Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23197 |
|---|---|
| ensemblid | ENSG00000113194.13 |
| hgncid | 24666 |
| symbol | FAF2 |
| name | Fas associated factor family member 2 |
| refseq_nuc | NM_014613.3 |
| refseq_prot | NP_055428.1 |
| ensembl_nuc | ENST00000261942.7 |
| ensembl_prot | ENSP00000261942.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 176448385 |
| end | 176510074 |
| strand | + |
| ver | v1.2 |
| region | chr5:176448385-176510074 |
| region5000 | chr5:176443385-176515074 |
| regionname0 | FAF2_chr5_176448385_176510074 |
| regionname5000 | FAF2_chr5_176443385_176515074 |
| 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 | 445 | 365 | 84 | 64 | 166 | 10 | 39 | 127 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0002 | 0/0 | 445 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0003 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0004 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0005 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0006 | 0/0 | 445 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| 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 | 1338 | 362 | 82 | 64 | 165 | 10 | 39 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0002 | 0/0 | 1338 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0003 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0004 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0005 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0006 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0007 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0008 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| 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 | 3148 | 107 | 5 | 24 | 56 | 3 | 18 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0002 | 1/0 | 3148 | 62 | 5 | 9 | 34 | 4 | 9 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0003 | 0/0 | 3149 | 56 | 1 | 10 | 36 | 0 | 9 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0004 | 0/0 | 3148 | 46 | 38 | 7 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0005 | 0/0 | 3148 | 29 | 1 | 2 | 24 | 1 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0006 | 0/0 | 3148 | 22 | 13 | 5 | 1 | 2 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0007 | 0/0 | 3150 | 7 | 4 | 3 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0008 | 0/0 | 3152 | 5 | 0 | 0 | 5 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0009 | 0/0 | 3149 | 4 | 3 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0010 | 0/0 | 3148 | 4 | 4 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0011 | 0/0 | 3148 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0012 | 0/0 | 3148 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0013 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0014 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0015 | 0/0 | 3149 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0016 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0017 | 0/0 | 3148 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0018 | 0/0 | 3148 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0019 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0020 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0021 | 0/0 | 3148 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0022 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0023 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0024 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0025 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0026 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0027 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0028 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0029 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0030 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0031 | 0/0 | 3148 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0032 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0033 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| t0034 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| 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 | 0 | 2 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0312 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| 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 | 1338 | 362 | 82 | 64 | 165 | 10 | 39 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0005 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0008 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0002c0002 | 0/0 | 1338 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0003c0003 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0004c0004 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0005c0006 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0006c0007 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4485 | 103 | 4 | 24 | 53 | 3 | 18 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0002 | 1/0 | 4485 | 58 | 4 | 9 | 32 | 4 | 8 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0003 | 0/0 | 4486 | 56 | 1 | 10 | 36 | 0 | 9 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0004 | 0/0 | 4485 | 45 | 37 | 7 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0005 | 0/0 | 4485 | 29 | 1 | 2 | 24 | 1 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0006 | 0/0 | 4485 | 22 | 13 | 5 | 1 | 2 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0007 | 0/0 | 4487 | 7 | 4 | 3 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0008 | 0/0 | 4489 | 5 | 0 | 0 | 5 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0009 | 0/0 | 4486 | 4 | 3 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0010 | 0/0 | 4485 | 4 | 4 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0011 | 0/0 | 4485 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0012 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0013 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0014 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0015 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0016 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0017 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0018 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0019 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0020 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0021 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0022 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0023 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0024 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0025 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0026 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0028 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0029 | 0/0 | 4487 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0030 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0031 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0032 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0033 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0001t0034 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0005t0001 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0008t0027 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0001c0009t0002 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0002c0002t0001 | 0/0 | 4485 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0003c0003t0002 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0004c0004t0002 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0005c0006t0004 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| a0006c0007t0002 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | copy fasta | chr5 | 176443385 | 176515074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0312 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0015g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0015g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0016g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0017g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0018g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0019g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0020g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0021g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0023g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0024g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0025g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0026g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0028g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0029g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0030g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0031g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0032g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0033g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0034g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0008t0027g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0009t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0003c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0004c0004t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0005c0006t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0006c0007t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0316 | EUR | FIN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0263 | EUR | FIN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0366 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0364 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0105 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0103 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0246 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0281 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01496 | hp1 | a0001 | c0001 | t0018 | g0204 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0108 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0109 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01891 | hp1 | a0001 | c0001 | t0024 | g0239 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0025 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0351 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0087 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02040 | hp1 | a0001 | c0001 | t0016 | g0174 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02040 | hp2 | a0001 | c0001 | t0030 | g0145 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02056 | hp2 | a0001 | c0001 | t0029 | g0093 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0271 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02132 | hp2 | a0001 | c0001 | t0026 | g0056 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0321 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0266 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0151 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02258 | hp2 | a0005 | c0006 | t0004 | g0353 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02451 | hp1 | a0004 | c0004 | t0002 | g0330 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0334 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02602 | hp2 | a0001 | c0001 | t0031 | g0138 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0369 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0083 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0362 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0368 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02886 | hp1 | a0001 | c0001 | t0022 | g0262 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02886 | hp2 | a0001 | c0001 | t0032 | g0097 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0020 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0367 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0232 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0259 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0096 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0257 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0283 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03486 | hp2 | a0001 | c0008 | t0027 | g0305 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0340 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03942 | hp1 | a0006 | c0007 | t0002 | g0348 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04115 | hp2 | a0001 | c0001 | t0028 | g0102 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18522 | hp1 | a0001 | c0001 | t0033 | g0306 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0226 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0365 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0041 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18951 | hp1 | a0001 | c0001 | t0020 | g0219 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18953 | hp2 | a0001 | c0001 | t0012 | g0224 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18969 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18997 | hp2 | a0001 | c0001 | t0015 | g0053 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18999 | hp2 | a0001 | c0001 | t0019 | g0300 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0247 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19060 | hp1 | a0001 | c0001 | t0011 | g0121 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19068 | hp2 | a0001 | c0001 | t0015 | g0054 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0363 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19077 | hp1 | a0001 | c0009 | t0002 | g0346 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0214 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | ASW | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ASW | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0315 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | GIH | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0197 | SAS | GIH | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01123 | hp1 | a0001 | c0001 | t0021 | g0314 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0104 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0082 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0242 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0312 | REF | REF | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176486391
|
G | A | 1 | a0003 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.169G>A | p.Val57Ile | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/11 | 192/4485 | 169/1338 | 57/445 | chr5 | 176486391 | ||
| chr5:176492223
|
C | A | 1 | a0004 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.374C>A | p.Pro125His | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/11 | 397/4485 | 374/1338 | 125/445 | chr5 | 176492223 | ||
| chr5:176496501
|
G | A | 1 | a0005 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.677G>A | p.Arg226Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 700/4485 | 677/1338 | 226/445 | chr5 | 176496501 | ||
| chr5:176496557
|
G | A | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.733G>A | p.Val245Met | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 756/4485 | 733/1338 | 245/445 | chr5 | 176496557 | ||
| chr5:176499030
|
G | A | 1 | a0002 | 3 | NA18974.hp1 NA19066.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.956G>A | p.Arg319Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/11 | 979/4485 | 956/1338 | 319/445 | chr5 | 176499030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176492323
|
G | A | 1 | a0001c0005 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.474G>A | p.Thr158Thr | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/11 | 497/4485 | 474/1338 | 158/445 | chr5 | 176492323 | ||
| chr5:176496637
|
T | G | 1 | a0001c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.813T>G | p.Thr271Thr | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 836/4485 | 813/1338 | 271/445 | chr5 | 176496637 | ||
| chr5:176498989
|
G | A | 1 | a0001c0009 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.915G>A | p.Gln305Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/11 | 938/4485 | 915/1338 | 305/445 | chr5 | 176498989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176507052
|
A | ATAT | 1 | a0001c0001t0008 | 5 | NA18947.hp2 NA18965.hp2 NA19004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*120dupTAT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 121 | INFO_REALIGN_3_PRIME | chr5 | 176507052 | ||||
| chr5:176507231
|
T | C | 1 | a0001c0001t0016 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 281 | chr5 | 176507231 | |||||
| chr5:176507255
|
C | T | 1 | a0001c0001t0011 | 3 | NA18969.hp1 NA19060.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 305 | chr5 | 176507255 | |||||
| chr5:176507526
|
A | AT | 1 | a0001c0001t0007 | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*583dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 584 | INFO_REALIGN_3_PRIME | chr5 | 176507526 | ||||
| chr5:176507528
|
T | A | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 578 | chr5 | 176507528 | |||||
| chr5:176507588
|
C | T | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 638 | chr5 | 176507588 | |||||
| chr5:176507621
|
G | A | 1 | a0001c0001t0018 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 671 | chr5 | 176507621 | |||||
| chr5:176507774
|
A | G | 1 | a0001c0001t0033 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 824 | chr5 | 176507774 | |||||
| chr5:176508024
|
C | T | 1 | a0001c0001t0032 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1074C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1074 | chr5 | 176508024 | |||||
| chr5:176508058
|
T | C | 1 | a0001c0001t0019 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1108 | chr5 | 176508058 | |||||
| chr5:176508140
|
C | G | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1190C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1190 | chr5 | 176508140 | |||||
| chr5:176508144
|
C | A | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1194C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1194 | chr5 | 176508144 | |||||
| chr5:176508315
|
T | C | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | 229 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1365T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1365 | chr5 | 176508315 | |||||
| chr5:176508392
|
C | CA | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(6): Show | 75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1442_*1443insA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1443 | chr5 | 176508392 | |||||
| chr5:176508577
|
T | C | 1 | a0001c0001t0012 | 2 | NA18942.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1627T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1627 | chr5 | 176508577 | |||||
| chr5:176508728
|
C | T | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1778C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1778 | chr5 | 176508728 | |||||
| chr5:176508734
|
A | G | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(1): Show | 53 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1784A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1784 | chr5 | 176508734 | |||||
| chr5:176508858
|
C | T | 4 | a0001c0001t0009a0001c0001t0013a0001c0001t0014others(1): Show | 9 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1908C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1908 | chr5 | 176508858 | |||||
| chr5:176508872
|
A | G | 1 | a0001c0001t0025 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1922 | chr5 | 176508872 | |||||
| chr5:176508959
|
A | AT | 3 | a0001c0001t0009a0001c0001t0029a0001c0001t0032 | 6 | HG01243.hp1 HG02056.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2019dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2020 | INFO_REALIGN_3_PRIME | chr5 | 176508959 | ||||
| chr5:176509121
|
T | C | 2 | a0001c0001t0015a0001c0001t0026 | 3 | HG02132.hp2 NA18997.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2171T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2171 | chr5 | 176509121 | |||||
| chr5:176509208
|
C | T | 1 | a0001c0001t0024 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2258C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2258 | chr5 | 176509208 | |||||
| chr5:176509209
|
G | C | 3 | a0001c0001t0009a0001c0001t0013a0001c0001t0032 | 7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2259G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2259 | chr5 | 176509209 | |||||
| chr5:176509316
|
C | A | 2 | a0001c0001t0005a0001c0001t0017 | 30 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2366C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2366 | chr5 | 176509316 | |||||
| chr5:176509515
|
T | C | 10 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(7): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2565T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2565 | chr5 | 176509515 | |||||
| chr5:176509527
|
G | A | 1 | a0001c0008t0027 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2577G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2577 | chr5 | 176509527 | |||||
| chr5:176509579
|
T | C | 1 | a0001c0001t0030 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2629T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2629 | chr5 | 176509579 | |||||
| chr5:176509617
|
G | C | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2667 | chr5 | 176509617 | |||||
| chr5:176509749
|
T | C | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2799 | chr5 | 176509749 | |||||
| chr5:176509763
|
A | G | 1 | a0001c0001t0028 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2813A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2813 | chr5 | 176509763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176448562
|
A | C | 1 | a0001c0001t0004g0369 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+92A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448562 | ||||||
| chr5:176448651
|
C | T | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+181C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448651 | ||||||
| chr5:176448671
|
G | C | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+201G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448671 | ||||||
| chr5:176448673
|
A | G | 4 | a0001c0001t0005g0363a0001c0001t0005g0364a0001c0001t0005g0365others(1): Show | 4 | HG00438.hp1 HG00609.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+203A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448673 | ||||||
| chr5:176448797
|
T | C | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+327T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448797 | ||||||
| chr5:176448800
|
A | G | 1 | a0001c0001t0010g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+330A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448800 | ||||||
| chr5:176448916
|
G | T | 1 | a0001c0001t0003g0362 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.63+446G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448916 | ||||||
| chr5:176448960
|
G | A | 1 | a0001c0001t0005g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.63+490G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448960 | ||||||
| chr5:176449077
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+607C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449077 | ||||||
| chr5:176449097
|
C | T | 1 | a0001c0001t0004g0369 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449097 | ||||||
| chr5:176449143
|
A | G | 2 | a0001c0001t0001g0360a0001c0001t0001g0361 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.63+673A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449143 | ||||||
| chr5:176449420
|
C | A | 69 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(66): Show | 70 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+950C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449420 | ||||||
| chr5:176449461
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.63+991G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449461 | ||||||
| chr5:176449596
|
C | T | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | NA18955.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1126C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449596 | ||||||
| chr5:176449713
|
TATTGATA others(69): Show |
T | 1 | a0001c0001t0001g0355 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+1244_63+1319del others(76): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449713 | ||||||
| chr5:176450055
|
A | ACAGTTGA others(45): Show |
1 | a0001c0001t0002g0095 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.63+1586_63+1637dup others(52): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176450055 | |||||
| chr5:176450109
|
C | G | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+1639C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450109 | ||||||
| chr5:176450268
|
T | C | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | NA18971.hp2 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.63+1798T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450268 | ||||||
| chr5:176450318
|
A | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+1848A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450318 | ||||||
| chr5:176450413
|
CAT | C | 3 | a0001c0001t0004g0021a0001c0001t0010g0004a0001c0001t0010g0005 | 3 | HG02257.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+1944_63+1945del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450413 | ||||||
| chr5:176450556
|
C | CT | 7 | a0001c0001t0004g0354a0001c0001t0007g0367a0001c0001t0007g0368others(4): Show | 7 | HG02056.hp2 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2100dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176450556 | |||||
| chr5:176450583
|
C | T | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2113C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450583 | ||||||
| chr5:176450788
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+2318C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450788 | ||||||
| chr5:176450955
|
A | G | 1 | a0005c0006t0004g0353 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+2485A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450955 | ||||||
| chr5:176451006
|
G | A | 297 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(294): Show | 300 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.63+2536G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451006 | ||||||
| chr5:176451006
|
G | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2536G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451006 | ||||||
| chr5:176451313
|
G | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+2843G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451313 | ||||||
| chr5:176451326
|
G | T | 2 | a0001c0001t0004g0003a0005c0006t0004g0353 | 3 | HG02258.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.63+2856G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451326 | ||||||
| chr5:176451414
|
G | A | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2944G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451414 | ||||||
| chr5:176451450
|
T | C | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.63+2980T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451450 | ||||||
| chr5:176451726
|
GAT | G | 3 | a0001c0001t0001g0285a0001c0001t0007g0367a0001c0001t0007g0368 | 3 | HG02809.hp2 HG03041.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.63+3267_63+3268del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451726 | |||||
| chr5:176451765
|
CATAT | C | 64 | a0001c0001t0002g0095a0001c0001t0003g0002a0001c0001t0003g0027others(61): Show | 65 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+3301_63+3304del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451765 | |||||
| chr5:176451770
|
ATATACG | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0030others(4): Show | 7 | HG00558.hp2 NA18942.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3302_63+3307del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451770 | |||||
| chr5:176451775
|
CGT | C | 23 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(20): Show | 23 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3316_63+3317del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451775 | |||||
| chr5:176451777
|
T | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0030others(4): Show | 7 | HG00558.hp2 NA18942.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3307T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451777 | ||||||
| chr5:176451784
|
GTGTATAT others(25): Show |
G | 64 | a0001c0001t0002g0095a0001c0001t0003g0002a0001c0001t0003g0027others(61): Show | 65 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+3316_63+3347del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451784 | |||||
| chr5:176451786
|
G | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3316G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451786 | ||||||
| chr5:176451797
|
T | C | 2 | a0001c0001t0010g0018a0001c0001t0010g0019 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3327T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451797 | ||||||
| chr5:176451799
|
CAT | C | 12 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0001t0006g0105others(9): Show | 12 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3339_63+3340del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451799 | |||||
| chr5:176451801
|
TATATATA others(39): Show |
T | 1 | a0001c0001t0010g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+3345_63+3390del others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451801 | |||||
| chr5:176451803
|
TATATATA others(37): Show |
T | 3 | a0001c0001t0004g0021a0001c0001t0010g0005a0001c0001t0013g0025 | 3 | HG01891.hp2 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+3341_63+3384del others(44): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451803 | |||||
| chr5:176451807
|
TATAC | T | 6 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0004g0022others(3): Show | 6 | HG02965.hp1 HG03209.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3339_63+3342del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451807 | |||||
| chr5:176451809
|
T | C | 1 | a0001c0001t0006g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+3339T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451809 | ||||||
| chr5:176451809
|
TACACACA others(27): Show |
T | 23 | a0001c0001t0004g0277a0001c0001t0004g0280a0001c0001t0005g0026others(20): Show | 23 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3345_63+3378del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451809 | |||||
| chr5:176451811
|
C | CACATATA others(197): Show |
1 | a0001c0001t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(204): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(171): Show |
1 | a0001c0001t0001g0132 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(173): Show |
1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(180): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(147): Show |
1 | a0001c0001t0001g0231 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(154): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(173): Show |
3 | a0001c0001t0001g0202a0001c0001t0004g0203a0001c0001t0018g0204 | 3 | HG01496.hp1 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.63+3344_63+3345ins others(180): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(199): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01257.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.63+3344_63+3345ins others(206): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | CACATATA others(172): Show |
1 | a0001c0001t0001g0355 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(179): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | |||||
| chr5:176451811
|
C | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0030others(13): Show | 16 | HG00558.hp2 HG00733.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+3341C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451811 | ||||||
| chr5:176451813
|
C | CATATATA others(13): Show |
1 | a0001c0001t0010g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(20): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | |||||
| chr5:176451813
|
C | CATATATA others(3): Show |
1 | a0001c0001t0004g0354 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | |||||
| chr5:176451813
|
C | CATATATA others(171): Show |
1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | |||||
| chr5:176451813
|
C | CATATATA others(197): Show |
1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(204): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | |||||
| chr5:176451813
|
CACAT | C | 32 | a0001c0001t0003g0092a0001c0001t0004g0003a0001c0001t0004g0114others(29): Show | 33 | HG01167.hp1 HG01361.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.63+3345_63+3348del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | |||||
| chr5:176451815
|
C | T | 126 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(123): Show | 127 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+3345C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451815 | ||||||
| chr5:176451815
|
CAT | C | 6 | a0001c0001t0002g0286a0001c0001t0002g0301a0001c0001t0002g0302others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3357_63+3358del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451815 | |||||
| chr5:176451815
|
CATAT | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0030 | 3 | NA18975.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+3355_63+3358del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451815 | |||||
| chr5:176451817
|
T | C | 8 | a0001c0001t0001g0173a0001c0001t0001g0201a0001c0001t0002g0289others(5): Show | 8 | HG00639.hp2 HG02280.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+3347T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451817 | ||||||
| chr5:176451817
|
T | TATATATA others(197): Show |
1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(204): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | |||||
| chr5:176451817
|
T | TATATATA others(159): Show |
1 | a0001c0001t0001g0285 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(166): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | |||||
| chr5:176451817
|
T | TATATATA others(171): Show |
1 | a0001c0001t0001g0116 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | |||||
| chr5:176451817
|
T | TATATATA others(145): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18944.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(152): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | |||||
| chr5:176451817
|
T | TATATATA others(29): Show |
4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | |||||
| chr5:176451819
|
T | TATACACA others(39): Show |
1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATACACA others(65): Show |
1 | a0001c0001t0010g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(72): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATACATA others(217): Show |
1 | a0001c0001t0004g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(224): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATACATA others(143): Show |
1 | a0001c0001t0001g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(150): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(157): Show |
1 | a0001c0001t0011g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(164): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(115): Show |
2 | a0001c0001t0001g0360a0001c0001t0001g0361 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(167): Show |
1 | a0001c0001t0001g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(191): Show |
1 | a0001c0001t0001g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(198): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(169): Show |
1 | a0001c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(176): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(115): Show |
1 | a0001c0001t0001g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(245): Show |
1 | a0001c0001t0001g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(252): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(167): Show |
1 | a0001c0001t0001g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(167): Show |
2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01070.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(91): Show |
1 | a0001c0001t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(98): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(115): Show |
2 | a0001c0001t0004g0137a0001c0001t0031g0138 | 2 | HG02602.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(141): Show |
1 | a0001c0001t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(193): Show |
1 | a0001c0001t0001g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(117): Show |
8 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0228others(5): Show | 8 | HG01109.hp2 HG01175.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(124): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(247): Show |
1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(254): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(141): Show |
1 | a0001c0001t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(143): Show |
24 | a0001c0001t0001g0094a0001c0001t0001g0200a0001c0001t0001g0205others(21): Show | 24 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(150): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(193): Show |
1 | a0001c0001t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(169): Show |
20 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(17): Show | 20 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(176): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(195): Show |
17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(202): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(219): Show |
1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(226): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(221): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG01257.hp1 HG01258.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(228): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(247): Show |
1 | a0001c0001t0001g0152 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(254): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(273): Show |
2 | a0001c0001t0001g0150a0001c0005t0001g0151 | 2 | HG01952.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(280): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(299): Show |
1 | a0001c0001t0004g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(306): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(155): Show |
1 | a0001c0001t0004g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(162): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451819
|
T | TATATACA others(119): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(126): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | |||||
| chr5:176451821
|
T | TATACATA others(63): Show |
1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(70): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(139): Show |
1 | a0001c0001t0001g0129 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(146): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(89): Show |
1 | a0001c0001t0034g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(96): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(141): Show |
1 | a0001c0001t0004g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(167): Show |
2 | a0001c0001t0016g0174a0001c0001t0030g0145 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(191): Show |
1 | a0001c0001t0001g0144 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(198): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(193): Show |
1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(219): Show |
1 | a0001c0001t0001g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(226): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451821
|
T | TATACATA others(195): Show |
1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(202): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | |||||
| chr5:176451823
|
T | TACATATA others(61): Show |
3 | a0001c0001t0004g0134a0001c0001t0004g0135a0001c0001t0004g0136 | 3 | HG02965.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(68): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451823 | |||||
| chr5:176451825
|
T | C | 8 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(5): Show | 8 | HG02135.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+3355T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451825 | ||||||
| chr5:176451827
|
T | C | 37 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0133others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.63+3357T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451827 | ||||||
| chr5:176451827
|
TAC | T | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | NA18942.hp1 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.63+3359_63+3360del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451827 | |||||
| chr5:176451829
|
C | T | 142 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(139): Show | 142 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+3359C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451829 | ||||||
| chr5:176451829
|
CAT | C | 8 | a0001c0001t0001g0231a0001c0001t0004g0003a0001c0001t0004g0238others(5): Show | 9 | HG01891.hp1 HG01928.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3371_63+3372del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451829 | |||||
| chr5:176451830
|
A | G | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+3360A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451830 | ||||||
| chr5:176451831
|
T | C | 125 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(122): Show | 126 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+3361T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451831 | ||||||
| chr5:176451831
|
T | TATATATA others(3): Show |
1 | a0001c0001t0004g0354 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+3370_63+3371ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451831 | |||||
| chr5:176451832
|
ATATATAT others(64): Show |
A | 1 | a0001c0001t0003g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+3364_63+3434del others(71): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451832 | |||||
| chr5:176451833
|
T | C | 14 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0147others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+3363T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451833 | ||||||
| chr5:176451833
|
T | TATACAC | 4 | a0001c0001t0004g0198a0001c0001t0004g0236a0001c0001t0004g0237others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3366_63+3367ins others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451833 | |||||
| chr5:176451837
|
TATATACA others(3): Show |
T | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+3373_63+3382del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451837 | |||||
| chr5:176451837
|
TATATACA others(31): Show |
T | 3 | a0001c0001t0004g0012a0001c0001t0014g0013a0001c0001t0014g0014 | 3 | HG02922.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+3373_63+3410del others(38): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451837 | |||||
| chr5:176451839
|
TATAC | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3371_63+3374del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451839 | |||||
| chr5:176451839
|
TATACACA others(29): Show |
T | 1 | a0001c0001t0004g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+3373_63+3408del others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451839 | |||||
| chr5:176451841
|
T | C | 2 | a0001c0001t0033g0306a0001c0008t0027g0305 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.63+3371T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451841 | ||||||
| chr5:176451841
|
TAC | T | 65 | a0001c0001t0002g0095a0001c0001t0003g0002a0001c0001t0003g0027others(62): Show | 66 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.63+3377_63+3378del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451841 | |||||
| chr5:176451841
|
TACACACA others(27): Show |
T | 3 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008 | 3 | HG00733.hp1 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63+3373_63+3406del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451841 | |||||
| chr5:176451843
|
C | T | 36 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0115others(33): Show | 36 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.63+3373C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451843 | ||||||
| chr5:176451845
|
C | CATAT | 3 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0019 | 3 | HG02809.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3376_63+3377ins others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451845 | |||||
| chr5:176451845
|
C | T | 6 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0007g0001others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3375C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451845 | ||||||
| chr5:176451845
|
CACATATA others(25): Show |
C | 2 | a0001c0001t0006g0111a0001c0001t0017g0281 | 2 | HG01433.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.63+3377_63+3408del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451845 | |||||
| chr5:176451847
|
C | T | 168 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(165): Show | 170 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.63+3377C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451847 | ||||||
| chr5:176451847
|
CATATATA others(25): Show |
C | 1 | a0001c0001t0004g0282 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+3387_63+3418del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451847 | |||||
| chr5:176451855
|
TACAC | T | 21 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0004g0022others(18): Show | 21 | HG02055.hp1 HG02080.hp1 HG02886.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+3387_63+3390del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451855 | |||||
| chr5:176451856
|
ACACATAT others(35): Show |
A | 3 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0092 | 3 | HG03834.hp2 NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.63+3387_63+3428del others(42): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | ||||||
| chr5:176451856
|
ACACATAT others(36): Show |
A | 1 | a0001c0001t0003g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.63+3387_63+3429del others(43): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | ||||||
| chr5:176451856
|
ACACATAT others(39): Show |
A | 2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.63+3387_63+3432del others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | ||||||
| chr5:176451857
|
C | T | 55 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(52): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.63+3387C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451857 | ||||||
| chr5:176451859
|
C | CAT | 37 | a0001c0001t0001g0343a0001c0001t0002g0286a0001c0001t0002g0287others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.63+3399_63+3400dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451859 | |||||
| chr5:176451859
|
C | T | 216 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(213): Show | 218 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.63+3389C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451859 | ||||||
| chr5:176451865
|
TATATACA others(3): Show |
T | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+3401_63+3410del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451865 | |||||
| chr5:176451867
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3397T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451867 | ||||||
| chr5:176451868
|
ATACACAC others(22): Show |
A | 6 | a0001c0001t0006g0105a0001c0001t0006g0106a0001c0001t0006g0107others(3): Show | 6 | HG00642.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3400_63+3428del others(29): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(23): Show |
A | 1 | a0001c0001t0006g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.63+3400_63+3429del others(30): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(25): Show |
A | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+3400_63+3431del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(26): Show |
A | 5 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0006g0257others(2): Show | 5 | HG02055.hp1 HG02080.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3400_63+3432del others(33): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(27): Show |
A | 2 | a0001c0001t0004g0256a0001c0001t0005g0255 | 2 | HG03098.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+3400_63+3433del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(28): Show |
A | 6 | a0001c0001t0005g0251a0001c0001t0005g0252a0001c0001t0005g0253others(3): Show | 6 | HG03486.hp1 NA18906.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3400_63+3434del others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(29): Show |
A | 1 | a0001c0001t0006g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+3400_63+3435del others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451868
|
ATACACAC others(30): Show |
A | 3 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246 | 3 | HG01167.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.63+3400_63+3436del others(37): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | |||||
| chr5:176451869
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3399T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451869 | ||||||
| chr5:176451869
|
T | TATAC | 4 | a0001c0001t0002g0291a0001c0001t0002g0317a0001c0001t0002g0322others(1): Show | 4 | NA18955.hp1 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+3400_63+3401ins others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451869 | |||||
| chr5:176451870
|
ACACACAT others(22): Show |
A | 1 | a0001c0001t0006g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.63+3401_63+3429del others(29): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | ||||||
| chr5:176451870
|
ACACACAT others(26): Show |
A | 5 | a0001c0001t0006g0249a0001c0001t0006g0250a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3401_63+3433del others(33): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | ||||||
| chr5:176451870
|
ACACACAT others(27): Show |
A | 1 | a0001c0001t0009g0098 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.63+3401_63+3434del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | ||||||
| chr5:176451870
|
ACACACAT others(28): Show |
A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0243 | 3 | HG01496.hp2 NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+3401_63+3435del others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | ||||||
| chr5:176451871
|
C | T | 242 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(239): Show | 244 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.63+3401C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451871 | ||||||
| chr5:176451873
|
C | T | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG02015.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3403C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451873 | ||||||
| chr5:176451875
|
C | T | 17 | a0001c0001t0001g0284a0001c0001t0002g0291a0001c0001t0002g0322others(14): Show | 18 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+3405C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451875 | ||||||
| chr5:176451877
|
T | C | 25 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(22): Show | 25 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.63+3407T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451877 | ||||||
| chr5:176451879
|
T | C | 1 | a0001c0001t0007g0368 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63+3409T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451879 | ||||||
| chr5:176451879
|
T | TATACACA others(161): Show |
1 | a0001c0001t0005g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+3412_63+3413ins others(168): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | |||||
| chr5:176451879
|
T | TATACACA others(163): Show |
1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+3412_63+3413ins others(170): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | |||||
| chr5:176451879
|
T | TATATATA others(3): Show |
1 | a0001c0001t0004g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+3416_63+3417ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | |||||
| chr5:176451885
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+3415T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451885 | ||||||
| chr5:176451886
|
A | G | 1 | a0001c0001t0004g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.63+3416A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451886 | ||||||
| chr5:176451886
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0009g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.63+3418_63+3438del others(21): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451886 | |||||
| chr5:176451890
|
ATATTTTT others(4): Show |
A | 3 | a0001c0001t0003g0085a0001c0001t0003g0086a0001c0001t0005g0087 | 3 | HG01952.hp1 NA18979.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.63+3422_63+3432del others(11): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451890 | |||||
| chr5:176451890
|
ATATTTTT others(5): Show |
A | 35 | a0001c0001t0003g0002a0001c0001t0003g0027a0001c0001t0003g0028others(32): Show | 36 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.63+3422_63+3433del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451890 | |||||
| chr5:176451892
|
A | AT | 6 | a0001c0001t0002g0288a0001c0001t0002g0316a0001c0001t0002g0347others(3): Show | 6 | HG00280.hp1 HG01928.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3451dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
A | T | 1 | a0001c0001t0002g0352 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.63+3422A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451892 | ||||||
| chr5:176451892
|
ATT | A | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(13): Show | 16 | HG00609.hp2 HG00733.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+3450_63+3451del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTT | A | 23 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0142others(20): Show | 23 | HG01993.hp2 HG02040.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3449_63+3451del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTT | A | 71 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0120others(68): Show | 71 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+3448_63+3451del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTTT | A | 29 | a0001c0001t0001g0094a0001c0001t0001g0125a0001c0001t0001g0131others(26): Show | 31 | HG00408.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.63+3447_63+3451del others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTTTT | A | 9 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0001g0359others(6): Show | 9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3446_63+3451del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTTTTT others(2): Show |
A | 23 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0277others(20): Show | 23 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3443_63+3451del others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTTTTT others(4): Show |
A | 17 | a0001c0001t0002g0095a0001c0001t0003g0044a0001c0001t0003g0045others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+3441_63+3451del others(11): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451892
|
ATTTTTTT others(5): Show |
A | 12 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(9): Show | 12 | HG00558.hp1 HG00621.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3440_63+3451del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | |||||
| chr5:176451893
|
T | TA | 10 | a0001c0001t0002g0289a0001c0001t0002g0308a0001c0001t0002g0309others(7): Show | 10 | HG01081.hp1 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+3423_63+3424ins others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451893 | ||||||
| chr5:176451893
|
T | TATACACA others(120): Show |
1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+3423_63+3424ins others(127): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451893 | ||||||
| chr5:176451894
|
T | A | 30 | a0001c0001t0001g0117a0001c0001t0001g0324a0001c0001t0002g0286others(27): Show | 30 | HG01256.hp2 HG01258.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.63+3424T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451894 | ||||||
| chr5:176451895
|
T | A | 7 | a0001c0001t0001g0284a0001c0001t0001g0355a0001c0001t0002g0289others(4): Show | 7 | HG02647.hp2 HG02897.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+3425T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451895 | ||||||
| chr5:176451896
|
T | A | 24 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00609.hp2 HG00733.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.63+3426T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451896 | ||||||
| chr5:176451897
|
T | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0142others(23): Show | 26 | HG01993.hp2 HG02040.hp2 HG02602.hp2 others(23): Show |
intron_variant | MODIFIER | c.63+3427T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451897 | ||||||
| chr5:176451898
|
T | A | 80 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(77): Show | 80 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.63+3428T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451898 | ||||||
| chr5:176451899
|
T | A | 32 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0152others(29): Show | 34 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+3429T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451899 | ||||||
| chr5:176451900
|
T | A | 14 | a0001c0001t0001g0115a0001c0001t0001g0128a0001c0001t0001g0130others(11): Show | 14 | HG00438.hp2 HG00621.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+3430T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451900 | ||||||
| chr5:176451901
|
T | A | 4 | a0001c0001t0003g0088a0001c0001t0004g0134a0001c0001t0004g0237others(1): Show | 4 | HG02647.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3431T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451901 | ||||||
| chr5:176451902
|
T | A | 6 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0003g0092others(3): Show | 6 | HG02280.hp1 HG03041.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3432T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451902 | ||||||
| chr5:176451903
|
T | A | 2 | a0001c0001t0004g0134a0001c0001t0013g0020 | 2 | HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.63+3433T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451903 | ||||||
| chr5:176451904
|
T | A | 2 | a0001c0001t0001g0205a0001c0001t0010g0018 | 2 | HG02280.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.63+3434T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451904 | ||||||
| chr5:176451905
|
T | A | 1 | a0001c0001t0032g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+3435T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451905 | ||||||
| chr5:176451962
|
C | T | 45 | a0001c0001t0004g0256a0001c0001t0004g0260a0001c0001t0004g0261others(42): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+3492C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451962 | ||||||
| chr5:176452055
|
A | G | 3 | a0001c0001t0002g0344a0001c0001t0002g0345a0004c0004t0002g0330 | 3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.63+3585A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452055 | ||||||
| chr5:176452261
|
T | A | 205 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(202): Show | 206 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.63+3791T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452261 | ||||||
| chr5:176452295
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3825T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452295 | ||||||
| chr5:176452469
|
T | G | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.63+3999T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452469 | ||||||
| chr5:176452643
|
G | C | 3 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035 | 3 | NA18965.hp2 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.63+4173G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452643 | ||||||
| chr5:176453064
|
A | G | 1 | a0001c0001t0005g0278 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.63+4594A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453064 | ||||||
| chr5:176453476
|
G | T | 1 | a0001c0001t0001g0355 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+5006G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453476 | ||||||
| chr5:176453616
|
G | T | 1 | a0001c0001t0001g0355 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+5146G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453616 | ||||||
| chr5:176453831
|
A | G | 8 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(5): Show | 8 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+5361A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453831 | ||||||
| chr5:176453873
|
G | A | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+5403G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453873 | ||||||
| chr5:176453988
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.63+5518G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453988 | ||||||
| chr5:176454013
|
A | G | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+5543A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454013 | ||||||
| chr5:176454042
|
A | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0172 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.63+5572A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454042 | ||||||
| chr5:176454048
|
TA | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0194a0001c0001t0002g0309others(3): Show | 6 | HG01081.hp1 HG02132.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+5591delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454048 | |||||
| chr5:176454190
|
C | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5720C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454190 | ||||||
| chr5:176454225
|
T | C | 1 | a0001c0001t0005g0263 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+5755T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454225 | ||||||
| chr5:176454406
|
TAAAAATA others(10): Show |
T | 1 | a0001c0001t0001g0116 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.63+5941_63+5957del others(17): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454406 | |||||
| chr5:176454533
|
G | A | 9 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0001t0006g0105others(6): Show | 9 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6063G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454533 | ||||||
| chr5:176454576
|
T | C | 4 | a0001c0001t0006g0244a0001c0001t0006g0245a0001c0001t0006g0246others(1): Show | 4 | HG01167.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6106T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454576 | ||||||
| chr5:176454576
|
T | G | 2 | a0001c0001t0006g0249a0001c0001t0006g0258 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63+6106T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454576 | ||||||
| chr5:176454577
|
G | GA | 35 | a0001c0001t0001g0324a0001c0001t0001g0359a0001c0001t0002g0288others(32): Show | 35 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+6141dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
G | GAA | 24 | a0001c0001t0001g0116a0001c0001t0002g0287a0001c0001t0002g0291others(21): Show | 24 | HG00544.hp2 HG00639.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+6140_63+6141dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
G | GAAAAAAA others(14): Show |
1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+6121_63+6141dup others(21): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GA | G | 8 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0108others(5): Show | 8 | HG01099.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6141delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0010others(6): Show | 10 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+6133_63+6141del others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+6130_63+6141del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(6): Show |
G | 10 | a0001c0001t0001g0094a0001c0001t0001g0129a0001c0001t0001g0153others(7): Show | 10 | HG00639.hp2 HG02165.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+6129_63+6141del others(13): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(7): Show |
G | 132 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(129): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.63+6128_63+6141del others(14): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(8): Show |
G | 3 | a0001c0001t0001g0166a0001c0001t0001g0231a0001c0001t0011g0121 | 3 | HG01256.hp1 HG03490.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.63+6127_63+6141del others(15): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(9): Show |
G | 4 | a0001c0001t0003g0044a0001c0001t0003g0057a0001c0001t0003g0362others(1): Show | 4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6126_63+6141del others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(10): Show |
G | 73 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0002g0095others(70): Show | 74 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.63+6125_63+6141del others(17): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454577
|
GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0005g0263 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+6124_63+6141del others(18): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | |||||
| chr5:176454634
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6164A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454634 | ||||||
| chr5:176454661
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6191A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454661 | ||||||
| chr5:176454673
|
A | T | 1 | a0001c0001t0002g0342 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6203A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454673 | ||||||
| chr5:176454695
|
T | C | 276 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(273): Show | 278 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.63+6225T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454695 | ||||||
| chr5:176454936
|
C | G | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+6466C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454936 | ||||||
| chr5:176454945
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+6475G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454945 | ||||||
| chr5:176454963
|
A | G | 8 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(5): Show | 8 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6493A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454963 | ||||||
| chr5:176455075
|
T | TA | 9 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6616dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455075 | |||||
| chr5:176455194
|
A | G | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6724A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455194 | ||||||
| chr5:176455221
|
G | C | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6751G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455221 | ||||||
| chr5:176455255
|
G | A | 42 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(39): Show | 42 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+6785G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455255 | ||||||
| chr5:176455448
|
C | CA | 17 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+6988dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455448 | |||||
| chr5:176455508
|
G | C | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+7038G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455508 | ||||||
| chr5:176455618
|
G | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0160others(5): Show | 8 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+7148G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455618 | ||||||
| chr5:176455708
|
T | C | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+7238T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455708 | ||||||
| chr5:176455770
|
A | G | 72 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0002g0095others(69): Show | 73 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.63+7300A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455770 | ||||||
| chr5:176455853
|
C | CTTTATGT others(28): Show |
3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+7391_63+7425dup others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455853 | |||||
| chr5:176456084
|
T | G | 1 | a0001c0001t0003g0036 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.63+7614T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456084 | ||||||
| chr5:176456137
|
T | A | 11 | a0001c0001t0004g0003a0001c0001t0004g0236a0001c0001t0004g0237others(8): Show | 12 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+7667T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456137 | ||||||
| chr5:176456196
|
C | G | 1 | a0001c0001t0002g0341 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.63+7726C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456196 | ||||||
| chr5:176456272
|
A | T | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7802A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456272 | ||||||
| chr5:176456516
|
A | G | 1 | a0001c0001t0010g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+8046A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456516 | ||||||
| chr5:176456576
|
C | CCA | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.63+8107_63+8108ins others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176456576 | |||||
| chr5:176456877
|
G | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+8407G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456877 | ||||||
| chr5:176456887
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.63+8417A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456887 | ||||||
| chr5:176457077
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+8607T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457077 | ||||||
| chr5:176457104
|
G | C | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+8634G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457104 | ||||||
| chr5:176457211
|
C | T | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+8741C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457211 | ||||||
| chr5:176457245
|
A | G | 1 | a0001c0001t0005g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+8775A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457245 | ||||||
| chr5:176457403
|
C | T | 1 | a0001c0001t0018g0204 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.63+8933C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457403 | ||||||
| chr5:176457486
|
C | T | 71 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(68): Show | 72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.63+9016C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457486 | ||||||
| chr5:176457596
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+9126T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457596 | ||||||
| chr5:176457653
|
G | GGT | 65 | a0001c0001t0002g0095a0001c0001t0004g0235a0001c0001t0004g0256others(62): Show | 65 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.63+9204_63+9205dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | |||||
| chr5:176457653
|
G | GGTGT | 141 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(138): Show | 142 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+9202_63+9205dup others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | |||||
| chr5:176457653
|
G | GGTGTGT | 5 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0001g0201others(2): Show | 5 | HG00639.hp2 HG02080.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9200_63+9205dup others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | |||||
| chr5:176457655
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+9185T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457655 | ||||||
| chr5:176457662
|
G | T | 10 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(7): Show | 10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9192G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457662 | ||||||
| chr5:176457714
|
T | C | 1 | a0001c0001t0003g0058 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.63+9244T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457714 | ||||||
| chr5:176457774
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG01975.hp1 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.63+9304A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457774 | ||||||
| chr5:176457844
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0184a0001c0001t0001g0194others(1): Show | 4 | HG02165.hp2 NA18941.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+9374T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457844 | ||||||
| chr5:176457902
|
G | A | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9432G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457902 | ||||||
| chr5:176458006
|
A | G | 10 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(7): Show | 10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9536A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458006 | ||||||
| chr5:176458079
|
CCTCTTCT others(5): Show |
C | 10 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(7): Show | 10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9618_63+9629del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458079 | |||||
| chr5:176458109
|
A | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+9639A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458109 | ||||||
| chr5:176458197
|
T | C | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9727T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458197 | ||||||
| chr5:176458228
|
C | T | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+9758C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458228 | ||||||
| chr5:176458407
|
C | T | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+9937C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458407 | ||||||
| chr5:176458408
|
C | CTTTTT | 8 | a0001c0001t0001g0131a0001c0001t0001g0188a0001c0001t0001g0205others(5): Show | 8 | HG01070.hp2 HG02897.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+9953_63+9957dup others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | |||||
| chr5:176458408
|
C | CTTTTTT | 227 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(224): Show | 229 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.63+9952_63+9957dup others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | |||||
| chr5:176458408
|
C | CTTTTTTT | 103 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0153others(100): Show | 104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.63+9951_63+9957dup others(7): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | |||||
| chr5:176458408
|
C | CTTTTTTT others(1): Show |
22 | a0001c0001t0001g0324a0001c0001t0002g0095a0001c0001t0002g0302others(19): Show | 22 | HG00733.hp1 HG01099.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+9950_63+9957dup others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | |||||
| chr5:176458408
|
CT | C | 6 | a0001c0001t0005g0276a0001c0001t0007g0367a0001c0001t0007g0368others(3): Show | 6 | HG02280.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9957delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | |||||
| chr5:176458433
|
G | A | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+9963G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458433 | ||||||
| chr5:176458436
|
GTCTCACT others(1): Show |
G | 20 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(17): Show | 21 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+9973_63+9980del others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458436 | |||||
| chr5:176458455
|
G | A | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9985G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458455 | ||||||
| chr5:176458473
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+10003G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458473 | ||||||
| chr5:176458639
|
C | T | 144 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(141): Show | 145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.63+10169C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458639 | ||||||
| chr5:176458824
|
C | A | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+10354C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458824 | ||||||
| chr5:176459143
|
G | GT | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10679dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459143 | |||||
| chr5:176459219
|
A | G | 4 | a0001c0001t0006g0243a0001c0001t0006g0247a0001c0001t0006g0248others(1): Show | 4 | HG01496.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+10749A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459219 | ||||||
| chr5:176459250
|
C | CT | 93 | a0001c0001t0001g0126a0001c0001t0001g0148a0001c0001t0001g0165others(90): Show | 94 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.63+10800dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | |||||
| chr5:176459250
|
C | CTT | 63 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(60): Show | 64 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+10799_63+10800d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | |||||
| chr5:176459250
|
C | CTTT | 8 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0075others(5): Show | 8 | HG02132.hp2 HG04184.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+10798_63+10800d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | |||||
| chr5:176459250
|
CT | C | 31 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0131others(28): Show | 32 | HG00438.hp2 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+10800delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | |||||
| chr5:176459297
|
T | C | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+10827T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459297 | ||||||
| chr5:176459413
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.63+10943C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459413 | ||||||
| chr5:176459503
|
G | A | 1 | a0001c0001t0002g0344 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+11033G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459503 | ||||||
| chr5:176459546
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+11076G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459546 | ||||||
| chr5:176459685
|
A | G | 2 | a0001c0001t0003g0059a0001c0001t0003g0060 | 2 | NA18951.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.63+11215A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459685 | ||||||
| chr5:176459706
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+11236T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459706 | ||||||
| chr5:176459747
|
A | G | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+11277A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459747 | ||||||
| chr5:176460055
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+11585A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460055 | ||||||
| chr5:176460153
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+11683T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460153 | ||||||
| chr5:176460155
|
C | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+11685C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460155 | ||||||
| chr5:176460250
|
A | T | 1 | a0001c0001t0002g0352 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.63+11780A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460250 | ||||||
| chr5:176460263
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.63+11793G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460263 | ||||||
| chr5:176460278
|
C | G | 3 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0013g0020 | 3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+11808C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460278 | ||||||
| chr5:176460502
|
A | G | 3 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0013g0020 | 3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+12032A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460502 | ||||||
| chr5:176460513
|
C | CGT | 159 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(156): Show | 160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.63+12082_63+12083d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
C | CGTGT | 47 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0131others(44): Show | 47 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+12080_63+12083d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
C | CGTGTGT | 21 | a0001c0001t0001g0120a0001c0001t0001g0210a0001c0001t0003g0072others(18): Show | 21 | HG00733.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+12078_63+12083d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
C | CGTGTGTG others(1): Show |
16 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0003g0055others(13): Show | 16 | HG00544.hp2 HG02074.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+12076_63+12083d others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0010g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+12070_63+12083d others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+12043C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460513 | ||||||
| chr5:176460513
|
CGT | C | 29 | a0001c0001t0001g0112a0001c0001t0002g0329a0001c0001t0002g0335others(26): Show | 30 | HG00280.hp2 HG00733.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+12082_63+12083d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
CGTGT | C | 10 | a0001c0001t0001g0284a0001c0001t0003g0079a0001c0001t0004g0021others(7): Show | 10 | HG01433.hp2 HG02080.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12080_63+12083d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
CGTGTGT | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+12078_63+12083d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
CGTGTGTG others(3): Show |
C | 4 | a0001c0001t0002g0344a0001c0001t0002g0345a0001c0001t0003g0061others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12074_63+12083d others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0158a0001c0001t0002g0338 | 2 | HG00423.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.63+12072_63+12083d others(14): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460513
|
CGTGTGTG others(13): Show |
C | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+12064_63+12083d others(22): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | |||||
| chr5:176460554
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.63+12084A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460554 | ||||||
| chr5:176460595
|
G | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12125G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460595 | ||||||
| chr5:176460614
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+12144C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460614 | ||||||
| chr5:176460675
|
G | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+12205G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460675 | ||||||
| chr5:176460685
|
C | G | 2 | a0001c0001t0001g0324a0001c0001t0002g0342 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.63+12215C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460685 | ||||||
| chr5:176460689
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+12219C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460689 | ||||||
| chr5:176460781
|
A | G | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+12311A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460781 | ||||||
| chr5:176460823
|
A | G | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+12353A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460823 | ||||||
| chr5:176461014
|
T | G | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+12544T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461014 | ||||||
| chr5:176461018
|
CT | C | 300 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(297): Show | 303 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.63+12560delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461018 | |||||
| chr5:176461097
|
C | T | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461097 | ||||||
| chr5:176461163
|
A | G | 3 | a0001c0001t0003g0058a0001c0001t0003g0076a0001c0001t0003g0077 | 3 | NA18983.hp1 NA18984.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.63+12693A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461163 | ||||||
| chr5:176461234
|
G | A | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+12764G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461234 | ||||||
| chr5:176461312
|
C | CT | 202 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(199): Show | 203 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.63+12866dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | |||||
| chr5:176461312
|
C | CTT | 111 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0126others(108): Show | 113 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.63+12865_63+12866d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | |||||
| chr5:176461312
|
C | CTTT | 8 | a0001c0001t0001g0032a0001c0001t0002g0345a0001c0001t0003g0072others(5): Show | 8 | HG02615.hp1 HG02922.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12864_63+12866d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | |||||
| chr5:176461484
|
A | AT | 11 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0303others(8): Show | 11 | HG00280.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+13022dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461484 | |||||
| chr5:176461498
|
A | T | 8 | a0001c0001t0006g0243a0001c0001t0006g0247a0001c0001t0006g0248others(5): Show | 8 | HG01496.hp2 HG03139.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13028A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461498 | ||||||
| chr5:176461502
|
T | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13032T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461502 | ||||||
| chr5:176461503
|
T | A | 141 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(138): Show | 142 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+13033T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461503 | ||||||
| chr5:176461622
|
C | T | 1 | a0001c0001t0004g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.63+13152C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461622 | ||||||
| chr5:176461626
|
C | A | 1 | a0001c0001t0003g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+13156C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461626 | ||||||
| chr5:176461651
|
G | GTTA | 7 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(4): Show | 8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+13196_63+13198d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461651 | |||||
| chr5:176461768
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+13298T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461768 | ||||||
| chr5:176461814
|
CT | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+13347delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461814 | |||||
| chr5:176461938
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.63+13468C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461938 | ||||||
| chr5:176461972
|
G | C | 1 | a0001c0001t0002g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.63+13502G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461972 | ||||||
| chr5:176462015
|
A | G | 301 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(298): Show | 304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.63+13545A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462015 | ||||||
| chr5:176462091
|
A | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0044others(13): Show | 16 | HG00558.hp2 HG01081.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+13621A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462091 | ||||||
| chr5:176462190
|
T | C | 368 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(365): Show | 371 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.63+13720T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462190 | ||||||
| chr5:176462201
|
A | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+13731A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462201 | ||||||
| chr5:176462256
|
G | A | 301 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(298): Show | 304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.63+13786G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462256 | ||||||
| chr5:176462315
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.63+13845A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462315 | ||||||
| chr5:176462425
|
A | T | 1 | a0001c0001t0002g0349 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.63+13955A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462425 | ||||||
| chr5:176462432
|
T | TG | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+13964dupG | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176462432 | |||||
| chr5:176462451
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+13981C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462451 | ||||||
| chr5:176462480
|
C | T | 206 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(203): Show | 207 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.63+14010C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462480 | ||||||
| chr5:176462601
|
C | T | 5 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(2): Show | 5 | HG02486.hp1 NA18955.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+14131C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462601 | ||||||
| chr5:176462916
|
G | A | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+14446G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462916 | ||||||
| chr5:176462969
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+14499A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462969 | ||||||
| chr5:176462974
|
G | A | 144 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(141): Show | 145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.63+14504G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462974 | ||||||
| chr5:176463041
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+14571G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463041 | ||||||
| chr5:176463384
|
C | CA | 9 | a0001c0001t0003g0072a0001c0001t0004g0006a0001c0001t0004g0007others(6): Show | 9 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+14926dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463384 | |||||
| chr5:176463425
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+14955T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463425 | ||||||
| chr5:176463724
|
G | GT | 24 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0146others(21): Show | 24 | HG00408.hp2 HG00621.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+15273dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463724 | |||||
| chr5:176463724
|
GT | G | 25 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0001g0211others(22): Show | 26 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+15273delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463724 | |||||
| chr5:176463730
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.63+15260T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463730 | ||||||
| chr5:176463731
|
T | G | 1 | a0001c0001t0019g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.63+15261T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463731 | ||||||
| chr5:176463766
|
G | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+15296G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463766 | ||||||
| chr5:176463847
|
A | G | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(67): Show | 71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-15341A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463847 | ||||||
| chr5:176463889
|
C | T | 21 | a0001c0001t0005g0026a0001c0001t0005g0101a0001c0001t0005g0251others(18): Show | 21 | HG00544.hp2 HG02015.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-15299C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463889 | ||||||
| chr5:176463918
|
C | T | 1 | a0001c0001t0010g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-15270C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463918 | ||||||
| chr5:176463966
|
G | A | 1 | a0001c0001t0005g0269 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64-15222G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463966 | ||||||
| chr5:176463996
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-15192C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463996 | ||||||
| chr5:176464017
|
A | G | 3 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0316 | 3 | HG00280.hp1 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.64-15171A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464017 | ||||||
| chr5:176464025
|
G | A | 12 | a0001c0001t0004g0137a0001c0001t0004g0149a0001c0001t0004g0169others(9): Show | 12 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-15163G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464025 | ||||||
| chr5:176464027
|
G | C | 1 | a0001c0001t0010g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-15161G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464027 | ||||||
| chr5:176464051
|
A | G | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.64-15137A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464051 | ||||||
| chr5:176464098
|
C | T | 9 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0001t0006g0105others(6): Show | 9 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-15090C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464098 | ||||||
| chr5:176464284
|
G | C | 1 | a0001c0001t0008g0035 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64-14904G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464284 | ||||||
| chr5:176464487
|
CT | C | 65 | a0001c0001t0001g0324a0001c0001t0001g0343a0001c0001t0001g0359others(62): Show | 65 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-14678delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | |||||
| chr5:176464487
|
CTT | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0132a0001c0001t0001g0142others(10): Show | 13 | HG00621.hp1 HG01361.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-14679_64-14678d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | |||||
| chr5:176464487
|
CTTT | C | 279 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(276): Show | 282 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.64-14680_64-14678d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | |||||
| chr5:176464525
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-14663C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464525 | ||||||
| chr5:176465107
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.64-14081T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465107 | ||||||
| chr5:176465221
|
C | T | 1 | a0001c0001t0004g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.64-13967C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465221 | ||||||
| chr5:176465366
|
C | CT | 11 | a0001c0001t0001g0220a0001c0001t0002g0340a0001c0001t0002g0351others(8): Show | 11 | HG01928.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-13804dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465366 | |||||
| chr5:176465366
|
CT | C | 249 | a0001c0001t0001g0031a0001c0001t0001g0094a0001c0001t0001g0112others(246): Show | 251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.64-13804delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465366 | |||||
| chr5:176465367
|
T | TTTC | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-13819_64-13818i others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465367 | |||||
| chr5:176465370
|
T | C | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-13818T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465370 | ||||||
| chr5:176465414
|
C | T | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(67): Show | 71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-13774C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465414 | ||||||
| chr5:176465648
|
T | A | 3 | a0001c0001t0002g0344a0001c0001t0002g0345a0004c0004t0002g0330 | 3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.64-13540T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465648 | ||||||
| chr5:176465873
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-13315C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465873 | ||||||
| chr5:176465980
|
T | G | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-13208T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465980 | ||||||
| chr5:176466030
|
T | C | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG00733.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13158T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466030 | ||||||
| chr5:176466062
|
G | A | 299 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(296): Show | 302 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.64-13126G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466062 | ||||||
| chr5:176466119
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-13069A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466119 | ||||||
| chr5:176466126
|
G | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0172 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-13062G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466126 | ||||||
| chr5:176466190
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.64-12998C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466190 | ||||||
| chr5:176466212
|
C | T | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12976C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466212 | ||||||
| chr5:176466460
|
C | T | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-12728C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466460 | ||||||
| chr5:176466575
|
T | G | 274 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(271): Show | 276 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.64-12613T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466575 | ||||||
| chr5:176466651
|
C | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12537C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466651 | ||||||
| chr5:176466658
|
A | C | 1 | a0001c0001t0009g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-12530A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466658 | ||||||
| chr5:176466813
|
G | GTAGGAAA others(30): Show |
8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12374_64-12338d others(39): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176466813 | |||||
| chr5:176466941
|
C | A | 143 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(140): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.64-12247C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466941 | ||||||
| chr5:176466948
|
G | A | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-12240G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466948 | ||||||
| chr5:176467038
|
G | C | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(67): Show | 71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-12150G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467038 | ||||||
| chr5:176467118
|
T | C | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-12070T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467118 | ||||||
| chr5:176467127
|
T | C | 1 | a0001c0001t0004g0240 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-12061T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467127 | ||||||
| chr5:176467128
|
C | T | 1 | a0001c0001t0005g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-12060C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467128 | ||||||
| chr5:176467129
|
CT | C | 112 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0002g0287others(109): Show | 113 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.64-12035delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | |||||
| chr5:176467129
|
CTT | C | 36 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(33): Show | 37 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.64-12036_64-12035d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | |||||
| chr5:176467129
|
CTTT | C | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12037_64-12035d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | |||||
| chr5:176467129
|
CTTTTTTT | C | 112 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(109): Show | 112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.64-12041_64-12035d others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | |||||
| chr5:176467131
|
T | C | 1 | a0001c0001t0005g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-12057T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467131 | ||||||
| chr5:176467135
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-12053T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467135 | ||||||
| chr5:176467136
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-12052T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467136 | ||||||
| chr5:176467330
|
G | GT | 6 | a0001c0001t0002g0337a0001c0001t0003g0030a0001c0001t0003g0061others(3): Show | 6 | HG01109.hp1 HG02056.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11850dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467330 | |||||
| chr5:176467330
|
G | T | 6 | a0001c0001t0004g0238a0001c0001t0007g0367a0001c0001t0007g0368others(3): Show | 6 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11858G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467330 | ||||||
| chr5:176467339
|
G | T | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-11849G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467339 | ||||||
| chr5:176467340
|
G | T | 1 | a0001c0001t0008g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.64-11848G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467340 | ||||||
| chr5:176467454
|
C | T | 3 | a0001c0001t0011g0121a0001c0001t0011g0213a0001c0001t0011g0214 | 3 | NA18969.hp1 NA19060.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.64-11734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467454 | ||||||
| chr5:176467499
|
C | T | 1 | a0001c0001t0017g0281 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.64-11689C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467499 | ||||||
| chr5:176467585
|
G | A | 4 | a0001c0001t0003g0062a0001c0001t0003g0072a0001c0001t0003g0074others(1): Show | 4 | NA18977.hp2 NA19056.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-11603G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467585 | ||||||
| chr5:176467632
|
A | G | 1 | a0004c0004t0002g0330 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-11556A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467632 | ||||||
| chr5:176467734
|
T | G | 5 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11454T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467734 | ||||||
| chr5:176467778
|
T | C | 5 | a0001c0001t0004g0256a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-11410T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467778 | ||||||
| chr5:176467806
|
AT | A | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11380delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467806 | |||||
| chr5:176467810
|
G | T | 2 | a0001c0001t0004g0238a0001c0001t0004g0354 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-11378G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467810 | ||||||
| chr5:176467861
|
A | C | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64-11327A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467861 | ||||||
| chr5:176467925
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64-11263G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467925 | ||||||
| chr5:176468022
|
G | A | 274 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(271): Show | 276 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.64-11166G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468022 | ||||||
| chr5:176468096
|
C | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-11092C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468096 | ||||||
| chr5:176468109
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-11079G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468109 | ||||||
| chr5:176468244
|
C | A | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-10944C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468244 | ||||||
| chr5:176468317
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-10871G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468317 | ||||||
| chr5:176468403
|
T | C | 1 | a0001c0001t0004g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-10785T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468403 | ||||||
| chr5:176468412
|
G | A | 10 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(7): Show | 11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-10776G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468412 | ||||||
| chr5:176468520
|
C | G | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(67): Show | 71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-10668C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468520 | ||||||
| chr5:176468785
|
C | CA | 9 | a0001c0001t0004g0119a0001c0001t0004g0236a0001c0001t0006g0108others(6): Show | 9 | HG01515.hp2 HG01517.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-10391dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176468785 | |||||
| chr5:176468785
|
CA | C | 16 | a0001c0001t0003g0072a0001c0001t0004g0006a0001c0001t0004g0007others(13): Show | 17 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-10391delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176468785 | |||||
| chr5:176468815
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-10373G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468815 | ||||||
| chr5:176468849
|
C | T | 3 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0013g0020 | 3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-10339C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468849 | ||||||
| chr5:176469232
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-9956G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469232 | ||||||
| chr5:176469482
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-9706C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469482 | ||||||
| chr5:176469645
|
A | G | 8 | a0001c0001t0001g0139a0001c0001t0001g0150a0001c0001t0001g0159others(5): Show | 8 | HG01934.hp1 HG01952.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9543A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469645 | ||||||
| chr5:176469760
|
C | T | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-9428C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469760 | ||||||
| chr5:176469773
|
T | G | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-9415T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469773 | ||||||
| chr5:176469861
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-9327G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469861 | ||||||
| chr5:176470219
|
C | G | 143 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(140): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.64-8969C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470219 | ||||||
| chr5:176470310
|
A | G | 300 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(297): Show | 303 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.64-8878A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470310 | ||||||
| chr5:176470368
|
G | A | 1 | a0006c0007t0002g0348 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64-8820G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470368 | ||||||
| chr5:176470420
|
A | G | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8768A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470420 | ||||||
| chr5:176470437
|
C | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8751C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470437 | ||||||
| chr5:176470460
|
C | A | 1 | a0001c0001t0004g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.64-8728C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470460 | ||||||
| chr5:176470475
|
G | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-8713G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470475 | ||||||
| chr5:176470532
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.64-8656G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470532 | ||||||
| chr5:176470541
|
C | T | 71 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0142others(68): Show | 72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-8647C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470541 | ||||||
| chr5:176470637
|
TCACA | T | 10 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(7): Show | 11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-8542_64-8539del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176470637 | |||||
| chr5:176470648
|
C | A | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-8540C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470648 | ||||||
| chr5:176471197
|
G | A | 1 | a0001c0001t0005g0253 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64-7991G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471197 | ||||||
| chr5:176471303
|
T | G | 7 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(4): Show | 8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-7885T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471303 | ||||||
| chr5:176471309
|
A | G | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-7879A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471309 | ||||||
| chr5:176471331
|
A | G | 1 | a0001c0001t0007g0017 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.64-7857A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471331 | ||||||
| chr5:176471375
|
C | CT | 9 | a0001c0001t0002g0291a0001c0001t0002g0294a0001c0001t0002g0299others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-7789dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471375
|
CTT | C | 6 | a0001c0001t0001g0031a0001c0001t0003g0057a0001c0001t0003g0075others(3): Show | 6 | HG01070.hp1 HG02145.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-7790_64-7789del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471375
|
CTTT | C | 78 | a0001c0001t0001g0032a0001c0001t0001g0142a0001c0001t0003g0002others(75): Show | 79 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-7791_64-7789del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471375
|
CTTTT | C | 16 | a0001c0001t0001g0122a0001c0001t0001g0146a0001c0001t0001g0163others(13): Show | 16 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-7792_64-7789del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471375
|
CTTTTT | C | 187 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(184): Show | 188 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.64-7793_64-7789del others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471375
|
CTTTTTT | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0358a0001c0001t0004g0114others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-7794_64-7789del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | |||||
| chr5:176471432
|
G | C | 1 | a0001c0001t0013g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-7756G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471432 | ||||||
| chr5:176471679
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-7509G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471679 | ||||||
| chr5:176471684
|
CT | C | 256 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(253): Show | 259 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.64-7488delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471684 | |||||
| chr5:176471704
|
A | T | 1 | a0001c0001t0004g0221 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-7484A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471704 | ||||||
| chr5:176471711
|
C | A | 6 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | HG01975.hp1 HG01993.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7477C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471711 | ||||||
| chr5:176471880
|
G | A | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(67): Show | 71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-7308G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471880 | ||||||
| chr5:176471973
|
C | T | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-7215C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471973 | ||||||
| chr5:176471981
|
C | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-7207C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471981 | ||||||
| chr5:176471996
|
C | A | 299 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(296): Show | 302 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.64-7192C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471996 | ||||||
| chr5:176472135
|
T | A | 1 | a0001c0001t0002g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64-7053T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472135 | ||||||
| chr5:176472147
|
T | G | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-7041T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472147 | ||||||
| chr5:176472277
|
G | T | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | NA18947.hp2 NA18965.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6911G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472277 | ||||||
| chr5:176472452
|
G | GT | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0010g0018others(2): Show | 5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6728dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472452 | |||||
| chr5:176472461
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.64-6727A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472461 | ||||||
| chr5:176472719
|
CA | C | 18 | a0001c0001t0001g0146a0001c0001t0002g0344a0001c0001t0002g0345others(15): Show | 18 | HG02451.hp1 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-6453delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472719 | |||||
| chr5:176472719
|
CAA | C | 285 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(282): Show | 288 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.64-6454_64-6453del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472719 | |||||
| chr5:176472735
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.64-6453A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472735 | ||||||
| chr5:176472810
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-6378A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472810 | ||||||
| chr5:176473114
|
T | A | 299 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(296): Show | 302 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.64-6074T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473114 | ||||||
| chr5:176473179
|
G | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-6009G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473179 | ||||||
| chr5:176473503
|
C | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(1): Show | 4 | HG00621.hp1 HG02071.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-5685C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473503 | ||||||
| chr5:176473527
|
A | G | 20 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(17): Show | 21 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-5661A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473527 | ||||||
| chr5:176473728
|
C | T | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5460C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473728 | ||||||
| chr5:176473729
|
G | A | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5459G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473729 | ||||||
| chr5:176473914
|
T | G | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | NA18971.hp2 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.64-5274T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473914 | ||||||
| chr5:176473955
|
G | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-5233G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473955 | ||||||
| chr5:176474070
|
C | T | 4 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(1): Show | 5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5118C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474070 | ||||||
| chr5:176474208
|
T | C | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-4980T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474208 | ||||||
| chr5:176474317
|
C | T | 1 | a0001c0001t0004g0003 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.64-4871C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474317 | ||||||
| chr5:176474391
|
A | T | 138 | a0001c0001t0001g0116a0001c0001t0001g0129a0001c0001t0001g0144others(135): Show | 141 | HG00408.hp1 HG00558.hp2 HG00642.hp2 others(138): Show |
intron_variant | MODIFIER | c.64-4797A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474391 | ||||||
| chr5:176474419
|
T | C | 2 | a0001c0001t0004g0023a0001c0001t0004g0024 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-4769T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474419 | ||||||
| chr5:176474446
|
AC | A | 24 | a0001c0001t0004g0119a0001c0001t0004g0134a0001c0001t0004g0135others(21): Show | 25 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-4736delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176474446 | |||||
| chr5:176474457
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-4731C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474457 | ||||||
| chr5:176474584
|
T | C | 10 | a0001c0001t0004g0003a0001c0001t0004g0236a0001c0001t0004g0237others(7): Show | 11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-4604T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474584 | ||||||
| chr5:176474619
|
A | G | 2 | a0001c0001t0002g0296a0001c0001t0002g0299 | 2 | NA18945.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.64-4569A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474619 | ||||||
| chr5:176475101
|
G | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0172 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4087G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475101 | ||||||
| chr5:176475137
|
G | GTTA | 76 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0223others(73): Show | 77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.64-4036_64-4034dup others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176475137 | |||||
| chr5:176475195
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-3993C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475195 | ||||||
| chr5:176475339
|
G | C | 1 | a0001c0001t0002g0301 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64-3849G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475339 | ||||||
| chr5:176475480
|
T | C | 2 | a0001c0001t0003g0062a0001c0001t0003g0085 | 2 | NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.64-3708T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475480 | ||||||
| chr5:176475596
|
C | T | 1 | a0001c0001t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64-3592C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475596 | ||||||
| chr5:176475611
|
T | C | 2 | a0001c0001t0004g0135a0001c0001t0004g0136 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-3577T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475611 | ||||||
| chr5:176475699
|
C | T | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3489C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475699 | ||||||
| chr5:176475880
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64-3308A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475880 | ||||||
| chr5:176475924
|
A | G | 1 | a0002c0002t0001g0179 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.64-3264A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475924 | ||||||
| chr5:176475951
|
A | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-3237A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475951 | ||||||
| chr5:176476124
|
G | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0081 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.64-3064G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476124 | ||||||
| chr5:176476129
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64-3059G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476129 | ||||||
| chr5:176476262
|
T | C | 2 | a0001c0001t0003g0057a0001c0001t0003g0067 | 2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.64-2926T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476262 | ||||||
| chr5:176476359
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-2829G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476359 | ||||||
| chr5:176476471
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0200 | 2 | NA18945.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.64-2717G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476471 | ||||||
| chr5:176476627
|
C | CT | 64 | a0001c0001t0001g0094a0001c0001t0001g0124a0001c0001t0001g0140others(61): Show | 65 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-2538dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476627
|
C | CTT | 12 | a0001c0001t0005g0255a0001c0001t0005g0264a0001c0001t0005g0269others(9): Show | 12 | HG00438.hp1 HG01167.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-2539_64-2538dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476627
|
CT | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 9 | HG01175.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-2538delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476627
|
CTT | C | 7 | a0001c0001t0003g0062a0001c0001t0003g0085a0001c0001t0007g0367others(4): Show | 7 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2539_64-2538del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476627
|
CTTT | C | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(63): Show | 67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-2540_64-2538del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476627
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0142a0001c0001t0001g0233a0001c0001t0031g0138 | 3 | HG02602.hp2 HG02683.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.64-2547_64-2538del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | |||||
| chr5:176476673
|
C | T | 27 | a0001c0001t0005g0026a0001c0001t0005g0251a0001c0001t0005g0252others(24): Show | 27 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.64-2515C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476673 | ||||||
| chr5:176476804
|
A | AT | 69 | a0001c0001t0001g0094a0001c0001t0001g0120a0001c0001t0001g0124others(66): Show | 69 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-2361dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | |||||
| chr5:176476804
|
A | ATT | 11 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0022others(8): Show | 12 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-2362_64-2361dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | |||||
| chr5:176476804
|
AT | A | 7 | a0001c0001t0001g0159a0001c0001t0001g0324a0001c0001t0002g0316others(4): Show | 7 | HG00280.hp1 HG01169.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2361delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | |||||
| chr5:176477029
|
C | T | 1 | a0006c0007t0002g0348 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64-2159C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477029 | ||||||
| chr5:176477043
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0195 | 2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.64-2145C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477043 | ||||||
| chr5:176477070
|
A | G | 148 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(145): Show | 149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-2118A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477070 | ||||||
| chr5:176477087
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-2101C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477087 | ||||||
| chr5:176477088
|
GTGAGCCA others(130): Show |
G | 1 | a0001c0001t0002g0328 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.64-2062_64-1926del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477088 | |||||
| chr5:176477098
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64-2090G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477098 | ||||||
| chr5:176477099
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-2089T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477099 | ||||||
| chr5:176477100
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-2088G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477100 | ||||||
| chr5:176477106
|
CCT | C | 3 | a0001c0001t0013g0025a0001c0001t0014g0013a0001c0001t0014g0014 | 3 | HG01891.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-2081_64-2080del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477106 | ||||||
| chr5:176477106
|
CCTT | C | 17 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(14): Show | 18 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-2081_64-2079del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477106 | ||||||
| chr5:176477107
|
C | CT | 33 | a0001c0001t0001g0178a0001c0001t0001g0192a0001c0001t0001g0225others(30): Show | 33 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.64-2063dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | |||||
| chr5:176477107
|
CTTTTTTT others(131): Show |
C | 2 | a0001c0001t0002g0335a0001c0001t0002g0339 | 2 | NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.64-2062_64-1925del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | |||||
| chr5:176477107
|
CTTTTTTT others(132): Show |
C | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.64-2058_64-1920del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | |||||
| chr5:176477136
|
G | A | 1 | a0001c0001t0002g0352 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.64-2052G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477136 | ||||||
| chr5:176477140
|
T | C | 139 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(136): Show | 139 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.64-2048T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477140 | ||||||
| chr5:176477172
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0218 | 2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.64-2016C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477172 | ||||||
| chr5:176477187
|
T | C | 1 | a0001c0001t0005g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-2001T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477187 | ||||||
| chr5:176477225
|
A | G | 2 | a0001c0001t0004g0260a0001c0001t0032g0097 | 2 | HG02080.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.64-1963A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477225 | ||||||
| chr5:176477235
|
G | A | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-1953G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477235 | ||||||
| chr5:176477236
|
T | C | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-1952T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477236 | ||||||
| chr5:176477243
|
C | CTTTTTTT others(126): Show |
1 | a0001c0001t0032g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-1945_64-1944ins others(133): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477243 | ||||||
| chr5:176477244
|
CT | C | 179 | a0001c0001t0001g0094a0001c0001t0001g0113a0001c0001t0001g0115others(176): Show | 179 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.64-1924delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477244 | |||||
| chr5:176477244
|
CTT | C | 80 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0112others(77): Show | 81 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-1925_64-1924del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477244 | |||||
| chr5:176477245
|
T | C | 1 | a0001c0001t0032g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-1943T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477245 | ||||||
| chr5:176477245
|
T | TTTTTTTT others(129): Show |
1 | a0001c0001t0004g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.64-1926_64-1925ins others(136): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477245 | |||||
| chr5:176477290
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.64-1898T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477290 | ||||||
| chr5:176477293
|
G | A | 1 | a0001c0001t0034g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-1895G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477293 | ||||||
| chr5:176477307
|
T | G | 278 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(275): Show | 280 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.64-1881T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477307 | ||||||
| chr5:176477345
|
C | T | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-1843C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477345 | ||||||
| chr5:176477417
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.64-1771C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477417 | ||||||
| chr5:176477485
|
G | A | 1 | a0001c0001t0010g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-1703G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477485 | ||||||
| chr5:176477569
|
CAAAGCCA others(9): Show |
C | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.64-1614_64-1599del others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477569 | |||||
| chr5:176477588
|
A | G | 1 | a0001c0001t0016g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-1600A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477588 | ||||||
| chr5:176478302
|
T | C | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.64-886T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478302 | ||||||
| chr5:176478359
|
G | A | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.64-829G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478359 | ||||||
| chr5:176478430
|
C | T | 81 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(78): Show | 82 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.64-758C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478430 | ||||||
| chr5:176478446
|
T | A | 3 | a0001c0001t0002g0307a0001c0001t0002g0310a0001c0001t0002g0311 | 3 | HG00639.hp1 HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.64-742T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478446 | ||||||
| chr5:176478506
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-682G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478506 | ||||||
| chr5:176478510
|
G | C | 1 | a0001c0001t0005g0271 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-678G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478510 | ||||||
| chr5:176478596
|
T | G | 9 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0147others(6): Show | 9 | HG00621.hp1 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-592T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478596 | ||||||
| chr5:176478646
|
C | G | 1 | a0001c0001t0005g0253 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64-542C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478646 | ||||||
| chr5:176478688
|
T | C | 1 | a0001c0008t0027g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-500T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478688 | ||||||
| chr5:176478731
|
A | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-457A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478731 | ||||||
| chr5:176479695
|
G | T | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+439G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479695 | ||||||
| chr5:176479756
|
G | A | 1 | a0001c0001t0003g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.132+500G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479756 | ||||||
| chr5:176479883
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.132+627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479883 | ||||||
| chr5:176479938
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.132+682G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479938 | ||||||
| chr5:176480195
|
G | T | 143 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(140): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.132+939G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480195 | ||||||
| chr5:176480261
|
G | A | 1 | a0001c0001t0004g0134 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.132+1005G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480261 | ||||||
| chr5:176480267
|
G | A | 1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.132+1011G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480267 | ||||||
| chr5:176480288
|
CT | C | 10 | a0001c0001t0002g0286a0001c0001t0002g0291a0001c0001t0002g0292others(7): Show | 10 | HG01993.hp1 NA18945.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+1041delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176480288 | |||||
| chr5:176480523
|
C | G | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+1267C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480523 | ||||||
| chr5:176480596
|
G | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.132+1340G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480596 | ||||||
| chr5:176480712
|
C | G | 1 | a0001c0001t0002g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.132+1456C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480712 | ||||||
| chr5:176480769
|
C | T | 2 | a0001c0001t0007g0367a0001c0001t0007g0368 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.132+1513C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480769 | ||||||
| chr5:176480960
|
A | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0042a0001c0001t0003g0362 | 4 | HG01168.hp2 HG02735.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1704A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480960 | ||||||
| chr5:176481006
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0025 | 2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+1750A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481006 | ||||||
| chr5:176481018
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.132+1762G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481018 | ||||||
| chr5:176481139
|
C | T | 1 | a0001c0001t0010g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.132+1883C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481139 | ||||||
| chr5:176481236
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0218 | 2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.132+1980C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481236 | ||||||
| chr5:176481323
|
G | A | 1 | a0001c0001t0002g0347 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.132+2067G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481323 | ||||||
| chr5:176481345
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.132+2089C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481345 | ||||||
| chr5:176481383
|
C | T | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.132+2127C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481383 | ||||||
| chr5:176481444
|
T | C | 10 | a0001c0001t0004g0003a0001c0001t0004g0236a0001c0001t0004g0238others(7): Show | 11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+2188T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481444 | ||||||
| chr5:176481489
|
C | A | 5 | a0001c0001t0006g0243a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG01496.hp2 HG03209.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2233C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481489 | ||||||
| chr5:176481610
|
A | G | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.132+2354A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481610 | ||||||
| chr5:176481751
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.132+2495G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481751 | ||||||
| chr5:176481797
|
G | A | 3 | a0001c0001t0003g0050a0001c0001t0003g0055a0001c0001t0003g0091 | 3 | HG00558.hp2 NA18939.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.132+2541G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481797 | ||||||
| chr5:176481802
|
C | T | 1 | a0001c0001t0004g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.132+2546C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481802 | ||||||
| chr5:176481824
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.132+2568G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481824 | ||||||
| chr5:176481861
|
T | C | 59 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(56): Show | 59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.132+2605T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481861 | ||||||
| chr5:176481932
|
C | G | 3 | a0002c0002t0001g0177a0002c0002t0001g0179a0002c0002t0001g0180 | 3 | NA18974.hp1 NA19066.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.132+2676C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481932 | ||||||
| chr5:176481977
|
C | G | 1 | a0001c0001t0021g0314 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.132+2721C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481977 | ||||||
| chr5:176482051
|
C | T | 74 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(71): Show | 76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.132+2795C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482051 | ||||||
| chr5:176482220
|
G | GT | 182 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0112others(179): Show | 184 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.132+2979dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482220 | |||||
| chr5:176482466
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+3210G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482466 | ||||||
| chr5:176482489
|
A | C | 76 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(73): Show | 78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.132+3233A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482489 | ||||||
| chr5:176482640
|
C | T | 226 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(223): Show | 227 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.132+3384C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482640 | ||||||
| chr5:176482790
|
C | A | 212 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(209): Show | 213 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.132+3534C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482790 | ||||||
| chr5:176482795
|
C | T | 1 | a0001c0001t0010g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.132+3539C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482795 | ||||||
| chr5:176482863
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133-3492A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482863 | ||||||
| chr5:176482895
|
T | TTTG | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0008g0035 | 3 | HG00408.hp2 NA18965.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.133-3439_133-3437d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482895 | |||||
| chr5:176482895
|
TTTGTTG | T | 62 | a0001c0001t0001g0126a0001c0001t0001g0228a0001c0001t0001g0343others(59): Show | 62 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.133-3442_133-3437d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482895 | |||||
| chr5:176482933
|
T | C | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133-3422T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482933 | ||||||
| chr5:176482973
|
G | C | 1 | a0001c0001t0003g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.133-3382G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482973 | ||||||
| chr5:176482976
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0218 | 2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.133-3379C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482976 | ||||||
| chr5:176483036
|
C | CT | 22 | a0001c0001t0002g0335a0001c0001t0002g0339a0001c0001t0005g0026others(19): Show | 22 | HG00544.hp2 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.133-3311dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176483036 | |||||
| chr5:176483044
|
T | A | 6 | a0001c0001t0002g0319a0001c0001t0004g0256a0001c0001t0004g0260others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-3311T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483044 | ||||||
| chr5:176483080
|
G | A | 2 | a0001c0001t0002g0337a0001c0001t0002g0350 | 2 | NA18995.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.133-3275G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483080 | ||||||
| chr5:176483163
|
C | T | 1 | a0001c0001t0005g0272 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.133-3192C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483163 | ||||||
| chr5:176483202
|
A | C | 1 | a0001c0001t0034g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133-3153A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483202 | ||||||
| chr5:176483217
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.133-3138G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483217 | ||||||
| chr5:176483251
|
T | C | 128 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(125): Show | 129 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.133-3104T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483251 | ||||||
| chr5:176483675
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.133-2680G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483675 | ||||||
| chr5:176483686
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133-2669T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483686 | ||||||
| chr5:176483798
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.133-2557C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483798 | ||||||
| chr5:176483799
|
G | A | 1 | a0001c0001t0005g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.133-2556G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483799 | ||||||
| chr5:176484075
|
A | T | 1 | a0001c0001t0005g0366 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.133-2280A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484075 | ||||||
| chr5:176484144
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.133-2211G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484144 | ||||||
| chr5:176484201
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133-2154G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484201 | ||||||
| chr5:176484311
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133-2044A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484311 | ||||||
| chr5:176484445
|
T | C | 3 | a0001c0001t0002g0344a0001c0001t0002g0345a0004c0004t0002g0330 | 3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.133-1910T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484445 | ||||||
| chr5:176484548
|
G | A | 1 | a0001c0001t0004g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-1807G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484548 | ||||||
| chr5:176484658
|
C | T | 74 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(71): Show | 76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.133-1697C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484658 | ||||||
| chr5:176484693
|
C | A | 1 | a0001c0001t0003g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133-1662C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484693 | ||||||
| chr5:176484806
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.133-1549G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484806 | ||||||
| chr5:176484870
|
C | A | 1 | a0001c0001t0002g0286 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.133-1485C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484870 | ||||||
| chr5:176484894
|
G | GA | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0132others(67): Show | 71 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-1446dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176484894 | |||||
| chr5:176484894
|
GA | G | 59 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(56): Show | 59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.133-1446delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176484894 | |||||
| chr5:176484917
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.133-1438G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484917 | ||||||
| chr5:176485145
|
C | T | 3 | a0001c0001t0002g0344a0001c0001t0002g0345a0004c0004t0002g0330 | 3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.133-1210C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485145 | ||||||
| chr5:176485223
|
C | G | 1 | a0001c0001t0017g0281 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-1132C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485223 | ||||||
| chr5:176485276
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.133-1079A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485276 | ||||||
| chr5:176485330
|
A | G | 58 | a0001c0001t0004g0256a0001c0001t0004g0260a0001c0001t0004g0261others(55): Show | 58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.133-1025A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485330 | ||||||
| chr5:176485754
|
G | A | 10 | a0001c0001t0006g0083a0001c0001t0006g0103a0001c0001t0006g0104others(7): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-601G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485754 | ||||||
| chr5:176485779
|
G | A | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-576G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485779 | ||||||
| chr5:176485862
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133-493C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485862 | ||||||
| chr5:176485923
|
G | A | 1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.133-432G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485923 | ||||||
| chr5:176485993
|
G | A | 76 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(73): Show | 78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.133-362G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485993 | ||||||
| chr5:176486081
|
A | G | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-274A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486081 | ||||||
| chr5:176486305
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133-50G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486305 | ||||||
| chr5:176486341
|
G | A | 1 | a0001c0001t0017g0281 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-14G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486341 | ||||||
| chr5:176486562
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.267+73C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176486562 | ||||||
| chr5:176486673
|
AT | A | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.267+194delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 176486673 | |||||
| chr5:176486759
|
T | C | 1 | a0001c0001t0002g0328 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.267+270T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176486759 | ||||||
| chr5:176487057
|
C | T | 295 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(292): Show | 298 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(295): Show |
intron_variant | MODIFIER | c.267+568C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487057 | ||||||
| chr5:176487215
|
C | T | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+726C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487215 | ||||||
| chr5:176487223
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.267+734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487223 | ||||||
| chr5:176487234
|
G | C | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.267+745G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487234 | ||||||
| chr5:176487364
|
G | A | 60 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(57): Show | 60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.267+875G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487364 | ||||||
| chr5:176487429
|
C | T | 4 | a0001c0001t0004g0198a0001c0001t0004g0222a0001c0001t0004g0234others(1): Show | 4 | HG02109.hp2 HG02647.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+940C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487429 | ||||||
| chr5:176487584
|
C | T | 143 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(140): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.267+1095C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487584 | ||||||
| chr5:176487590
|
C | T | 1 | a0001c0001t0005g0252 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.267+1101C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487590 | ||||||
| chr5:176487828
|
A | C | 1 | a0001c0001t0004g0021 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.268-1123A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487828 | ||||||
| chr5:176488166
|
C | T | 2 | a0001c0001t0010g0004a0001c0001t0010g0005 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.268-785C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488166 | ||||||
| chr5:176488449
|
A | C | 59 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(56): Show | 59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.268-502A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488449 | ||||||
| chr5:176488479
|
T | C | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.268-472T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488479 | ||||||
| chr5:176488483
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.268-468G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488483 | ||||||
| chr5:176488623
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0189a0001c0001t0001g0193 | 3 | NA18954.hp2 NA19000.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.268-328G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488623 | ||||||
| chr5:176488711
|
C | T | 60 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(57): Show | 60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.268-240C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488711 | ||||||
| chr5:176488834
|
C | T | 364 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(361): Show | 367 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(364): Show |
intron_variant | MODIFIER | c.268-117C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488834 | ||||||
| chr5:176488854
|
T | C | 1 | a0001c0001t0005g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268-97T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488854 | ||||||
| chr5:176488860
|
G | A | 75 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(72): Show | 77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.268-91G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488860 | ||||||
| chr5:176489059
|
A | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0217 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.344+32A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489059 | ||||||
| chr5:176489076
|
C | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.344+49C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489076 | ||||||
| chr5:176489082
|
T | C | 60 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(57): Show | 60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+55T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489082 | ||||||
| chr5:176489154
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.344+127C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489154 | ||||||
| chr5:176489167
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.344+140A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489167 | ||||||
| chr5:176489181
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344+154G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489181 | ||||||
| chr5:176489248
|
T | C | 221 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(218): Show | 224 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.344+221T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489248 | ||||||
| chr5:176489292
|
T | TC | 43 | a0001c0001t0002g0095a0001c0001t0002g0288a0001c0001t0002g0289others(40): Show | 43 | HG00544.hp2 HG01099.hp2 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.344+274dupC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176489292 | |||||
| chr5:176489292
|
TC | T | 182 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(179): Show | 185 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.344+274delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176489292 | |||||
| chr5:176489470
|
T | A | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+443T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489470 | ||||||
| chr5:176489640
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+613C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489640 | ||||||
| chr5:176489715
|
T | G | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+688T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489715 | ||||||
| chr5:176490077
|
T | C | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.344+1050T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490077 | ||||||
| chr5:176490078
|
G | A | 3 | a0001c0001t0004g0114a0001c0001t0006g0283a0001c0001t0022g0262 | 3 | HG02886.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.344+1051G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490078 | ||||||
| chr5:176490087
|
G | A | 1 | a0001c0001t0030g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.344+1060G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490087 | ||||||
| chr5:176490227
|
C | G | 1 | a0001c0001t0028g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.344+1200C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490227 | ||||||
| chr5:176490234
|
C | G | 1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.344+1207C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490234 | ||||||
| chr5:176490236
|
G | T | 10 | a0001c0001t0006g0083a0001c0001t0006g0103a0001c0001t0006g0104others(7): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+1209G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490236 | ||||||
| chr5:176490276
|
A | C | 2 | a0001c0001t0004g0282a0001c0001t0024g0239 | 2 | HG01361.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.344+1249A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490276 | ||||||
| chr5:176490291
|
A | C | 78 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(75): Show | 79 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.344+1264A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490291 | ||||||
| chr5:176490305
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+1278C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490305 | ||||||
| chr5:176490310
|
C | CA | 93 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0140others(90): Show | 95 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.344+1297dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176490310 | |||||
| chr5:176490331
|
G | T | 10 | a0001c0001t0006g0083a0001c0001t0006g0103a0001c0001t0006g0104others(7): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+1304G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490331 | ||||||
| chr5:176490337
|
A | G | 13 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+1310A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490337 | ||||||
| chr5:176490341
|
T | C | 3 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0048 | 3 | HG01175.hp2 HG01934.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.344+1314T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490341 | ||||||
| chr5:176490384
|
G | A | 11 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(8): Show | 11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+1357G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490384 | ||||||
| chr5:176490532
|
GC | G | 152 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(149): Show | 154 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.344+1507delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176490532 | |||||
| chr5:176490778
|
T | C | 1 | a0001c0001t0010g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.345-1416T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490778 | ||||||
| chr5:176490788
|
C | A | 91 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(88): Show | 93 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.345-1406C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490788 | ||||||
| chr5:176490857
|
G | C | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.345-1337G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490857 | ||||||
| chr5:176490998
|
A | G | 58 | a0001c0001t0004g0256a0001c0001t0004g0260a0001c0001t0004g0261others(55): Show | 58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.345-1196A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490998 | ||||||
| chr5:176491047
|
A | T | 67 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(64): Show | 68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.345-1147A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491047 | ||||||
| chr5:176491181
|
C | T | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-1013C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491181 | ||||||
| chr5:176491261
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-933T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491261 | ||||||
| chr5:176491643
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0011g0121a0001c0001t0011g0213others(1): Show | 4 | HG02165.hp1 NA18969.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-551C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491643 | ||||||
| chr5:176491768
|
G | GTA | 10 | a0001c0001t0006g0083a0001c0001t0006g0103a0001c0001t0006g0104others(7): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-424_345-423dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176491768 | |||||
| chr5:176491877
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-317G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491877 | ||||||
| chr5:176491913
|
T | C | 1 | a0001c0001t0019g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.345-281T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491913 | ||||||
| chr5:176492065
|
A | C | 2 | a0001c0001t0013g0020a0001c0001t0013g0025 | 2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.345-129A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176492065 | ||||||
| chr5:176492095
|
C | T | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-99C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176492095 | ||||||
| chr5:176492454
|
C | T | 1 | a0001c0001t0002g0331 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.483+122C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492454 | ||||||
| chr5:176492514
|
G | T | 1 | a0001c0001t0002g0338 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.483+182G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492514 | ||||||
| chr5:176492605
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483+273C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492605 | ||||||
| chr5:176492638
|
C | G | 1 | a0001c0001t0003g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.483+306C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492638 | ||||||
| chr5:176492652
|
T | C | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+320T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492652 | ||||||
| chr5:176492708
|
G | A | 49 | a0001c0001t0004g0114a0001c0001t0004g0256a0001c0001t0004g0260others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.483+376G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492708 | ||||||
| chr5:176492773
|
A | G | 2 | a0001c0001t0004g0238a0001c0001t0004g0354 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.483+441A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492773 | ||||||
| chr5:176492834
|
A | G | 2 | a0001c0001t0010g0018a0001c0001t0010g0019 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+502A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492834 | ||||||
| chr5:176492870
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0018g0204 | 3 | HG01257.hp2 HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.483+538A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492870 | ||||||
| chr5:176492916
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483+584A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492916 | ||||||
| chr5:176492969
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.483+637A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492969 | ||||||
| chr5:176492978
|
A | G | 3 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0316 | 3 | HG00280.hp1 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.483+646A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492978 | ||||||
| chr5:176493119
|
C | G | 90 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(87): Show | 92 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.483+787C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493119 | ||||||
| chr5:176493289
|
A | G | 146 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(143): Show | 147 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.484-710A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493289 | ||||||
| chr5:176493401
|
C | T | 13 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-598C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493401 | ||||||
| chr5:176493440
|
T | G | 145 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(142): Show | 146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.484-559T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493440 | ||||||
| chr5:176493489
|
C | A | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.484-510C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493489 | ||||||
| chr5:176493501
|
A | G | 13 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-498A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493501 | ||||||
| chr5:176493526
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.484-473G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493526 | ||||||
| chr5:176493723
|
T | G | 4 | a0001c0001t0006g0243a0001c0001t0006g0247a0001c0001t0006g0248others(1): Show | 4 | HG01496.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-276T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493723 | ||||||
| chr5:176493919
|
G | A | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.484-80G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493919 | ||||||
| chr5:176494149
|
AGTT | A | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(63): Show | 67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.570-31_570-29delGT others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 176494149 | |||||
| chr5:176494350
|
A | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.661+75A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494350 | ||||||
| chr5:176494385
|
G | A | 11 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(8): Show | 11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+110G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494385 | ||||||
| chr5:176494407
|
T | A | 11 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(8): Show | 11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+132T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494407 | ||||||
| chr5:176494460
|
T | C | 220 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(217): Show | 223 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.661+185T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494460 | ||||||
| chr5:176494461
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0218 | 2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.661+186G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494461 | ||||||
| chr5:176494565
|
A | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+290A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494565 | ||||||
| chr5:176494712
|
G | A | 8 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0001t0006g0105others(5): Show | 8 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+437G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494712 | ||||||
| chr5:176494782
|
A | G | 145 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(142): Show | 146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.661+507A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494782 | ||||||
| chr5:176494911
|
G | C | 1 | a0001c0008t0027g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+636G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494911 | ||||||
| chr5:176494935
|
A | G | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(63): Show | 67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.661+660A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494935 | ||||||
| chr5:176495016
|
G | A | 1 | a0001c0008t0027g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+741G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495016 | ||||||
| chr5:176495024
|
CAG | C | 7 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+752_661+753del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495024 | |||||
| chr5:176495154
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661+879G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495154 | ||||||
| chr5:176495225
|
T | C | 1 | a0001c0001t0004g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.661+950T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495225 | ||||||
| chr5:176495409
|
AT | A | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-1068delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495409 | |||||
| chr5:176495505
|
C | A | 97 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(94): Show | 99 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.662-981C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495505 | ||||||
| chr5:176495510
|
AT | A | 23 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0211others(20): Show | 24 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.662-957delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | |||||
| chr5:176495510
|
ATT | A | 211 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(208): Show | 212 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.662-958_662-957del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | |||||
| chr5:176495510
|
ATTT | A | 69 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0158others(66): Show | 70 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.662-959_662-957del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | |||||
| chr5:176495624
|
G | A | 7 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-862G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495624 | ||||||
| chr5:176495793
|
G | GT | 75 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(72): Show | 77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.662-693_662-692ins others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495793 | ||||||
| chr5:176495879
|
G | A | 1 | a0001c0001t0010g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-607G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495879 | ||||||
| chr5:176495954
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.662-532G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495954 | ||||||
| chr5:176496079
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.662-407C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496079 | ||||||
| chr5:176496124
|
C | G | 13 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-362C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496124 | ||||||
| chr5:176496139
|
C | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0205 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.662-347C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496139 | ||||||
| chr5:176496353
|
G | A | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.662-133G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496353 | ||||||
| chr5:176496430
|
G | A | 145 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(142): Show | 146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.662-56G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496430 | ||||||
| chr5:176496704
|
G | A | 1 | a0001c0001t0004g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.839+41G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176496704 | ||||||
| chr5:176496846
|
G | C | 8 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(5): Show | 9 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.839+183G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176496846 | ||||||
| chr5:176497039
|
G | A | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.839+376G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497039 | ||||||
| chr5:176497047
|
G | A | 73 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(70): Show | 75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.839+384G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497047 | ||||||
| chr5:176497073
|
G | A | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+410G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497073 | ||||||
| chr5:176497111
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+448A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497111 | ||||||
| chr5:176497138
|
T | C | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.839+475T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497138 | ||||||
| chr5:176497249
|
T | TA | 19 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(16): Show | 20 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.839+596dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176497249 | |||||
| chr5:176497297
|
T | A | 7 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.839+634T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497297 | ||||||
| chr5:176497366
|
A | T | 307 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(304): Show | 310 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(307): Show |
intron_variant | MODIFIER | c.839+703A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497366 | ||||||
| chr5:176497374
|
C | G | 1 | a0001c0001t0003g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.839+711C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497374 | ||||||
| chr5:176497401
|
T | A | 3 | a0001c0001t0003g0057a0001c0001t0003g0067a0001c0001t0003g0075 | 3 | HG03654.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.839+738T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497401 | ||||||
| chr5:176497410
|
A | G | 2 | a0001c0001t0003g0039a0001c0001t0003g0064 | 2 | HG00558.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.839+747A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497410 | ||||||
| chr5:176497421
|
A | G | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+758A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497421 | ||||||
| chr5:176497872
|
G | A | 1 | a0001c0001t0005g0253 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.840-1042G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497872 | ||||||
| chr5:176498220
|
C | T | 65 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.840-694C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498220 | ||||||
| chr5:176498408
|
TTG | T | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.840-504_840-503del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176498408 | |||||
| chr5:176498820
|
T | TAC | 3 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358 | 3 | NA18990.hp2 NA19002.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.840-78_840-77dupCA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176498820 | |||||
| chr5:176498848
|
A | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.840-66A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498848 | ||||||
| chr5:176498911
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.840-3C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498911 | ||||||
| chr5:176499317
|
G | A | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1011+232G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499317 | ||||||
| chr5:176499382
|
C | T | 1 | a0001c0001t0017g0281 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1011+297C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499382 | ||||||
| chr5:176499600
|
T | C | 86 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(83): Show | 88 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1012-403T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499600 | ||||||
| chr5:176499656
|
A | G | 2 | a0001c0001t0005g0251a0001c0001t0005g0252 | 2 | NA18946.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1012-347A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499656 | ||||||
| chr5:176499745
|
G | C | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.1012-258G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499745 | ||||||
| chr5:176499792
|
C | T | 2 | a0001c0001t0002g0318a0006c0007t0002g0348 | 2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1012-211C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499792 | ||||||
| chr5:176500261
|
C | CAG | 20 | a0001c0001t0006g0083a0001c0001t0006g0103a0001c0001t0006g0104others(17): Show | 20 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1155+133_1155+134d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176500261 | |||||
| chr5:176500307
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1155+161A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500307 | ||||||
| chr5:176500362
|
A | G | 1 | a0001c0001t0003g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1155+216A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500362 | ||||||
| chr5:176500528
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1155+382C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500528 | ||||||
| chr5:176500617
|
C | T | 9 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+471C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500617 | ||||||
| chr5:176500780
|
TAGTC | T | 10 | a0001c0001t0004g0003a0001c0001t0004g0237a0001c0001t0004g0238others(7): Show | 11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+638_1155+641d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176500780 | |||||
| chr5:176500893
|
G | A | 1 | a0001c0001t0002g0328 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1155+747G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500893 | ||||||
| chr5:176501052
|
G | A | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155+906G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501052 | ||||||
| chr5:176501092
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1155+946A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501092 | ||||||
| chr5:176501128
|
A | T | 3 | a0001c0001t0004g0222a0001c0001t0006g0283a0001c0001t0026g0056 | 3 | HG02109.hp2 HG02132.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1155+982A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501128 | ||||||
| chr5:176501132
|
T | A | 12 | a0001c0001t0004g0114a0001c0001t0005g0363a0001c0001t0006g0243others(9): Show | 13 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1155+986T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501132 | ||||||
| chr5:176501133
|
A | T | 8 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(5): Show | 9 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+987A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501133 | ||||||
| chr5:176501133
|
AAATAAT | A | 67 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(64): Show | 68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1155+998_1155+1003 others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176501133 | |||||
| chr5:176501305
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1155+1159G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501305 | ||||||
| chr5:176501382
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1155+1236G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501382 | ||||||
| chr5:176501557
|
C | T | 1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1155+1411C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501557 | ||||||
| chr5:176501564
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1155+1418G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501564 | ||||||
| chr5:176501967
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1155+1821G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501967 | ||||||
| chr5:176501976
|
C | T | 203 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(200): Show | 204 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1155+1830C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501976 | ||||||
| chr5:176502101
|
C | T | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.1155+1955C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502101 | ||||||
| chr5:176502151
|
C | T | 1 | a0001c0001t0006g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1155+2005C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502151 | ||||||
| chr5:176502237
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1155+2091C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502237 | ||||||
| chr5:176502256
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1155+2110A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502256 | ||||||
| chr5:176502309
|
T | C | 1 | a0001c0001t0005g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1155+2163T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502309 | ||||||
| chr5:176502346
|
C | T | 12 | a0001c0001t0004g0137a0001c0001t0004g0149a0001c0001t0004g0169others(9): Show | 12 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1155+2200C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502346 | ||||||
| chr5:176502468
|
G | T | 76 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(73): Show | 78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1155+2322G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502468 | ||||||
| chr5:176502499
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1155+2353G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502499 | ||||||
| chr5:176502521
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1155+2375G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502521 | ||||||
| chr5:176502838
|
A | G | 1 | a0001c0001t0003g0060 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1155+2692A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502838 | ||||||
| chr5:176502997
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1155+2851G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502997 | ||||||
| chr5:176503047
|
CA | C | 76 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0123others(73): Show | 78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1155+2911delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503047 | |||||
| chr5:176503277
|
G | A | 13 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1155+3131G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503277 | ||||||
| chr5:176503329
|
C | T | 6 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(3): Show | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155+3183C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503329 | ||||||
| chr5:176503381
|
C | T | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155+3235C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503381 | ||||||
| chr5:176503486
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0025 | 2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1156-3282C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503486 | ||||||
| chr5:176503487
|
G | A | 144 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0113others(141): Show | 145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1156-3281G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503487 | ||||||
| chr5:176503555
|
CA | C | 273 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(270): Show | 276 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.1156-3196delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503555 | |||||
| chr5:176503555
|
CAA | C | 13 | a0001c0001t0001g0144a0001c0001t0003g0065a0001c0001t0003g0077others(10): Show | 13 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-3197_1156-319 others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503555 | |||||
| chr5:176503884
|
G | A | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1156-2884G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503884 | ||||||
| chr5:176503884
|
G | C | 67 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(64): Show | 68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1156-2884G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503884 | ||||||
| chr5:176504056
|
G | A | 1 | a0001c0001t0010g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1156-2712G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504056 | ||||||
| chr5:176504128
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1156-2640C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504128 | ||||||
| chr5:176504228
|
G | C | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.1156-2540G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504228 | ||||||
| chr5:176504247
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1156-2521G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504247 | ||||||
| chr5:176504305
|
C | T | 1 | a0001c0001t0006g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1156-2463C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504305 | ||||||
| chr5:176504325
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1156-2443C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504325 | ||||||
| chr5:176504451
|
G | T | 1 | a0001c0001t0005g0366 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1156-2317G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504451 | ||||||
| chr5:176504456
|
C | T | 1 | a0001c0001t0022g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1156-2312C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504456 | ||||||
| chr5:176504498
|
C | T | 2 | a0001c0001t0010g0018a0001c0001t0010g0019 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1156-2270C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504498 | ||||||
| chr5:176504532
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-2236C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504532 | ||||||
| chr5:176504743
|
G | T | 1 | a0001c0008t0027g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1156-2025G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504743 | ||||||
| chr5:176504769
|
C | T | 302 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(299): Show | 305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.1156-1999C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504769 | ||||||
| chr5:176504921
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1156-1847G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504921 | ||||||
| chr5:176505001
|
C | T | 7 | a0001c0001t0003g0002a0001c0001t0003g0042a0001c0001t0003g0052others(4): Show | 8 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1156-1767C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505001 | ||||||
| chr5:176505009
|
C | T | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(63): Show | 67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1156-1759C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505009 | ||||||
| chr5:176505010
|
A | G | 364 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(361): Show | 367 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(364): Show |
intron_variant | MODIFIER | c.1156-1758A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505010 | ||||||
| chr5:176505013
|
AC | A | 75 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(72): Show | 76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1156-1753delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505013 | |||||
| chr5:176505015
|
C | G | 75 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0002others(72): Show | 76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1156-1753C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505015 | ||||||
| chr5:176505023
|
G | GA | 7 | a0001c0001t0001g0126a0001c0001t0001g0196a0001c0001t0002g0309others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-1727dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505023 | |||||
| chr5:176505023
|
GA | G | 71 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0156others(68): Show | 72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1156-1727delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505023 | |||||
| chr5:176505024
|
A | G | 2 | a0001c0001t0007g0017a0006c0007t0002g0348 | 2 | HG02896.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1156-1744A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505024 | ||||||
| chr5:176505213
|
A | G | 1 | a0001c0001t0010g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1156-1555A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505213 | ||||||
| chr5:176505375
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1156-1393T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505375 | ||||||
| chr5:176505455
|
A | G | 9 | a0001c0001t0001g0126a0001c0001t0009g0096a0001c0001t0009g0098others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1156-1313A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505455 | ||||||
| chr5:176505467
|
G | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-1301G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505467 | ||||||
| chr5:176505646
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG01975.hp1 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1156-1122A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505646 | ||||||
| chr5:176505692
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0228a0001c0001t0004g0198 | 3 | HG02976.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1156-1076A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505692 | ||||||
| chr5:176505703
|
G | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-1065G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505703 | ||||||
| chr5:176505709
|
T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0147others(1): Show | 4 | NA18612.hp1 NA18939.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-1059T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505709 | ||||||
| chr5:176505957
|
G | A | 1 | a0001c0001t0010g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1156-811G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505957 | ||||||
| chr5:176506024
|
G | A | 303 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(300): Show | 306 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.1156-744G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506024 | ||||||
| chr5:176506034
|
C | T | 5 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156-734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506034 | ||||||
| chr5:176506059
|
C | T | 148 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(145): Show | 149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1156-709C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506059 | ||||||
| chr5:176506192
|
C | CA | 13 | a0001c0001t0001g0161a0001c0001t0001g0182a0001c0001t0001g0215others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-562dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506192 | |||||
| chr5:176506194
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | NA18955.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-560_1156-548d others(15): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506194 | |||||
| chr5:176506201
|
A | AC | 3 | a0001c0001t0010g0004a0001c0001t0010g0005a0001c0001t0010g0019 | 3 | HG02486.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1156-567_1156-566i others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506201 | ||||||
| chr5:176506204
|
A | AC | 20 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(17): Show | 20 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1156-564_1156-563i others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506204 | ||||||
| chr5:176506204
|
A | C | 10 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(7): Show | 11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-564A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506204 | ||||||
| chr5:176506205
|
A | C | 66 | a0001c0001t0001g0117a0001c0001t0003g0002a0001c0001t0003g0027others(63): Show | 67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1156-563A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506205 | ||||||
| chr5:176506206
|
AC | A | 7 | a0001c0001t0007g0001a0001c0001t0007g0015a0001c0001t0007g0016others(4): Show | 8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1156-561delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506206 | ||||||
| chr5:176506207
|
C | A | 74 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0215others(71): Show | 75 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1156-561C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506207 | ||||||
| chr5:176506208
|
A | C | 1 | a0001c0001t0005g0269 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1156-560A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506208 | ||||||
| chr5:176506209
|
A | C | 73 | a0001c0001t0001g0117a0001c0001t0003g0002a0001c0001t0003g0027others(70): Show | 75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1156-559A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506209 | ||||||
| chr5:176506210
|
A | C | 10 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-558A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506210 | ||||||
| chr5:176506359
|
A | G | 1 | a0001c0001t0033g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1156-409A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506359 | ||||||
| chr5:176506543
|
G | T | 7 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0009g0099others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-225G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506543 | ||||||
| chr5:176506588
|
T | C | 1 | a0001c0008t0027g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1156-180T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506588 | ||||||
| chr5:176506690
|
TGTGTGTG others(1): Show |
T | 204 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0094others(201): Show | 205 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1156-62_1156-55del others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506690 | |||||
| chr5:176506699
|
G | T | 4 | a0001c0001t0005g0026a0001c0001t0005g0270a0001c0001t0005g0275others(1): Show | 4 | NA18953.hp1 NA18965.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-69G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506699 | ||||||
| chr5:176506707
|
G | A | 1 | a0001c0001t0005g0101 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1156-61G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506707 |