968223
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-16021A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968223 | ||||||
| chr2:174968413
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.20-16211T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968413 | ||||||
| chr2:174968658
|
C | T | 146 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.20-16456G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968658 | ||||||
| chr2:174968794
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-16592T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968794 | ||||||
| chr2:174968800
|
A | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-16598T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968800 | ||||||
| chr2:174968905
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-16703A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968905 | ||||||
| chr2:174968986
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-16784T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174968986 | ||||||
| chr2:174969176
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.20-16974C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969176 | ||||||
| chr2:174969405
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG00735.hp1 HG01070.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.20-17203C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969405 | ||||||
| chr2:174969770
|
T | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-17568A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969770 | ||||||
| chr2:174969794
|
G | A | 3 | a0001c0001t0007g0030a0001c0001t0007g0033a0001c0001t0007g0035 | 3 | HG01361.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.20-17592C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969794 | ||||||
| chr2:174969811
|
G | C | 1 | a0001c0001t0003g0010 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.20-17609C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969811 | ||||||
| chr2:174969880
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.20-17678A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969880 | ||||||
| chr2:174969901
|
T | C | 18 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-17699A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174969901 | ||||||
| chr2:174970323
|
T | G | 2 | a0001c0001t0005g0100a0001c0001t0005g0101 | 2 | HG02071.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.20-18121A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970323 | ||||||
| chr2:174970651
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.20-18449A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970651 | ||||||
| chr2:174970698
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-18496G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970698 | ||||||
| chr2:174970736
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-18534A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970736 | ||||||
| chr2:174970761
|
T | C | 38 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(35): Show | 38 | HG00735.hp2 HG01361.hp2 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.20-18559A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970761 | ||||||
| chr2:174970805
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-18603G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970805 | ||||||
| chr2:174970814
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0002g0182others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-18612T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174970814 | ||||||
| chr2:174971046
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-18844A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971046 | ||||||
| chr2:174971243
|
G | A | 1 | a0001c0001t0006g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.20-19041C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971243 | ||||||
| chr2:174971305
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0128a0001c0001t0001g0133 | 3 | NA18956.hp1 NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.20-19103C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971305 | ||||||
| chr2:174971313
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG00735.hp1 HG01070.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.20-19111C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971313 | ||||||
| chr2:174971346
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-19144C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971346 | ||||||
| chr2:174971381
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-19179A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971381 | ||||||
| chr2:174971439
|
A | G | 1 | a0001c0001t0003g0012 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.20-19237T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971439 | ||||||
| chr2:174971525
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00609.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.20-19323T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971525 | ||||||
| chr2:174971861
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.20-19659G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174971861 | ||||||
| chr2:174972021
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20-19819G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972021 | ||||||
| chr2:174972078
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-19876T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972078 | ||||||
| chr2:174972115
|
T | C | 90 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.20-19913A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972115 | ||||||
| chr2:174972156
|
C | A | 87 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.20-19954G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972156 | ||||||
| chr2:174972389
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20-20187C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972389 | ||||||
| chr2:174972422
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-20220A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972422 | ||||||
| chr2:174972430
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.20-20228T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972430 | ||||||
| chr2:174972485
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-20283G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972485 | ||||||
| chr2:174972529
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-20327T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972529 | ||||||
| chr2:174972597
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.20-20395C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972597 | ||||||
| chr2:174972735
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-20533C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972735 | ||||||
| chr2:174972749
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-20547G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972749 | ||||||
| chr2:174972810
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-20608T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972810 | ||||||
| chr2:174972815
|
TAAGG | T | 7 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0002g0110others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-20617_20-20614d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972815 | ||||||
| chr2:174972850
|
G | T | 1 | a0001c0001t0006g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.20-20648C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972850 | ||||||
| chr2:174972873
|
A | G | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.20-20671T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972873 | ||||||
| chr2:174972885
|
C | T | 251 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.20-20683G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972885 | ||||||
| chr2:174972971
|
C | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02071.hp1 NA18947.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-20769G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174972971 | ||||||
| chr2:174973254
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-21052A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973254 | ||||||
| chr2:174973292
|
C | T | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-21090G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973292 | ||||||
| chr2:174973334
|
G | A | 13 | a0001c0001t0001g0028a0001c0001t0006g0027a0001c0001t0006g0031others(10): Show | 13 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.20-21132C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973334 | ||||||
| chr2:174973468
|
G | A | 153 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.20-21266C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973468 | ||||||
| chr2:174973581
|
C | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18951.hp1 NA18978.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-21379G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973581 | ||||||
| chr2:174973850
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-21648A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174973850 | ||||||
| chr2:174974218
|
G | C | 1 | a0001c0001t0007g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.20-22016C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974218 | ||||||
| chr2:174974344
|
T | C | 1 | a0001c0001t0005g0180 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.20-22142A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974344 | ||||||
| chr2:174974457
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.20-22255T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974457 | ||||||
| chr2:174974458
|
GCAATGAA others(2682): Show |
G | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.20-24945_20-22257d others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974458 | ||||||
| chr2:174974844
|
T | C | 1 | a0001c0001t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.20-22642A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974844 | ||||||
| chr2:174974887
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.20-22685C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974887 | ||||||
| chr2:174974894
|
T | TAC | 34 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(31): Show | 34 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.20-22693_20-22692i others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974894
|
T | TACAC | 18 | a0001c0001t0001g0036a0001c0001t0001g0198a0001c0001t0001g0199others(15): Show | 18 | HG01361.hp1 HG02083.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.20-22693_20-22692i others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974894
|
T | TACACAC | 12 | a0001c0001t0001g0202a0001c0001t0001g0211a0001c0001t0001g0230others(9): Show | 12 | HG00438.hp1 HG00558.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-22693_20-22692i others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974894
|
T | TACACACA others(1): Show |
5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | NA18944.hp1 NA18959.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-22693_20-22692i others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974894
|
TTA | T | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(4): Show | 7 | HG01069.hp1 HG01070.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-22694_20-22693d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974894
|
TTAATACA others(5): Show |
T | 1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.20-22704_20-22693d others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974894 | ||||||
| chr2:174974895
|
T | A | 80 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.20-22693A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974895 | ||||||
| chr2:174974896
|
A | C | 80 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.20-22694T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974896 | ||||||
| chr2:174974898
|
T | C | 87 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.20-22696A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TAC | 40 | a0001c0001t0001g0042a0001c0001t0001g0086a0001c0001t0001g0108others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.20-22698_20-22697d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TACAC | 25 | a0001c0001t0001g0037a0001c0001t0001g0088a0001c0001t0001g0102others(22): Show | 25 | HG02257.hp1 HG02300.hp2 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.20-22700_20-22697d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TACACAC | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0067others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-22702_20-22697d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TACACACA others(1): Show |
32 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-22704_20-22697d others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TACACACA others(3): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0120 | 3 | HG01496.hp2 HG02300.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.20-22706_20-22697d others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-22712_20-22697d others(18): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
TAC | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01070.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-22698_20-22697d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0001g0203others(2): Show | 5 | HG00609.hp1 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-22706_20-22697d others(12): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974898
|
TACACACA others(5): Show |
T | 13 | a0001c0001t0002g0117a0001c0001t0005g0068a0001c0001t0005g0089others(10): Show | 13 | HG00423.hp2 HG01433.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-22708_20-22697d others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974898 | ||||||
| chr2:174974936
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.20-22735_20-22734i others(13): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974936 | ||||||
| chr2:174974938
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-22736C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174974938 | ||||||
| chr2:174975096
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.20-22894A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975096 | ||||||
| chr2:174975299
|
T | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | HG00735.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-23097A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975299 | ||||||
| chr2:174975369
|
T | C | 94 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.20-23167A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975369 | ||||||
| chr2:174975386
|
C | A | 1 | a0001c0001t0006g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.20-23184G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975386 | ||||||
| chr2:174975476
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-23274G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975476 | ||||||
| chr2:174975651
|
C | CA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-23450dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975651 | ||||||
| chr2:174975655
|
C | CA | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0051others(12): Show | 15 | HG00438.hp2 HG00558.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-23454dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975655 | ||||||
| chr2:174975658
|
A | AC | 25 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0169others(22): Show | 25 | HG01891.hp2 HG02015.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-23457_20-23456i others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975658 | ||||||
| chr2:174975659
|
A | C | 102 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0042others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.20-23457T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975659 | ||||||
| chr2:174975660
|
A | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-23458T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975660 | ||||||
| chr2:174975918
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.20-23716C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975918 | ||||||
| chr2:174975964
|
CA | C | 134 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.20-23763delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975964 | ||||||
| chr2:174975980
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.20-23778C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975980 | ||||||
| chr2:174975987
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-23785T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174975987 | ||||||
| chr2:174976126
|
C | CA | 12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0060others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-23925dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976126 | ||||||
| chr2:174976126
|
CA | C | 116 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.20-23925delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976126 | ||||||
| chr2:174976126
|
CAA | C | 79 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.20-23926_20-23925d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976126 | ||||||
| chr2:174976126
|
CAAA | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0195others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-23927_20-23925d others(5): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976126 | ||||||
| chr2:174976126
|
CAAAA | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(6): Show | 9 | HG02559.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-23928_20-23925d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976126 | ||||||
| chr2:174976176
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.20-23974A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976176 | ||||||
| chr2:174976367
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-24165T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976367 | ||||||
| chr2:174976428
|
G | A | 20 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(17): Show | 20 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.20-24226C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976428 | ||||||
| chr2:174976729
|
C | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-24527G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976729 | ||||||
| chr2:174976878
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.20-24676G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976878 | ||||||
| chr2:174976928
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-24726A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174976928 | ||||||
| chr2:174977148
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.20-24946G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977148 | ||||||
| chr2:174977150
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.20-24948C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977150 | ||||||
| chr2:174977283
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.20-25081T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977283 | ||||||
| chr2:174977527
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-25325A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977527 | ||||||
| chr2:174977641
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.20-25439A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977641 | ||||||
| chr2:174977872
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.20-25670G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977872 | ||||||
| chr2:174977904
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.20-25702T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977904 | ||||||
| chr2:174977999
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.20-25797T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174977999 | ||||||
| chr2:174978000
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.20-25798A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978000 | ||||||
| chr2:174978070
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.20-25868A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978070 | ||||||
| chr2:174978073
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.20-25871C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978073 | ||||||
| chr2:174978074
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.20-25872G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978074 | ||||||
| chr2:174978133
|
G | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-25931C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978133 | ||||||
| chr2:174978193
|
C | T | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.20-25991G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978193 | ||||||
| chr2:174978729
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.19+26165A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978729 | ||||||
| chr2:174978859
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.19+26035A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978859 | ||||||
| chr2:174978910
|
CCATCAAT others(30): Show |
C | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25947_19+25983d others(39): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978910 | ||||||
| chr2:174978949
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25945A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978949 | ||||||
| chr2:174978950
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25944G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978950 | ||||||
| chr2:174978954
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25940G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978954 | ||||||
| chr2:174978955
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25939T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978955 | ||||||
| chr2:174978956
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25938A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978956 | ||||||
| chr2:174978958
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25936G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978958 | ||||||
| chr2:174978959
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25935T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174978959 | ||||||
| chr2:174979254
|
TGA | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+25638_19+25639d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979254 | ||||||
| chr2:174979398
|
A | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0185 | 2 | HG00609.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.19+25496T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979398 | ||||||
| chr2:174979509
|
A | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18968.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.19+25385T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979509 | ||||||
| chr2:174979543
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.19+25351C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979543 | ||||||
| chr2:174979663
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.19+25231T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979663 | ||||||
| chr2:174979747
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+25147C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979747 | ||||||
| chr2:174979753
|
C | A | 1 | a0001c0001t0003g0012 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.19+25141G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979753 | ||||||
| chr2:174979865
|
A | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0169a0001c0001t0001g0170others(25): Show | 28 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.19+25029T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979865 | ||||||
| chr2:174979880
|
A | AAAAAC | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+25009_19+25013d others(7): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174979880 | ||||||
| chr2:174980013
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+24881A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980013 | ||||||
| chr2:174980023
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+24871T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980023 | ||||||
| chr2:174980027
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+24867C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980027 | ||||||
| chr2:174980078
|
C | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0006g0027others(11): Show | 14 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.19+24816G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980078 | ||||||
| chr2:174980496
|
T | C | 94 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.19+24398A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980496 | ||||||
| chr2:174980547
|
T | C | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00438.hp1 HG02083.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+24347A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980547 | ||||||
| chr2:174980716
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.19+24178A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980716 | ||||||
| chr2:174980777
|
T | C | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+24117A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980777 | ||||||
| chr2:174980803
|
G | A | 93 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.19+24091C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174980803 | ||||||
| chr2:174981075
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+23819A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981075 | ||||||
| chr2:174981431
|
TA | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+23462delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981431 | ||||||
| chr2:174981453
|
A | T | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19+23441T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981453 | ||||||
| chr2:174981648
|
T | G | 5 | a0001c0001t0002g0099a0001c0001t0002g0117a0001c0001t0002g0160others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+23246A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981648 | ||||||
| chr2:174981655
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.19+23239T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981655 | ||||||
| chr2:174981713
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19+23181A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981713 | ||||||
| chr2:174981776
|
C | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+23118G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981776 | ||||||
| chr2:174981792
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.19+23102G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981792 | ||||||
| chr2:174981843
|
C | T | 90 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.19+23051G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174981843 | ||||||
| chr2:174982010
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19+22884A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982010 | ||||||
| chr2:174982042
|
C | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 15 | HG00639.hp2 HG01081.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+22852G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982042 | ||||||
| chr2:174982043
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+22851C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982043 | ||||||
| chr2:174982101
|
C | T | 151 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.19+22793G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982101 | ||||||
| chr2:174982123
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.19+22771C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982123 | ||||||
| chr2:174982138
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.19+22756A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982138 | ||||||
| chr2:174982260
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19+22634T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982260 | ||||||
| chr2:174982319
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+22575T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982319 | ||||||
| chr2:174982367
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+22527A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982367 | ||||||
| chr2:174982411
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+22483G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982411 | ||||||
| chr2:174982417
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.19+22477C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982417 | ||||||
| chr2:174982431
|
C | T | 4 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0014others(1): Show | 4 | HG00558.hp2 HG02015.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+22463G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982431 | ||||||
| chr2:174982516
|
A | T | 113 | a0001c0001t0001g0042a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.19+22378T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982516 | ||||||
| chr2:174982739
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.19+22155G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982739 | ||||||
| chr2:174982826
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0053 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19+22068A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982826 | ||||||
| chr2:174982990
|
G | C | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19+21904C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982990 | ||||||
| chr2:174982999
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19+21895C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174982999 | ||||||
| chr2:174983129
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19+21765T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983129 | ||||||
| chr2:174983161
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.19+21733A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983161 | ||||||
| chr2:174983254
|
G | C | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+21640C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983254 | ||||||
| chr2:174983275
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.19+21619G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983275 | ||||||
| chr2:174983279
|
T | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG00735.hp1 HG01070.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.19+21615A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983279 | ||||||
| chr2:174983349
|
T | G | 22 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(19): Show | 22 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.19+21545A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983349 | ||||||
| chr2:174983467
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19+21427C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983467 | ||||||
| chr2:174983656
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+21238G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983656 | ||||||
| chr2:174983829
|
A | AAAAT | 14 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0044others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+21061_19+21064d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983829 | ||||||
| chr2:174983841
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19+21053A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983841 | ||||||
| chr2:174983898
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+20996A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174983898 | ||||||
| chr2:174984055
|
G | GT | 7 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0128others(4): Show | 7 | HG01517.hp1 HG03098.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+20838dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984055 | ||||||
| chr2:174984136
|
T | C | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+20758A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984136 | ||||||
| chr2:174984185
|
C | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+20709G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984185 | ||||||
| chr2:174984366
|
C | CT | 27 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(24): Show | 27 | HG00438.hp2 HG01175.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.19+20527dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984366 | ||||||
| chr2:174984366
|
CT | C | 5 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0169others(2): Show | 5 | HG00673.hp1 HG01069.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+20527delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984366 | ||||||
| chr2:174984432
|
G | A | 1 | a0002c0002t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19+20462C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984432 | ||||||
| chr2:174984479
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.19+20415G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984479 | ||||||
| chr2:174984665
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0009g0001 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.19+20229G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174984665 | ||||||
| chr2:174985020
|
A | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+19874T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985020 | ||||||
| chr2:174985228
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.19+19666G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985228 | ||||||
| chr2:174985490
|
AAC | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+19402_19+19403d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985490 | ||||||
| chr2:174985525
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+19369A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985525 | ||||||
| chr2:174985703
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+19191G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985703 | ||||||
| chr2:174985727
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+19167C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985727 | ||||||
| chr2:174985791
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.19+19103G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174985791 | ||||||
| chr2:174986277
|
T | C | 93 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.19+18617A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174986277 | ||||||
| chr2:174986517
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18968.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.19+18377G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174986517 | ||||||
| chr2:174986622
|
G | GT | 93 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.19+18271dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174986622 | ||||||
| chr2:174987044
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+17850A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987044 | ||||||
| chr2:174987045
|
A | G | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+17849T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987045 | ||||||
| chr2:174987406
|
C | CT | 16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+17487dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987406 | ||||||
| chr2:174987406
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+17488G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987406 | ||||||
| chr2:174987477
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.19+17417C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987477 | ||||||
| chr2:174987497
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19+17397A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987497 | ||||||
| chr2:174987521
|
C | A | 1 | a0001c0001t0001g0135 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.19+17373G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987521 | ||||||
| chr2:174987557
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+17337T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987557 | ||||||
| chr2:174987632
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.19+17262G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987632 | ||||||
| chr2:174987725
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+17169A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987725 | ||||||
| chr2:174987746
|
C | A | 1 | a0001c0001t0003g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19+17148G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987746 | ||||||
| chr2:174987886
|
T | C | 4 | a0001c0001t0002g0069a0001c0001t0002g0082a0001c0001t0002g0083others(1): Show | 4 | HG02155.hp1 NA18612.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+17008A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987886 | ||||||
| chr2:174987982
|
C | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+16912G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174987982 | ||||||
| chr2:174988090
|
T | G | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0213others(5): Show | 8 | NA18942.hp2 NA18967.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+16804A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988090 | ||||||
| chr2:174988097
|
C | T | 11 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+16797G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988097 | ||||||
| chr2:174988121
|
A | AG | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+16772dupC | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988121 | ||||||
| chr2:174988125
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+16769T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988125 | ||||||
| chr2:174988225
|
T | C | 178 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(175): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.19+16669A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988225 | ||||||
| chr2:174988313
|
C | T | 23 | a0001c0001t0001g0042a0001c0001t0001g0169a0001c0001t0001g0170others(20): Show | 23 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.19+16581G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988313 | ||||||
| chr2:174988356
|
C | CA | 16 | a0001c0001t0001g0042a0001c0001t0001g0135a0001c0001t0001g0158others(13): Show | 16 | HG02155.hp1 HG02559.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+16537dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988356 | ||||||
| chr2:174988501
|
G | A | 93 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.19+16393C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988501 | ||||||
| chr2:174988558
|
C | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+16336G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988558 | ||||||
| chr2:174988639
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19+16255A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174988639 | ||||||
| chr2:174989014
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19+15880T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989014 | ||||||
| chr2:174989016
|
T | TAGTAGTA others(15): Show |
1 | a0001c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19+15877_19+15878i others(24): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989016 | ||||||
| chr2:174989017
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19+15877G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989017 | ||||||
| chr2:174989212
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+15682G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989212 | ||||||
| chr2:174989364
|
A | G | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+15530T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989364 | ||||||
| chr2:174989370
|
C | A | 1 | a0001c0001t0006g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19+15524G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989370 | ||||||
| chr2:174989402
|
G | A | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+15492C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989402 | ||||||
| chr2:174989492
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.19+15402A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989492 | ||||||
| chr2:174989541
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.19+15353A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989541 | ||||||
| chr2:174989622
|
T | C | 13 | a0001c0001t0001g0036a0001c0001t0006g0027a0001c0001t0006g0031others(10): Show | 13 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+15272A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989622 | ||||||
| chr2:174989654
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19+15240C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989654 | ||||||
| chr2:174989656
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.19+15238C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989656 | ||||||
| chr2:174989659
|
T | A | 146 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.19+15235A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174989659 | ||||||
| chr2:174990210
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+14684G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990210 | ||||||
| chr2:174990233
|
C | CTG | 26 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0079others(23): Show | 26 | HG00735.hp1 HG01070.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.19+14659_19+14660d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990233 | ||||||
| chr2:174990233
|
CTG | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0136others(9): Show | 12 | HG00438.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.19+14659_19+14660d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990233 | ||||||
| chr2:174990233
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0159 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.19+14649_19+14660d others(14): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990233 | ||||||
| chr2:174990233
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.19+14647_19+14660d others(16): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990233 | ||||||
| chr2:174990260
|
T | TGAGA | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+14633_19+14634i others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990260 | ||||||
| chr2:174990260
|
TGTGA | T | 5 | a0001c0001t0005g0109a0001c0001t0006g0038a0001c0001t0006g0039others(2): Show | 5 | HG01433.hp2 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+14630_19+14633d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990260 | ||||||
| chr2:174990262
|
T | A | 55 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0092others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.19+14632A>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990262
|
T | TGA | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0004g0271others(1): Show | 4 | HG02970.hp2 NA18948.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+14630_19+14631d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990262
|
TGA | T | 11 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG00735.hp2 HG02300.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+14630_19+14631d others(4): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990262
|
TGAGA | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0197others(6): Show | 9 | HG02257.hp1 HG03017.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+14628_19+14631d others(6): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990262
|
TGAGAGA | T | 83 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.19+14626_19+14631d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990262
|
TGAGAGAG others(1): Show |
T | 3 | a0001c0001t0001g0195a0001c0001t0001g0207a0001c0001t0001g0255 | 3 | HG03225.hp2 HG04115.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19+14624_19+14631d others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990262 | ||||||
| chr2:174990264
|
A | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0108others(1): Show | 4 | HG02809.hp2 HG03098.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+14630T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990264 | ||||||
| chr2:174990268
|
A | T | 5 | a0001c0001t0001g0197a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG03017.hp1 HG04184.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+14626T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990268 | ||||||
| chr2:174990270
|
A | T | 85 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.19+14624T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990270 | ||||||
| chr2:174990272
|
A | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG00738.hp1 HG01517.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.19+14622T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990272 | ||||||
| chr2:174990274
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19+14620T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990274 | ||||||
| chr2:174990317
|
G | GC | 5 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+14576_19+14577i others(3): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990317 | ||||||
| chr2:174990318
|
T | C | 127 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.19+14576A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990318 | ||||||
| chr2:174990318
|
T | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+14576A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990318 | ||||||
| chr2:174990909
|
G | T | 132 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.19+13985C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990909 | ||||||
| chr2:174990968
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19+13926G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990968 | ||||||
| chr2:174990992
|
T | C | 4 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+13902A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174990992 | ||||||
| chr2:174991134
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.19+13760G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991134 | ||||||
| chr2:174991142
|
A | C | 90 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.19+13752T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991142 | ||||||
| chr2:174991424
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.19+13470C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991424 | ||||||
| chr2:174991519
|
ATGTAAC | A | 5 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(2): Show | 5 | NA18943.hp1 NA18965.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+13369_19+13374d others(8): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991519 | ||||||
| chr2:174991785
|
T | C | 1 | a0001c0001t0006g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19+13109A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991785 | ||||||
| chr2:174991984
|
G | A | 1 | a0001c0001t0010g0002 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.19+12910C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174991984 | ||||||
| chr2:174992064
|
G | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+12830C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992064 | ||||||
| chr2:174992157
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+12737C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992157 | ||||||
| chr2:174992229
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19+12665A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992229 | ||||||
| chr2:174992262
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19+12632A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992262 | ||||||
| chr2:174992288
|
T | G | 1 | a0001c0001t0003g0021 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.19+12606A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992288 | ||||||
| chr2:174992446
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0009g0001 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.19+12448T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992446 | ||||||
| chr2:174992486
|
A | G | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+12408T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992486 | ||||||
| chr2:174992630
|
C | A | 1 | a0001c0001t0001g0249 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.19+12264G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992630 | ||||||
| chr2:174992804
|
CT | C | 24 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0169others(21): Show | 24 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.19+12089delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992804 | ||||||
| chr2:174992846
|
G | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+12048C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992846 | ||||||
| chr2:174992981
|
A | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+11913T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992981 | ||||||
| chr2:174992986
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+11908G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174992986 | ||||||
| chr2:174993333
|
CA | C | 132 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.19+11560delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174993333 | ||||||
| chr2:174993512
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+11382A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174993512 | ||||||
| chr2:174993574
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+11320C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174993574 | ||||||
| chr2:174993774
|
G | C | 90 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.19+11120C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174993774 | ||||||
| chr2:174994518
|
A | G | 1 | a0001c0001t0004g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19+10376T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994518 | ||||||
| chr2:174994566
|
G | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+10328C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994566 | ||||||
| chr2:174994636
|
G | T | 117 | a0001c0001t0001g0042a0001c0001t0001g0094a0001c0001t0001g0095others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.19+10258C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994636 | ||||||
| chr2:174994778
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.19+10116A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994778 | ||||||
| chr2:174994876
|
GGACTTAA others(4): Show |
G | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+10007_19+10017d others(13): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994876 | ||||||
| chr2:174994950
|
A | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+9944T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174994950 | ||||||
| chr2:174995074
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.19+9820C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174995074 | ||||||
| chr2:174995425
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+9469C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174995425 | ||||||
| chr2:174995497
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18951.hp1 NA18978.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+9397C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174995497 | ||||||
| chr2:174995594
|
G | A | 90 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.19+9300C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174995594 | ||||||
| chr2:174995934
|
G | A | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+8960C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174995934 | ||||||
| chr2:174996034
|
G | GA | 94 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.19+8859dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996034 | ||||||
| chr2:174996045
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19+8849C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996045 | ||||||
| chr2:174996150
|
C | T | 2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.19+8744G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996150 | ||||||
| chr2:174996235
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+8659A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996235 | ||||||
| chr2:174996356
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+8538C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996356 | ||||||
| chr2:174996492
|
A | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 15 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+8402T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996492 | ||||||
| chr2:174996597
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.19+8297C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996597 | ||||||
| chr2:174996633
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+8261T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996633 | ||||||
| chr2:174996663
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+8231C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996663 | ||||||
| chr2:174996735
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.19+8159G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996735 | ||||||
| chr2:174996909
|
C | A | 1 | a0001c0001t0004g0272 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19+7985G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996909 | ||||||
| chr2:174996958
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.19+7936C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174996958 | ||||||
| chr2:174997312
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+7582A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997312 | ||||||
| chr2:174997326
|
C | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0181others(3): Show | 6 | HG01496.hp2 HG02622.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+7568G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997326 | ||||||
| chr2:174997754
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+7140C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997754 | ||||||
| chr2:174997797
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.19+7097G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997797 | ||||||
| chr2:174997828
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19+7066C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997828 | ||||||
| chr2:174997901
|
C | T | 19 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+6993G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997901 | ||||||
| chr2:174997941
|
G | C | 137 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.19+6953C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997941 | ||||||
| chr2:174997986
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.19+6908G>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997986 | ||||||
| chr2:174997986
|
C | T | 89 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.19+6908G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174997986 | ||||||
| chr2:174998040
|
T | C | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+6854A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998040 | ||||||
| chr2:174998132
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19+6762C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998132 | ||||||
| chr2:174998163
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19+6731G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998163 | ||||||
| chr2:174998302
|
C | CA | 95 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.19+6591dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998302 | ||||||
| chr2:174998302
|
C | CAA | 10 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(7): Show | 10 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+6590_19+6591dup others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998302 | ||||||
| chr2:174998302
|
CA | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0048others(14): Show | 17 | HG01361.hp2 HG02300.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.19+6591delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998302 | ||||||
| chr2:174998333
|
TA | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0004g0262others(13): Show | 16 | HG02257.hp2 HG02615.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+6560delT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998333 | ||||||
| chr2:174998417
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19+6477C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998417 | ||||||
| chr2:174998570
|
A | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+6324T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998570 | ||||||
| chr2:174998600
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19+6294A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998600 | ||||||
| chr2:174998690
|
T | C | 94 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.19+6204A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998690 | ||||||
| chr2:174998782
|
G | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 15 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+6112C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998782 | ||||||
| chr2:174998841
|
T | C | 13 | a0001c0001t0001g0036a0001c0001t0006g0027a0001c0001t0006g0031others(10): Show | 13 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+6053A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998841 | ||||||
| chr2:174998860
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19+6034A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998860 | ||||||
| chr2:174998868
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19+6026G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174998868 | ||||||
| chr2:174999060
|
C | CT | 4 | a0001c0001t0001g0103a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG02559.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+5833dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999060 | ||||||
| chr2:174999104
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+5790A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999104 | ||||||
| chr2:174999237
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.19+5657T>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999237 | ||||||
| chr2:174999424
|
C | T | 2 | a0001c0001t0005g0100a0001c0001t0005g0101 | 2 | HG02071.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.19+5470G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999424 | ||||||
| chr2:174999845
|
G | A | 1 | a0001c0001t0005g0180 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.19+5049C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999845 | ||||||
| chr2:174999855
|
T | C | 95 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.19+5039A>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999855 | ||||||
| chr2:174999961
|
C | T | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+4933G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 174999961 | ||||||
| chr2:175000081
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19+4813T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000081 | ||||||
| chr2:175000107
|
A | T | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00438.hp1 HG02083.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4787T>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000107 | ||||||
| chr2:175000137
|
A | AT | 9 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0193others(6): Show | 9 | HG02622.hp1 HG03017.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+4756dupA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000137 | ||||||
| chr2:175000137
|
AT | A | 150 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0036others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.19+4756delA | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000137 | ||||||
| chr2:175000328
|
G | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG02559.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+4566C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000328 | ||||||
| chr2:175000429
|
C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+4465G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000429 | ||||||
| chr2:175000664
|
G | A | 16 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(13): Show | 16 | HG02257.hp1 HG02257.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+4230C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000664 | ||||||
| chr2:175000696
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02055.hp1 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19+4198C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000696 | ||||||
| chr2:175000988
|
G | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3906C>G | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175000988 | ||||||
| chr2:175001119
|
AC | A | 5 | a0001c0001t0001g0037a0001c0001t0006g0038a0001c0001t0006g0039others(2): Show | 5 | HG02258.hp1 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3774delG | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175001119 | ||||||
| chr2:175001230
|
G | T | 16 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(13): Show | 16 | HG02257.hp1 HG02257.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+3664C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175001230 | ||||||
| chr2:175001359
|
C | A | 1 | a0001c0001t0010g0002 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.19+3535G>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175001359 | ||||||
| chr2:175001415
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19+3479G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175001415 | ||||||
| chr2:175001784
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+3110T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175001784 | ||||||
| chr2:175002241
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0185 | 2 | HG00609.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.19+2653C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175002241 | ||||||
| chr2:175002913
|
A | G | 1 | a0001c0001t0015g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19+1981T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175002913 | ||||||
| chr2:175003029
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.19+1865A>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175003029 | ||||||
| chr2:175003969
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.19+925T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175003969 | ||||||
| chr2:175004016
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.19+878C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004016 | ||||||
| chr2:175004045
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19+849G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004045 | ||||||
| chr2:175004089
|
T | TA | 19 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 19 | HG02257.hp1 HG02257.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+804dupT | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004089 | ||||||
| chr2:175004450
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+444G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004450 | ||||||
| chr2:175004523
|
AAAAT | A | 7 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+367_19+370delAT others(2): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004523 | ||||||
| chr2:175004641
|
C | T | 15 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 15 | HG01361.hp2 HG02258.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+253G>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004641 | ||||||
| chr2:175004667
|
G | A | 91 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.19+227C>T | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004667 | ||||||
| chr2:175004740
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.19+154C>A | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004740 | ||||||
| chr2:175004821
|
CCCCCCAG others(7): Show |
C | 4 | a0001c0001t0004g0273a0001c0001t0004g0274a0001c0001t0004g0275others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+59_19+72delCGGG others(10): Show |
CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004821 | ||||||
| chr2:175004827
|
A | G | 12 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+67T>C | CHN1 | ENSG00000128656.15 | transcript | ENST00000409900.9 | protein_coding | 1/12 | chr2 | 175004827 |