| geneid | 55137 |
|---|---|
| ensemblid | ENSG00000182263.14 |
| hgncid | 13285 |
| symbol | FIGN |
| name | fidgetin, microtubule severing factor |
| refseq_nuc | NM_018086.4 |
| refseq_prot | NP_060556.2 |
| ensembl_nuc | ENST00000333129.4 |
| ensembl_prot | ENSP00000333836.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 163602611 |
| end | 163736008 |
| strand | - |
| ver | v1.2 |
| region | chr2:163602611-163736008 |
| region5000 | chr2:163597611-163741008 |
| regionname0 | FIGN_chr2_163602611_163736008 |
| regionname5000 | FIGN_chr2_163597611_163741008 |
| 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 | 759 | 263 | 80 | 33 | 114 | 8 | 26 | 85 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0002 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0003 | 0/0 | 759 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0004 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| 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 | 2280 | 238 | 66 | 30 | 106 | 8 | 26 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0002 | 0/0 | 2280 | 15 | 14 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0003 | 0/0 | 2280 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0004 | 0/0 | 2280 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0005 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0006 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0007 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0008 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| c0009 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 7264 | 54 | 9 | 12 | 18 | 5 | 9 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0002 | 0/0 | 7266 | 29 | 0 | 0 | 27 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0003 | 1/0 | 7258 | 14 | 13 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0004 | 0/0 | 7265 | 10 | 4 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0005 | 0/0 | 7264 | 10 | 4 | 0 | 4 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0006 | 0/0 | 7265 | 10 | 3 | 5 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0007 | 0/0 | 7255 | 7 | 7 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0008 | 0/0 | 7259 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0009 | 0/0 | 7263 | 5 | 2 | 0 | 3 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0010 | 0/0 | 7267 | 5 | 0 | 0 | 5 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0011 | 0/0 | 7265 | 5 | 4 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0012 | 0/0 | 7265 | 4 | 0 | 0 | 0 | 0 | 4 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0013 | 0/0 | 7267 | 3 | 3 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0014 | 0/0 | 7266 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0015 | 0/0 | 7262 | 3 | 3 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0016 | 0/0 | 7264 | 3 | 2 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0017 | 0/0 | 7264 | 3 | 0 | 0 | 3 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0018 | 0/0 | 7265 | 3 | 0 | 0 | 3 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0019 | 0/0 | 7264 | 3 | 0 | 3 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0020 | 0/0 | 7264 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0021 | 0/0 | 7267 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0022 | 0/0 | 7265 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0023 | 0/0 | 7264 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0024 | 0/0 | 7262 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0025 | 0/0 | 7264 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0026 | 0/0 | 7264 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0027 | 0/0 | 7265 | 2 | 1 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0028 | 0/0 | 7256 | 2 | 1 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0029 | 0/0 | 7266 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0030 | 0/0 | 7263 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0031 | 0/0 | 7264 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0032 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0033 | 0/0 | 7262 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0034 | 0/0 | 7263 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0035 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0036 | 0/0 | 7266 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0037 | 0/0 | 7265 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0038 | 0/0 | 7266 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0039 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0040 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0041 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0042 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0043 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0044 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0045 | 0/0 | 7266 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0046 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0047 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0048 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0049 | 0/0 | 7266 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0050 | 0/0 | 7267 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0051 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0052 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0053 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0054 | 0/0 | 7262 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0055 | 0/0 | 7262 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0056 | 0/0 | 7260 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0057 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0058 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0059 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0060 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0061 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0062 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0063 | 0/0 | 7269 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0064 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0065 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0066 | 0/0 | 7259 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0067 | 0/0 | 7258 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0068 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0069 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0070 | 0/0 | 7266 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0071 | 0/0 | 7263 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0072 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0073 | 0/0 | 7257 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0074 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0075 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0076 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0077 | 0/0 | 7257 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0078 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0079 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0080 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0081 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0082 | 0/0 | 7266 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0083 | 0/0 | 7260 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0084 | 0/0 | 7267 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0085 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| t0086 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| 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 | 2280 | 238 | 66 | 30 | 106 | 8 | 26 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002 | 0/0 | 2280 | 15 | 14 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003 | 0/0 | 2280 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0004 | 0/0 | 2280 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0008 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0009 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0002c0006 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0003c0005 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0004c0007 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 9543 | 54 | 9 | 12 | 18 | 5 | 9 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0002 | 0/0 | 9545 | 27 | 0 | 0 | 25 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0003 | 1/0 | 9537 | 13 | 12 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0004 | 0/0 | 9544 | 9 | 3 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0005 | 0/0 | 9543 | 9 | 4 | 0 | 3 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0006 | 0/0 | 9544 | 10 | 3 | 5 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0007 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0008 | 0/0 | 9538 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0009 | 0/0 | 9542 | 3 | 1 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0010 | 0/0 | 9546 | 5 | 0 | 0 | 5 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0011 | 0/0 | 9544 | 3 | 2 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0012 | 0/0 | 9544 | 4 | 0 | 0 | 0 | 0 | 4 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0013 | 0/0 | 9546 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0014 | 0/0 | 9545 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0015 | 0/0 | 9541 | 3 | 3 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0016 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0017 | 0/0 | 9543 | 3 | 0 | 0 | 3 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0018 | 0/0 | 9544 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0019 | 0/0 | 9543 | 3 | 0 | 3 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0020 | 0/0 | 9543 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0021 | 0/0 | 9546 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0022 | 0/0 | 9544 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0023 | 0/0 | 9543 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0024 | 0/0 | 9541 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0025 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0026 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0027 | 0/0 | 9544 | 2 | 1 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0029 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0030 | 0/0 | 9542 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0031 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0032 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0034 | 0/0 | 9542 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0035 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0036 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0037 | 0/0 | 9544 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0038 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0039 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0040 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0041 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0042 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0043 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0044 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0045 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0046 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0047 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0048 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0049 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0050 | 0/0 | 9546 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0051 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0052 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0053 | 0/0 | 9543 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0055 | 0/0 | 9541 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0056 | 0/0 | 9539 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0057 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0058 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0059 | 0/0 | 9550 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0060 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0061 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0062 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0063 | 0/0 | 9548 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0064 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0065 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0066 | 0/0 | 9538 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0067 | 0/0 | 9537 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0069 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0070 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0071 | 0/0 | 9542 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0072 | 0/0 | 9541 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0073 | 0/0 | 9536 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0074 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0075 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0076 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0077 | 0/0 | 9536 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0078 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0079 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0080 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0081 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0082 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0083 | 0/0 | 9539 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0001t0084 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0003 | 0/0 | 9537 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0004 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0007 | 0/0 | 9534 | 5 | 5 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0009 | 0/0 | 9542 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0011 | 0/0 | 9544 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0013 | 0/0 | 9546 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0016 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0002t0028 | 0/0 | 9535 | 2 | 1 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003t0002 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003t0018 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003t0032 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003t0068 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0003t0085 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0004t0033 | 0/0 | 9541 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0008t0035 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0001c0009t0005 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0002c0006t0009 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0003c0005t0054 | 0/0 | 9541 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| a0004c0007t0086 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | copy fasta | chr2 | 163597611 | 163741008 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0011g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0012g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0016g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0017g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0017g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0018g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0018g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0019g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0019g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0020g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0021g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0022g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0022g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0023g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0023g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0024g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0025g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0025g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0026g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0027g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0027g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0029g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0029g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0031g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0031g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0032g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0034g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0034g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0035g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0036g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0036g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0037g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0037g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0038g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0039g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0040g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0041g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0042g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0043g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0044g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0045g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0046g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0047g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0048g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0049g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0050g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0051g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0052g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0053g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0055g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0056g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0057g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0058g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0059g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0060g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0061g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0062g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0063g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0064g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0065g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0066g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0067g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0069g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0070g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0071g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0072g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0073g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0074g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0075g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0076g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0077g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0078g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0079g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0080g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0081g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0082g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0083g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0001t0084g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0028g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0002t0028g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0032g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0068g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0003t0085g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0004t0033g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0004t0033g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0008t0035g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0001c0009t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0002c0006t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0003c0005t0054g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| a0004c0007t0086g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00323 | hp1 | a0001 | c0001 | t0082 | g0259 | EUR | FIN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00323 | hp2 | a0001 | c0001 | t0055 | g0046 | EUR | FIN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00408 | hp2 | a0001 | c0001 | t0052 | g0215 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0226 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0069 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00639 | hp1 | a0001 | c0001 | t0077 | g0051 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00639 | hp2 | a0003 | c0005 | t0054 | g0024 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00735 | hp2 | a0001 | c0001 | t0011 | g0114 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG00741 | hp2 | a0001 | c0001 | t0083 | g0253 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01070 | hp1 | a0001 | c0004 | t0033 | g0138 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01070 | hp2 | a0001 | c0001 | t0019 | g0255 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01071 | hp1 | a0001 | c0004 | t0033 | g0174 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01175 | hp1 | a0001 | c0002 | t0028 | g0187 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01261 | hp1 | a0001 | c0001 | t0016 | g0130 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0169 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01358 | hp2 | a0001 | c0001 | t0037 | g0265 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01361 | hp2 | a0001 | c0001 | t0019 | g0257 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01433 | hp2 | a0001 | c0001 | t0019 | g0258 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01496 | hp1 | a0001 | c0001 | t0065 | g0238 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01496 | hp2 | a0001 | c0001 | t0023 | g0155 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01515 | hp2 | a0001 | c0001 | t0067 | g0194 | EUR | IBS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01884 | hp2 | a0001 | c0001 | t0081 | g0261 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01891 | hp1 | a0001 | c0001 | t0047 | g0185 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01978 | hp1 | a0001 | c0001 | t0022 | g0079 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02040 | hp1 | a0001 | c0001 | t0060 | g0060 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02056 | hp2 | a0001 | c0001 | t0074 | g0179 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02074 | hp1 | a0001 | c0001 | t0034 | g0251 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02129 | hp1 | a0001 | c0001 | t0064 | g0237 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02132 | hp2 | a0002 | c0006 | t0009 | g0216 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02135 | hp1 | a0001 | c0001 | t0022 | g0217 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02135 | hp2 | a0001 | c0001 | t0041 | g0017 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CDX | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02257 | hp2 | a0001 | c0001 | t0071 | g0242 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0243 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02280 | hp1 | a0001 | c0001 | t0056 | g0121 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02280 | hp2 | a0001 | c0001 | t0031 | g0131 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02293 | hp1 | a0001 | c0001 | t0023 | g0165 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02293 | hp2 | a0001 | c0001 | t0075 | g0009 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02451 | hp1 | a0001 | c0001 | t0026 | g0095 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02572 | hp1 | a0001 | c0002 | t0011 | g0128 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0244 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02647 | hp1 | a0001 | c0002 | t0009 | g0120 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02647 | hp2 | a0001 | c0001 | t0026 | g0094 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0071 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02723 | hp1 | a0001 | c0001 | t0045 | g0176 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0140 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02735 | hp2 | a0001 | c0001 | t0012 | g0122 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02809 | hp1 | a0001 | c0001 | t0070 | g0103 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0193 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02886 | hp2 | a0001 | c0002 | t0011 | g0092 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0124 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02965 | hp2 | a0001 | c0002 | t0016 | g0067 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02970 | hp1 | a0001 | c0001 | t0059 | g0093 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02970 | hp2 | a0001 | c0001 | t0024 | g0001 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0104 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0078 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03098 | hp1 | a0001 | c0002 | t0013 | g0190 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03130 | hp2 | a0001 | c0001 | t0030 | g0127 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03139 | hp1 | a0001 | c0001 | t0025 | g0107 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0240 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0102 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03209 | hp2 | a0001 | c0001 | t0027 | g0108 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0136 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03225 | hp2 | a0001 | c0001 | t0057 | g0109 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0183 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03486 | hp1 | a0001 | c0002 | t0028 | g0134 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0038 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03492 | hp1 | a0001 | c0001 | t0020 | g0256 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03540 | hp1 | a0001 | c0001 | t0072 | g0160 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03540 | hp2 | a0001 | c0001 | t0053 | g0125 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03579 | hp1 | a0001 | c0002 | t0016 | g0132 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03579 | hp2 | a0001 | c0001 | t0030 | g0096 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03669 | hp2 | a0001 | c0001 | t0014 | g0045 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0015 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03710 | hp1 | a0001 | c0001 | t0027 | g0166 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03710 | hp2 | a0001 | c0001 | t0069 | g0082 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03831 | hp1 | a0001 | c0001 | t0042 | g0177 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03831 | hp2 | a0001 | c0001 | t0049 | g0020 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03927 | hp2 | a0001 | c0001 | t0020 | g0247 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0018 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0184 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18612 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18612 | hp2 | a0001 | c0001 | t0018 | g0203 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18941 | hp1 | a0001 | c0001 | t0009 | g0196 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18943 | hp1 | a0001 | c0001 | t0044 | g0016 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18944 | hp1 | a0001 | c0001 | t0020 | g0263 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18959 | hp2 | a0001 | c0001 | t0079 | g0170 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18960 | hp1 | a0001 | c0001 | t0029 | g0037 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18961 | hp1 | a0001 | c0001 | t0017 | g0148 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18961 | hp2 | a0004 | c0007 | t0086 | g0250 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18964 | hp1 | a0001 | c0001 | t0078 | g0058 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18964 | hp2 | a0001 | c0001 | t0034 | g0252 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18968 | hp1 | a0001 | c0001 | t0018 | g0028 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18973 | hp2 | a0001 | c0003 | t0002 | g0207 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18982 | hp1 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18982 | hp2 | a0001 | c0001 | t0043 | g0209 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18983 | hp1 | a0001 | c0001 | t0040 | g0210 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18983 | hp2 | a0001 | c0008 | t0035 | g0248 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18985 | hp1 | a0001 | c0001 | t0063 | g0233 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0061 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18988 | hp2 | a0001 | c0003 | t0018 | g0221 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0213 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18993 | hp1 | a0001 | c0001 | t0035 | g0246 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18993 | hp2 | a0001 | c0003 | t0032 | g0086 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18994 | hp1 | a0001 | c0001 | t0080 | g0264 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0064 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18995 | hp1 | a0001 | c0001 | t0048 | g0208 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18995 | hp2 | a0001 | c0001 | t0037 | g0260 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19000 | hp1 | a0001 | c0001 | t0051 | g0084 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19003 | hp1 | a0001 | c0003 | t0085 | g0262 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19004 | hp2 | a0001 | c0001 | t0014 | g0204 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19005 | hp1 | a0001 | c0001 | t0076 | g0022 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19006 | hp1 | a0001 | c0003 | t0068 | g0050 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19007 | hp1 | a0001 | c0001 | t0084 | g0254 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0073 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19030 | hp1 | a0001 | c0001 | t0031 | g0091 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0100 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19055 | hp2 | a0001 | c0001 | t0017 | g0151 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19056 | hp2 | a0001 | c0009 | t0005 | g0236 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19065 | hp1 | a0001 | c0001 | t0029 | g0214 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19065 | hp2 | a0001 | c0001 | t0066 | g0029 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19066 | hp1 | a0001 | c0001 | t0058 | g0156 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19066 | hp2 | a0001 | c0001 | t0036 | g0245 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19068 | hp2 | a0001 | c0001 | t0061 | g0149 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19070 | hp2 | a0001 | c0001 | t0017 | g0147 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19076 | hp1 | a0001 | c0001 | t0073 | g0011 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19076 | hp2 | a0001 | c0001 | t0062 | g0225 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19079 | hp2 | a0001 | c0001 | t0036 | g0249 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19083 | hp1 | a0001 | c0001 | t0039 | g0230 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19083 | hp2 | a0001 | c0001 | t0032 | g0014 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ASW | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0172 | AFR | ASW | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0229 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0126 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02486 | hp2 | a0001 | c0001 | t0046 | g0013 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG02559 | hp2 | a0001 | c0001 | t0050 | g0171 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0123 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20300 | hp1 | a0001 | c0002 | t0007 | g0135 | AFR | USA | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| NA20300 | hp2 | a0001 | c0001 | t0024 | g0001 | AFR | USA | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0113 | REF | REF | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:163602611
|
T | C | 1 | a0001 | 3 | HG02886.hp1 HG03098.hp1 HG03209.hp1 |
splice_region_variant | LOW | c.*6941A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | chr2 | 163602611 | ||||||
| chr2:163609662
|
C | T | 1 | a0002 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.2170G>A | p.Val724Ile | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2486/9537 | 2170/2280 | 724/759 | chr2 | 163609662 | ||
| chr2:163610148
|
C | T | 1 | a0003 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1684G>A | p.Glu562Lys | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2000/9537 | 1684/2280 | 562/759 | chr2 | 163610148 | ||
| chr2:163610300
|
G | A | 1 | a0004 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.1532C>T | p.Ala511Val | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1848/9537 | 1532/2280 | 511/759 | chr2 | 163610300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:163609663
|
G | A | 1 | a0001c0003 | 6 | NA18973.hp2 NA18988.hp2 NA18993.hp2 others(3): Show |
synonymous_variant | LOW | c.2169C>T | p.Pro723Pro | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2485/9537 | 2169/2280 | 723/759 | chr2 | 163609663 | ||
| chr2:163609720
|
G | A | 1 | a0001c0004 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2112C>T | p.Pro704Pro | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2428/9537 | 2112/2280 | 704/759 | chr2 | 163609720 | ||
| chr2:163610977
|
T | A | 1 | a0001c0002 | 15 | HG01175.hp1 HG02572.hp1 HG02630.hp2 others(12): Show |
synonymous_variant | LOW | c.855A>T | p.Leu285Leu | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1171/9537 | 855/2280 | 285/759 | chr2 | 163610977 | ||
| chr2:163611511
|
T | C | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.321A>G | p.Glu107Glu | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 637/9537 | 321/2280 | 107/759 | chr2 | 163611511 | ||
| chr2:163611685
|
G | C | 1 | a0001c0009 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.147C>G | p.Thr49Thr | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 463/9537 | 147/2280 | 49/759 | chr2 | 163611685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:163602871
|
A | G | 9 | a0001c0001t0012a0001c0001t0014a0001c0001t0038others(6): Show | 14 | HG00323.hp1 HG02559.hp2 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6681T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6681 | chr2 | 163602871 | |||||
| chr2:163602880
|
T | A | 2 | a0001c0001t0025a0001c0001t0031 | 4 | HG02109.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6672A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6672 | chr2 | 163602880 | |||||
| chr2:163602912
|
G | T | 32 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(29): Show | 76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6640C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6640 | chr2 | 163602912 | |||||
| chr2:163603217
|
A | T | 2 | a0001c0001t0032a0001c0003t0032 | 2 | NA18993.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6335T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6335 | chr2 | 163603217 | |||||
| chr2:163603432
|
C | G | 1 | a0001c0001t0026 | 2 | HG02451.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6120G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6120 | chr2 | 163603432 | |||||
| chr2:163603706
|
A | C | 1 | a0001c0001t0066 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5846T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5846 | chr2 | 163603706 | |||||
| chr2:163604118
|
A | G | 2 | a0001c0001t0055a0003c0005t0054 | 2 | HG00323.hp2 HG00639.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5434T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5434 | chr2 | 163604118 | |||||
| chr2:163604247
|
T | G | 1 | a0001c0001t0064 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5305A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5305 | chr2 | 163604247 | |||||
| chr2:163604367
|
G | A | 4 | a0001c0001t0055a0001c0001t0056a0001c0001t0057others(1): Show | 4 | HG00323.hp2 HG00639.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5185C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5185 | chr2 | 163604367 | |||||
| chr2:163604437
|
A | G | 34 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(31): Show | 78 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5115T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5115 | chr2 | 163604437 | |||||
| chr2:163604659
|
T | C | 1 | a0003c0005t0054 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4893A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4893 | chr2 | 163604659 | |||||
| chr2:163604802
|
C | CAG | 32 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(29): Show | 76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*4748_*4749dupCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4749 | chr2 | 163604802 | |||||
| chr2:163604802
|
C | CAGAG | 5 | a0001c0001t0055a0001c0001t0059a0001c0001t0063others(2): Show | 5 | HG00323.hp2 HG00639.hp2 HG00741.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4746_*4749dupCTCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4749 | chr2 | 163604802 | |||||
| chr2:163604849
|
G | A | 1 | a0001c0001t0065 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4703C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4703 | chr2 | 163604849 | |||||
| chr2:163604936
|
C | CTTTTT | 16 | a0001c0001t0009a0001c0001t0013a0001c0001t0015others(13): Show | 28 | HG00323.hp2 HG00639.hp2 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4611_*4615dupAAAA others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
C | CTTTTTT | 16 | a0001c0001t0005a0001c0001t0018a0001c0001t0019others(13): Show | 28 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4610_*4615dupAAAA others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
C | CTTTTTTT | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | 138 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*4609_*4615dupAAAA others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0006a0001c0001t0010a0001c0001t0037others(5): Show | 22 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4608_*4615dupAAAA others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0012a0001c0001t0014a0001c0001t0038others(4): Show | 12 | HG00323.hp1 HG02698.hp1 HG02735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4607_*4615dupAAAA others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0048a0001c0001t0049a0001c0001t0058 | 3 | HG03831.hp2 NA18995.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4606_*4615dupAAAA others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
CT | C | 4 | a0001c0001t0067a0001c0001t0077a0001c0001t0083others(1): Show | 5 | HG00639.hp1 HG00741.hp2 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4615delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | |||||
| chr2:163604936
|
CTT | C | 2 | a0001c0001t0007a0001c0002t0007 | 7 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4614_*4615delAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4614 | chr2 | 163604936 | |||||
| chr2:163604984
|
T | C | 9 | a0001c0001t0007a0001c0001t0015a0001c0001t0026others(6): Show | 18 | HG00323.hp2 HG00639.hp2 HG01175.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4568A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4568 | chr2 | 163604984 | |||||
| chr2:163605443
|
G | A | 1 | a0001c0001t0074 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4109 | chr2 | 163605443 | |||||
| chr2:163605454
|
A | C | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4098T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4098 | chr2 | 163605454 | |||||
| chr2:163605488
|
A | G | 1 | a0001c0001t0055 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4064T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4064 | chr2 | 163605488 | |||||
| chr2:163605695
|
G | A | 1 | a0001c0003t0068 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3857C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3857 | chr2 | 163605695 | |||||
| chr2:163605897
|
AT | A | 44 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(41): Show | 100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3654delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3654 | chr2 | 163605897 | |||||
| chr2:163605897
|
ATT | A | 2 | a0001c0001t0012a0001c0001t0049 | 5 | HG02698.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3653_*3654delAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3653 | chr2 | 163605897 | |||||
| chr2:163605931
|
C | T | 1 | a0001c0001t0026 | 2 | HG02451.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3621G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3621 | chr2 | 163605931 | |||||
| chr2:163606014
|
T | C | 1 | a0001c0001t0075 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3538 | chr2 | 163606014 | |||||
| chr2:163606145
|
A | T | 1 | a0001c0001t0062 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3407 | chr2 | 163606145 | |||||
| chr2:163606168
|
C | T | 1 | a0001c0001t0030 | 2 | HG03130.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3384G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3384 | chr2 | 163606168 | |||||
| chr2:163606297
|
A | G | 2 | a0001c0001t0043a0001c0001t0080 | 2 | NA18982.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3255T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3255 | chr2 | 163606297 | |||||
| chr2:163606611
|
C | G | 1 | a0003c0005t0054 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2941G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2941 | chr2 | 163606611 | |||||
| chr2:163606623
|
C | T | 2 | a0001c0001t0017a0001c0001t0061 | 4 | NA18961.hp1 NA19055.hp2 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2929G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2929 | chr2 | 163606623 | |||||
| chr2:163606782
|
T | C | 1 | a0001c0001t0050 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2770 | chr2 | 163606782 | |||||
| chr2:163606904
|
A | T | 2 | a0001c0001t0035a0001c0008t0035 | 2 | NA18983.hp2 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2648T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2648 | chr2 | 163606904 | |||||
| chr2:163606976
|
T | A | 31 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(28): Show | 75 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2576A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2576 | chr2 | 163606976 | |||||
| chr2:163606981
|
G | A | 7 | a0001c0001t0009a0001c0001t0030a0001c0001t0034others(4): Show | 12 | HG01070.hp1 HG01071.hp1 HG02074.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2571C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2571 | chr2 | 163606981 | |||||
| chr2:163607131
|
C | T | 1 | a0001c0001t0069 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2421G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2421 | chr2 | 163607131 | |||||
| chr2:163607528
|
CTATGT | C | 4 | a0001c0001t0055a0001c0001t0056a0001c0001t0057others(1): Show | 4 | HG00323.hp2 HG00639.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2019_*2023delACAT others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2019 | chr2 | 163607528 | |||||
| chr2:163607546
|
A | G | 27 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(24): Show | 97 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2006T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2006 | chr2 | 163607546 | |||||
| chr2:163607588
|
G | GA | 3 | a0001c0001t0011a0001c0001t0045a0001c0002t0011 | 6 | HG00735.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1963dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1963 | chr2 | 163607588 | |||||
| chr2:163607593
|
A | C | 1 | a0001c0004t0033 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1959T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1959 | chr2 | 163607593 | |||||
| chr2:163607647
|
T | A | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1905A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1905 | chr2 | 163607647 | |||||
| chr2:163607722
|
A | C | 2 | a0001c0001t0025a0001c0001t0031 | 4 | HG02109.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1830T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1830 | chr2 | 163607722 | |||||
| chr2:163608027
|
T | C | 1 | a0001c0001t0031 | 2 | HG02280.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1525A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1525 | chr2 | 163608027 | |||||
| chr2:163608045
|
T | C | 2 | a0001c0001t0046a0001c0001t0081 | 2 | HG01884.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1507A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1507 | chr2 | 163608045 | |||||
| chr2:163608087
|
T | C | 1 | a0001c0001t0058 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1465A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1465 | chr2 | 163608087 | |||||
| chr2:163608256
|
G | GAT | 3 | a0001c0001t0013a0001c0001t0047a0001c0002t0013 | 4 | HG01891.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1294_*1295dupAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1295 | chr2 | 163608256 | |||||
| chr2:163608267
|
G | A | 61 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(58): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1285C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1285 | chr2 | 163608267 | |||||
| chr2:163608793
|
G | T | 1 | a0001c0001t0038 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 759 | chr2 | 163608793 | |||||
| chr2:163608842
|
T | A | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*710A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 710 | chr2 | 163608842 | |||||
| chr2:163609119
|
T | C | 1 | a0001c0001t0078 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 433 | chr2 | 163609119 | |||||
| chr2:163609206
|
G | A | 23 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(20): Show | 63 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*346C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 346 | chr2 | 163609206 | |||||
| chr2:163609522
|
T | C | 2 | a0001c0001t0079a0004c0007t0086 | 2 | NA18959.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*30A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 30 | chr2 | 163609522 | |||||
| chr2:163609529
|
AT | A | 19 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(16): Show | 88 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*22delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 22 | chr2 | 163609529 | |||||
| chr2:163735859
|
C | T | 14 | a0001c0001t0019a0001c0001t0020a0001c0001t0034others(11): Show | 21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-167G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/3 | 932 | chr2 | 163735859 | |||||
| chr2:163735905
|
G | C | 14 | a0001c0001t0019a0001c0001t0020a0001c0001t0034others(11): Show | 21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-213C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/3 | chr2 | 163735905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:163611818
|
G | T | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-12C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611818 | ||||||
| chr2:163611824
|
A | G | 1 | a0001c0001t0025g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-18T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611824 | ||||||
| chr2:163611850
|
A | G | 106 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(103): Show | 106 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.26-44T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611850 | ||||||
| chr2:163611904
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-98A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611904 | ||||||
| chr2:163611933
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0004g0042a0001c0001t0004g0223 | 3 | NA18955.hp1 NA18977.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.26-127G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611933 | ||||||
| chr2:163611951
|
T | C | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-145A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611951 | ||||||
| chr2:163612046
|
A | G | 1 | a0001c0001t0004g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-240T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612046 | ||||||
| chr2:163612096
|
T | A | 21 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0175others(18): Show | 21 | HG00323.hp1 HG01106.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-290A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612096 | ||||||
| chr2:163612317
|
C | A | 2 | a0001c0004t0033g0138a0001c0004t0033g0174 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.26-511G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612317 | ||||||
| chr2:163612587
|
G | GA | 22 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0077others(19): Show | 23 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.26-782dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612587 | ||||||
| chr2:163612665
|
C | T | 1 | a0001c0001t0047g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.26-859G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612665 | ||||||
| chr2:163612676
|
G | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-870C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612676 | ||||||
| chr2:163612692
|
A | ATG | 85 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0056others(82): Show | 85 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-888_26-887dupCA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | ||||||
| chr2:163612692
|
A | ATGTG | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0023others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.26-890_26-887dupCA others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | ||||||
| chr2:163612692
|
A | ATGTGTG | 12 | a0001c0001t0001g0119a0001c0001t0002g0205a0001c0001t0003g0097others(9): Show | 13 | HG01261.hp1 HG01496.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-892_26-887dupCA others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | ||||||
| chr2:163612692
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0077a0001c0001t0009g0064a0001c0001t0034g0252others(2): Show | 5 | HG02559.hp2 HG03579.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-894_26-887dupCA others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | ||||||
| chr2:163612692
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-896_26-887dupCA others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | ||||||
| chr2:163612749
|
C | CAT | 7 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0003g0241others(4): Show | 7 | HG00639.hp2 HG01257.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-945_26-944dupAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | ||||||
| chr2:163612749
|
CAT | C | 130 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0023others(127): Show | 131 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.26-945_26-944delAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | ||||||
| chr2:163612749
|
CATAT | C | 19 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0144others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-947_26-944delAT others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | ||||||
| chr2:163612785
|
A | AAG | 117 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(114): Show | 117 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.26-981_26-980dupCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612785 | ||||||
| chr2:163612849
|
T | C | 29 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(26): Show | 29 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-1043A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612849 | ||||||
| chr2:163612853
|
T | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | NA18943.hp2 NA18959.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-1047A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612853 | ||||||
| chr2:163613126
|
C | T | 1 | a0001c0001t0071g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-1320G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613126 | ||||||
| chr2:163613534
|
C | T | 57 | a0001c0001t0001g0056a0001c0001t0001g0142a0001c0001t0001g0144others(54): Show | 57 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.26-1728G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613534 | ||||||
| chr2:163613602
|
G | A | 1 | a0001c0001t0022g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-1796C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613602 | ||||||
| chr2:163614238
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-2432T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614238 | ||||||
| chr2:163614353
|
C | A | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-2547G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614353 | ||||||
| chr2:163614467
|
T | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0077others(20): Show | 24 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.26-2661A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614467 | ||||||
| chr2:163614634
|
C | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.26-2828G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614634 | ||||||
| chr2:163614686
|
G | A | 22 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0077others(19): Show | 23 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.26-2880C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614686 | ||||||
| chr2:163614709
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-2903G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614709 | ||||||
| chr2:163614823
|
T | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.26-3017A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614823 | ||||||
| chr2:163614833
|
CAGG | C | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0005g0178 | 3 | NA18945.hp2 NA18969.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.26-3030_26-3028del others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614833 | ||||||
| chr2:163614870
|
A | T | 63 | a0001c0001t0001g0056a0001c0001t0001g0142a0001c0001t0001g0144others(60): Show | 63 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-3064T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614870 | ||||||
| chr2:163614912
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26-3106T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614912 | ||||||
| chr2:163614922
|
A | G | 1 | a0001c0001t0004g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-3116T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614922 | ||||||
| chr2:163614948
|
G | A | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-3142C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614948 | ||||||
| chr2:163615046
|
A | T | 5 | a0001c0001t0021g0183a0001c0001t0021g0243a0001c0001t0025g0107others(2): Show | 5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-3240T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615046 | ||||||
| chr2:163615077
|
T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-3271A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615077 | ||||||
| chr2:163615216
|
A | G | 5 | a0001c0001t0021g0183a0001c0001t0021g0243a0001c0001t0025g0107others(2): Show | 5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-3410T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615216 | ||||||
| chr2:163615345
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-3539A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615345 | ||||||
| chr2:163615475
|
A | T | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-3669T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615475 | ||||||
| chr2:163615578
|
T | A | 2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-3772A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615578 | ||||||
| chr2:163615595
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(187): Show | 190 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.26-3789A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615595 | ||||||
| chr2:163615764
|
T | A | 17 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0164others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-3958A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615764 | ||||||
| chr2:163615912
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0083others(6): Show | 9 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-4106T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615912 | ||||||
| chr2:163616058
|
GT | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0083others(6): Show | 9 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-4253delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616058 | ||||||
| chr2:163616060
|
A | G | 66 | a0001c0001t0001g0056a0001c0001t0001g0142a0001c0001t0001g0144others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.26-4254T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616060 | ||||||
| chr2:163616139
|
A | G | 1 | a0001c0001t0004g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.26-4333T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616139 | ||||||
| chr2:163616726
|
G | C | 1 | a0001c0001t0004g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-4920C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616726 | ||||||
| chr2:163616936
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(233): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.26-5130T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616936 | ||||||
| chr2:163617007
|
G | A | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26-5201C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617007 | ||||||
| chr2:163617149
|
C | T | 3 | a0001c0001t0003g0097a0001c0001t0013g0193a0001c0001t0031g0131 | 3 | HG02280.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.26-5343G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617149 | ||||||
| chr2:163617243
|
A | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.26-5437T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617243 | ||||||
| chr2:163617371
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0077a0001c0001t0014g0045 | 3 | HG03669.hp2 HG03927.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.26-5565A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617371 | ||||||
| chr2:163617712
|
T | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-5906A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617712 | ||||||
| chr2:163617714
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26-5908C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617714 | ||||||
| chr2:163617759
|
A | C | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-5953T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617759 | ||||||
| chr2:163618127
|
G | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-6321C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618127 | ||||||
| chr2:163618414
|
C | CT | 39 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(36): Show | 39 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.26-6609dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618414 | ||||||
| chr2:163618414
|
CT | C | 6 | a0001c0001t0001g0144a0001c0001t0002g0005a0001c0001t0002g0075others(3): Show | 6 | NA18945.hp2 NA18946.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-6609delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618414 | ||||||
| chr2:163618680
|
T | C | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-6874A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618680 | ||||||
| chr2:163619171
|
A | G | 1 | a0001c0001t0063g0233 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.26-7365T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619171 | ||||||
| chr2:163619313
|
T | G | 1 | a0001c0001t0003g0186 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-7507A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619313 | ||||||
| chr2:163619448
|
C | T | 1 | a0001c0001t0010g0213 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.26-7642G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619448 | ||||||
| chr2:163619576
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-7770C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619576 | ||||||
| chr2:163619805
|
T | A | 1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-7999A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619805 | ||||||
| chr2:163619854
|
A | T | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-8048T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619854 | ||||||
| chr2:163619980
|
A | T | 2 | a0001c0001t0019g0255a0001c0001t0027g0166 | 2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.26-8174T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619980 | ||||||
| chr2:163619984
|
A | G | 1 | a0001c0002t0016g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26-8178T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619984 | ||||||
| chr2:163620036
|
T | A | 1 | a0001c0001t0061g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-8230A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620036 | ||||||
| chr2:163620266
|
C | T | 1 | a0001c0001t0082g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-8460G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620266 | ||||||
| chr2:163620377
|
G | T | 1 | a0001c0001t0013g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.26-8571C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620377 | ||||||
| chr2:163620407
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-8601A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620407 | ||||||
| chr2:163620590
|
T | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.26-8784A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620590 | ||||||
| chr2:163620705
|
C | T | 1 | a0001c0001t0022g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-8899G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620705 | ||||||
| chr2:163620851
|
T | TTG | 53 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0141others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.26-9047_26-9046dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
T | TTGTG | 29 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(26): Show | 29 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-9049_26-9046dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
T | TTGTGTG | 29 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0055others(26): Show | 29 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-9051_26-9046dup others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
T | TTGTGTGT others(1): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0003g0182others(15): Show | 18 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.26-9053_26-9046dup others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
T | TTGTGTGT others(3): Show |
63 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0027others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-9055_26-9046dup others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
T | TTGTGTGT others(5): Show |
7 | a0001c0001t0002g0088a0001c0001t0005g0078a0001c0001t0008g0072others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-9057_26-9046dup others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
TTG | T | 2 | a0001c0001t0004g0191a0001c0001t0024g0001 | 3 | HG02970.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-9047_26-9046del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620851
|
TTGTG | T | 24 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0077others(21): Show | 24 | HG00558.hp1 HG01070.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.26-9049_26-9046del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | ||||||
| chr2:163620879
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0076g0022 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.26-9074_26-9073ins others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620879 | ||||||
| chr2:163621211
|
A | G | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-9405T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621211 | ||||||
| chr2:163621262
|
G | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0110others(93): Show | 96 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.26-9456C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621262 | ||||||
| chr2:163621268
|
T | C | 5 | a0001c0001t0015g0123a0001c0001t0015g0124a0001c0001t0015g0126others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-9462A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621268 | ||||||
| chr2:163621341
|
C | T | 136 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0047others(133): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.26-9535G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621341 | ||||||
| chr2:163621901
|
G | A | 10 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0002g0003others(7): Show | 10 | HG02027.hp1 NA18612.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-10095C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621901 | ||||||
| chr2:163621926
|
C | T | 1 | a0001c0001t0081g0261 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-10120G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621926 | ||||||
| chr2:163622137
|
G | A | 1 | a0001c0002t0007g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.26-10331C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622137 | ||||||
| chr2:163622287
|
A | G | 1 | a0001c0001t0048g0208 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.26-10481T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622287 | ||||||
| chr2:163622319
|
G | A | 6 | a0001c0001t0017g0147a0001c0001t0017g0148a0001c0001t0017g0151others(3): Show | 6 | NA18959.hp2 NA18961.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-10513C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622319 | ||||||
| chr2:163622334
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0031g0091a0001c0001t0059g0093 | 3 | HG02970.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-10528T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622334 | ||||||
| chr2:163622358
|
G | T | 8 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0015g0126others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-10552C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622358 | ||||||
| chr2:163622441
|
C | T | 10 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0005g0158others(7): Show | 10 | HG00408.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-10635G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622441 | ||||||
| chr2:163622618
|
G | T | 6 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0021g0243others(3): Show | 6 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-10812C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622618 | ||||||
| chr2:163622699
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.26-10893G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622699 | ||||||
| chr2:163622776
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.26-10970C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622776 | ||||||
| chr2:163622921
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0002g0089 | 2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.26-11115T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622921 | ||||||
| chr2:163623271
|
A | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.26-11465T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623271 | ||||||
| chr2:163623291
|
A | C | 3 | a0001c0001t0005g0040a0001c0001t0035g0246a0001c0008t0035g0248 | 3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-11485T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623291 | ||||||
| chr2:163623334
|
T | C | 15 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0005g0158others(12): Show | 15 | HG00408.hp1 HG00558.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-11528A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623334 | ||||||
| chr2:163623397
|
T | C | 1 | a0001c0001t0021g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-11591A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623397 | ||||||
| chr2:163623447
|
C | T | 20 | a0001c0001t0001g0118a0001c0001t0001g0218a0001c0001t0003g0186others(17): Show | 20 | HG00735.hp2 HG01175.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-11641G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623447 | ||||||
| chr2:163623570
|
T | C | 1 | a0001c0001t0006g0041 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26-11764A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623570 | ||||||
| chr2:163623808
|
C | T | 5 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0029g0214others(2): Show | 5 | HG00558.hp1 HG03942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-12002G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623808 | ||||||
| chr2:163623869
|
T | C | 8 | a0001c0001t0001g0111a0001c0001t0001g0152a0001c0001t0001g0162others(5): Show | 8 | HG00140.hp2 HG01070.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-12063A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623869 | ||||||
| chr2:163623935
|
C | T | 2 | a0001c0001t0011g0114a0001c0001t0011g0188 | 2 | HG00735.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.26-12129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623935 | ||||||
| chr2:163624065
|
TTGATA | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.26-12264_26-12260d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624065 | ||||||
| chr2:163624119
|
C | G | 5 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(2): Show | 5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-12313G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624119 | ||||||
| chr2:163624179
|
T | C | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-12373A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624179 | ||||||
| chr2:163624691
|
C | CAT | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(105): Show | 108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.26-12887_26-12886d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | ||||||
| chr2:163624691
|
C | CATAT | 13 | a0001c0001t0001g0142a0001c0001t0002g0003a0001c0001t0003g0241others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-12889_26-12886d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | ||||||
| chr2:163624691
|
C | CATATAT | 5 | a0001c0001t0011g0114a0001c0001t0011g0188a0001c0001t0013g0102others(2): Show | 5 | HG00735.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-12891_26-12886d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | ||||||
| chr2:163624708
|
A | ATAT | 6 | a0001c0001t0002g0074a0001c0001t0006g0239a0001c0001t0018g0028others(3): Show | 6 | HG01175.hp1 HG02074.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-12903_26-12902i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | ||||||
| chr2:163624708
|
A | T | 5 | a0001c0001t0001g0175a0001c0001t0003g0192a0001c0001t0005g0158others(2): Show | 5 | HG01106.hp1 HG01515.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-12902T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | ||||||
| chr2:163624708
|
AT | A | 7 | a0001c0001t0001g0119a0001c0001t0007g0068a0001c0001t0047g0185others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-12903delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | ||||||
| chr2:163624709
|
T | TA | 24 | a0001c0001t0001g0112a0001c0001t0001g0220a0001c0001t0002g0146others(21): Show | 24 | HG00323.hp1 HG00609.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-12904_26-12903i others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624709 | ||||||
| chr2:163624709
|
T | TATA | 49 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0141others(46): Show | 49 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.26-12904_26-12903i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624709 | ||||||
| chr2:163624710
|
T | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(104): Show | 107 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.26-12904A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624710 | ||||||
| chr2:163624711
|
T | A | 3 | a0001c0001t0002g0044a0001c0001t0074g0179a0001c0002t0009g0120 | 3 | HG02056.hp2 HG02132.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.26-12905A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624711 | ||||||
| chr2:163624712
|
T | A | 4 | a0001c0001t0005g0040a0001c0001t0006g0041a0001c0001t0009g0129others(1): Show | 4 | HG00408.hp1 HG02257.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-12906A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624712 | ||||||
| chr2:163624922
|
T | C | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.26-13116A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624922 | ||||||
| chr2:163624951
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-13145T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624951 | ||||||
| chr2:163624978
|
G | T | 1 | a0001c0001t0018g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.26-13172C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624978 | ||||||
| chr2:163624996
|
C | A | 3 | a0001c0001t0004g0191a0001c0001t0007g0068a0001c0002t0011g0092 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-13190G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624996 | ||||||
| chr2:163625129
|
C | T | 9 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0015g0126others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-13323G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625129 | ||||||
| chr2:163625227
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0077 | 2 | HG01167.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.26-13421T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625227 | ||||||
| chr2:163625257
|
C | A | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-13451G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625257 | ||||||
| chr2:163625278
|
G | C | 1 | a0001c0001t0005g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.26-13472C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625278 | ||||||
| chr2:163625358
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 47 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-13552T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625358 | ||||||
| chr2:163625427
|
T | C | 2 | a0001c0001t0029g0037a0001c0001t0051g0084 | 2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-13621A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625427 | ||||||
| chr2:163625458
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0014g0045 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-13652A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625458 | ||||||
| chr2:163625489
|
G | A | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-13683C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625489 | ||||||
| chr2:163625632
|
A | G | 13 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0005g0158others(10): Show | 13 | HG00408.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-13826T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625632 | ||||||
| chr2:163625936
|
A | C | 1 | a0001c0001t0043g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-14130T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625936 | ||||||
| chr2:163626179
|
A | G | 6 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(3): Show | 6 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-14373T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626179 | ||||||
| chr2:163626204
|
TC | T | 3 | a0001c0001t0005g0040a0001c0001t0035g0246a0001c0008t0035g0248 | 3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-14399delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626204 | ||||||
| chr2:163626421
|
A | G | 1 | a0001c0003t0002g0207 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26-14615T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626421 | ||||||
| chr2:163626779
|
C | G | 1 | a0001c0001t0060g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-14973G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626779 | ||||||
| chr2:163626819
|
C | T | 2 | a0001c0001t0005g0153a0001c0001t0005g0159 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-15013G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626819 | ||||||
| chr2:163626878
|
C | T | 1 | a0001c0001t0058g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.26-15072G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626878 | ||||||
| chr2:163626953
|
G | A | 17 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(14): Show | 17 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-15147C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626953 | ||||||
| chr2:163626973
|
A | G | 21 | a0001c0001t0002g0026a0001c0001t0003g0106a0001c0001t0005g0040others(18): Show | 21 | HG00408.hp1 HG00558.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-15167T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626973 | ||||||
| chr2:163627062
|
G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-15256C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627062 | ||||||
| chr2:163627445
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(106): Show | 109 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.26-15639A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627445 | ||||||
| chr2:163627610
|
C | A | 5 | a0001c0001t0001g0220a0001c0001t0025g0229a0001c0002t0007g0135others(2): Show | 5 | HG02109.hp2 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-15804G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627610 | ||||||
| chr2:163627693
|
C | G | 17 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(14): Show | 17 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-15887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627693 | ||||||
| chr2:163627796
|
T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.26-15990A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627796 | ||||||
| chr2:163627838
|
T | TTGAAGGC others(6): Show |
1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-16045_26-16033d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627838 | ||||||
| chr2:163628248
|
TG | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(65): Show | 69 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.26-16443delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628248 | ||||||
| chr2:163628649
|
T | A | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-16843A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628649 | ||||||
| chr2:163628761
|
A | T | 1 | a0001c0001t0007g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-16955T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628761 | ||||||
| chr2:163628923
|
T | A | 5 | a0001c0001t0013g0102a0001c0001t0021g0243a0001c0001t0025g0107others(2): Show | 5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-17117A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628923 | ||||||
| chr2:163629038
|
G | A | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-17232C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629038 | ||||||
| chr2:163629087
|
C | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(65): Show | 69 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.26-17281G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629087 | ||||||
| chr2:163629344
|
A | G | 1 | a0001c0001t0045g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.26-17538T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629344 | ||||||
| chr2:163629455
|
G | T | 11 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0123others(8): Show | 11 | HG00558.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-17649C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629455 | ||||||
| chr2:163629952
|
C | CT | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(53): Show | 57 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.26-18147dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
C | CTT | 9 | a0001c0001t0001g0012a0001c0001t0003g0186a0001c0001t0006g0006others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-18148_26-18147d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0015g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26-18159_26-18147d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-18160_26-18147d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CT | C | 29 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0081others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.26-18147delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTT | C | 5 | a0001c0001t0001g0168a0001c0001t0003g0241a0001c0001t0050g0171others(2): Show | 5 | HG00140.hp2 HG01891.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-18148_26-18147d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTTTT | C | 5 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0029g0214others(2): Show | 5 | HG00558.hp1 HG03942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-18150_26-18147d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(2): Show | 5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-18154_26-18147d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-18156_26-18147d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-18160_26-18147d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163629952
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0021g0183a0001c0001t0056g0121 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-18164_26-18147d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | ||||||
| chr2:163630036
|
C | T | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-18230G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630036 | ||||||
| chr2:163630043
|
C | T | 1 | a0001c0001t0007g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-18237G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630043 | ||||||
| chr2:163630118
|
C | A | 11 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0123others(8): Show | 11 | HG00558.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-18312G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630118 | ||||||
| chr2:163630129
|
C | A | 2 | a0001c0001t0019g0255a0001c0001t0027g0166 | 2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.26-18323G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630129 | ||||||
| chr2:163630328
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0011g0114a0001c0001t0011g0188others(1): Show | 4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-18522A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630328 | ||||||
| chr2:163630339
|
T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.26-18533A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630339 | ||||||
| chr2:163630349
|
T | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0150 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.26-18543A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630349 | ||||||
| chr2:163630369
|
G | A | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-18563C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630369 | ||||||
| chr2:163630510
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(128): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.26-18704G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630510 | ||||||
| chr2:163630573
|
C | T | 2 | a0001c0001t0036g0245a0004c0007t0086g0250 | 2 | NA18961.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.26-18767G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630573 | ||||||
| chr2:163630675
|
A | AG | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(48): Show | 52 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.26-18870dupC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630675 | ||||||
| chr2:163630683
|
G | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-18877C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630683 | ||||||
| chr2:163630938
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0014g0045 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-19132G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630938 | ||||||
| chr2:163631060
|
G | A | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-19254C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631060 | ||||||
| chr2:163631374
|
C | T | 2 | a0001c0004t0033g0138a0001c0004t0033g0174 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.26-19568G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631374 | ||||||
| chr2:163631504
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-19698A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631504 | ||||||
| chr2:163631733
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-19927T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631733 | ||||||
| chr2:163631865
|
A | C | 9 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(6): Show | 9 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-20059T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631865 | ||||||
| chr2:163631883
|
C | T | 2 | a0001c0001t0021g0243a0001c0002t0007g0240 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.26-20077G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631883 | ||||||
| chr2:163632016
|
C | T | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-20210G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632016 | ||||||
| chr2:163632031
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(179): Show | 183 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.26-20225G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632031 | ||||||
| chr2:163632299
|
G | A | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26-20493C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632299 | ||||||
| chr2:163632425
|
G | T | 1 | a0001c0003t0002g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.26-20619C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632425 | ||||||
| chr2:163632504
|
T | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-20698A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632504 | ||||||
| chr2:163632556
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20750G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632556 | ||||||
| chr2:163632565
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20759A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632565 | ||||||
| chr2:163632586
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20780T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632586 | ||||||
| chr2:163632590
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20784T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632590 | ||||||
| chr2:163632592
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20786A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632592 | ||||||
| chr2:163632594
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20788G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632594 | ||||||
| chr2:163632595
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20789T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632595 | ||||||
| chr2:163632600
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20794G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632600 | ||||||
| chr2:163632601
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20795T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632601 | ||||||
| chr2:163632602
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20796A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632602 | ||||||
| chr2:163632605
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20799T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632605 | ||||||
| chr2:163632606
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20800T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632606 | ||||||
| chr2:163632607
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20801A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632607 | ||||||
| chr2:163632609
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20803A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632609 | ||||||
| chr2:163632614
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20808T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632614 | ||||||
| chr2:163632615
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20809A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632615 | ||||||
| chr2:163632616
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20810T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632616 | ||||||
| chr2:163632617
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20811T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632617 | ||||||
| chr2:163632618
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20812T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632618 | ||||||
| chr2:163632619
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20813T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632619 | ||||||
| chr2:163632620
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20814T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632620 | ||||||
| chr2:163632636
|
T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.26-20830A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632636 | ||||||
| chr2:163632636
|
T | C | 1 | a0001c0001t0060g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-20830A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632636 | ||||||
| chr2:163632637
|
T | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(136): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.26-20831A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632637 | ||||||
| chr2:163632676
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20870G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632676 | ||||||
| chr2:163632690
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20884A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632690 | ||||||
| chr2:163632704
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20898A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632704 | ||||||
| chr2:163632774
|
C | T | 9 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0123others(6): Show | 9 | HG00558.hp1 HG02280.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-20968G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632774 | ||||||
| chr2:163632958
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-21152T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632958 | ||||||
| chr2:163633051
|
G | C | 5 | a0001c0001t0003g0101a0001c0001t0009g0129a0001c0002t0003g0100others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-21245C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633051 | ||||||
| chr2:163633427
|
T | C | 1 | a0001c0001t0043g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-21621A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633427 | ||||||
| chr2:163633487
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21681A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633487 | ||||||
| chr2:163633491
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21685A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633491 | ||||||
| chr2:163633495
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21689G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633495 | ||||||
| chr2:163633498
|
G | C | 1 | a0001c0001t0023g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.26-21692C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633498 | ||||||
| chr2:163633514
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21708G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633514 | ||||||
| chr2:163633517
|
CCTCCACA others(17): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21735_26-21712d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633517 | ||||||
| chr2:163633549
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21743G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633549 | ||||||
| chr2:163633556
|
A | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(136): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.26-21750T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633556 | ||||||
| chr2:163633565
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21759A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633565 | ||||||
| chr2:163633570
|
T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21764A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633570 | ||||||
| chr2:163633574
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21768T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633574 | ||||||
| chr2:163633576
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21770G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633576 | ||||||
| chr2:163633586
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21780G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633586 | ||||||
| chr2:163633587
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21781G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633587 | ||||||
| chr2:163633592
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21786G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633592 | ||||||
| chr2:163633603
|
G | T | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-21797C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633603 | ||||||
| chr2:163633613
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21807T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633613 | ||||||
| chr2:163633624
|
G | A | 3 | a0001c0001t0004g0191a0001c0001t0007g0068a0001c0002t0011g0092 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-21818C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633624 | ||||||
| chr2:163633731
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(42): Show | 46 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.26-21925G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633731 | ||||||
| chr2:163634019
|
A | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 200 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.26-22213T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634019 | ||||||
| chr2:163634086
|
A | ATGCG | 6 | a0001c0001t0017g0147a0001c0001t0017g0148a0001c0001t0017g0151others(3): Show | 6 | NA18959.hp2 NA18961.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-22284_26-22281d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634086 | ||||||
| chr2:163634089
|
C | CGT | 25 | a0001c0001t0001g0047a0001c0001t0001g0118a0001c0001t0001g0137others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-22285_26-22284d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634089
|
C | CGTGT | 105 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.26-22287_26-22284d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634089
|
C | CGTGTGT | 18 | a0001c0001t0001g0080a0001c0001t0001g0111a0001c0001t0001g0162others(15): Show | 18 | HG00408.hp2 HG01261.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-22289_26-22284d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634089
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0002a0001c0001t0002g0228a0001c0001t0063g0233 | 3 | HG01175.hp2 NA18985.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-22293_26-22284d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634089
|
CGT | C | 11 | a0001c0001t0005g0117a0001c0001t0007g0068a0001c0001t0008g0167others(8): Show | 11 | HG00558.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-22285_26-22284d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634089
|
CGTGT | C | 6 | a0001c0001t0004g0191a0001c0001t0015g0123a0001c0001t0015g0124others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-22287_26-22284d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | ||||||
| chr2:163634114
|
G | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(29): Show | 33 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-22308C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634114 | ||||||
| chr2:163634413
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-22607A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634413 | ||||||
| chr2:163634723
|
C | T | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-22917G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634723 | ||||||
| chr2:163634794
|
T | C | 3 | a0001c0001t0002g0228a0001c0001t0052g0215a0001c0001t0064g0237 | 3 | HG00408.hp2 HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-22988A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634794 | ||||||
| chr2:163634958
|
G | T | 1 | a0001c0001t0003g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-23152C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634958 | ||||||
| chr2:163635106
|
A | G | 5 | a0001c0001t0003g0101a0001c0001t0009g0129a0001c0002t0003g0100others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-23300T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635106 | ||||||
| chr2:163635175
|
G | A | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-23369C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635175 | ||||||
| chr2:163635532
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.26-23726G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635532 | ||||||
| chr2:163635681
|
T | C | 1 | a0001c0001t0082g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-23875A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635681 | ||||||
| chr2:163635884
|
C | G | 5 | a0001c0001t0003g0101a0001c0001t0009g0129a0001c0002t0003g0100others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-24078G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635884 | ||||||
| chr2:163635967
|
A | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-24161T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635967 | ||||||
| chr2:163636088
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-24282T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636088 | ||||||
| chr2:163636426
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.26-24620G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636426 | ||||||
| chr2:163636594
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.26-24788T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636594 | ||||||
| chr2:163636653
|
T | C | 1 | a0002c0006t0009g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-24847A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636653 | ||||||
| chr2:163636733
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-24927A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636733 | ||||||
| chr2:163636944
|
T | C | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.26-25138A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636944 | ||||||
| chr2:163636951
|
C | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0142others(16): Show | 19 | HG00423.hp1 HG02027.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-25145G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636951 | ||||||
| chr2:163636976
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0010g0061 | 2 | NA18985.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.26-25170C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636976 | ||||||
| chr2:163636977
|
G | A | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-25171C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636977 | ||||||
| chr2:163636987
|
G | A | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-25181C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636987 | ||||||
| chr2:163637097
|
C | T | 4 | a0001c0001t0015g0123a0001c0001t0015g0124a0001c0001t0021g0183others(1): Show | 4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-25291G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637097 | ||||||
| chr2:163637222
|
C | T | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-25416G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637222 | ||||||
| chr2:163637328
|
G | C | 2 | a0001c0001t0003g0182a0001c0001t0011g0172 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.26-25522C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637328 | ||||||
| chr2:163637520
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-25714T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637520 | ||||||
| chr2:163637533
|
T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.26-25727A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637533 | ||||||
| chr2:163637667
|
C | CT | 8 | a0001c0001t0001g0218a0001c0001t0002g0074a0001c0001t0003g0186others(5): Show | 8 | HG01175.hp1 HG02040.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-25862dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637667 | ||||||
| chr2:163637667
|
CT | C | 12 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0015g0123others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-25862delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637667 | ||||||
| chr2:163637721
|
C | T | 4 | a0001c0001t0015g0123a0001c0001t0015g0124a0001c0001t0021g0183others(1): Show | 4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-25915G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637721 | ||||||
| chr2:163637776
|
A | G | 1 | a0001c0002t0028g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.26-25970T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637776 | ||||||
| chr2:163637930
|
TG | T | 5 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(2): Show | 5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-26125delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637930 | ||||||
| chr2:163638012
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-26206G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638012 | ||||||
| chr2:163638215
|
G | A | 1 | a0001c0001t0081g0261 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-26409C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638215 | ||||||
| chr2:163638262
|
A | T | 4 | a0001c0001t0015g0123a0001c0001t0015g0124a0001c0001t0021g0183others(1): Show | 4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-26456T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638262 | ||||||
| chr2:163638713
|
G | C | 5 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(2): Show | 5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-26907C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638713 | ||||||
| chr2:163638748
|
C | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-26942G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638748 | ||||||
| chr2:163638917
|
AC | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0006g0062others(3): Show | 6 | HG00735.hp1 HG01167.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-27112delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638917 | ||||||
| chr2:163638942
|
A | C | 3 | a0001c0001t0001g0055a0001c0001t0008g0072a0001c0001t0009g0196 | 3 | NA18747.hp2 NA18941.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.26-27136T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638942 | ||||||
| chr2:163639125
|
T | C | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26-27319A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639125 | ||||||
| chr2:163639150
|
C | A | 7 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0021g0243others(4): Show | 7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-27344G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639150 | ||||||
| chr2:163639320
|
G | T | 3 | a0001c0001t0002g0228a0001c0001t0052g0215a0001c0001t0064g0237 | 3 | HG00408.hp2 HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-27514C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639320 | ||||||
| chr2:163639436
|
T | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(28): Show | 32 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-27630A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639436 | ||||||
| chr2:163639490
|
A | T | 1 | a0001c0001t0003g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-27684T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639490 | ||||||
| chr2:163639511
|
T | C | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-27705A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639511 | ||||||
| chr2:163639558
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.26-27752C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639558 | ||||||
| chr2:163639802
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0098 | 2 | HG02818.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.26-27996A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639802 | ||||||
| chr2:163639825
|
T | G | 1 | a0001c0001t0022g0079 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.26-28019A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639825 | ||||||
| chr2:163639857
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(142): Show | 145 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.26-28051A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639857 | ||||||
| chr2:163640169
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0060g0060 | 3 | HG02040.hp1 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-28363A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163640169 | ||||||
| chr2:163640291
|
G | T | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-28485C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163640291 | ||||||
| chr2:163641078
|
C | T | 9 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0126others(6): Show | 9 | HG00558.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-29272G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641078 | ||||||
| chr2:163641098
|
G | A | 1 | a0001c0001t0002g0198 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.26-29292C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641098 | ||||||
| chr2:163641110
|
A | T | 20 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0152others(17): Show | 20 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-29304T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641110 | ||||||
| chr2:163641139
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0060g0060 | 3 | HG02040.hp1 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-29333T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641139 | ||||||
| chr2:163641167
|
G | A | 4 | a0001c0001t0015g0123a0001c0001t0015g0124a0001c0001t0021g0183others(1): Show | 4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-29361C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641167 | ||||||
| chr2:163641281
|
G | A | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-29475C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641281 | ||||||
| chr2:163641388
|
AG | A | 7 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0021g0243others(4): Show | 7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-29583delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641388 | ||||||
| chr2:163641436
|
C | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(190): Show | 194 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.26-29630G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641436 | ||||||
| chr2:163641525
|
C | T | 11 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0123others(8): Show | 11 | HG00558.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-29719G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641525 | ||||||
| chr2:163641663
|
G | A | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-29857C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641663 | ||||||
| chr2:163641739
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-29933T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641739 | ||||||
| chr2:163641809
|
T | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-30003A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641809 | ||||||
| chr2:163641873
|
A | G | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-30067T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641873 | ||||||
| chr2:163641918
|
C | A | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-30112G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641918 | ||||||
| chr2:163642394
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0011g0114a0001c0001t0011g0188others(1): Show | 4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-30588A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642394 | ||||||
| chr2:163642417
|
G | C | 1 | a0001c0001t0015g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.26-30611C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642417 | ||||||
| chr2:163642534
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0011g0114a0001c0001t0011g0188others(1): Show | 4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-30728A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642534 | ||||||
| chr2:163642576
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-30770A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642576 | ||||||
| chr2:163642793
|
T | A | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-30987A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642793 | ||||||
| chr2:163643005
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 200 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.26-31199T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643005 | ||||||
| chr2:163643273
|
G | A | 1 | a0001c0001t0007g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.26-31467C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643273 | ||||||
| chr2:163643414
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-31608C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643414 | ||||||
| chr2:163643549
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-31743C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643549 | ||||||
| chr2:163643644
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-31838G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643644 | ||||||
| chr2:163643650
|
C | CA | 26 | a0001c0001t0001g0118a0001c0001t0001g0218a0001c0001t0002g0212others(23): Show | 26 | HG00323.hp1 HG00735.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-31845dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643650 | ||||||
| chr2:163643650
|
CA | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0030others(24): Show | 27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.26-31845delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643650 | ||||||
| chr2:163643691
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.26-31885A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643691 | ||||||
| chr2:163643733
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.26-31927G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643733 | ||||||
| chr2:163643765
|
C | A | 7 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0021g0243others(4): Show | 7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-31959G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643765 | ||||||
| chr2:163643904
|
G | T | 3 | a0001c0001t0004g0191a0001c0001t0007g0068a0001c0002t0011g0092 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-32098C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643904 | ||||||
| chr2:163643905
|
C | A | 3 | a0001c0001t0004g0191a0001c0001t0007g0068a0001c0002t0011g0092 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-32099G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643905 | ||||||
| chr2:163643919
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.26-32113G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643919 | ||||||
| chr2:163643932
|
C | CA | 16 | a0001c0001t0001g0110a0001c0001t0001g0220a0001c0001t0003g0087others(13): Show | 16 | HG01433.hp2 HG02109.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-32127dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAA | 6 | a0001c0001t0004g0189a0001c0001t0013g0102a0001c0001t0021g0243others(3): Show | 6 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-32129_26-32127d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAA | 7 | a0001c0001t0001g0066a0001c0001t0001g0139a0001c0001t0001g0219others(4): Show | 7 | HG00735.hp1 HG02293.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-32132_26-32127d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0098a0001c0001t0001g0152a0001c0001t0002g0052others(10): Show | 13 | HG01070.hp2 HG01261.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-32135_26-32127d others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(3): Show |
43 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0027others(40): Show | 43 | HG00140.hp2 HG00609.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.26-32136_26-32127d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(4): Show |
46 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0057others(43): Show | 46 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.26-32137_26-32127d others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0036others(14): Show | 17 | HG00741.hp1 HG01106.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-32138_26-32127d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(6): Show |
10 | a0001c0001t0001g0083a0001c0001t0002g0212a0001c0001t0003g0106others(7): Show | 10 | HG01106.hp2 HG01891.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-32139_26-32127d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0026a0001c0001t0026g0095 | 2 | HG02451.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.26-32140_26-32127d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26-32143_26-32127d others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-32144_26-32127d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
CA | C | 15 | a0001c0001t0001g0137a0001c0001t0001g0218a0001c0001t0002g0146others(12): Show | 15 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-32127delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643932
|
CAAAAAAA | C | 15 | a0001c0001t0001g0142a0001c0001t0001g0195a0001c0001t0001g0197others(12): Show | 15 | HG00408.hp1 HG00423.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-32133_26-32127d others(9): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | ||||||
| chr2:163643957
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0006g0006 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.26-32152_26-32151i others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643957 | ||||||
| chr2:163644008
|
C | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 200 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.26-32202G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644008 | ||||||
| chr2:163644099
|
G | T | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-32293C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644099 | ||||||
| chr2:163644382
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0001g0197a0001c0001t0001g0199others(6): Show | 9 | HG02155.hp1 NA18612.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-32576A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644382 | ||||||
| chr2:163644706
|
A | T | 5 | a0001c0001t0003g0101a0001c0001t0009g0129a0001c0002t0003g0100others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-32900T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644706 | ||||||
| chr2:163644796
|
T | G | 1 | a0001c0001t0007g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.26-32990A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644796 | ||||||
| chr2:163645124
|
A | G | 11 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0015g0123others(8): Show | 11 | HG00558.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-33318T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645124 | ||||||
| chr2:163645152
|
T | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-33346A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645152 | ||||||
| chr2:163645161
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-33355T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645161 | ||||||
| chr2:163645245
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(191): Show | 195 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.26-33439T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645245 | ||||||
| chr2:163645263
|
C | A | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-33457G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645263 | ||||||
| chr2:163645263
|
C | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(132): Show | 135 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.26-33457G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645263 | ||||||
| chr2:163645510
|
T | C | 5 | a0001c0001t0013g0102a0001c0001t0021g0243a0001c0001t0025g0107others(2): Show | 5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-33704A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645510 | ||||||
| chr2:163645574
|
G | A | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-33768C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645574 | ||||||
| chr2:163645991
|
G | C | 1 | a0001c0001t0003g0241 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-34185C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645991 | ||||||
| chr2:163646180
|
C | T | 3 | a0001c0001t0005g0040a0001c0001t0035g0246a0001c0008t0035g0248 | 3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-34374G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646180 | ||||||
| chr2:163646312
|
A | T | 1 | a0001c0001t0029g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.26-34506T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646312 | ||||||
| chr2:163646330
|
C | G | 7 | a0001c0001t0001g0218a0001c0001t0003g0186a0001c0001t0004g0133others(4): Show | 7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-34524G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646330 | ||||||
| chr2:163646777
|
A | G | 2 | a0001c0001t0031g0091a0001c0001t0059g0093 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-34971T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646777 | ||||||
| chr2:163646949
|
C | T | 2 | a0001c0001t0050g0171a0001c0001t0057g0109 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-35143G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646949 | ||||||
| chr2:163647046
|
G | C | 122 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(119): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.26-35240C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647046 | ||||||
| chr2:163647107
|
G | A | 1 | a0001c0001t0002g0003 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.26-35301C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647107 | ||||||
| chr2:163647191
|
G | A | 56 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0112others(53): Show | 56 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-35385C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647191 | ||||||
| chr2:163647279
|
A | C | 5 | a0001c0001t0002g0026a0001c0001t0005g0040a0001c0001t0014g0015others(2): Show | 5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-35473T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647279 | ||||||
| chr2:163647368
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0003g0186 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-35562G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647368 | ||||||
| chr2:163647411
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-35605A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647411 | ||||||
| chr2:163647627
|
G | A | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(31): Show | 35 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.26-35821C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647627 | ||||||
| chr2:163647678
|
A | C | 61 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0112others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.26-35872T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647678 | ||||||
| chr2:163647792
|
T | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(31): Show | 35 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.26-35986A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647792 | ||||||
| chr2:163647810
|
A | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 41 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.26-36004T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647810 | ||||||
| chr2:163647852
|
A | G | 4 | a0001c0001t0029g0037a0001c0001t0037g0260a0001c0001t0051g0084others(1): Show | 4 | NA18960.hp1 NA18995.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-36046T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647852 | ||||||
| chr2:163648026
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0083others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-36220G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648026 | ||||||
| chr2:163648073
|
T | G | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-36267A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648073 | ||||||
| chr2:163648129
|
C | A | 3 | a0001c0001t0003g0106a0001c0001t0026g0094a0001c0001t0026g0095 | 3 | HG02451.hp1 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-36323G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648129 | ||||||
| chr2:163648213
|
C | A | 17 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0002g0146others(14): Show | 17 | HG00323.hp1 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-36407G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648213 | ||||||
| chr2:163648450
|
C | G | 1 | a0001c0001t0006g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26-36644G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648450 | ||||||
| chr2:163648793
|
T | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(216): Show | 220 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.26-36987A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648793 | ||||||
| chr2:163648897
|
A | G | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-37091T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648897 | ||||||
| chr2:163648967
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(183): Show | 187 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.26-37161T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648967 | ||||||
| chr2:163648974
|
A | T | 12 | a0001c0001t0001g0118a0001c0001t0001g0163a0001c0001t0001g0218others(9): Show | 12 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-37168T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648974 | ||||||
| chr2:163649133
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 158 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.26-37327T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649133 | ||||||
| chr2:163649225
|
G | A | 3 | a0001c0001t0006g0099a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02055.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-37419C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649225 | ||||||
| chr2:163649255
|
G | A | 5 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0023g0155others(2): Show | 5 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-37449C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649255 | ||||||
| chr2:163649300
|
A | G | 1 | a0001c0001t0043g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-37494T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649300 | ||||||
| chr2:163649428
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.26-37622A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649428 | ||||||
| chr2:163649568
|
G | A | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-37762C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649568 | ||||||
| chr2:163649649
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(107): Show | 110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.26-37843A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649649 | ||||||
| chr2:163649675
|
A | T | 1 | a0001c0001t0019g0255 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.26-37869T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649675 | ||||||
| chr2:163649968
|
G | A | 10 | a0001c0001t0001g0118a0001c0001t0001g0163a0001c0001t0001g0218others(7): Show | 10 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-38162C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649968 | ||||||
| chr2:163650086
|
A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-38280T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650086 | ||||||
| chr2:163650169
|
T | G | 25 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0004g0133others(22): Show | 25 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-38363A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650169 | ||||||
| chr2:163650211
|
C | T | 2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-38405G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650211 | ||||||
| chr2:163650330
|
A | T | 10 | a0001c0001t0001g0118a0001c0001t0001g0163a0001c0001t0001g0218others(7): Show | 10 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-38524T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650330 | ||||||
| chr2:163650363
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-38557A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650363 | ||||||
| chr2:163650431
|
T | C | 26 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0139others(23): Show | 27 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-38625A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650431 | ||||||
| chr2:163650467
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(183): Show | 187 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.26-38661T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650467 | ||||||
| chr2:163650880
|
A | G | 23 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0139others(20): Show | 24 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-39074T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650880 | ||||||
| chr2:163650927
|
C | A | 1 | a0001c0001t0003g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-39121G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650927 | ||||||
| chr2:163650984
|
C | A | 3 | a0001c0001t0003g0106a0001c0001t0026g0094a0001c0001t0026g0095 | 3 | HG02451.hp1 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-39178G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650984 | ||||||
| chr2:163651054
|
A | AGAT | 4 | a0001c0001t0001g0030a0001c0001t0002g0005a0001c0001t0032g0014others(1): Show | 4 | NA18969.hp2 NA19065.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-39251_26-39249d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651054 | ||||||
| chr2:163651064
|
A | G | 11 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0163others(8): Show | 11 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-39258T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651064 | ||||||
| chr2:163651286
|
C | A | 1 | a0001c0001t0018g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.26-39480G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651286 | ||||||
| chr2:163651385
|
C | T | 1 | a0001c0001t0030g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-39579G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651385 | ||||||
| chr2:163651405
|
G | A | 3 | a0001c0001t0003g0186a0001c0001t0015g0126a0001c0002t0016g0067 | 3 | HG02257.hp1 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.26-39599C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651405 | ||||||
| chr2:163651724
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.26-39918A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651724 | ||||||
| chr2:163652343
|
A | AAC | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(35): Show | 38 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.26-40539_26-40538d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | ||||||
| chr2:163652343
|
A | AACAC | 27 | a0001c0001t0001g0047a0001c0001t0001g0111a0001c0001t0001g0118others(24): Show | 28 | HG00408.hp2 HG01361.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.26-40541_26-40538d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | ||||||
| chr2:163652343
|
A | AACACAC | 4 | a0001c0001t0005g0153a0001c0001t0005g0159a0001c0001t0016g0130others(1): Show | 4 | HG01261.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-40543_26-40538d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | ||||||
| chr2:163652343
|
A | AACACACA others(1): Show |
2 | a0001c0001t0001g0218a0001c0001t0003g0097 | 2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-40545_26-40538d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | ||||||
| chr2:163652345
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0006g0239 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-40555_26-40540d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652345 | ||||||
| chr2:163652355
|
CACACAA | C | 3 | a0001c0001t0005g0040a0001c0001t0015g0123a0001c0001t0015g0124 | 3 | HG00408.hp1 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-40555_26-40550d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652355 | ||||||
| chr2:163652357
|
CACAA | C | 12 | a0001c0001t0001g0112a0001c0001t0002g0063a0001c0001t0003g0106others(9): Show | 12 | HG00423.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-40555_26-40552d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652357 | ||||||
| chr2:163652359
|
CAA | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0002g0031others(9): Show | 12 | HG01071.hp2 HG02155.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-40555_26-40554d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652359 | ||||||
| chr2:163652361
|
A | AAC | 7 | a0001c0001t0001g0220a0001c0001t0013g0193a0001c0001t0020g0263others(4): Show | 7 | HG01496.hp1 HG01496.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-40557_26-40556d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652361
|
A | AACAC | 66 | a0001c0001t0001g0023a0001c0001t0001g0137a0001c0001t0001g0141others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.26-40559_26-40556d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652361
|
A | AACACAC | 11 | a0001c0001t0001g0057a0001c0001t0003g0182a0001c0001t0007g0181others(8): Show | 11 | HG00558.hp1 HG01515.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-40561_26-40556d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652361
|
A | AACACACA others(1): Show |
6 | a0001c0001t0001g0119a0001c0001t0006g0099a0001c0001t0014g0045others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-40563_26-40556d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652361
|
A | AACACACA others(3): Show |
1 | a0001c0001t0004g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-40565_26-40556d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652361
|
A | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(129): Show | 133 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.26-40555T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | ||||||
| chr2:163652481
|
C | CA | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.26-40676dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652481 | ||||||
| chr2:163652634
|
T | C | 1 | a0001c0001t0075g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.26-40828A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652634 | ||||||
| chr2:163652744
|
A | T | 15 | a0001c0001t0001g0057a0001c0001t0001g0119a0001c0001t0001g0175others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-40938T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652744 | ||||||
| chr2:163652796
|
A | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-40990T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652796 | ||||||
| chr2:163652914
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-41108A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652914 | ||||||
| chr2:163652918
|
G | A | 3 | a0001c0001t0014g0015a0001c0001t0035g0246a0001c0008t0035g0248 | 3 | HG03688.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-41112C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652918 | ||||||
| chr2:163653129
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0014g0045 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-41323A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653129 | ||||||
| chr2:163653386
|
T | C | 4 | a0001c0001t0003g0182a0001c0001t0006g0099a0001c0001t0007g0181others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-41580A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653386 | ||||||
| chr2:163653501
|
T | C | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-41695A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653501 | ||||||
| chr2:163653749
|
G | C | 5 | a0001c0001t0003g0182a0001c0001t0006g0099a0001c0001t0007g0181others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-41943C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653749 | ||||||
| chr2:163653823
|
T | A | 1 | a0001c0001t0015g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.26-42017A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653823 | ||||||
| chr2:163653995
|
G | A | 3 | a0001c0001t0014g0015a0001c0001t0035g0246a0001c0008t0035g0248 | 3 | HG03688.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-42189C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653995 | ||||||
| chr2:163654005
|
A | C | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-42199T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654005 | ||||||
| chr2:163654128
|
T | C | 1 | a0001c0001t0027g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.26-42322A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654128 | ||||||
| chr2:163654214
|
C | A | 1 | a0001c0001t0021g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-42408G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654214 | ||||||
| chr2:163654419
|
T | C | 22 | a0001c0001t0001g0139a0001c0001t0003g0097a0001c0001t0003g0101others(19): Show | 22 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.26-42613A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654419 | ||||||
| chr2:163654605
|
T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.26-42799A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654605 | ||||||
| chr2:163654778
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.26-42972A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654778 | ||||||
| chr2:163654841
|
C | T | 3 | a0001c0001t0004g0133a0001c0001t0027g0108a0001c0001t0050g0171 | 3 | HG02559.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-43035G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654841 | ||||||
| chr2:163654911
|
AAGG | A | 7 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(4): Show | 7 | HG02280.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-43108_26-43106d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654911 | ||||||
| chr2:163655039
|
G | A | 1 | a0001c0001t0077g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-43233C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655039 | ||||||
| chr2:163655111
|
T | TAAGAAAT others(237): Show |
1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-43306_26-43305i others(246): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655111 | ||||||
| chr2:163655260
|
C | T | 3 | a0001c0001t0003g0192a0001c0001t0015g0123a0001c0001t0015g0124 | 3 | HG02809.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-43454G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655260 | ||||||
| chr2:163655292
|
T | C | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-43486A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655292 | ||||||
| chr2:163655344
|
G | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-43538C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655344 | ||||||
| chr2:163655369
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0023g0165a0001c0001t0067g0194 | 3 | HG01515.hp2 HG02293.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.26-43563G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655369 | ||||||
| chr2:163655437
|
T | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0150 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.26-43631A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655437 | ||||||
| chr2:163655550
|
T | A | 1 | a0001c0001t0001g0235 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.26-43744A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655550 | ||||||
| chr2:163655597
|
G | T | 1 | a0001c0003t0002g0207 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26-43791C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655597 | ||||||
| chr2:163655731
|
A | G | 7 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(4): Show | 7 | HG02280.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-43925T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655731 | ||||||
| chr2:163655785
|
G | GCA | 34 | a0001c0001t0001g0081a0001c0001t0001g0197a0001c0001t0001g0199others(31): Show | 34 | HG00408.hp2 HG00609.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-43981_26-43980d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655785 | ||||||
| chr2:163655785
|
G | GCACA | 17 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0195others(14): Show | 17 | HG00423.hp1 HG02027.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-43983_26-43980d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655785 | ||||||
| chr2:163655804
|
C | CACACAGA others(1): Show |
6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CACAG | 4 | a0001c0001t0003g0106a0001c0001t0025g0107a0001c0001t0031g0131others(1): Show | 4 | HG02280.hp2 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CACAGAG | 17 | a0001c0001t0001g0139a0001c0001t0003g0097a0001c0001t0003g0101others(14): Show | 17 | HG01175.hp1 HG01261.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CACAGAGA others(1): Show |
3 | a0001c0001t0003g0192a0001c0001t0015g0123a0001c0001t0015g0124 | 3 | HG02809.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-43999_26-43998i others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CACAGAGA others(3): Show |
3 | a0001c0001t0001g0118a0001c0001t0004g0189a0001c0002t0013g0190 | 3 | HG03098.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.26-43999_26-43998i others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CAG | 3 | a0001c0001t0006g0039a0001c0001t0045g0176a0001c0001t0057g0109 | 3 | HG01884.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.26-44000_26-43999d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CAGAG | 11 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-44002_26-43999d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | CAGAGAG | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-44004_26-43999d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655804
|
C | G | 2 | a0001c0001t0029g0037a0001c0001t0051g0084 | 2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-43998G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | ||||||
| chr2:163655806
|
G | C | 4 | a0001c0001t0001g0141a0001c0001t0002g0206a0001c0001t0012g0038others(1): Show | 4 | HG03491.hp1 HG03831.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-44000C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655806 | ||||||
| chr2:163655810
|
G | C | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-44004C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655810 | ||||||
| chr2:163655937
|
G | A | 2 | a0001c0001t0029g0037a0001c0001t0051g0084 | 2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-44131C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655937 | ||||||
| chr2:163656049
|
T | C | 1 | a0001c0001t0006g0041 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26-44243A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656049 | ||||||
| chr2:163656108
|
C | A | 73 | a0001c0001t0001g0023a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.26-44302G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656108 | ||||||
| chr2:163656185
|
G | T | 2 | a0001c0001t0008g0167a0001c0001t0008g0180 | 2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.26-44379C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656185 | ||||||
| chr2:163656241
|
C | T | 31 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0139others(28): Show | 31 | HG00735.hp2 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.26-44435G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656241 | ||||||
| chr2:163656330
|
T | C | 1 | a0001c0001t0038g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.26-44524A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656330 | ||||||
| chr2:163656354
|
A | G | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-44548T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656354 | ||||||
| chr2:163656360
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.26-44554C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656360 | ||||||
| chr2:163656372
|
G | A | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-44566C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656372 | ||||||
| chr2:163656623
|
G | A | 1 | a0001c0001t0004g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.26-44817C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656623 | ||||||
| chr2:163656685
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.26-44879C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656685 | ||||||
| chr2:163656799
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.26-44993A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656799 | ||||||
| chr2:163657091
|
G | A | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-45285C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657091 | ||||||
| chr2:163657104
|
C | A | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-45298G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657104 | ||||||
| chr2:163657115
|
G | GA | 63 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0110others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.26-45310dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657115 | ||||||
| chr2:163657115
|
GA | G | 5 | a0001c0001t0006g0076a0001c0001t0024g0001a0001c0001t0035g0246others(2): Show | 6 | HG01978.hp2 HG02970.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-45310delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657115 | ||||||
| chr2:163657500
|
C | CTG | 9 | a0001c0001t0001g0083a0001c0001t0001g0142a0001c0001t0006g0099others(6): Show | 9 | HG00323.hp2 HG01106.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-45696_26-45695d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
C | CTGTG | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.26-45698_26-45695d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
C | CTGTGTG | 41 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0175others(38): Show | 42 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.26-45700_26-45695d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0118a0001c0001t0001g0201a0001c0001t0002g0052others(4): Show | 7 | HG02015.hp1 HG02027.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-45702_26-45695d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
C | CTGTGTGT others(3): Show |
17 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(14): Show | 17 | HG00423.hp1 HG02027.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-45704_26-45695d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0002g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.26-45706_26-45695d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
CTG | C | 26 | a0001c0001t0001g0139a0001c0001t0003g0101a0001c0001t0003g0241others(23): Show | 26 | HG00558.hp1 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-45696_26-45695d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657500
|
CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-45704_26-45695d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | ||||||
| chr2:163657551
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.26-45745A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657551 | ||||||
| chr2:163657627
|
A | C | 3 | a0001c0002t0007g0135a0001c0002t0007g0136a0001c0002t0028g0134 | 3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-45821T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657627 | ||||||
| chr2:163657729
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(193): Show | 197 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.26-45923A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657729 | ||||||
| chr2:163657746
|
A | G | 1 | a0001c0001t0052g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.26-45940T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657746 | ||||||
| chr2:163657821
|
T | C | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-46015A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657821 | ||||||
| chr2:163657930
|
T | C | 5 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(2): Show | 5 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-46124A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657930 | ||||||
| chr2:163658087
|
C | G | 1 | a0001c0001t0015g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26-46281G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658087 | ||||||
| chr2:163658123
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.26-46317G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658123 | ||||||
| chr2:163658364
|
G | GCT | 9 | a0001c0001t0001g0141a0001c0001t0005g0153a0001c0001t0006g0239others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-46560_26-46559d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCT | 5 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0012g0122others(2): Show | 5 | HG01261.hp1 HG02451.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-46562_26-46559d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCTCT | 8 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0005g0159others(5): Show | 8 | HG01175.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-46564_26-46559d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCTCTC others(1): Show |
5 | a0001c0001t0003g0241a0001c0001t0023g0155a0001c0001t0071g0242others(2): Show | 5 | HG01496.hp2 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-46566_26-46559d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCTCTC others(5): Show |
1 | a0001c0001t0058g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.26-46570_26-46559d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCTCTC others(7): Show |
1 | a0001c0001t0005g0158 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.26-46572_26-46559d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
G | GCTCTCTC others(9): Show |
1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-46574_26-46559d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCT | G | 22 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0142others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-46560_26-46559d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCT | G | 20 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0019g0255others(17): Show | 20 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-46562_26-46559d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCT | G | 13 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0219others(10): Show | 13 | HG00558.hp2 HG01433.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-46564_26-46559d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(3): Show |
G | 2 | a0001c0001t0001g0027a0001c0001t0001g0056 | 2 | HG01255.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.26-46568_26-46559d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(5): Show |
G | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.26-46570_26-46559d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(7): Show |
G | 10 | a0001c0001t0001g0057a0001c0001t0001g0119a0001c0001t0003g0105others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-46572_26-46559d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(9): Show |
G | 12 | a0001c0001t0001g0175a0001c0001t0002g0075a0001c0001t0003g0182others(9): Show | 13 | HG01106.hp1 HG02258.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-46574_26-46559d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(11): Show |
G | 4 | a0001c0001t0001g0118a0001c0001t0003g0106a0001c0001t0031g0131others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-46576_26-46559d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(13): Show |
G | 9 | a0001c0001t0003g0116a0001c0001t0004g0133a0001c0001t0004g0189others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-46578_26-46559d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658364
|
GCTCTCTC others(15): Show |
G | 47 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-46580_26-46559d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | ||||||
| chr2:163658380
|
T | G | 2 | a0001c0001t0008g0167a0001c0001t0008g0180 | 2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.26-46574A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658380 | ||||||
| chr2:163658400
|
T | G | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-46594A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658400 | ||||||
| chr2:163658410
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0018g0203 | 2 | NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26-46604C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658410 | ||||||
| chr2:163658425
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26-46619C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658425 | ||||||
| chr2:163658518
|
T | C | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-46712A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658518 | ||||||
| chr2:163658524
|
C | T | 26 | a0001c0001t0001g0139a0001c0001t0003g0097a0001c0001t0003g0101others(23): Show | 26 | HG00558.hp1 HG01175.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-46718G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658524 | ||||||
| chr2:163658678
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.26-46872C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658678 | ||||||
| chr2:163658730
|
C | G | 23 | a0001c0001t0001g0139a0001c0001t0003g0097a0001c0001t0003g0101others(20): Show | 23 | HG00558.hp1 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.26-46924G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658730 | ||||||
| chr2:163658970
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0018g0028 | 2 | NA18941.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.26-47164C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658970 | ||||||
| chr2:163659027
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.26-47221C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659027 | ||||||
| chr2:163659054
|
C | T | 32 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0003g0097others(29): Show | 32 | HG00558.hp1 HG00735.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-47248G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659054 | ||||||
| chr2:163659073
|
C | G | 4 | a0001c0001t0003g0192a0001c0001t0015g0123a0001c0001t0015g0124others(1): Show | 4 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-47267G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659073 | ||||||
| chr2:163659184
|
G | C | 5 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-47378C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659184 | ||||||
| chr2:163659261
|
G | A | 1 | a0001c0001t0027g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26-47455C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659261 | ||||||
| chr2:163659270
|
G | T | 2 | a0001c0001t0001g0152a0001c0001t0027g0166 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.26-47464C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659270 | ||||||
| chr2:163659504
|
G | T | 1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.26-47698C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659504 | ||||||
| chr2:163659645
|
C | T | 1 | a0001c0001t0071g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-47839G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659645 | ||||||
| chr2:163659754
|
C | G | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-47948G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659754 | ||||||
| chr2:163659802
|
G | C | 4 | a0001c0001t0003g0192a0001c0001t0015g0123a0001c0001t0015g0124others(1): Show | 4 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-47996C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659802 | ||||||
| chr2:163660101
|
AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-48312_26-48296d others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660101 | ||||||
| chr2:163660288
|
G | A | 51 | a0001c0001t0001g0047a0001c0001t0001g0197a0001c0001t0001g0199others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.26-48482C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660288 | ||||||
| chr2:163660353
|
T | C | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-48547A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660353 | ||||||
| chr2:163660528
|
A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-48722T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660528 | ||||||
| chr2:163660562
|
T | A | 65 | a0001c0001t0001g0047a0001c0001t0001g0115a0001c0001t0001g0175others(62): Show | 66 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.26-48756A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660562 | ||||||
| chr2:163660670
|
C | CAT | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 88 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-48866_26-48865d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660670 | ||||||
| chr2:163660670
|
CAT | C | 8 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-48866_26-48865d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660670 | ||||||
| chr2:163660672
|
TATATATA others(37): Show |
T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-48910_26-48867d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660672 | ||||||
| chr2:163660679
|
ATATATAC others(17): Show |
A | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-48897_26-48874d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660679 | ||||||
| chr2:163660681
|
A | ATACACAT others(57): Show |
2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-48876_26-48875i others(66): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660681
|
A | ATATACAC others(15): Show |
19 | a0001c0001t0001g0227a0001c0001t0001g0235a0001c0001t0002g0052others(16): Show | 19 | HG00408.hp2 HG00609.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-48897_26-48876d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660681
|
A | ATATACAC others(37): Show |
1 | a0001c0001t0002g0198 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.26-48919_26-48876d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660681
|
ATATACAC others(15): Show |
A | 9 | a0001c0001t0001g0163a0001c0001t0003g0192a0001c0001t0004g0189others(6): Show | 9 | HG02723.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-48897_26-48876d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660681
|
ATATACAC others(37): Show |
A | 7 | a0001c0001t0001g0142a0001c0001t0002g0202a0001c0001t0014g0204others(4): Show | 7 | HG00423.hp1 HG02155.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-48919_26-48876d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660681
|
ATATACAC others(59): Show |
A | 5 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(2): Show | 5 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-48941_26-48876d others(68): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | ||||||
| chr2:163660684
|
T | C | 2 | a0001c0001t0006g0099a0001c0002t0004g0184 | 2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-48878A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660684 | ||||||
| chr2:163660685
|
ACACATAT others(33): Show |
A | 1 | a0001c0001t0077g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-48919_26-48880d others(42): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660685 | ||||||
| chr2:163660686
|
C | T | 2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-48880G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660686 | ||||||
| chr2:163660694
|
C | T | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-48888G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660694 | ||||||
| chr2:163660703
|
G | A | 4 | a0001c0001t0002g0089a0001c0001t0035g0246a0001c0003t0002g0073others(1): Show | 4 | NA18983.hp2 NA18988.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-48897C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660703 | ||||||
| chr2:163660703
|
GTATACAC others(125): Show |
G | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49029_26-48898d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660703 | ||||||
| chr2:163660705
|
ATACACAT others(175): Show |
A | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-49081_26-48900d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660705 | ||||||
| chr2:163660708
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.26-48902G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660708 | ||||||
| chr2:163660713
|
A | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0006g0169 | 3 | HG00140.hp2 HG01358.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.26-48907T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660713 | ||||||
| chr2:163660716
|
C | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-48910G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660716 | ||||||
| chr2:163660716
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-48934_26-48911d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660716 | ||||||
| chr2:163660722
|
T | A | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-48916A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660722 | ||||||
| chr2:163660724
|
TGTATACA others(127): Show |
T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-49052_26-48919d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660724 | ||||||
| chr2:163660726
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0007g0181others(1): Show | 4 | HG01106.hp1 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-48920A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660726 | ||||||
| chr2:163660730
|
C | CACATAT | 3 | a0001c0001t0019g0255a0001c0001t0082g0259a0001c0001t0083g0253 | 3 | HG00323.hp1 HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.26-48930_26-48925d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660730 | ||||||
| chr2:163660730
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(107): Show | 111 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.26-48924G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660730 | ||||||
| chr2:163660732
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-48927_26-48926i others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660732 | ||||||
| chr2:163660733
|
A | G | 1 | a0001c0001t0005g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-48927T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660733 | ||||||
| chr2:163660752
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.26-48946G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660752 | ||||||
| chr2:163660754
|
C | CATATACA others(3): Show |
2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-48958_26-48949d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660754 | ||||||
| chr2:163660755
|
A | G | 2 | a0001c0001t0005g0153a0001c0001t0005g0159 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-48949T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660755 | ||||||
| chr2:163660768
|
TGTATAC | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(81): Show | 84 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-48968_26-48963d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660768 | ||||||
| chr2:163660769
|
G | A | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48963C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660769 | ||||||
| chr2:163660774
|
C | T | 39 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0118others(36): Show | 40 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.26-48968G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660774 | ||||||
| chr2:163660774
|
CACATATA others(27): Show |
C | 1 | a0001c0001t0001g0030 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.26-49002_26-48969d others(36): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660774 | ||||||
| chr2:163660775
|
A | G | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48969T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660775 | ||||||
| chr2:163660776
|
C | CATATACA others(3): Show |
3 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117 | 3 | HG02896.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-48980_26-48971d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | ||||||
| chr2:163660776
|
C | CATATACA others(35): Show |
1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-48971_26-48970i others(44): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | ||||||
| chr2:163660776
|
C | T | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48970G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | ||||||
| chr2:163660777
|
A | G | 3 | a0001c0001t0005g0153a0001c0001t0005g0159a0001c0001t0022g0079 | 3 | HG01978.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-48971T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660777 | ||||||
| chr2:163660782
|
C | T | 1 | a0001c0001t0021g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-48976G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660782 | ||||||
| chr2:163660788
|
T | C | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48982A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660788 | ||||||
| chr2:163660791
|
G | A | 13 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0139others(10): Show | 13 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48985C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(205): Show |
1 | a0001c0001t0013g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(214): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(185): Show |
1 | a0001c0002t0007g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(194): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(245): Show |
1 | a0001c0001t0005g0158 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(254): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(183): Show |
2 | a0001c0001t0003g0101a0001c0002t0003g0100 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.26-48986_26-48985i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(185): Show |
3 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0002t0007g0244 | 3 | HG01891.hp2 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.26-48986_26-48985i others(194): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(209): Show |
1 | a0001c0001t0071g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(218): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(223): Show |
1 | a0001c0001t0021g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(232): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATACAC others(207): Show |
1 | a0001c0001t0005g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(216): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
G | GTATATAC others(207): Show |
1 | a0001c0001t0005g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(216): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660791
|
GTATATAG others(1): Show |
G | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(81): Show | 84 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-48993_26-48986d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | ||||||
| chr2:163660792
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-48986A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660792 | ||||||
| chr2:163660796
|
T | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-48990A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660796 | ||||||
| chr2:163660798
|
G | C | 36 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0118others(33): Show | 37 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.26-48992C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660798 | ||||||
| chr2:163660798
|
G | T | 13 | a0001c0001t0001g0139a0001c0001t0003g0101a0001c0001t0003g0241others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48992C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660798 | ||||||
| chr2:163660799
|
A | ATATACAT others(183): Show |
5 | a0001c0001t0003g0097a0001c0001t0023g0155a0001c0001t0031g0091others(2): Show | 5 | HG01175.hp1 HG01496.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-48994_26-48993i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | ||||||
| chr2:163660799
|
A | ATATACAT others(183): Show |
1 | a0001c0001t0016g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.26-48994_26-48993i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | ||||||
| chr2:163660799
|
A | G | 13 | a0001c0001t0001g0139a0001c0001t0003g0101a0001c0001t0003g0241others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48993T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | ||||||
| chr2:163660802
|
TAC | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-48998_26-48997d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660802 | ||||||
| chr2:163660808
|
T | TATATGTA others(145): Show |
1 | a0001c0002t0007g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26-49003_26-49002i others(154): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660808 | ||||||
| chr2:163660808
|
T | TATATGTA others(167): Show |
2 | a0001c0002t0007g0135a0001c0002t0028g0134 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-49003_26-49002i others(176): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660808 | ||||||
| chr2:163660809
|
A | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49003T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660809 | ||||||
| chr2:163660810
|
TATAC | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(80): Show | 83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-49008_26-49005d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660810 | ||||||
| chr2:163660813
|
A | G | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49007T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660813 | ||||||
| chr2:163660814
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49008G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660814 | ||||||
| chr2:163660815
|
A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-49009T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660815 | ||||||
| chr2:163660816
|
TATAC | T | 3 | a0001c0001t0022g0079a0001c0001t0063g0233a0002c0006t0009g0216 | 3 | HG01978.hp1 HG02132.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.26-49014_26-49011d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660816 | ||||||
| chr2:163660818
|
T | C | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49012A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660818 | ||||||
| chr2:163660820
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(9): Show | 12 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-49014G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660820 | ||||||
| chr2:163660823
|
A | ATATATGT others(9): Show |
3 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117 | 3 | HG02896.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-49018_26-49017i others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660823 | ||||||
| chr2:163660823
|
A | G | 2 | a0001c0001t0031g0131a0001c0002t0016g0132 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49017T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660823 | ||||||
| chr2:163660826
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49020A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660826 | ||||||
| chr2:163660828
|
TGTATAC | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(79): Show | 82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.26-49028_26-49023d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660828 | ||||||
| chr2:163660829
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49023C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660829 | ||||||
| chr2:163660830
|
T | TATATACA others(231): Show |
1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-49025_26-49024i others(240): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660830 | ||||||
| chr2:163660834
|
C | CAT | 47 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-49030_26-49029d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | ||||||
| chr2:163660834
|
C | CATAT | 25 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0003g0097others(22): Show | 26 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-49032_26-49029d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | ||||||
| chr2:163660834
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0175others(9): Show | 12 | HG00639.hp1 HG01106.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-49028G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | ||||||
| chr2:163660837
|
A | ATATACAT others(7): Show |
1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.26-49032_26-49031i others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | ||||||
| chr2:163660837
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-49032_26-49031i others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | ||||||
| chr2:163660837
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.26-49031T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | ||||||
| chr2:163660837
|
ATATACAT others(9): Show |
A | 1 | a0002c0006t0009g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-49047_26-49032d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | ||||||
| chr2:163660837
|
ATATACAT others(44): Show |
A | 1 | a0001c0001t0077g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-49082_26-49032d others(53): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | ||||||
| chr2:163660840
|
TACATATA others(11): Show |
T | 1 | a0001c0001t0063g0233 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.26-49052_26-49035d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660840 | ||||||
| chr2:163660842
|
C | T | 6 | a0001c0001t0002g0059a0001c0001t0014g0015a0001c0001t0022g0079others(3): Show | 6 | HG01978.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49036G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660842 | ||||||
| chr2:163660844
|
T | C | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-49038A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660844 | ||||||
| chr2:163660844
|
T | TAC | 3 | a0001c0002t0007g0135a0001c0002t0007g0136a0001c0002t0028g0134 | 3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-49039_26-49038i others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660844 | ||||||
| chr2:163660845
|
A | G | 3 | a0001c0001t0002g0059a0001c0001t0014g0015a0001c0001t0022g0079 | 3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49039T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660845 | ||||||
| chr2:163660850
|
T | C | 3 | a0001c0001t0002g0059a0001c0001t0014g0015a0001c0001t0022g0079 | 3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49044A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660850 | ||||||
| chr2:163660853
|
G | A | 8 | a0001c0001t0002g0059a0001c0001t0003g0106a0001c0001t0003g0116others(5): Show | 8 | HG01978.hp1 HG02280.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-49047C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660853 | ||||||
| chr2:163660854
|
T | A | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49048A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660854 | ||||||
| chr2:163660858
|
C | CAT | 3 | a0001c0001t0013g0102a0001c0001t0024g0001a0001c0001t0050g0171 | 4 | HG02559.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-49054_26-49053d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | CATAT | 5 | a0001c0001t0001g0115a0001c0001t0003g0101a0001c0001t0011g0114others(2): Show | 5 | HG00735.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-49056_26-49053d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | CATATAT | 7 | a0001c0001t0005g0173a0001c0001t0013g0193a0001c0001t0031g0091others(4): Show | 7 | HG01175.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-49058_26-49053d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | CATATATA others(1): Show |
4 | a0001c0001t0001g0139a0001c0001t0005g0158a0001c0001t0016g0130others(1): Show | 4 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49060_26-49053d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | CATATATA others(3): Show |
1 | a0001c0001t0071g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-49062_26-49053d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | CATATATA others(5): Show |
1 | a0001c0001t0021g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26-49064_26-49053d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
C | T | 9 | a0001c0001t0002g0059a0001c0001t0003g0106a0001c0001t0003g0116others(6): Show | 9 | HG01978.hp1 HG02132.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-49052G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660858
|
CAT | C | 4 | a0001c0001t0001g0220a0001c0001t0003g0161a0001c0001t0008g0021others(1): Show | 4 | HG01496.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49054_26-49053d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | ||||||
| chr2:163660863
|
A | G | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49057T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660863 | ||||||
| chr2:163660865
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0006g0099a0001c0001t0008g0072 | 3 | HG02055.hp2 NA18747.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.26-49059T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660865 | ||||||
| chr2:163660865
|
A | T | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-49059T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660865 | ||||||
| chr2:163660867
|
A | G | 3 | a0001c0001t0004g0133a0001c0001t0004g0189a0001c0002t0013g0190 | 3 | HG02976.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-49061T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660867 | ||||||
| chr2:163660871
|
A | G | 3 | a0001c0001t0002g0059a0001c0001t0014g0015a0001c0001t0022g0079 | 3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49065T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660871 | ||||||
| chr2:163660873
|
A | G | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-49067T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660873 | ||||||
| chr2:163660877
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0035 | 2 | HG01167.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.26-49071T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660877 | ||||||
| chr2:163660878
|
TA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.26-49073delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660878 | ||||||
| chr2:163660879
|
A | AT | 6 | a0001c0001t0003g0106a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49074dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | ATATAT | 8 | a0001c0001t0001g0197a0001c0001t0001g0235a0001c0001t0006g0234others(5): Show | 8 | HG00609.hp1 NA18941.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0005g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.26-49074_26-49073i others(27): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | ATATATT | 6 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02056.hp1 HG02109.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | ATATTT | 5 | a0001c0001t0002g0228a0001c0001t0003g0186a0001c0001t0015g0126others(2): Show | 5 | HG00408.hp2 HG02129.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | ATATTTT | 11 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0202others(8): Show | 11 | HG00423.hp1 HG02630.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0043 | 2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.26-49073T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
A | T | 1 | a0001c0002t0011g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.26-49073T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
AT | A | 35 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0137others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.26-49074delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660879
|
ATT | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0142others(20): Show | 23 | HG00140.hp1 HG00558.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.26-49075_26-49074d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | ||||||
| chr2:163660880
|
T | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.26-49074A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | ||||||
| chr2:163660880
|
T | TATATA | 3 | a0001c0001t0002g0222a0001c0001t0003g0097a0001c0001t0070g0103 | 3 | HG02027.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.26-49075_26-49074i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | ||||||
| chr2:163660880
|
T | TATATATA | 4 | a0001c0001t0005g0153a0001c0001t0005g0159a0001c0004t0033g0138others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49075_26-49074i others(9): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | ||||||
| chr2:163660880
|
T | TATATATA others(12): Show |
1 | a0001c0001t0006g0239 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-49075_26-49074i others(21): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | ||||||
| chr2:163660880
|
T | TG | 7 | a0001c0001t0001g0118a0001c0001t0002g0005a0001c0001t0003g0105others(4): Show | 7 | HG00408.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-49075_26-49074i others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | ||||||
| chr2:163660881
|
T | A | 19 | a0001c0001t0001g0115a0001c0001t0002g0026a0001c0001t0002g0043others(16): Show | 20 | HG01175.hp1 HG01261.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-49075A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660881 | ||||||
| chr2:163660881
|
T | G | 1 | a0001c0001t0008g0021 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.26-49075A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660881 | ||||||
| chr2:163660882
|
T | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.26-49076A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660882 | ||||||
| chr2:163660883
|
T | A | 24 | a0001c0001t0001g0157a0001c0001t0001g0175a0001c0001t0002g0026others(21): Show | 25 | HG00558.hp2 HG01106.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-49077A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660883 | ||||||
| chr2:163660884
|
T | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.26-49078A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660884 | ||||||
| chr2:163660885
|
T | A | 15 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0003g0101others(12): Show | 16 | HG02015.hp2 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-49079A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660885 | ||||||
| chr2:163660886
|
T | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-49080A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660886 | ||||||
| chr2:163660887
|
T | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0008g0021others(4): Show | 7 | HG02015.hp2 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-49081A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660887 | ||||||
| chr2:163660888
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 85 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-49082A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660888 | ||||||
| chr2:163660889
|
T | A | 6 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0008g0021others(3): Show | 6 | HG02015.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49083A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660889 | ||||||
| chr2:163660890
|
T | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0002g0074others(6): Show | 9 | HG01884.hp2 HG02074.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-49084A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660890 | ||||||
| chr2:163661033
|
G | A | 2 | a0001c0001t0007g0068a0001c0002t0016g0067 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.26-49227C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661033 | ||||||
| chr2:163661233
|
T | TTTA | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49430_26-49428d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661233 | ||||||
| chr2:163661519
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0003g0105a0001c0001t0004g0191others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-49713G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661519 | ||||||
| chr2:163661657
|
T | C | 1 | a0001c0002t0007g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26-49851A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661657 | ||||||
| chr2:163661774
|
G | A | 1 | a0001c0001t0041g0017 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.26-49968C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661774 | ||||||
| chr2:163661784
|
T | C | 5 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-49978A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661784 | ||||||
| chr2:163661786
|
T | G | 6 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0005g0117others(3): Show | 6 | HG02280.hp2 HG02735.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-49980A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661786 | ||||||
| chr2:163661808
|
G | T | 2 | a0001c0001t0002g0228a0001c0001t0052g0215 | 2 | HG00408.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.26-50002C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661808 | ||||||
| chr2:163661822
|
A | T | 3 | a0001c0001t0004g0133a0001c0001t0006g0099a0001c0002t0004g0184 | 3 | HG02055.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-50016T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661822 | ||||||
| chr2:163661875
|
A | G | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-50069T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661875 | ||||||
| chr2:163661888
|
C | T | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01175.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-50082G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661888 | ||||||
| chr2:163661899
|
T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-50093A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661899 | ||||||
| chr2:163662027
|
T | C | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50221A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662027 | ||||||
| chr2:163662039
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-50233C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662039 | ||||||
| chr2:163662133
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-50327A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662133 | ||||||
| chr2:163662202
|
G | A | 1 | a0001c0001t0004g0085 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-50396C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662202 | ||||||
| chr2:163662267
|
A | G | 2 | a0001c0001t0003g0105a0001c0001t0004g0191 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-50461T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662267 | ||||||
| chr2:163662421
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0005g0153a0001c0001t0005g0158others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50615C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662421 | ||||||
| chr2:163662542
|
T | G | 3 | a0001c0001t0001g0119a0001c0001t0024g0001a0001c0002t0009g0120 | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50736A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662542 | ||||||
| chr2:163662598
|
G | A | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.26-50792C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662598 | ||||||
| chr2:163662655
|
T | G | 2 | a0001c0001t0001g0118a0001c0002t0004g0184 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.26-50849A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662655 | ||||||
| chr2:163662771
|
G | A | 45 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.26-50965C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662771 | ||||||
| chr2:163663325
|
T | TTTTG | 17 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(14): Show | 17 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-51523_26-51520d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663325 | ||||||
| chr2:163663365
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.26-51559C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663365 | ||||||
| chr2:163663518
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0004g0191 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-51712C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663518 | ||||||
| chr2:163663605
|
G | A | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.26-51799C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663605 | ||||||
| chr2:163663898
|
G | GA | 28 | a0001c0001t0001g0137a0001c0001t0003g0106a0001c0001t0003g0116others(25): Show | 28 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.26-52093dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663898 | ||||||
| chr2:163663911
|
T | C | 113 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.26-52105A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663911 | ||||||
| chr2:163663925
|
G | A | 2 | a0001c0001t0029g0037a0001c0001t0051g0084 | 2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-52119C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663925 | ||||||
| chr2:163664138
|
T | C | 1 | a0001c0001t0014g0045 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.26-52332A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664138 | ||||||
| chr2:163664258
|
C | G | 2 | a0001c0001t0004g0189a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-52452G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664258 | ||||||
| chr2:163664269
|
C | A | 1 | a0001c0001t0025g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-52463G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664269 | ||||||
| chr2:163664342
|
T | C | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.26-52536A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664342 | ||||||
| chr2:163664485
|
C | T | 1 | a0001c0004t0033g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.26-52679G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664485 | ||||||
| chr2:163664591
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-52785G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664591 | ||||||
| chr2:163664984
|
T | C | 2 | a0001c0001t0003g0105a0001c0001t0004g0191 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-53178A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664984 | ||||||
| chr2:163664998
|
G | GT | 86 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0141others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.26-53193dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664998 | ||||||
| chr2:163665005
|
A | G | 4 | a0001c0001t0025g0107a0001c0001t0027g0108a0001c0001t0045g0176others(1): Show | 4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-53199T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665005 | ||||||
| chr2:163665034
|
G | A | 16 | a0001c0001t0001g0098a0001c0001t0001g0139a0001c0001t0001g0175others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-53228C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665034 | ||||||
| chr2:163665242
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-53436G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665242 | ||||||
| chr2:163665384
|
C | T | 2 | a0001c0001t0015g0126a0001c0001t0030g0127 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-53578G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665384 | ||||||
| chr2:163665556
|
T | G | 1 | a0001c0001t0001g0197 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.26-53750A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665556 | ||||||
| chr2:163665892
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.26-54086G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665892 | ||||||
| chr2:163666055
|
A | G | 1 | a0001c0001t0026g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26-54249T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666055 | ||||||
| chr2:163666398
|
A | G | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0007g0244 | 3 | HG02630.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-54592T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666398 | ||||||
| chr2:163666442
|
G | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0142others(18): Show | 21 | HG00140.hp1 HG00558.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-54636C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666442 | ||||||
| chr2:163666690
|
G | A | 1 | a0001c0001t0004g0085 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-54884C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666690 | ||||||
| chr2:163666717
|
T | C | 12 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-54911A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666717 | ||||||
| chr2:163666765
|
GC | G | 17 | a0001c0001t0001g0227a0001c0001t0001g0235a0001c0001t0002g0222others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-54960delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666765 | ||||||
| chr2:163666766
|
C | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(240): Show | 244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.26-54960G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666766 | ||||||
| chr2:163666894
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-55088T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666894 | ||||||
| chr2:163666901
|
T | TA | 126 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0098others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.26-55096dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666901 | ||||||
| chr2:163667235
|
C | A | 25 | a0001c0001t0001g0137a0001c0001t0003g0116a0001c0001t0005g0117others(22): Show | 25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-55429G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667235 | ||||||
| chr2:163667291
|
C | T | 89 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0139others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.26-55485G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667291 | ||||||
| chr2:163667338
|
C | CA | 112 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0118others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.26-55533dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | ||||||
| chr2:163667338
|
C | CAA | 34 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0110others(31): Show | 34 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-55534_26-55533d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | ||||||
| chr2:163667338
|
C | CAAA | 21 | a0001c0001t0001g0137a0001c0001t0003g0116a0001c0001t0005g0117others(18): Show | 21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-55535_26-55533d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | ||||||
| chr2:163667503
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.26-55697A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667503 | ||||||
| chr2:163667579
|
T | C | 3 | a0001c0001t0021g0183a0001c0001t0050g0171a0001c0002t0013g0190 | 3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-55773A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667579 | ||||||
| chr2:163667726
|
A | G | 1 | a0001c0001t0060g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-55920T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667726 | ||||||
| chr2:163667740
|
G | A | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-55934C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667740 | ||||||
| chr2:163667809
|
A | G | 1 | a0001c0001t0083g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.26-56003T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667809 | ||||||
| chr2:163667883
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-56077C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667883 | ||||||
| chr2:163667913
|
G | A | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-56107C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667913 | ||||||
| chr2:163667952
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0014g0204 | 2 | HG00423.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.26-56146G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667952 | ||||||
| chr2:163668014
|
A | AC | 30 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0003g0182others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.26-56209dupG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | ||||||
| chr2:163668014
|
A | ACC | 25 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(22): Show | 25 | HG01106.hp1 HG01515.hp2 HG02293.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-56210_26-56209d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | ||||||
| chr2:163668014
|
A | ACCC | 42 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0157others(39): Show | 42 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.26-56211_26-56209d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | ||||||
| chr2:163668014
|
A | ACCCC | 31 | a0001c0001t0001g0023a0001c0001t0001g0144a0001c0001t0001g0152others(28): Show | 31 | HG00140.hp2 HG00423.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.26-56212_26-56209d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | ||||||
| chr2:163668023
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0012g0071 | 2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.26-56217G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668023 | ||||||
| chr2:163668025
|
C | CA | 3 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0016g0132 | 3 | HG02280.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-56220dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668025 | ||||||
| chr2:163668026
|
A | C | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-56220T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668026 | ||||||
| chr2:163668229
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-56423C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668229 | ||||||
| chr2:163668316
|
A | C | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-56510T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668316 | ||||||
| chr2:163668355
|
G | A | 20 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0106others(17): Show | 20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-56549C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668355 | ||||||
| chr2:163668525
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-56719G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668525 | ||||||
| chr2:163668739
|
G | A | 2 | a0001c0001t0041g0017a0001c0001t0073g0011 | 2 | HG02135.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.26-56933C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668739 | ||||||
| chr2:163668935
|
C | T | 2 | a0001c0001t0005g0153a0001c0001t0005g0159 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-57129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668935 | ||||||
| chr2:163668970
|
T | C | 2 | a0001c0001t0015g0126a0001c0001t0030g0127 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-57164A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668970 | ||||||
| chr2:163669015
|
A | AAT | 112 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0047others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.26-57211_26-57210d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATAT | 6 | a0001c0001t0001g0163a0001c0001t0002g0143a0001c0001t0026g0094others(3): Show | 6 | HG02647.hp2 NA18946.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-57213_26-57210d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATAT | 8 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-57215_26-57210d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(1): Show |
2 | a0001c0001t0001g0152a0001c0001t0003g0105 | 2 | HG02818.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.26-57217_26-57210d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(3): Show |
5 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02698.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-57219_26-57210d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(5): Show |
7 | a0001c0001t0003g0106a0001c0001t0003g0116a0001c0001t0004g0189others(4): Show | 7 | HG01496.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-57221_26-57210d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(7): Show |
8 | a0001c0001t0059g0093a0001c0002t0007g0104a0001c0002t0007g0135others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-57223_26-57210d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(9): Show |
7 | a0001c0001t0003g0101a0001c0001t0003g0241a0001c0001t0005g0173others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-57225_26-57210d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(11): Show |
2 | a0001c0001t0013g0102a0001c0001t0013g0193 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26-57227_26-57210d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(13): Show |
2 | a0001c0001t0003g0097a0001c0001t0006g0239 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.26-57229_26-57210d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(15): Show |
5 | a0001c0001t0001g0118a0001c0001t0006g0099a0001c0001t0007g0181others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-57210_26-57209i others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(17): Show |
3 | a0001c0001t0001g0175a0001c0001t0011g0172a0001c0001t0021g0243 | 3 | HG01106.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.26-57210_26-57209i others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
A | AATATATA others(19): Show |
2 | a0001c0001t0003g0182a0001c0002t0007g0244 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.26-57210_26-57209i others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669015
|
AAT | A | 6 | a0001c0001t0001g0002a0001c0001t0019g0257a0001c0001t0019g0258others(3): Show | 6 | HG01175.hp2 HG01361.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-57211_26-57210d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | ||||||
| chr2:163669035
|
T | TATATATA others(5): Show |
3 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0058g0156 | 3 | HG00558.hp1 NA18951.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.26-57230_26-57229i others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669035 | ||||||
| chr2:163669073
|
A | G | 1 | a0001c0001t0023g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-57267T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669073 | ||||||
| chr2:163669116
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.26-57310T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669116 | ||||||
| chr2:163669143
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-57337G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669143 | ||||||
| chr2:163669288
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.26-57482C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669288 | ||||||
| chr2:163669360
|
T | C | 1 | a0001c0001t0006g0039 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-57554A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669360 | ||||||
| chr2:163669464
|
C | G | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-57658G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669464 | ||||||
| chr2:163669585
|
G | GTAGAT | 8 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-57784_26-57780d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669585 | ||||||
| chr2:163669791
|
C | A | 1 | a0001c0001t0057g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-57985G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669791 | ||||||
| chr2:163669922
|
C | T | 1 | a0001c0001t0039g0230 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26-58116G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669922 | ||||||
| chr2:163670075
|
A | G | 2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-58269T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670075 | ||||||
| chr2:163670177
|
C | T | 20 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0116others(17): Show | 20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-58371G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670177 | ||||||
| chr2:163670249
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-58443G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670249 | ||||||
| chr2:163670315
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-58509T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670315 | ||||||
| chr2:163670550
|
A | G | 3 | a0001c0001t0021g0183a0001c0001t0050g0171a0001c0002t0013g0190 | 3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-58744T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670550 | ||||||
| chr2:163670587
|
A | T | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58781T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670587 | ||||||
| chr2:163670589
|
T | G | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-58783A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670589 | ||||||
| chr2:163670591
|
T | A | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58785A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670591 | ||||||
| chr2:163670592
|
A | G | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58786T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670592 | ||||||
| chr2:163670917
|
G | A | 1 | a0001c0001t0070g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26-59111C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670917 | ||||||
| chr2:163671073
|
G | A | 2 | a0001c0001t0004g0223a0001c0001t0004g0224 | 2 | NA18951.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.26-59267C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671073 | ||||||
| chr2:163671121
|
G | A | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-59315C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671121 | ||||||
| chr2:163671228
|
C | G | 6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-59422G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671228 | ||||||
| chr2:163671462
|
G | T | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-59656C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671462 | ||||||
| chr2:163671600
|
TA | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-59795delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671600 | ||||||
| chr2:163671602
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.26-59796C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671602 | ||||||
| chr2:163672251
|
T | TA | 104 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0118others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.26-60446dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | ||||||
| chr2:163672251
|
T | TAA | 32 | a0001c0001t0001g0047a0001c0001t0001g0137a0001c0001t0002g0222others(29): Show | 32 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-60447_26-60446d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | ||||||
| chr2:163672251
|
TA | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0048a0001c0001t0001g0081others(14): Show | 17 | HG00408.hp1 HG01884.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-60446delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | ||||||
| chr2:163672341
|
G | T | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-60535C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672341 | ||||||
| chr2:163672462
|
A | G | 6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-60656T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672462 | ||||||
| chr2:163672560
|
T | C | 20 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0106others(17): Show | 20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-60754A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672560 | ||||||
| chr2:163672878
|
AATGAG | A | 2 | a0001c0001t0003g0106a0001c0001t0004g0189 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-61077_26-61073d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672878 | ||||||
| chr2:163672891
|
T | C | 3 | a0001c0001t0021g0183a0001c0001t0050g0171a0001c0002t0013g0190 | 3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-61085A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672891 | ||||||
| chr2:163673018
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.26-61212G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673018 | ||||||
| chr2:163673134
|
C | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-61328G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673134 | ||||||
| chr2:163673223
|
G | A | 25 | a0001c0001t0001g0137a0001c0001t0003g0116a0001c0001t0005g0117others(22): Show | 25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-61417C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673223 | ||||||
| chr2:163673265
|
C | T | 1 | a0001c0001t0055g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.26-61459G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673265 | ||||||
| chr2:163673266
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-61460C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673266 | ||||||
| chr2:163673682
|
T | C | 114 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.25+61221A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673682 | ||||||
| chr2:163673748
|
T | C | 22 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0106others(19): Show | 22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+61155A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673748 | ||||||
| chr2:163674166
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25+60737T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674166 | ||||||
| chr2:163674239
|
T | C | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+60664A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674239 | ||||||
| chr2:163674273
|
C | A | 12 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60630G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674273 | ||||||
| chr2:163674273
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+60630G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674273 | ||||||
| chr2:163674295
|
TTG | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+60606_25+60607d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674295 | ||||||
| chr2:163674326
|
T | A | 12 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60577A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674326 | ||||||
| chr2:163674365
|
T | C | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+60538A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674365 | ||||||
| chr2:163674650
|
A | G | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+60253T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674650 | ||||||
| chr2:163674694
|
G | A | 14 | a0001c0001t0001g0048a0001c0001t0002g0026a0001c0001t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+60209C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674694 | ||||||
| chr2:163674705
|
T | C | 12 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60198A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674705 | ||||||
| chr2:163674737
|
G | A | 45 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0141others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.25+60166C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674737 | ||||||
| chr2:163674795
|
T | A | 94 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0139others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+60108A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674795 | ||||||
| chr2:163674936
|
C | A | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+59967G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674936 | ||||||
| chr2:163675036
|
A | G | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+59867T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675036 | ||||||
| chr2:163675352
|
A | G | 170 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0098others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.25+59551T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675352 | ||||||
| chr2:163675427
|
A | G | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25+59476T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675427 | ||||||
| chr2:163675453
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+59450A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675453 | ||||||
| chr2:163675478
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0007g0181others(1): Show | 4 | HG01106.hp1 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+59425A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675478 | ||||||
| chr2:163675504
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0004g0191 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+59399C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675504 | ||||||
| chr2:163675653
|
C | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0002g0005others(2): Show | 5 | NA18964.hp1 NA18969.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+59250G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675653 | ||||||
| chr2:163675706
|
C | CT | 37 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0119others(34): Show | 37 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.25+59196dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | ||||||
| chr2:163675706
|
CT | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0030others(29): Show | 32 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.25+59196delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | ||||||
| chr2:163675706
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+59187_25+59196d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | ||||||
| chr2:163675711
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+59192A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675711 | ||||||
| chr2:163675775
|
C | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.25+59128G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675775 | ||||||
| chr2:163675918
|
G | A | 3 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0016g0132 | 3 | HG02280.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.25+58985C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675918 | ||||||
| chr2:163676016
|
C | G | 1 | a0001c0003t0068g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.25+58887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676016 | ||||||
| chr2:163676029
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+58874A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676029 | ||||||
| chr2:163676033
|
G | A | 2 | a0001c0001t0003g0106a0001c0001t0004g0189 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+58870C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676033 | ||||||
| chr2:163676089
|
C | A | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+58814G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676089 | ||||||
| chr2:163676116
|
C | G | 1 | a0001c0001t0029g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.25+58787G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676116 | ||||||
| chr2:163676270
|
C | A | 44 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+58633G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676270 | ||||||
| chr2:163676434
|
A | AAT | 11 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0083others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+58467_25+58468d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
A | AATAT | 6 | a0001c0001t0001g0157a0001c0001t0002g0145a0001c0001t0005g0158others(3): Show | 6 | HG00558.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58465_25+58468d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
A | AATATAT | 6 | a0001c0001t0001g0118a0001c0001t0001g0142a0001c0001t0002g0044others(3): Show | 6 | HG01978.hp2 HG02132.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+58463_25+58468d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
A | AATATATA others(3): Show |
1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25+58459_25+58468d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AAT | A | 24 | a0001c0001t0001g0110a0001c0001t0001g0137a0001c0001t0001g0139others(21): Show | 24 | HG00558.hp1 HG01255.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+58467_25+58468d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATAT | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0111a0001c0001t0001g0152others(18): Show | 21 | HG00140.hp2 HG01358.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+58465_25+58468d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATAT | A | 14 | a0001c0001t0004g0191a0001c0001t0005g0153a0001c0001t0015g0126others(11): Show | 14 | HG02486.hp1 HG02895.hp2 HG03130.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+58463_25+58468d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0003g0192a0001c0001t0003g0241a0001c0001t0004g0133others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+58461_25+58468d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0004g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25+58459_25+58468d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0007g0181a0001c0002t0016g0132 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.25+58457_25+58468d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(7): Show |
A | 10 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0105others(7): Show | 10 | HG01106.hp1 HG02280.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+58455_25+58468d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(9): Show |
A | 9 | a0001c0001t0003g0116a0001c0001t0003g0186a0001c0001t0005g0117others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+58453_25+58468d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(11): Show |
A | 6 | a0001c0001t0001g0115a0001c0001t0002g0146a0001c0001t0002g0150others(3): Show | 6 | HG00735.hp2 HG01891.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58451_25+58468d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(13): Show |
A | 1 | a0001c0002t0028g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+58449_25+58468d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676434
|
AATATATA others(19): Show |
A | 44 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+58443_25+58468d others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | ||||||
| chr2:163676454
|
TATATATA others(23): Show |
T | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+58419_25+58448d others(32): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676454 | ||||||
| chr2:163676456
|
TATATATA others(21): Show |
T | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.25+58419_25+58446d others(30): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676456 | ||||||
| chr2:163676463
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+58440T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676463 | ||||||
| chr2:163676464
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0002a0001c0002t0013g0190 | 2 | HG01175.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+58419_25+58438d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676464 | ||||||
| chr2:163676466
|
T | TATATATA others(28): Show |
1 | a0001c0001t0021g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25+58436_25+58437i others(37): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676466 | ||||||
| chr2:163676466
|
T | TATATATA others(24): Show |
1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+58436_25+58437i others(33): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676466 | ||||||
| chr2:163676470
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0078g0058 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+58419_25+58432d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676470 | ||||||
| chr2:163676472
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0008g0021 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25+58419_25+58430d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676472 | ||||||
| chr2:163676476
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0057a0001c0001t0002g0005a0001c0001t0002g0052others(3): Show | 6 | HG03669.hp2 HG03927.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58419_25+58426d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676476 | ||||||
| chr2:163676478
|
TATATAA | T | 11 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0002g0075others(8): Show | 11 | HG00323.hp2 HG00408.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+58419_25+58424d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676478 | ||||||
| chr2:163676480
|
TATAA | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0035others(13): Show | 16 | HG01257.hp2 HG01261.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+58419_25+58422d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676480 | ||||||
| chr2:163676482
|
TAA | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0034others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+58419_25+58420d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676482 | ||||||
| chr2:163676484
|
A | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(21): Show | 24 | HG00741.hp1 HG01071.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+58419T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676484 | ||||||
| chr2:163676923
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+57980T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676923 | ||||||
| chr2:163676935
|
A | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(261): Show | 265 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.25+57968T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676935 | ||||||
| chr2:163677348
|
A | T | 88 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0139others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+57555T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677348 | ||||||
| chr2:163677377
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.25+57526A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677377 | ||||||
| chr2:163677581
|
T | C | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+57322A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677581 | ||||||
| chr2:163677734
|
T | C | 1 | a0001c0001t0014g0204 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+57169A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677734 | ||||||
| chr2:163677924
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(104): Show | 108 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.25+56979C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677924 | ||||||
| chr2:163678346
|
G | A | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+56557C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678346 | ||||||
| chr2:163678427
|
G | C | 1 | a0001c0001t0026g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.25+56476C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678427 | ||||||
| chr2:163678512
|
C | T | 1 | a0001c0001t0023g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+56391G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678512 | ||||||
| chr2:163678548
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25+56355A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678548 | ||||||
| chr2:163678664
|
G | C | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+56239C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678664 | ||||||
| chr2:163678958
|
T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+55945A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678958 | ||||||
| chr2:163679220
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+55683C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679220 | ||||||
| chr2:163679259
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+55644G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679259 | ||||||
| chr2:163679260
|
G | A | 2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+55643C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679260 | ||||||
| chr2:163679338
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+55565A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679338 | ||||||
| chr2:163679365
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0033others(7): Show | 10 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+55538C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679365 | ||||||
| chr2:163679474
|
C | T | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+55429G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679474 | ||||||
| chr2:163679495
|
C | CA | 102 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0118others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.25+55407dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679495 | ||||||
| chr2:163679495
|
C | CAA | 41 | a0001c0001t0001g0047a0001c0001t0001g0152a0001c0001t0001g0195others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.25+55406_25+55407d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679495 | ||||||
| chr2:163679511
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+55392A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679511 | ||||||
| chr2:163679668
|
G | A | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+55235C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679668 | ||||||
| chr2:163679812
|
C | T | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+55091G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679812 | ||||||
| chr2:163679940
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0027g0166 | 3 | HG03669.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.25+54963C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679940 | ||||||
| chr2:163679980
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25+54923C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679980 | ||||||
| chr2:163680309
|
A | G | 2 | a0001c0001t0009g0129a0001c0002t0011g0128 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+54594T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680309 | ||||||
| chr2:163680350
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.25+54553G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680350 | ||||||
| chr2:163680356
|
A | G | 35 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+54547T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680356 | ||||||
| chr2:163680376
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(79): Show | 82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.25+54527C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680376 | ||||||
| chr2:163680386
|
C | G | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+54517G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680386 | ||||||
| chr2:163680512
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+54391C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680512 | ||||||
| chr2:163680710
|
A | G | 2 | a0001c0001t0006g0234a0001c0001t0062g0225 | 2 | NA19076.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.25+54193T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680710 | ||||||
| chr2:163680732
|
C | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+54171G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680732 | ||||||
| chr2:163680874
|
A | G | 1 | a0001c0001t0072g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.25+54029T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680874 | ||||||
| chr2:163680946
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(92): Show | 96 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+53957A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680946 | ||||||
| chr2:163680983
|
A | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(92): Show | 96 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+53920T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680983 | ||||||
| chr2:163681201
|
T | G | 4 | a0001c0001t0030g0096a0001c0002t0007g0135a0001c0002t0007g0136others(1): Show | 4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+53702A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681201 | ||||||
| chr2:163681273
|
A | AAAT | 6 | a0001c0001t0001g0139a0001c0001t0003g0161a0001c0001t0005g0153others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+53629_25+53630i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681273 | ||||||
| chr2:163681389
|
T | G | 1 | a0001c0001t0065g0238 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.25+53514A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681389 | ||||||
| chr2:163681454
|
T | C | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+53449A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681454 | ||||||
| chr2:163681521
|
G | C | 2 | a0001c0001t0015g0126a0001c0001t0030g0127 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.25+53382C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681521 | ||||||
| chr2:163681542
|
C | T | 44 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+53361G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681542 | ||||||
| chr2:163681556
|
AAAGTGAC others(5): Show |
A | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0083others(2): Show | 5 | HG00741.hp1 HG01106.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+53335_25+53346d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681556 | ||||||
| chr2:163681603
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+53300C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681603 | ||||||
| chr2:163681632
|
G | A | 1 | a0001c0001t0076g0022 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.25+53271C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681632 | ||||||
| chr2:163682192
|
C | G | 44 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+52711G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682192 | ||||||
| chr2:163682309
|
T | C | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+52594A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682309 | ||||||
| chr2:163682361
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+52542G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682361 | ||||||
| chr2:163682372
|
C | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+52531G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682372 | ||||||
| chr2:163682394
|
CACA | C | 116 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.25+52506_25+52508d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682394 | ||||||
| chr2:163682423
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(80): Show | 83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.25+52480A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682423 | ||||||
| chr2:163682461
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.25+52442C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682461 | ||||||
| chr2:163682528
|
C | G | 116 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.25+52375G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682528 | ||||||
| chr2:163682773
|
C | T | 1 | a0001c0001t0077g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25+52130G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682773 | ||||||
| chr2:163683067
|
G | A | 23 | a0001c0001t0001g0137a0001c0001t0012g0122a0001c0001t0019g0255others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+51836C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683067 | ||||||
| chr2:163683179
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0006g0062 | 2 | HG00735.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.25+51724C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683179 | ||||||
| chr2:163683186
|
A | G | 1 | a0001c0002t0028g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+51717T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683186 | ||||||
| chr2:163683463
|
A | C | 2 | a0001c0001t0070g0103a0001c0002t0007g0104 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+51440T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683463 | ||||||
| chr2:163683814
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.25+51089G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683814 | ||||||
| chr2:163684166
|
T | TAC | 22 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0106others(19): Show | 22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+50735_25+50736d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684166 | ||||||
| chr2:163684257
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.25+50646G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684257 | ||||||
| chr2:163684608
|
A | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+50295T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684608 | ||||||
| chr2:163684743
|
C | T | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+50160G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684743 | ||||||
| chr2:163684895
|
C | A | 3 | a0001c0001t0001g0098a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+50008G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684895 | ||||||
| chr2:163684939
|
A | AT | 23 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0026others(20): Show | 23 | HG01496.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+49963dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | ||||||
| chr2:163684939
|
AT | A | 22 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0197others(19): Show | 22 | HG01070.hp1 HG01071.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.25+49963delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | ||||||
| chr2:163684939
|
ATTTTTT | A | 34 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0141others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.25+49958_25+49963d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | ||||||
| chr2:163685075
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.25+49828C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685075 | ||||||
| chr2:163685115
|
G | T | 2 | a0001c0001t0034g0252a0001c0001t0080g0264 | 2 | NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.25+49788C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685115 | ||||||
| chr2:163685752
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+49151C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685752 | ||||||
| chr2:163685755
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+49148A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685755 | ||||||
| chr2:163685851
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+49052T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685851 | ||||||
| chr2:163685982
|
A | G | 34 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(31): Show | 34 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.25+48921T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685982 | ||||||
| chr2:163686298
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+48605G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686298 | ||||||
| chr2:163686385
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+48518A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686385 | ||||||
| chr2:163686438
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0003g0105 | 2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.25+48465T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686438 | ||||||
| chr2:163686479
|
T | C | 90 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0139others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.25+48424A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686479 | ||||||
| chr2:163686526
|
A | C | 34 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(31): Show | 34 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.25+48377T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686526 | ||||||
| chr2:163686660
|
A | T | 91 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0139others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.25+48243T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686660 | ||||||
| chr2:163686737
|
C | A | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+48166G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686737 | ||||||
| chr2:163686758
|
G | GTA | 25 | a0001c0001t0001g0137a0001c0001t0003g0116a0001c0001t0005g0117others(22): Show | 25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.25+48143_25+48144d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686758 | ||||||
| chr2:163686760
|
A | G | 1 | a0001c0001t0004g0019 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.25+48143T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686760 | ||||||
| chr2:163686777
|
T | TAC | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.25+48124_25+48125d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686777 | ||||||
| chr2:163686777
|
T | TACAC | 20 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0002g0043others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.25+48122_25+48125d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686777 | ||||||
| chr2:163686795
|
CATAT | C | 4 | a0001c0001t0025g0107a0001c0001t0027g0108a0001c0001t0045g0176others(1): Show | 4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+48104_25+48107d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686795 | ||||||
| chr2:163686797
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0047others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.25+48106A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686797 | ||||||
| chr2:163686799
|
T | C | 110 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.25+48104A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686799 | ||||||
| chr2:163686828
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(90): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+48075A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686828 | ||||||
| chr2:163686953
|
T | C | 19 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0116others(16): Show | 19 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+47950A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686953 | ||||||
| chr2:163687012
|
T | TAC | 6 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | HG02280.hp1 HG02698.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+47889_25+47890d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687012 | ||||||
| chr2:163687012
|
TAC | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0164others(9): Show | 12 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+47889_25+47890d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687012 | ||||||
| chr2:163687168
|
A | C | 1 | a0003c0005t0054g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+47735T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687168 | ||||||
| chr2:163687187
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.25+47716G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687187 | ||||||
| chr2:163687599
|
T | C | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+47304A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687599 | ||||||
| chr2:163687996
|
T | C | 3 | a0001c0002t0007g0135a0001c0002t0007g0136a0001c0002t0028g0134 | 3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25+46907A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687996 | ||||||
| chr2:163688000
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+46903G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688000 | ||||||
| chr2:163688117
|
A | G | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+46786T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688117 | ||||||
| chr2:163688173
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.25+46730C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688173 | ||||||
| chr2:163688200
|
G | C | 20 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0116others(17): Show | 20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+46703C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688200 | ||||||
| chr2:163688250
|
A | T | 21 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0142others(18): Show | 21 | HG00140.hp1 HG00558.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+46653T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688250 | ||||||
| chr2:163688572
|
A | G | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+46331T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688572 | ||||||
| chr2:163688817
|
C | T | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+46086G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688817 | ||||||
| chr2:163688892
|
G | T | 1 | a0001c0001t0042g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.25+46011C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688892 | ||||||
| chr2:163689173
|
A | AACACAC | 2 | a0001c0001t0003g0097a0001c0001t0003g0105 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.25+45724_25+45729d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(1): Show |
8 | a0001c0001t0005g0040a0001c0001t0005g0173a0001c0001t0030g0096others(5): Show | 8 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+45722_25+45729d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(3): Show |
23 | a0001c0001t0002g0053a0001c0001t0003g0101a0001c0001t0003g0192others(20): Show | 23 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+45720_25+45729d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(5): Show |
21 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0115others(18): Show | 21 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+45718_25+45729d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(7): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(75): Show | 78 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.25+45716_25+45729d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(9): Show |
51 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0118others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.25+45714_25+45729d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(11): Show |
66 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0119others(63): Show | 67 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.25+45712_25+45729d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(13): Show |
9 | a0001c0001t0001g0201a0001c0001t0002g0228a0001c0001t0004g0223others(6): Show | 9 | HG00408.hp2 HG02129.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+45710_25+45729d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(15): Show |
2 | a0001c0001t0002g0232a0001c0001t0045g0176 | 2 | HG02015.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.25+45708_25+45729d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689173
|
A | AACACACA others(25): Show |
1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+45729_25+45730i others(34): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | ||||||
| chr2:163689274
|
A | T | 1 | a0001c0001t0081g0261 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+45629T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689274 | ||||||
| chr2:163689426
|
A | G | 12 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+45477T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689426 | ||||||
| chr2:163689451
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+45452A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689451 | ||||||
| chr2:163689687
|
T | G | 120 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0119others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.25+45216A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689687 | ||||||
| chr2:163689996
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+44907A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689996 | ||||||
| chr2:163690180
|
T | C | 3 | a0001c0001t0021g0183a0001c0001t0050g0171a0001c0002t0013g0190 | 3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+44723A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690180 | ||||||
| chr2:163690377
|
A | C | 2 | a0001c0001t0001g0057a0001c0001t0014g0045 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.25+44526T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690377 | ||||||
| chr2:163690408
|
G | A | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+44495C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690408 | ||||||
| chr2:163690432
|
C | T | 5 | a0001c0001t0031g0131a0001c0002t0007g0135a0001c0002t0007g0136others(2): Show | 5 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+44471G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690432 | ||||||
| chr2:163690562
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0006g0154 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.25+44341A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690562 | ||||||
| chr2:163690583
|
CAGTCT | C | 4 | a0001c0001t0002g0031a0001c0001t0002g0052a0001c0001t0004g0019others(1): Show | 4 | HG02155.hp2 NA18977.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+44315_25+44319d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690583 | ||||||
| chr2:163690588
|
T | C | 35 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+44315A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690588 | ||||||
| chr2:163690802
|
C | CAAAAATG others(1): Show |
22 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0106others(19): Show | 22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+44093_25+44100d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690802 | ||||||
| chr2:163690830
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+44073G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690830 | ||||||
| chr2:163690919
|
A | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+43984T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690919 | ||||||
| chr2:163690930
|
T | C | 24 | a0001c0001t0001g0137a0001c0001t0012g0122a0001c0001t0019g0255others(21): Show | 24 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+43973A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690930 | ||||||
| chr2:163691088
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0006g0154 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.25+43815G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691088 | ||||||
| chr2:163691281
|
C | T | 4 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0023g0155others(1): Show | 4 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+43622G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691281 | ||||||
| chr2:163691490
|
T | C | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+43413A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691490 | ||||||
| chr2:163691614
|
G | A | 6 | a0001c0001t0002g0043a0001c0001t0004g0032a0001c0001t0004g0042others(3): Show | 6 | HG02015.hp2 NA18943.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+43289C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691614 | ||||||
| chr2:163691689
|
A | G | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+43214T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691689 | ||||||
| chr2:163691693
|
A | G | 3 | a0001c0001t0005g0173a0001c0004t0033g0138a0001c0004t0033g0174 | 3 | HG01070.hp1 HG01071.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.25+43210T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691693 | ||||||
| chr2:163691766
|
TA | T | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+43136delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691766 | ||||||
| chr2:163691799
|
G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+43104C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691799 | ||||||
| chr2:163691867
|
G | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0164others(1): Show | 4 | HG00140.hp1 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+43036C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691867 | ||||||
| chr2:163692219
|
T | C | 2 | a0001c0001t0003g0106a0001c0001t0004g0189 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+42684A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692219 | ||||||
| chr2:163692230
|
T | G | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+42673A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692230 | ||||||
| chr2:163692324
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+42579T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692324 | ||||||
| chr2:163692400
|
G | A | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.25+42503C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692400 | ||||||
| chr2:163692719
|
T | A | 1 | a0001c0001t0045g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+42184A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692719 | ||||||
| chr2:163692740
|
C | T | 2 | a0001c0001t0048g0208a0001c0003t0002g0207 | 2 | NA18973.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.25+42163G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692740 | ||||||
| chr2:163693009
|
G | A | 1 | a0001c0001t0008g0021 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25+41894C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693009 | ||||||
| chr2:163693103
|
G | T | 1 | a0001c0001t0023g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+41800C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693103 | ||||||
| chr2:163693115
|
C | T | 1 | a0001c0001t0047g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25+41788G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693115 | ||||||
| chr2:163693243
|
C | T | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+41660G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693243 | ||||||
| chr2:163693291
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.25+41612C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693291 | ||||||
| chr2:163693388
|
C | T | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+41515G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693388 | ||||||
| chr2:163693582
|
G | A | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+41321C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693582 | ||||||
| chr2:163693693
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+41210A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693693 | ||||||
| chr2:163693811
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.25+41092G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693811 | ||||||
| chr2:163693968
|
G | T | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+40935C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693968 | ||||||
| chr2:163694001
|
T | C | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+40902A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694001 | ||||||
| chr2:163694131
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 115 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.25+40772T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694131 | ||||||
| chr2:163694365
|
T | A | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+40538A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694365 | ||||||
| chr2:163694460
|
C | T | 23 | a0001c0001t0001g0137a0001c0001t0012g0122a0001c0001t0019g0255others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+40443G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694460 | ||||||
| chr2:163694475
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.25+40428C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694475 | ||||||
| chr2:163694639
|
C | T | 35 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+40264G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694639 | ||||||
| chr2:163694699
|
T | G | 1 | a0001c0001t0004g0223 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.25+40204A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694699 | ||||||
| chr2:163694868
|
G | C | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+40035C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694868 | ||||||
| chr2:163695020
|
T | G | 1 | a0001c0002t0007g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25+39883A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695020 | ||||||
| chr2:163695070
|
GTC | G | 112 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0137others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.25+39831_25+39832d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695070 | ||||||
| chr2:163695225
|
C | A | 33 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(30): Show | 33 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.25+39678G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695225 | ||||||
| chr2:163695583
|
C | T | 1 | a0001c0001t0078g0058 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+39320G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695583 | ||||||
| chr2:163695593
|
C | A | 1 | a0001c0002t0007g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25+39310G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695593 | ||||||
| chr2:163695749
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+39154C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695749 | ||||||
| chr2:163695845
|
C | G | 1 | a0001c0001t0012g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.25+39058G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695845 | ||||||
| chr2:163696171
|
T | C | 35 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0175others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+38732A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696171 | ||||||
| chr2:163696283
|
T | C | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+38620A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696283 | ||||||
| chr2:163696364
|
GA | G | 6 | a0001c0001t0001g0139a0001c0001t0003g0161a0001c0001t0005g0153others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+38538delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696364 | ||||||
| chr2:163696377
|
G | C | 7 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | NA18747.hp1 NA18941.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+38526C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696377 | ||||||
| chr2:163696433
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+38470T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696433 | ||||||
| chr2:163696732
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+38171C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696732 | ||||||
| chr2:163696834
|
A | AT | 7 | a0001c0001t0001g0235a0001c0001t0003g0192a0001c0001t0004g0191others(4): Show | 7 | HG02647.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+38068dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696834 | ||||||
| chr2:163696834
|
AT | A | 38 | a0001c0001t0001g0030a0001c0001t0001g0098a0001c0001t0001g0175others(35): Show | 38 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.25+38068delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696834 | ||||||
| chr2:163697026
|
C | T | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+37877G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697026 | ||||||
| chr2:163697027
|
G | A | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37876C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697027 | ||||||
| chr2:163697100
|
C | CT | 26 | a0001c0001t0001g0115a0001c0001t0003g0097a0001c0001t0003g0101others(23): Show | 26 | HG00558.hp1 HG00735.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+37802dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | ||||||
| chr2:163697100
|
C | CTT | 4 | a0001c0001t0031g0091a0001c0001t0059g0093a0001c0002t0007g0244others(1): Show | 4 | HG01175.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+37801_25+37802d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | ||||||
| chr2:163697100
|
CTTTCTTT others(5): Show |
C | 3 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0066g0029 | 3 | NA19004.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.25+37791_25+37802d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | ||||||
| chr2:163697102
|
TTC | T | 10 | a0001c0001t0001g0139a0001c0001t0002g0146a0001c0001t0004g0224others(7): Show | 10 | HG01070.hp2 HG01496.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+37799_25+37800d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697102 | ||||||
| chr2:163697103
|
TC | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.25+37799delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697103 | ||||||
| chr2:163697104
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(135): Show | 139 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.25+37799G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697104 | ||||||
| chr2:163697105
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+37798A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697105 | ||||||
| chr2:163697194
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 91 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.25+37709C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697194 | ||||||
| chr2:163697218
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+37685T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697218 | ||||||
| chr2:163697220
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+37683G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697220 | ||||||
| chr2:163697274
|
T | C | 1 | a0001c0001t0067g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+37629A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697274 | ||||||
| chr2:163697293
|
G | A | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37610C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697293 | ||||||
| chr2:163697348
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(90): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+37555C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697348 | ||||||
| chr2:163697441
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+37462C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697441 | ||||||
| chr2:163697470
|
GC | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0164others(1): Show | 4 | HG00140.hp1 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+37432delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697470 | ||||||
| chr2:163697489
|
G | A | 7 | a0001c0001t0004g0133a0001c0001t0030g0096a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37414C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697489 | ||||||
| chr2:163697668
|
C | A | 2 | a0001c0001t0031g0091a0001c0001t0059g0093 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.25+37235G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697668 | ||||||
| chr2:163697738
|
C | T | 4 | a0001c0001t0025g0107a0001c0001t0027g0108a0001c0001t0045g0176others(1): Show | 4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+37165G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697738 | ||||||
| chr2:163697818
|
T | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0141others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.25+37085A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697818 | ||||||
| chr2:163698023
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+36880G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698023 | ||||||
| chr2:163698363
|
T | C | 1 | a0001c0001t0027g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.25+36540A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698363 | ||||||
| chr2:163698464
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+36439G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698464 | ||||||
| chr2:163698501
|
T | A | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0003g0182others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+36402A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698501 | ||||||
| chr2:163698696
|
G | C | 1 | a0001c0001t0075g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.25+36207C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698696 | ||||||
| chr2:163698718
|
G | A | 1 | a0001c0001t0059g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.25+36185C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698718 | ||||||
| chr2:163698881
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+36022C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698881 | ||||||
| chr2:163698930
|
T | C | 44 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0001g0197others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+35973A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698930 | ||||||
| chr2:163699244
|
A | G | 1 | a0001c0001t0016g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.25+35659T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699244 | ||||||
| chr2:163699258
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+35645C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699258 | ||||||
| chr2:163699287
|
A | AT | 4 | a0001c0001t0005g0173a0001c0001t0006g0041a0001c0004t0033g0138others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+35615dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699287 | ||||||
| chr2:163699456
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+35447A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699456 | ||||||
| chr2:163699465
|
T | C | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+35438A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699465 | ||||||
| chr2:163699510
|
T | TGTACTGG others(2): Show |
227 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.25+35392_25+35393i others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699510 | ||||||
| chr2:163699568
|
C | A | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+35335G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699568 | ||||||
| chr2:163699988
|
A | C | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+34915T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699988 | ||||||
| chr2:163700059
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+34844C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700059 | ||||||
| chr2:163700072
|
A | G | 1 | a0001c0001t0009g0196 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.25+34831T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700072 | ||||||
| chr2:163700074
|
G | A | 1 | a0001c0001t0009g0196 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.25+34829C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700074 | ||||||
| chr2:163700095
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+34808G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700095 | ||||||
| chr2:163700160
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+34743A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700160 | ||||||
| chr2:163700197
|
T | G | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+34706A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700197 | ||||||
| chr2:163700280
|
A | T | 2 | a0001c0001t0001g0080a0001c0001t0005g0078 | 2 | HG01261.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.25+34623T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700280 | ||||||
| chr2:163700409
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.25+34494C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700409 | ||||||
| chr2:163700446
|
G | A | 1 | a0001c0001t0022g0079 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+34457C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700446 | ||||||
| chr2:163700553
|
T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+34350A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700553 | ||||||
| chr2:163700663
|
T | C | 1 | a0001c0002t0028g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+34240A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700663 | ||||||
| chr2:163700826
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.25+34077C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700826 | ||||||
| chr2:163700833
|
G | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+34070C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700833 | ||||||
| chr2:163700950
|
C | T | 23 | a0001c0001t0001g0137a0001c0001t0012g0122a0001c0001t0019g0255others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+33953G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700950 | ||||||
| chr2:163701013
|
A | G | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+33890T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701013 | ||||||
| chr2:163701074
|
A | G | 13 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0004g0133others(10): Show | 13 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+33829T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701074 | ||||||
| chr2:163701471
|
C | T | 4 | a0001c0001t0003g0097a0001c0001t0031g0091a0001c0001t0059g0093others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+33432G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701471 | ||||||
| chr2:163701493
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.25+33410G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701493 | ||||||
| chr2:163701658
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+33245T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701658 | ||||||
| chr2:163701713
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(90): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+33190G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701713 | ||||||
| chr2:163701801
|
C | A | 4 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0089others(1): Show | 4 | HG02074.hp2 NA18946.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+33102G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701801 | ||||||
| chr2:163701852
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+33051G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701852 | ||||||
| chr2:163701919
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 85 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.25+32984T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701919 | ||||||
| chr2:163702280
|
G | A | 1 | a0001c0001t0071g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25+32623C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702280 | ||||||
| chr2:163702350
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.25+32553G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702350 | ||||||
| chr2:163702426
|
C | T | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+32477G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702426 | ||||||
| chr2:163702719
|
C | A | 3 | a0001c0001t0002g0228a0001c0001t0022g0217a0001c0001t0052g0215 | 3 | HG00408.hp2 HG02135.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.25+32184G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702719 | ||||||
| chr2:163702741
|
C | T | 1 | a0001c0009t0005g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.25+32162G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702741 | ||||||
| chr2:163702822
|
C | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(88): Show | 92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.25+32081G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702822 | ||||||
| chr2:163702961
|
G | A | 18 | a0001c0001t0003g0097a0001c0001t0003g0101a0001c0001t0003g0241others(15): Show | 18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+31942C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702961 | ||||||
| chr2:163703030
|
C | CT | 7 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0006g0239others(4): Show | 7 | HG02109.hp1 HG02135.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+31872dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703030 | ||||||
| chr2:163703115
|
A | G | 1 | a0001c0001t0010g0054 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.25+31788T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703115 | ||||||
| chr2:163703123
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25+31780A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703123 | ||||||
| chr2:163703196
|
T | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+31707A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703196 | ||||||
| chr2:163703455
|
C | A | 7 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(4): Show | 7 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+31448G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703455 | ||||||
| chr2:163703479
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+31424G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703479 | ||||||
| chr2:163703702
|
A | G | 1 | a0001c0001t0032g0014 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.25+31201T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703702 | ||||||
| chr2:163703801
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.25+31102C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703801 | ||||||
| chr2:163704029
|
G | A | 2 | a0001c0001t0021g0243a0001c0002t0007g0240 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.25+30874C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704029 | ||||||
| chr2:163704185
|
G | A | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+30718C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704185 | ||||||
| chr2:163704370
|
T | C | 16 | a0001c0001t0001g0115a0001c0001t0003g0106a0001c0001t0003g0186others(13): Show | 16 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+30533A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704370 | ||||||
| chr2:163704370
|
T | G | 3 | a0001c0001t0025g0107a0001c0001t0027g0108a0001c0001t0057g0109 | 3 | HG03139.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+30533A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704370 | ||||||
| chr2:163704503
|
T | C | 10 | a0001c0001t0001g0115a0001c0001t0003g0106a0001c0001t0003g0186others(7): Show | 10 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+30400A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704503 | ||||||
| chr2:163704615
|
G | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.25+30288C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704615 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(4): Show |
3 | a0001c0001t0001g0036a0001c0001t0004g0189a0003c0005t0054g0024 | 3 | HG00639.hp2 HG03130.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(6): Show |
2 | a0001c0001t0001g0048a0001c0001t0006g0041 | 2 | NA18991.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(8): Show |
1 | a0001c0001t0002g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.25+30277_25+30278i others(17): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(10): Show |
1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+30277_25+30278i others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(12): Show |
4 | a0001c0001t0001g0218a0001c0001t0005g0173a0001c0002t0007g0104others(1): Show | 4 | HG01071.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+30277_25+30278i others(21): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TCTCTCTC others(14): Show |
2 | a0001c0001t0003g0101a0001c0002t0003g0100 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(23): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTC | 29 | a0001c0001t0001g0027a0001c0001t0001g0141a0001c0001t0001g0152others(26): Show | 29 | HG00558.hp1 HG01358.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.25+30276_25+30277d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTC | 16 | a0001c0001t0001g0110a0001c0001t0001g0142a0001c0001t0001g0157others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.25+30274_25+30277d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTC | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0043g0209 | 3 | NA18945.hp2 NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.25+30272_25+30277d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(1): Show |
14 | a0001c0001t0001g0012a0001c0001t0001g0077a0001c0001t0001g0080others(11): Show | 14 | HG01106.hp2 HG01167.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+30270_25+30277d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(3): Show |
21 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0056others(18): Show | 21 | HG00323.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+30268_25+30277d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(5): Show |
27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0023others(24): Show | 27 | HG00423.hp1 HG01071.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.25+30266_25+30277d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(7): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0049others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+30264_25+30277d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(9): Show |
15 | a0001c0001t0001g0081a0001c0001t0002g0043a0001c0001t0002g0052others(12): Show | 15 | HG02015.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+30262_25+30277d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(11): Show |
13 | a0001c0001t0001g0098a0001c0001t0001g0220a0001c0001t0001g0235others(10): Show | 13 | HG00408.hp2 HG01891.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+30260_25+30277d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(13): Show |
5 | a0001c0001t0004g0224a0001c0001t0006g0099a0001c0001t0006g0234others(2): Show | 5 | HG01070.hp1 HG02055.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30258_25+30277d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(15): Show |
5 | a0001c0001t0003g0087a0001c0001t0003g0116a0001c0001t0005g0117others(2): Show | 5 | HG02132.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30256_25+30277d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(17): Show |
4 | a0001c0001t0001g0057a0001c0001t0003g0070a0001c0001t0004g0223others(1): Show | 4 | HG02135.hp1 HG03139.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+30254_25+30277d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704625
|
T | TTCTCTCT others(19): Show |
1 | a0001c0001t0013g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25+30252_25+30277d others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | ||||||
| chr2:163704656
|
T | TCTCTCTC others(7): Show |
3 | a0001c0001t0002g0206a0001c0001t0003g0106a0001c0003t0002g0207 | 3 | NA18973.hp2 NA18977.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+30246_25+30247i others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | ||||||
| chr2:163704656
|
T | TCTCTCTC others(9): Show |
1 | a0001c0001t0001g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.25+30246_25+30247i others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | ||||||
| chr2:163704656
|
TCA | T | 15 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+30245_25+30246d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | ||||||
| chr2:163704656
|
TCACA | T | 8 | a0001c0001t0015g0126a0001c0001t0016g0130a0001c0001t0023g0165others(5): Show | 8 | HG01261.hp1 HG01515.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+30243_25+30246d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | ||||||
| chr2:163704656
|
TCACACA | T | 4 | a0001c0001t0001g0119a0001c0001t0024g0001a0001c0001t0056g0121others(1): Show | 5 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30241_25+30246d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | ||||||
| chr2:163704658
|
A | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.25+30245T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704658 | ||||||
| chr2:163704660
|
A | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.25+30243T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704660 | ||||||
| chr2:163704662
|
A | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0137others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.25+30241T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704662 | ||||||
| chr2:163704664
|
A | T | 17 | a0001c0001t0019g0255a0001c0001t0020g0247a0001c0001t0020g0256others(14): Show | 17 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+30239T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704664 | ||||||
| chr2:163704798
|
G | T | 23 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0019g0255others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+30105C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704798 | ||||||
| chr2:163705049
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+29854A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705049 | ||||||
| chr2:163705300
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.25+29603G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705300 | ||||||
| chr2:163705417
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25+29486A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705417 | ||||||
| chr2:163705478
|
A | T | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+29425T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705478 | ||||||
| chr2:163705607
|
T | A | 1 | a0001c0003t0032g0086 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.25+29296A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705607 | ||||||
| chr2:163705830
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+29073T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705830 | ||||||
| chr2:163705904
|
A | C | 1 | a0001c0003t0068g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.25+28999T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705904 | ||||||
| chr2:163705904
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+28999T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705904 | ||||||
| chr2:163705985
|
G | T | 1 | a0001c0002t0004g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+28918C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705985 | ||||||
| chr2:163706106
|
T | A | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0004g0184 | 3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+28797A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706106 | ||||||
| chr2:163706156
|
A | G | 2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+28747T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706156 | ||||||
| chr2:163706189
|
A | G | 12 | a0001c0001t0001g0115a0001c0001t0003g0106a0001c0001t0003g0186others(9): Show | 12 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+28714T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706189 | ||||||
| chr2:163706279
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+28624C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706279 | ||||||
| chr2:163706624
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.25+28279T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706624 | ||||||
| chr2:163706761
|
T | C | 2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+28142A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706761 | ||||||
| chr2:163706914
|
C | T | 3 | a0001c0001t0025g0107a0001c0001t0027g0108a0001c0001t0057g0109 | 3 | HG03139.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+27989G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706914 | ||||||
| chr2:163707174
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.25+27729G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707174 | ||||||
| chr2:163707184
|
CA | C | 4 | a0001c0001t0020g0263a0001c0001t0036g0245a0001c0001t0084g0254others(1): Show | 4 | NA18944.hp1 NA18961.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+27718delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707184 | ||||||
| chr2:163707354
|
CA | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0175a0001c0001t0002g0052others(9): Show | 12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+27548delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707354 | ||||||
| chr2:163707354
|
CAA | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(245): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.25+27547_25+27548d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707354 | ||||||
| chr2:163707419
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.25+27484C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707419 | ||||||
| chr2:163708056
|
T | C | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+26847A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708056 | ||||||
| chr2:163708258
|
C | A | 11 | a0001c0001t0003g0192a0001c0001t0004g0133a0001c0001t0004g0191others(8): Show | 11 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+26645G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708258 | ||||||
| chr2:163708271
|
CTTAA | C | 23 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0019g0255others(20): Show | 23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+26628_25+26631d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708271 | ||||||
| chr2:163708322
|
T | C | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.25+26581A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708322 | ||||||
| chr2:163708453
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+26450A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708453 | ||||||
| chr2:163708636
|
T | C | 1 | a0001c0001t0063g0233 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.25+26267A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708636 | ||||||
| chr2:163708650
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+26253A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708650 | ||||||
| chr2:163708734
|
G | A | 1 | a0003c0005t0054g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+26169C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708734 | ||||||
| chr2:163708853
|
G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+26050C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708853 | ||||||
| chr2:163708905
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+25998C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708905 | ||||||
| chr2:163709018
|
G | A | 3 | a0001c0001t0021g0183a0001c0001t0030g0096a0001c0002t0013g0190 | 3 | HG03098.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.25+25885C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709018 | ||||||
| chr2:163709025
|
C | T | 2 | a0001c0001t0009g0129a0001c0002t0011g0128 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+25878G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709025 | ||||||
| chr2:163709124
|
C | T | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+25779G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709124 | ||||||
| chr2:163709133
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+25770G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709133 | ||||||
| chr2:163709154
|
C | T | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+25749G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709154 | ||||||
| chr2:163709346
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.25+25557A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709346 | ||||||
| chr2:163709461
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0010g0054 | 2 | HG02129.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25+25442C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709461 | ||||||
| chr2:163709650
|
C | T | 1 | a0001c0001t0083g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+25253G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709650 | ||||||
| chr2:163709713
|
A | G | 5 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0158others(2): Show | 5 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+25190T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709713 | ||||||
| chr2:163709784
|
GA | G | 5 | a0001c0001t0031g0131a0001c0002t0007g0135a0001c0002t0007g0136others(2): Show | 5 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+25118delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709784 | ||||||
| chr2:163709797
|
T | C | 1 | a0001c0001t0010g0054 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.25+25106A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709797 | ||||||
| chr2:163709898
|
A | G | 1 | a0001c0001t0045g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+25005T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709898 | ||||||
| chr2:163710276
|
G | A | 2 | a0001c0001t0003g0161a0001c0001t0072g0160 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.25+24627C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710276 | ||||||
| chr2:163710332
|
C | G | 85 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.25+24571G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710332 | ||||||
| chr2:163710354
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+24549A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710354 | ||||||
| chr2:163710374
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0087a0001c0001t0007g0068others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+24529G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710374 | ||||||
| chr2:163710905
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.25+23998G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710905 | ||||||
| chr2:163711129
|
C | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+23774G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711129 | ||||||
| chr2:163711151
|
G | T | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+23752C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711151 | ||||||
| chr2:163711171
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.25+23732C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711171 | ||||||
| chr2:163711179
|
T | C | 85 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.25+23724A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711179 | ||||||
| chr2:163711316
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.25+23587C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711316 | ||||||
| chr2:163711393
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+23510C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711393 | ||||||
| chr2:163711524
|
G | A | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0004g0184 | 3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+23379C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711524 | ||||||
| chr2:163711657
|
C | CA | 197 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.25+23245dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711657 | ||||||
| chr2:163711657
|
C | CAA | 19 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0057others(16): Show | 19 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+23244_25+23245d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711657 | ||||||
| chr2:163711791
|
C | T | 1 | a0003c0005t0054g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+23112G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711791 | ||||||
| chr2:163711865
|
C | G | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0004g0184 | 3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+23038G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711865 | ||||||
| chr2:163711939
|
C | T | 1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25+22964G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711939 | ||||||
| chr2:163712016
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+22887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712016 | ||||||
| chr2:163712071
|
G | A | 1 | a0001c0002t0028g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+22832C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712071 | ||||||
| chr2:163712280
|
GA | G | 3 | a0001c0001t0001g0098a0001c0001t0070g0103a0001c0002t0007g0104 | 3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+22622delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712280 | ||||||
| chr2:163712580
|
C | T | 1 | a0001c0001t0045g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+22323G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712580 | ||||||
| chr2:163712819
|
G | C | 1 | a0001c0001t0021g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25+22084C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712819 | ||||||
| chr2:163713027
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+21876T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713027 | ||||||
| chr2:163713130
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+21773A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713130 | ||||||
| chr2:163713242
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+21661T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713242 | ||||||
| chr2:163713448
|
C | CCA | 8 | a0001c0001t0002g0059a0001c0001t0002g0088a0001c0001t0003g0105others(5): Show | 8 | HG02040.hp1 HG02040.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+21453_25+21454d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713448 | ||||||
| chr2:163713448
|
CCA | C | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+21453_25+21454d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713448 | ||||||
| chr2:163713483
|
G | A | 43 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0199others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+21420C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713483 | ||||||
| chr2:163713515
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25+21388C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713515 | ||||||
| chr2:163713524
|
C | T | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+21379G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713524 | ||||||
| chr2:163713702
|
C | T | 1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25+21201G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713702 | ||||||
| chr2:163713890
|
C | T | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+21013G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713890 | ||||||
| chr2:163713923
|
G | A | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+20980C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713923 | ||||||
| chr2:163714018
|
G | C | 8 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+20885C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714018 | ||||||
| chr2:163714235
|
C | A | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+20668G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714235 | ||||||
| chr2:163714303
|
C | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(246): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.25+20600G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714303 | ||||||
| chr2:163714453
|
C | G | 4 | a0001c0001t0008g0167a0001c0001t0008g0180a0001c0001t0023g0155others(1): Show | 4 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+20450G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714453 | ||||||
| chr2:163714488
|
A | G | 2 | a0001c0001t0015g0126a0001c0001t0030g0127 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.25+20415T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714488 | ||||||
| chr2:163714609
|
C | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+20294G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714609 | ||||||
| chr2:163714780
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+20123G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714780 | ||||||
| chr2:163714984
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+19919G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714984 | ||||||
| chr2:163715111
|
C | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+19792G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715111 | ||||||
| chr2:163715225
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+19678C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715225 | ||||||
| chr2:163715861
|
T | C | 2 | a0001c0001t0009g0129a0001c0002t0011g0128 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+19042A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715861 | ||||||
| chr2:163715949
|
C | T | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+18954G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715949 | ||||||
| chr2:163715971
|
A | G | 1 | a0001c0001t0002g0089 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.25+18932T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715971 | ||||||
| chr2:163716152
|
C | T | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+18751G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716152 | ||||||
| chr2:163716153
|
G | T | 1 | a0001c0001t0001g0235 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.25+18750C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716153 | ||||||
| chr2:163716154
|
T | C | 1 | a0001c0001t0005g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.25+18749A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716154 | ||||||
| chr2:163716442
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+18461T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716442 | ||||||
| chr2:163716860
|
C | T | 1 | a0001c0003t0002g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.25+18043G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716860 | ||||||
| chr2:163717203
|
T | C | 2 | a0001c0001t0021g0183a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+17700A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717203 | ||||||
| chr2:163717306
|
A | G | 1 | a0001c0001t0032g0014 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.25+17597T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717306 | ||||||
| chr2:163717320
|
A | T | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+17583T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717320 | ||||||
| chr2:163717337
|
C | G | 110 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0139others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.25+17566G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717337 | ||||||
| chr2:163717441
|
G | C | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+17462C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717441 | ||||||
| chr2:163717506
|
T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+17397A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717506 | ||||||
| chr2:163717512
|
G | A | 1 | a0001c0001t0036g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.25+17391C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717512 | ||||||
| chr2:163717609
|
G | A | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+17294C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717609 | ||||||
| chr2:163717760
|
C | T | 8 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+17143G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717760 | ||||||
| chr2:163717804
|
A | G | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+17099T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717804 | ||||||
| chr2:163717834
|
T | C | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+17069A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717834 | ||||||
| chr2:163718392
|
T | G | 2 | a0001c0001t0008g0167a0001c0001t0008g0180 | 2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.25+16511A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718392 | ||||||
| chr2:163718457
|
C | T | 1 | a0001c0001t0006g0234 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.25+16446G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718457 | ||||||
| chr2:163718652
|
A | G | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+16251T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718652 | ||||||
| chr2:163718783
|
G | A | 1 | a0001c0001t0036g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.25+16120C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718783 | ||||||
| chr2:163718838
|
A | AGC | 116 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0118others(113): Show | 117 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.25+16064_25+16065i others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718838 | ||||||
| chr2:163718840
|
T | A | 116 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0118others(113): Show | 117 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.25+16063A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718840 | ||||||
| chr2:163718840
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.25+16063A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718840 | ||||||
| chr2:163718956
|
T | C | 8 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+15947A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718956 | ||||||
| chr2:163719006
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15897T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719006 | ||||||
| chr2:163719129
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15774A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719129 | ||||||
| chr2:163719274
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02630.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.25+15629A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719274 | ||||||
| chr2:163719581
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15322C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719581 | ||||||
| chr2:163719666
|
G | A | 4 | a0001c0001t0002g0063a0001c0001t0005g0065a0001c0001t0009g0064others(1): Show | 4 | HG00423.hp2 NA18994.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+15237C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719666 | ||||||
| chr2:163719675
|
TG | T | 5 | a0001c0001t0003g0101a0001c0001t0006g0099a0001c0001t0013g0102others(2): Show | 5 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+15227delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719675 | ||||||
| chr2:163719774
|
C | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+15129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719774 | ||||||
| chr2:163719821
|
T | A | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+15082A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719821 | ||||||
| chr2:163719985
|
T | A | 1 | a0001c0001t0023g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+14918A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719985 | ||||||
| chr2:163719986
|
A | T | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+14917T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719986 | ||||||
| chr2:163719989
|
C | A | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+14914G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719989 | ||||||
| chr2:163720233
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+14670G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720233 | ||||||
| chr2:163720331
|
C | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 90 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.25+14572G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720331 | ||||||
| chr2:163720358
|
C | T | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+14545G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720358 | ||||||
| chr2:163720407
|
T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+14496A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720407 | ||||||
| chr2:163720616
|
G | T | 6 | a0001c0001t0003g0105a0001c0001t0003g0192a0001c0001t0004g0191others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+14287C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720616 | ||||||
| chr2:163720791
|
C | T | 1 | a0001c0001t0007g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25+14112G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720791 | ||||||
| chr2:163720963
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+13940T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720963 | ||||||
| chr2:163720971
|
A | AAAAT | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0004g0184 | 3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+13928_25+13931d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720971 | ||||||
| chr2:163720986
|
G | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+13917C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720986 | ||||||
| chr2:163721002
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.25+13901C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721002 | ||||||
| chr2:163721059
|
G | A | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+13844C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721059 | ||||||
| chr2:163721129
|
A | G | 5 | a0001c0001t0003g0192a0001c0001t0004g0191a0001c0001t0015g0123others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+13774T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721129 | ||||||
| chr2:163721139
|
A | G | 1 | a0001c0001t0006g0006 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.25+13764T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721139 | ||||||
| chr2:163721191
|
A | G | 88 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+13712T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721191 | ||||||
| chr2:163721198
|
T | C | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+13705A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721198 | ||||||
| chr2:163721223
|
C | T | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+13680G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721223 | ||||||
| chr2:163721820
|
T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+13083A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721820 | ||||||
| chr2:163722213
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.25+12690T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722213 | ||||||
| chr2:163722244
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0006g0076a0003c0005t0054g0024 | 3 | HG00639.hp2 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.25+12659G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722244 | ||||||
| chr2:163722325
|
A | G | 17 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(14): Show | 17 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.25+12578T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722325 | ||||||
| chr2:163722415
|
C | T | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+12488G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722415 | ||||||
| chr2:163722478
|
G | GA | 3 | a0001c0001t0005g0173a0001c0004t0033g0138a0001c0004t0033g0174 | 3 | HG01070.hp1 HG01071.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.25+12424dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722478 | ||||||
| chr2:163722655
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.25+12248A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722655 | ||||||
| chr2:163722742
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.25+12161T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722742 | ||||||
| chr2:163722754
|
G | A | 1 | a0001c0001t0012g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+12149C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722754 | ||||||
| chr2:163722844
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+12059A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722844 | ||||||
| chr2:163722879
|
A | T | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+12024T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722879 | ||||||
| chr2:163722887
|
A | T | 1 | a0001c0001t0007g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25+12016T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722887 | ||||||
| chr2:163722925
|
G | A | 1 | a0001c0001t0029g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.25+11978C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722925 | ||||||
| chr2:163722948
|
A | T | 2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+11955T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722948 | ||||||
| chr2:163722993
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+11910G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722993 | ||||||
| chr2:163723013
|
T | C | 119 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0139others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.25+11890A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723013 | ||||||
| chr2:163723140
|
G | C | 1 | a0001c0001t0004g0224 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.25+11763C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723140 | ||||||
| chr2:163723187
|
T | A | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+11716A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723187 | ||||||
| chr2:163723193
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+11710T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723193 | ||||||
| chr2:163723204
|
A | ATAC | 6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+11698_25+11699i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723204 | ||||||
| chr2:163723213
|
TAATAA | T | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.25+11685_25+11689d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723213 | ||||||
| chr2:163723241
|
G | C | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+11662C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723241 | ||||||
| chr2:163723297
|
A | T | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11606T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723297 | ||||||
| chr2:163723423
|
G | A | 43 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0199others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+11480C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723423 | ||||||
| chr2:163723426
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0005g0117 | 2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+11477C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723426 | ||||||
| chr2:163723489
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0115others(7): Show | 10 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+11414G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723489 | ||||||
| chr2:163723636
|
C | A | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11267G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723636 | ||||||
| chr2:163723827
|
T | A | 1 | a0001c0001t0017g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.25+11076A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723827 | ||||||
| chr2:163723875
|
ATCATCTC others(2): Show |
A | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11019_25+11027d others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723875 | ||||||
| chr2:163723916
|
T | G | 1 | a0001c0001t0017g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.25+10987A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723916 | ||||||
| chr2:163724138
|
C | T | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+10765G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724138 | ||||||
| chr2:163724510
|
A | ATTAT | 119 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0139others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.25+10389_25+10392d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724510 | ||||||
| chr2:163724583
|
T | C | 1 | a0001c0001t0022g0079 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+10320A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724583 | ||||||
| chr2:163724731
|
T | G | 119 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0139others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.25+10172A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724731 | ||||||
| chr2:163724811
|
A | T | 43 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0199others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+10092T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724811 | ||||||
| chr2:163724843
|
G | C | 36 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.25+10060C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724843 | ||||||
| chr2:163724851
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.25+10052T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724851 | ||||||
| chr2:163725070
|
T | C | 2 | a0001c0001t0003g0105a0001c0002t0007g0104 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9833A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725070 | ||||||
| chr2:163725071
|
T | G | 2 | a0001c0001t0003g0105a0001c0002t0007g0104 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9832A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725071 | ||||||
| chr2:163725087
|
T | G | 15 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0157others(12): Show | 15 | HG00558.hp2 HG02056.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.25+9816A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725087 | ||||||
| chr2:163725250
|
A | C | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9653T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725250 | ||||||
| chr2:163725254
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9649A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725254 | ||||||
| chr2:163725280
|
A | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9623T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725280 | ||||||
| chr2:163725300
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | NA18943.hp2 NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.25+9603G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725300 | ||||||
| chr2:163725302
|
G | A | 16 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(13): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+9601C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725302 | ||||||
| chr2:163725481
|
A | G | 88 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+9422T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725481 | ||||||
| chr2:163725556
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+9347G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725556 | ||||||
| chr2:163725725
|
A | T | 2 | a0001c0001t0003g0105a0001c0002t0007g0104 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9178T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725725 | ||||||
| chr2:163725764
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+9139G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725764 | ||||||
| chr2:163725954
|
T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+8949A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725954 | ||||||
| chr2:163726086
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8817A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726086 | ||||||
| chr2:163726467
|
A | G | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+8436T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726467 | ||||||
| chr2:163726475
|
A | G | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+8428T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726475 | ||||||
| chr2:163726617
|
A | G | 2 | a0001c0001t0034g0252a0001c0001t0080g0264 | 2 | NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.25+8286T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726617 | ||||||
| chr2:163726618
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0077 | 2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.25+8285G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726618 | ||||||
| chr2:163726623
|
A | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+8280T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726623 | ||||||
| chr2:163726850
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8053A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726850 | ||||||
| chr2:163726852
|
C | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8051G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726852 | ||||||
| chr2:163726854
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8049A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726854 | ||||||
| chr2:163726859
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8044A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726859 | ||||||
| chr2:163726860
|
G | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8043C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726860 | ||||||
| chr2:163726862
|
A | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8041T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726862 | ||||||
| chr2:163726865
|
G | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8038C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726865 | ||||||
| chr2:163726868
|
C | T | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+8035G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726868 | ||||||
| chr2:163726870
|
A | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8033T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726870 | ||||||
| chr2:163726871
|
A | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8032T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726871 | ||||||
| chr2:163726884
|
AAAG | A | 3 | a0001c0001t0001g0115a0001c0001t0011g0114a0001c0001t0011g0188 | 3 | HG00735.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.25+8016_25+8018del others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726884 | ||||||
| chr2:163726886
|
A | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8017T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726886 | ||||||
| chr2:163726888
|
A | C | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8015T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726888 | ||||||
| chr2:163726890
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8013A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726890 | ||||||
| chr2:163726891
|
A | T | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8012T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726891 | ||||||
| chr2:163726899
|
T | G | 1 | a0001c0002t0016g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.25+8004A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726899 | ||||||
| chr2:163726906
|
T | C | 9 | a0001c0001t0001g0175a0001c0001t0003g0182a0001c0001t0005g0173others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+7997A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726906 | ||||||
| chr2:163726907
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7996A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726907 | ||||||
| chr2:163726910
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7993A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726910 | ||||||
| chr2:163726915
|
T | A | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7988A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726915 | ||||||
| chr2:163726916
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7987A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726916 | ||||||
| chr2:163726927
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+7976C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726927 | ||||||
| chr2:163726934
|
G | T | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7969C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726934 | ||||||
| chr2:163726936
|
G | T | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7967C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726936 | ||||||
| chr2:163726944
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7959A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726944 | ||||||
| chr2:163726945
|
G | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+7958C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726945 | ||||||
| chr2:163726955
|
T | G | 1 | a0001c0001t0062g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7948A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726955 | ||||||
| chr2:163727143
|
T | C | 3 | a0001c0001t0002g0232a0001c0001t0064g0237a0001c0001t0076g0022 | 3 | HG02015.hp1 HG02129.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.25+7760A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727143 | ||||||
| chr2:163727175
|
C | G | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7728G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727175 | ||||||
| chr2:163727300
|
A | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+7603T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727300 | ||||||
| chr2:163727383
|
TA | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.25+7519delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727383 | ||||||
| chr2:163727397
|
AT | A | 7 | a0001c0001t0004g0133a0001c0001t0012g0140a0001c0001t0031g0131others(4): Show | 7 | HG02280.hp2 HG02735.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7505delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727397 | ||||||
| chr2:163727404
|
T | C | 21 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+7499A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727404 | ||||||
| chr2:163727552
|
T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+7351A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727552 | ||||||
| chr2:163727632
|
C | CCCCACTT others(13): Show |
1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+7251_25+7270dup others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727632 | ||||||
| chr2:163727640
|
T | G | 2 | a0001c0001t0021g0183a0001c0002t0013g0190 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+7263A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727640 | ||||||
| chr2:163727646
|
C | G | 36 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.25+7257G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727646 | ||||||
| chr2:163727854
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7049C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727854 | ||||||
| chr2:163728116
|
T | C | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6787A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728116 | ||||||
| chr2:163728175
|
C | G | 3 | a0001c0001t0002g0198a0001c0001t0009g0196a0001c0001t0043g0209 | 3 | NA18941.hp1 NA18944.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.25+6728G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728175 | ||||||
| chr2:163728244
|
G | T | 1 | a0001c0001t0050g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+6659C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728244 | ||||||
| chr2:163728254
|
T | TA | 137 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0137others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.25+6648dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728254 | ||||||
| chr2:163728397
|
A | AAC | 4 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0003g0182others(1): Show | 4 | HG02698.hp2 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+6504_25+6505dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728397
|
A | AACAC | 13 | a0001c0001t0004g0133a0001c0001t0011g0172a0001c0001t0019g0257others(10): Show | 13 | HG01361.hp2 HG01433.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+6502_25+6505dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728397
|
AAC | A | 18 | a0001c0001t0001g0080a0001c0001t0001g0197a0001c0001t0002g0005others(15): Show | 18 | HG01261.hp2 HG01496.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+6504_25+6505del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728397
|
AACAC | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.25+6502_25+6505del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728397
|
AACACAC | A | 6 | a0001c0001t0003g0116a0001c0001t0005g0117a0001c0001t0007g0068others(3): Show | 6 | HG00609.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6500_25+6505del others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728397
|
AACACACA others(1): Show |
A | 18 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(15): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.25+6498_25+6505del others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | ||||||
| chr2:163728483
|
A | G | 43 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0199others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+6420T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728483 | ||||||
| chr2:163728491
|
T | C | 6 | a0001c0001t0001g0139a0001c0001t0003g0161a0001c0001t0005g0153others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6412A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728491 | ||||||
| chr2:163728494
|
G | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(159): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.25+6409C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728494 | ||||||
| chr2:163728520
|
G | A | 3 | a0001c0001t0003g0106a0001c0001t0004g0189a0001c0002t0004g0184 | 3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+6383C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728520 | ||||||
| chr2:163728561
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+6342T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728561 | ||||||
| chr2:163728636
|
G | A | 2 | a0001c0001t0003g0105a0001c0002t0007g0104 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+6267C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728636 | ||||||
| chr2:163728774
|
C | T | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+6129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728774 | ||||||
| chr2:163728796
|
T | C | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+6107A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728796 | ||||||
| chr2:163728882
|
G | A | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+6021C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728882 | ||||||
| chr2:163728986
|
C | T | 2 | a0001c0001t0003g0105a0001c0002t0007g0104 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+5917G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728986 | ||||||
| chr2:163729086
|
A | C | 22 | a0001c0001t0001g0137a0001c0001t0019g0255a0001c0001t0019g0257others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+5817T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729086 | ||||||
| chr2:163729109
|
T | C | 1 | a0001c0002t0007g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25+5794A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729109 | ||||||
| chr2:163729122
|
T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG00140.hp1 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+5781A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729122 | ||||||
| chr2:163729146
|
C | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+5757G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729146 | ||||||
| chr2:163729193
|
G | T | 24 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(21): Show | 24 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+5710C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729193 | ||||||
| chr2:163729324
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+5579T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729324 | ||||||
| chr2:163729586
|
A | T | 2 | a0001c0001t0009g0129a0001c0002t0011g0128 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+5317T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729586 | ||||||
| chr2:163729722
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25+5181A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729722 | ||||||
| chr2:163729801
|
A | G | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+5102T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729801 | ||||||
| chr2:163729964
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.25+4939A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729964 | ||||||
| chr2:163730155
|
T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(213): Show | 217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.25+4748A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730155 | ||||||
| chr2:163730172
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0016g0130a0001c0001t0024g0001others(2): Show | 6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+4731C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730172 | ||||||
| chr2:163730376
|
A | G | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+4527T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730376 | ||||||
| chr2:163730485
|
T | C | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+4418A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730485 | ||||||
| chr2:163730500
|
G | A | 20 | a0001c0001t0019g0255a0001c0001t0019g0257a0001c0001t0019g0258others(17): Show | 20 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+4403C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730500 | ||||||
| chr2:163730504
|
T | G | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.25+4399A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
T | TTG | 48 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0142others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.25+4397_25+4398dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
T | TTGTG | 54 | a0001c0001t0001g0111a0001c0001t0001g0139a0001c0001t0001g0195others(51): Show | 54 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.25+4395_25+4398dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
T | TTGTGTG | 17 | a0001c0001t0001g0235a0001c0001t0002g0222a0001c0001t0004g0223others(14): Show | 17 | HG00558.hp1 HG00609.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.25+4393_25+4398dup others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0175a0001c0001t0001g0227a0001c0001t0003g0182others(6): Show | 9 | HG01106.hp1 HG02056.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+4391_25+4398dup others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
TTG | T | 8 | a0001c0001t0001g0137a0001c0001t0004g0189a0001c0001t0012g0122others(5): Show | 8 | HG01255.hp1 HG01261.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+4397_25+4398del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
TTGTG | T | 6 | a0001c0001t0004g0133a0001c0001t0031g0131a0001c0002t0007g0135others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+4395_25+4398del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730504
|
TTGTGTG | T | 8 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+4393_25+4398del others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | ||||||
| chr2:163730524
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+4379C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730524 | ||||||
| chr2:163730662
|
T | G | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25+4241A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730662 | ||||||
| chr2:163730687
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25+4216T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730687 | ||||||
| chr2:163730762
|
A | G | 136 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0139others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.25+4141T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730762 | ||||||
| chr2:163730769
|
A | G | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+4134T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730769 | ||||||
| chr2:163730826
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0032g0014 | 2 | NA18969.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.25+4077T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730826 | ||||||
| chr2:163730884
|
C | T | 3 | a0001c0001t0003g0182a0001c0001t0007g0181a0001c0001t0011g0172 | 3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+4019G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730884 | ||||||
| chr2:163730937
|
A | G | 21 | a0001c0001t0019g0255a0001c0001t0019g0257a0001c0001t0019g0258others(18): Show | 21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+3966T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730937 | ||||||
| chr2:163730985
|
G | A | 3 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0002t0007g0104 | 3 | HG02818.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+3918C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730985 | ||||||
| chr2:163730991
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0077 | 2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.25+3912T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730991 | ||||||
| chr2:163731031
|
C | CA | 6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+3871dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731031 | ||||||
| chr2:163731035
|
T | C | 1 | a0001c0001t0008g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.25+3868A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731035 | ||||||
| chr2:163731450
|
T | C | 136 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0139others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.25+3453A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731450 | ||||||
| chr2:163731455
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+3448G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731455 | ||||||
| chr2:163731594
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0003g0186a0001c0001t0011g0114others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+3309C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731594 | ||||||
| chr2:163731612
|
A | G | 2 | a0001c0001t0026g0094a0001c0001t0026g0095 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+3291T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731612 | ||||||
| chr2:163731714
|
GA | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0115a0001c0001t0001g0139others(34): Show | 37 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.25+3188delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731714 | ||||||
| chr2:163731791
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+3112T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731791 | ||||||
| chr2:163731999
|
CA | C | 21 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+2903delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731999 | ||||||
| chr2:163732179
|
C | T | 2 | a0001c0001t0035g0246a0001c0008t0035g0248 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+2724G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732179 | ||||||
| chr2:163732401
|
TA | T | 21 | a0001c0001t0001g0098a0001c0001t0003g0097a0001c0001t0003g0101others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+2501delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732401 | ||||||
| chr2:163732457
|
T | C | 88 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+2446A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732457 | ||||||
| chr2:163732699
|
C | A | 1 | a0001c0001t0004g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25+2204G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732699 | ||||||
| chr2:163732705
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25+2198A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732705 | ||||||
| chr2:163733098
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(125): Show | 128 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.25+1805A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733098 | ||||||
| chr2:163733109
|
AC | A | 4 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0089others(1): Show | 4 | HG02074.hp2 NA18946.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1793delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733109 | ||||||
| chr2:163733202
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+1701C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733202 | ||||||
| chr2:163733256
|
C | T | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+1647G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733256 | ||||||
| chr2:163733378
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+1525G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733378 | ||||||
| chr2:163733613
|
G | A | 3 | a0001c0001t0003g0182a0001c0001t0007g0181a0001c0001t0011g0172 | 3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+1290C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733613 | ||||||
| chr2:163733746
|
C | T | 3 | a0001c0001t0003g0182a0001c0001t0007g0181a0001c0001t0011g0172 | 3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+1157G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733746 | ||||||
| chr2:163733804
|
G | C | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+1099C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733804 | ||||||
| chr2:163733942
|
C | CA | 21 | a0001c0001t0001g0118a0001c0001t0019g0255a0001c0001t0019g0257others(18): Show | 21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+960dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | ||||||
| chr2:163733942
|
CA | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(163): Show | 166 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.25+960delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | ||||||
| chr2:163733942
|
CAA | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0110a0001c0001t0001g0119others(22): Show | 26 | HG01167.hp1 HG01261.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+959_25+960delTT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | ||||||
| chr2:163734115
|
C | CT | 35 | a0001c0001t0001g0098a0001c0001t0001g0195a0001c0001t0001g0197others(32): Show | 35 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.25+787dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734115 | ||||||
| chr2:163734115
|
C | CTT | 9 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+786_25+787dupAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734115 | ||||||
| chr2:163734341
|
GC | G | 45 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+561delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734341 | ||||||
| chr2:163734350
|
A | C | 25 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0003g0097others(22): Show | 25 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.25+553T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734350 | ||||||
| chr2:163734541
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+362G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734541 | ||||||
| chr2:163734557
|
C | CA | 14 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0003g0116others(11): Show | 15 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+345dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | ||||||
| chr2:163734557
|
C | CAA | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(37): Show | 40 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.25+344_25+345dupTT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | ||||||
| chr2:163734557
|
C | CAAA | 151 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0023others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.25+343_25+345dupTT others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | ||||||
| chr2:163734557
|
C | CAAAA | 22 | a0001c0001t0001g0235a0001c0001t0002g0088a0001c0001t0002g0089others(19): Show | 22 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+342_25+345dupTT others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | ||||||
| chr2:163734557
|
C | CAAAAA | 7 | a0001c0001t0003g0186a0001c0001t0004g0189a0001c0001t0011g0188others(4): Show | 7 | HG01175.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+341_25+345dupTT others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | ||||||
| chr2:163734628
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0004g0191 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+275A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734628 | ||||||
| chr2:163734771
|
T | C | 1 | a0001c0001t0013g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+132A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734771 | ||||||
| chr2:163734781
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+122T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734781 | ||||||
| chr2:163735277
|
C | A | 1 | a0001c0001t0067g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-145-205G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735277 | ||||||
| chr2:163735316
|
AC | A | 43 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0199others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-145-245delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735316 | ||||||
| chr2:163735317
|
C | A | 1 | a0001c0001t0065g0238 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-145-245G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735317 | ||||||
| chr2:163735377
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-145-305G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735377 | ||||||
| chr2:163735774
|
T | G | 6 | a0001c0001t0003g0241a0001c0001t0006g0239a0001c0001t0021g0243others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146+64A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735774 |