Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3426 |
|---|---|
| ensemblid | ENSG00000205403.15 |
| hgncid | 5394 |
| symbol | CFI |
| name | complement factor I |
| refseq_nuc | NM_000204.5 |
| refseq_prot | NP_000195.3 |
| ensembl_nuc | ENST00000394634.7 |
| ensembl_prot | ENSP00000378130.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 109740695 |
| end | 109801999 |
| strand | - |
| ver | v1.2 |
| region | chr4:109740695-109801999 |
| region5000 | chr4:109735695-109806999 |
| regionname0 | CFI_chr4_109740695_109801999 |
| regionname5000 | CFI_chr4_109735695_109806999 |
| 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 | 0/1 | 583 | 310 | 77 | 63 | 134 | 14 | 21 | 108 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0002 | 0/0 | 583 | 17 | 0 | 0 | 15 | 0 | 2 | 9 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0003 | 1/0 | 583 | 15 | 13 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0004 | 0/0 | 583 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0005 | 0/0 | 583 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0006 | 0/0 | 583 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0007 | 0/0 | 583 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0008 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0009 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0010 | 0/0 | 583 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0011 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| 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 | 0/1 | 1752 | 182 | 48 | 32 | 72 | 12 | 17 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0002 | 0/0 | 1752 | 124 | 25 | 31 | 62 | 2 | 4 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0003 | 0/0 | 1752 | 17 | 0 | 0 | 15 | 0 | 2 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0004 | 1/0 | 1752 | 15 | 13 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0005 | 0/0 | 1752 | 4 | 0 | 0 | 4 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0006 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0007 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0008 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0009 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0010 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0011 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0012 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0013 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| c0014 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| 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 | 227 | 330 | 73 | 64 | 154 | 14 | 24 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| t0002 | 1/0 | 227 | 13 | 11 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| t0003 | 0/0 | 227 | 6 | 6 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| t0004 | 0/0 | 227 | 3 | 0 | 3 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| t0005 | 0/0 | 227 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| 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 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| 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 | 0/1 | 1752 | 182 | 48 | 32 | 72 | 12 | 17 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0002 | 0/0 | 1752 | 124 | 25 | 31 | 62 | 2 | 4 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0006 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0008 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0002c0003 | 0/0 | 1752 | 17 | 0 | 0 | 15 | 0 | 2 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0003c0004 | 1/0 | 1752 | 15 | 13 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0004c0005 | 0/0 | 1752 | 4 | 0 | 0 | 4 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0005c0007 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0006c0014 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0007c0010 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0008c0012 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0009c0011 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0010c0013 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0011c0009 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1978 | 174 | 40 | 32 | 72 | 12 | 17 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0001t0002 | 0/0 | 1978 | 3 | 3 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0001t0003 | 0/0 | 1978 | 5 | 5 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0002t0001 | 0/0 | 1978 | 114 | 19 | 27 | 62 | 2 | 4 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0002t0002 | 0/0 | 1978 | 6 | 5 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0002t0003 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0002t0004 | 0/0 | 1978 | 3 | 0 | 3 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0006t0005 | 0/0 | 1978 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0008t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0001c0008t0002 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0002c0003t0001 | 0/0 | 1978 | 17 | 0 | 0 | 15 | 0 | 2 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0003c0004t0001 | 0/0 | 1978 | 12 | 11 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0003c0004t0002 | 1/0 | 1978 | 3 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0004c0005t0001 | 0/0 | 1978 | 4 | 0 | 0 | 4 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0005c0007t0001 | 0/0 | 1978 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0006c0014t0001 | 0/0 | 1978 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0007c0010t0001 | 0/0 | 1978 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0008c0012t0001 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0009c0011t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0010c0013t0001 | 0/0 | 1978 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| a0011c0009t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | copy fasta | chr4 | 109735695 | 109806999 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0006t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0006t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0008t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0008t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0005c0007t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0005c0007t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0006c0014t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0007c0010t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0008c0012t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0009c0011t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0010c0013t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0011c0009t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | GBR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0061 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0309 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0150 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01074 | hp1 | a0005 | c0007 | t0001 | g0070 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01081 | hp1 | a0005 | c0007 | t0001 | g0069 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01106 | hp2 | a0006 | c0014 | t0001 | g0064 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01891 | hp2 | a0003 | c0004 | t0002 | g0029 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01975 | hp1 | a0010 | c0013 | t0001 | g0297 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0306 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0308 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0013 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0321 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02615 | hp1 | a0009 | c0011 | t0001 | g0113 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0034 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0014 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02647 | hp1 | a0001 | c0006 | t0005 | g0041 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0020 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02738 | hp2 | a0007 | c0010 | t0001 | g0062 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0296 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0149 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0030 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0152 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03041 | hp1 | a0001 | c0006 | t0005 | g0042 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03130 | hp2 | a0003 | c0004 | t0002 | g0033 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0337 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0322 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03516 | hp2 | a0001 | c0008 | t0002 | g0269 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03579 | hp1 | a0001 | c0008 | t0001 | g0293 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0304 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0324 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0314 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18941 | hp2 | a0004 | c0005 | t0001 | g0101 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0317 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0316 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0320 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18989 | hp2 | a0008 | c0012 | t0001 | g0189 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18999 | hp2 | a0004 | c0005 | t0001 | g0103 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19000 | hp1 | a0004 | c0005 | t0001 | g0109 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0318 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19070 | hp2 | a0004 | c0005 | t0001 | g0102 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0325 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ASW | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0060 | EUR | TSI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0348 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20300 | hp2 | a0011 | c0009 | t0001 | g0106 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0229 | REF | REF | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| homoSapiens_grch38 | hp1 | a0003 | c0004 | t0002 | g0032 | REF | REF | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109740897
|
A | G | 1 | a0008 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1748T>C | p.Val583Ala | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 1776/1978 | 1748/1752 | 583/583 | chr4 | 109740897 | ||
| chr4:109740964
|
T | C | 1 | a0007 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1681A>G | p.Lys561Glu | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 1709/1978 | 1681/1752 | 561/583 | chr4 | 109740964 | ||
| chr4:109746405
|
T | G | 1 | a0009 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1246A>C | p.Ile416Leu | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1274/1978 | 1246/1752 | 416/583 | chr4 | 109746405 | ||
| chr4:109746434
|
C | T | 1 | a0002 | 17 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(14): Show |
missense_variant | MODERATE | c.1217G>A | p.Arg406His | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1245/1978 | 1217/1752 | 406/583 | chr4 | 109746434 | ||
| chr4:109752492
|
T | C | 1 | a0010 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.916A>G | p.Ile306Val | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/13 | 944/1978 | 916/1752 | 306/583 | chr4 | 109752492 | ||
| chr4:109757769
|
T | C | 10 | a0001a0002a0004others(7): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
missense_variant | MODERATE | c.898A>G | p.Thr300Ala | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/13 | 926/1978 | 898/1752 | 300/583 | chr4 | 109757769 | ||
| chr4:109760294
|
C | T | 1 | a0011 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.859G>A | p.Gly287Arg | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/13 | 887/1978 | 859/1752 | 287/583 | chr4 | 109760294 | ||
| chr4:109761572
|
T | G | 1 | a0004 | 4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
missense_variant | MODERATE | c.603A>C | p.Arg201Ser | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 631/1978 | 603/1752 | 201/583 | chr4 | 109761572 | ||
| chr4:109761605
|
C | A | 1 | a0006 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.570G>T | p.Glu190Asp | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 598/1978 | 570/1752 | 190/583 | chr4 | 109761605 | ||
| chr4:109761673
|
T | C | 1 | a0005 | 2 | HG01074.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.502A>G | p.Arg168Gly | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 530/1978 | 502/1752 | 168/583 | chr4 | 109761673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109746445
|
G | A | 1 | a0001c0006 | 2 | HG02647.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.1206C>T | p.Pro402Pro | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1234/1978 | 1206/1752 | 402/583 | chr4 | 109746445 | ||
| chr4:109760349
|
C | T | 9 | a0001c0002a0001c0006a0001c0008others(6): Show | 138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
synonymous_variant | LOW | c.804G>A | p.Ser268Ser | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/13 | 832/1978 | 804/1752 | 268/583 | chr4 | 109760349 | ||
| chr4:109766567
|
T | A | 1 | a0001c0008 | 2 | HG03516.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.315A>T | p.Thr105Thr | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/13 | 343/1978 | 315/1752 | 105/583 | chr4 | 109766567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109740749
|
A | G | 1 | a0001c0006t0005 | 2 | HG02647.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 144 | chr4 | 109740749 | |||||
| chr4:109740781
|
G | A | 17 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(14): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*112C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 112 | chr4 | 109740781 | |||||
| chr4:109740886
|
C | A | 2 | a0001c0001t0003a0001c0002t0003 | 6 | HG02258.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 7 | chr4 | 109740886 | |||||
| chr4:109801984
|
C | T | 1 | a0001c0002t0004 | 3 | HG01070.hp1 HG01071.hp1 HG01257.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/13 | 13 | chr4 | 109801984 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109741297
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0249 | 2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1535-187G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741297 | ||||||
| chr4:109741593
|
A | G | 9 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0332others(6): Show | 9 | HG01975.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1535-483T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741593 | ||||||
| chr4:109741777
|
T | C | 3 | a0003c0004t0001g0149a0003c0004t0001g0150a0003c0004t0001g0304 | 3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1535-667A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741777 | ||||||
| chr4:109741982
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0251 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1534+509T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741982 | ||||||
| chr4:109741993
|
A | AATTTACT others(37): Show |
1 | a0001c0001t0001g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1534+454_1534+497d others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741993 | ||||||
| chr4:109742038
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1534+453T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742038 | ||||||
| chr4:109742250
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1534+241C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742250 | ||||||
| chr4:109742285
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1534+206G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742285 | ||||||
| chr4:109742313
|
T | A | 1 | a0001c0002t0001g0145 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1534+178A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742313 | ||||||
| chr4:109742354
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1534+137C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742354 | ||||||
| chr4:109742708
|
A | G | 5 | a0001c0001t0001g0164a0001c0001t0001g0188a0001c0001t0001g0193others(2): Show | 5 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1430-113T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742708 | ||||||
| chr4:109742735
|
G | A | 1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1430-140C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742735 | ||||||
| chr4:109742841
|
T | C | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(344): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1430-246A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742841 | ||||||
| chr4:109742901
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0223a0001c0001t0001g0228 | 3 | HG02155.hp2 NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1430-306T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742901 | ||||||
| chr4:109743047
|
G | T | 5 | a0001c0002t0001g0175a0001c0002t0001g0176a0003c0004t0001g0149others(2): Show | 5 | HG00738.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1430-452C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743047 | ||||||
| chr4:109743474
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(260): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1430-879A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743474 | ||||||
| chr4:109743480
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1430-885C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743480 | ||||||
| chr4:109743561
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0197others(5): Show | 8 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-966A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743561 | ||||||
| chr4:109743641
|
C | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0151others(26): Show | 30 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1430-1046G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743641 | ||||||
| chr4:109743727
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1430-1132G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743727 | ||||||
| chr4:109743859
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1430-1264T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743859 | ||||||
| chr4:109743903
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1430-1308A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743903 | ||||||
| chr4:109744056
|
CCATTCTC others(21): Show |
C | 1 | a0001c0002t0001g0008 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1430-1489_1430-146 others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744056 | ||||||
| chr4:109744073
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0131 | 3 | HG02723.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1430-1478A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744073 | ||||||
| chr4:109744085
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1430-1490T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744085 | ||||||
| chr4:109744091
|
A | C | 19 | a0001c0001t0001g0196a0001c0001t0001g0313a0002c0003t0001g0259others(16): Show | 19 | HG00544.hp2 HG00673.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1430-1496T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744091 | ||||||
| chr4:109744254
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1430-1659C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744254 | ||||||
| chr4:109744325
|
T | C | 103 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0163others(100): Show | 104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1430-1730A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744325 | ||||||
| chr4:109744393
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0195 | 2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1430-1798G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744393 | ||||||
| chr4:109744486
|
A | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG00438.hp1 NA18945.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1429+1736T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744486 | ||||||
| chr4:109744622
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0239 | 2 | HG00438.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1429+1600G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744622 | ||||||
| chr4:109745015
|
T | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1429+1207A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745015 | ||||||
| chr4:109745115
|
C | T | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1429+1107G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745115 | ||||||
| chr4:109745136
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1429+1086C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745136 | ||||||
| chr4:109745152
|
A | G | 3 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0001g0181 | 3 | HG00735.hp2 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1429+1070T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745152 | ||||||
| chr4:109745171
|
C | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1429+1051G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745171 | ||||||
| chr4:109745275
|
C | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1429+947G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745275 | ||||||
| chr4:109745326
|
G | C | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1429+896C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745326 | ||||||
| chr4:109745392
|
T | A | 1 | a0009c0011t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+830A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745392 | ||||||
| chr4:109745687
|
G | A | 2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1429+535C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745687 | ||||||
| chr4:109745723
|
C | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0120a0003c0004t0001g0030others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+499G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745723 | ||||||
| chr4:109746144
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1429+78C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109746144 | ||||||
| chr4:109746189
|
T | C | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(41): Show | 44 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+33A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109746189 | ||||||
| chr4:109746530
|
A | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1149-28T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746530 | ||||||
| chr4:109746663
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | NA18979.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1149-161C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746663 | ||||||
| chr4:109746710
|
G | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1149-208C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746710 | ||||||
| chr4:109746806
|
G | C | 1 | a0001c0002t0001g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1149-304C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746806 | ||||||
| chr4:109746972
|
T | C | 3 | a0003c0004t0001g0149a0003c0004t0001g0150a0003c0004t0001g0304 | 3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1149-470A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746972 | ||||||
| chr4:109746998
|
C | A | 1 | a0001c0001t0001g0209 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1149-496G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746998 | ||||||
| chr4:109747150
|
C | T | 3 | a0001c0002t0004g0005a0001c0002t0004g0006a0001c0002t0004g0007 | 3 | HG01070.hp1 HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1149-648G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747150 | ||||||
| chr4:109747158
|
C | T | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149-656G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747158 | ||||||
| chr4:109747172
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1149-670C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747172 | ||||||
| chr4:109747354
|
T | TA | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149-853dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747354 | ||||||
| chr4:109747361
|
A | AT | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1149-860dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747361 | ||||||
| chr4:109747373
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149-871T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747373 | ||||||
| chr4:109747495
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1149-993C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747495 | ||||||
| chr4:109747531
|
T | A | 1 | a0001c0002t0001g0179 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1149-1029A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747531 | ||||||
| chr4:109747564
|
T | G | 1 | a0001c0002t0001g0008 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1149-1062A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747564 | ||||||
| chr4:109747566
|
G | T | 1 | a0001c0002t0001g0008 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1149-1064C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747566 | ||||||
| chr4:109747744
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149-1242C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747744 | ||||||
| chr4:109747801
|
G | A | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1149-1299C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747801 | ||||||
| chr4:109747824
|
C | G | 342 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1149-1322G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747824 | ||||||
| chr4:109747992
|
G | C | 1 | a0002c0003t0001g0314 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1148+1226C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747992 | ||||||
| chr4:109748045
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1148+1173G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748045 | ||||||
| chr4:109748105
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1148+1113T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748105 | ||||||
| chr4:109748199
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1148+1019C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748199 | ||||||
| chr4:109748264
|
T | C | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1148+954A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748264 | ||||||
| chr4:109748457
|
C | A | 1 | a0001c0002t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1148+761G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748457 | ||||||
| chr4:109748639
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148+579C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748639 | ||||||
| chr4:109748644
|
A | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1148+574T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748644 | ||||||
| chr4:109748692
|
G | A | 1 | a0002c0003t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1148+526C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748692 | ||||||
| chr4:109748696
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1148+522G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748696 | ||||||
| chr4:109748769
|
G | A | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1148+449C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748769 | ||||||
| chr4:109748818
|
T | C | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1148+400A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748818 | ||||||
| chr4:109748876
|
C | T | 4 | a0001c0001t0001g0156a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG01256.hp1 HG03491.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+342G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748876 | ||||||
| chr4:109749183
|
C | T | 3 | a0001c0001t0003g0347a0001c0001t0003g0348a0010c0013t0001g0297 | 3 | HG01975.hp1 HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1148+35G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109749183 | ||||||
| chr4:109749651
|
G | C | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(336): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.941-49C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749651 | ||||||
| chr4:109749747
|
C | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-145G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749747 | ||||||
| chr4:109749873
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-271G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749873 | ||||||
| chr4:109750003
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.941-401A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750003 | ||||||
| chr4:109750027
|
C | T | 1 | a0001c0001t0003g0347 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.941-425G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750027 | ||||||
| chr4:109750082
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.941-480G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750082 | ||||||
| chr4:109750154
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096 | 3 | HG01069.hp1 HG01071.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.941-552C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750154 | ||||||
| chr4:109750280
|
A | G | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.941-678T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750280 | ||||||
| chr4:109750384
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-782T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750384 | ||||||
| chr4:109750385
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.941-783A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750385 | ||||||
| chr4:109750545
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.941-943G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750545 | ||||||
| chr4:109750567
|
C | G | 2 | a0005c0007t0001g0069a0005c0007t0001g0070 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.941-965G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750567 | ||||||
| chr4:109750577
|
A | T | 1 | a0001c0001t0001g0162 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.941-975T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750577 | ||||||
| chr4:109750709
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.941-1107G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750709 | ||||||
| chr4:109750722
|
G | T | 3 | a0001c0002t0001g0119a0001c0002t0001g0126a0001c0002t0001g0217 | 3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.941-1120C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750722 | ||||||
| chr4:109750770
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(12): Show | 16 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.941-1168T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750770 | ||||||
| chr4:109751039
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.940+1429T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751039 | ||||||
| chr4:109751070
|
CACAGACC others(27): Show |
C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+1364_940+1397d others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751070 | ||||||
| chr4:109751128
|
C | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.940+1340G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751128 | ||||||
| chr4:109751129
|
A | G | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.940+1339T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751129 | ||||||
| chr4:109751384
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0239 | 2 | HG00438.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.940+1084C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751384 | ||||||
| chr4:109751413
|
A | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.940+1055T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751413 | ||||||
| chr4:109751426
|
C | T | 2 | a0001c0001t0001g0313a0008c0012t0001g0189 | 2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.940+1042G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751426 | ||||||
| chr4:109751438
|
C | CT | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.940+1029dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | ||||||
| chr4:109751438
|
C | CTT | 38 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0185others(35): Show | 38 | HG00544.hp1 HG00673.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.940+1028_940+1029d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | ||||||
| chr4:109751438
|
CT | C | 80 | a0001c0002t0001g0001a0001c0002t0001g0022a0001c0002t0001g0035others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.940+1029delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | ||||||
| chr4:109751614
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.940+854T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751614 | ||||||
| chr4:109751629
|
T | A | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.940+839A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751629 | ||||||
| chr4:109751646
|
G | GGCCAGGC others(10): Show |
1 | a0002c0003t0001g0306 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.940+805_940+821dup others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751646 | ||||||
| chr4:109752041
|
C | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(55): Show | 58 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.940+427G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109752041 | ||||||
| chr4:109752158
|
C | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.940+310G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109752158 | ||||||
| chr4:109752647
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-144C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752647 | ||||||
| chr4:109752729
|
CTA | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-228_905-227del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752729 | ||||||
| chr4:109752797
|
C | G | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(331): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.905-294G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752797 | ||||||
| chr4:109752864
|
A | G | 9 | a0001c0001t0001g0098a0001c0001t0001g0270a0001c0001t0001g0327others(6): Show | 9 | HG01109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-361T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752864 | ||||||
| chr4:109752882
|
A | ATATAATA others(25): Show |
4 | a0001c0001t0001g0344a0001c0001t0003g0148a0001c0002t0001g0046others(1): Show | 4 | HG03041.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-411_905-380dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752882 | ||||||
| chr4:109752890
|
T | TATATTTA others(25): Show |
1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-388_905-387ins others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752890 | ||||||
| chr4:109752927
|
T | C | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-424A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752927 | ||||||
| chr4:109752935
|
TA | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-433delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752935 | ||||||
| chr4:109752936
|
A | ATTTATTA others(4): Show |
84 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(81): Show | 84 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.905-434_905-433ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752936 | ||||||
| chr4:109752936
|
A | G | 20 | a0001c0001t0001g0208a0001c0001t0001g0312a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-433T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752936 | ||||||
| chr4:109752938
|
A | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-435T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752938 | ||||||
| chr4:109752940
|
A | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-437T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752940 | ||||||
| chr4:109752942
|
A | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-439T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752942 | ||||||
| chr4:109752946
|
T | A | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-443A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752946 | ||||||
| chr4:109752947
|
TA | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-445delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752947 | ||||||
| chr4:109752949
|
T | G | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-446A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752949 | ||||||
| chr4:109752951
|
ATACATAT others(4): Show |
A | 36 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0100others(33): Show | 36 | HG00438.hp2 HG00544.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.905-459_905-449del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752951 | ||||||
| chr4:109752953
|
A | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-450T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752953 | ||||||
| chr4:109752954
|
C | A | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-451G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | ||||||
| chr4:109752954
|
C | G | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.905-451G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | ||||||
| chr4:109752954
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.905-451G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | ||||||
| chr4:109752962
|
T | TAA | 5 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0075others(2): Show | 6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-460_905-459ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | ||||||
| chr4:109752962
|
T | TTATATAA others(14): Show |
80 | a0001c0001t0001g0009a0001c0001t0001g0215a0001c0002t0001g0008others(77): Show | 80 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.905-460_905-459ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | ||||||
| chr4:109752962
|
T | TTATATAA others(46): Show |
3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-460_905-459ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | ||||||
| chr4:109752962
|
T | TTATATGA others(57): Show |
1 | a0001c0001t0001g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.905-460_905-459ins others(64): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | ||||||
| chr4:109752965
|
T | TATGAATA others(1): Show |
17 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(14): Show | 17 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(14): Show |
intron_variant | MODIFIER | c.905-463_905-462ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752965 | ||||||
| chr4:109752974
|
T | A | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-471A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752974 | ||||||
| chr4:109752977
|
A | ATATAT | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-475_905-474ins others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752977 | ||||||
| chr4:109752979
|
G | A | 90 | a0001c0001t0001g0174a0001c0001t0001g0241a0001c0001t0001g0275others(87): Show | 91 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.905-476C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752979 | ||||||
| chr4:109752979
|
G | T | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-476C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752979 | ||||||
| chr4:109752981
|
A | T | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-478T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752981 | ||||||
| chr4:109752984
|
A | T | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-481T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752984 | ||||||
| chr4:109752992
|
T | TTATATA | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-490_905-489ins others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752992 | ||||||
| chr4:109752994
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.905-502_905-492del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752994 | ||||||
| chr4:109752997
|
T | A | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-494A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752997 | ||||||
| chr4:109753005
|
T | TAA | 18 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-503_905-502ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | ||||||
| chr4:109753005
|
T | TTATATAA others(14): Show |
6 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG00558.hp1 HG02559.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-503_905-502ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | ||||||
| chr4:109753005
|
T | TTATATAT others(25): Show |
55 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0098others(52): Show | 56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.905-534_905-503dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | ||||||
| chr4:109753014
|
TA | T | 3 | a0001c0002t0001g0059a0001c0002t0001g0063a0001c0002t0001g0078 | 3 | HG01993.hp2 NA18945.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.905-512delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753014 | ||||||
| chr4:109753015
|
AT | A | 75 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(72): Show | 76 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.905-513delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753015 | ||||||
| chr4:109753022
|
A | G | 59 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(56): Show | 59 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.905-519T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753022 | ||||||
| chr4:109753025
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-522A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753025 | ||||||
| chr4:109753048
|
T | TTATATAA others(14): Show |
11 | a0001c0002t0001g0057a0001c0002t0001g0061a0001c0002t0001g0065others(8): Show | 11 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(110): Show |
1 | a0001c0008t0001g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-546_905-545ins others(117): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(142): Show |
1 | a0001c0008t0002g0269 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.905-546_905-545ins others(149): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(46): Show |
5 | a0001c0002t0001g0142a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(14): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(78): Show |
2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(85): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(120): Show |
8 | a0002c0003t0001g0306a0002c0003t0001g0307a0002c0003t0001g0309others(5): Show | 8 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(127): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(87): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0195 | 2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(55): Show |
81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(78): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(62): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(87): Show |
11 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0262others(8): Show | 11 | HG00741.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(119): Show |
1 | a0001c0001t0001g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.905-546_905-545ins others(126): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
T | TTATATAA others(87): Show |
1 | a0001c0001t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753048
|
TTATATAT others(3): Show |
T | 67 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0331others(64): Show | 68 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.905-555_905-546del others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | ||||||
| chr4:109753049
|
T | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-546A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753049 | ||||||
| chr4:109753058
|
A | AT | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(136): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.905-556dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATAAA others(195): Show |
1 | a0001c0002t0001g0047 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.905-556_905-555ins others(202): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATATA others(163): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-556_905-555ins others(170): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATATA others(195): Show |
39 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(36): Show | 39 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.905-556_905-555ins others(202): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATATA others(227): Show |
1 | a0001c0002t0001g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.905-556_905-555ins others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATATA others(132): Show |
1 | a0002c0003t0001g0318 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.905-556_905-555ins others(139): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753058
|
A | ATTATGTA others(99): Show |
1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-556_905-555ins others(106): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | ||||||
| chr4:109753063
|
TA | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0098others(64): Show | 68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.905-561delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753063 | ||||||
| chr4:109753067
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(137): Show | 143 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.905-564A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753067 | ||||||
| chr4:109753095
|
TA | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-593delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753095 | ||||||
| chr4:109753099
|
C | CAAATATT others(25): Show |
5 | a0003c0004t0001g0013a0003c0004t0001g0014a0003c0004t0001g0030others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-628_905-597dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | ||||||
| chr4:109753099
|
C | CAAATATT others(24): Show |
1 | a0003c0004t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.905-597_905-596ins others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | ||||||
| chr4:109753099
|
C | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(252): Show | 258 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.905-596G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | ||||||
| chr4:109753125
|
TATAA | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-626_905-623del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753125 | ||||||
| chr4:109753128
|
A | ATTTATAT others(2): Show |
8 | a0001c0001t0001g0018a0001c0002t0001g0054a0001c0002t0001g0119others(5): Show | 8 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-626_905-625ins others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753128 | ||||||
| chr4:109753131
|
T | C | 10 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(7): Show | 10 | HG02155.hp1 HG02523.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.905-628A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753131 | ||||||
| chr4:109753134
|
ATATTTAT others(10): Show |
A | 9 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-648_905-632del others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753134 | ||||||
| chr4:109753150
|
TTTA | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-650_905-648del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753150 | ||||||
| chr4:109753151
|
T | G | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-648A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753151 | ||||||
| chr4:109753159
|
TA | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-657delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753159 | ||||||
| chr4:109753160
|
A | G | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-657T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753160 | ||||||
| chr4:109753163
|
T | C | 9 | a0001c0001t0001g0018a0001c0002t0001g0054a0001c0002t0001g0119others(6): Show | 9 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-660A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753163 | ||||||
| chr4:109753174
|
A | AAC | 9 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AAT | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.905-673_905-672dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(42): Show |
1 | a0001c0001t0001g0017 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.905-672_905-671ins others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(106): Show |
1 | a0001c0008t0001g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(113): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(74): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0292 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.905-672_905-671ins others(81): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(138): Show |
6 | a0001c0001t0001g0277a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(145): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(170): Show |
1 | a0002c0003t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(177): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(106): Show |
5 | a0001c0001t0001g0160a0001c0001t0001g0218a0001c0001t0001g0220others(2): Show | 5 | HG00735.hp1 HG00738.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(113): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753174
|
A | AATATATA others(112): Show |
1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(119): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | ||||||
| chr4:109753181
|
T | G | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-678A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753181 | ||||||
| chr4:109753183
|
A | C | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0195others(2): Show | 5 | HG01175.hp1 HG01256.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-680T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753183 | ||||||
| chr4:109753189
|
TA | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-687delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753189 | ||||||
| chr4:109753193
|
T | C | 8 | a0001c0001t0001g0018a0001c0002t0001g0054a0001c0002t0001g0119others(5): Show | 8 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-690A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753193 | ||||||
| chr4:109753195
|
AATATTTA others(6): Show |
A | 1 | a0003c0004t0001g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.905-705_905-693del others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753195 | ||||||
| chr4:109753200
|
T | TA | 63 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(60): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-698_905-697ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753200 | ||||||
| chr4:109753203
|
T | TA | 63 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(60): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-701dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753203 | ||||||
| chr4:109753204
|
AAT | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-703_905-702del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753204 | ||||||
| chr4:109753206
|
TATATATT others(4): Show |
T | 3 | a0001c0002t0001g0054a0001c0002t0001g0136a0003c0004t0001g0150 | 3 | HG00738.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-714_905-704del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753206 | ||||||
| chr4:109753208
|
T | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(60): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-705A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753208 | ||||||
| chr4:109753213
|
T | G | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-710A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753213 | ||||||
| chr4:109753215
|
A | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(80): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.905-712T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753215 | ||||||
| chr4:109753216
|
T | TTATATAA others(14): Show |
5 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0126others(2): Show | 5 | HG01074.hp2 HG01243.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | ||||||
| chr4:109753216
|
T | TTATATAA others(14): Show |
16 | a0001c0001t0001g0018a0001c0001t0001g0098a0001c0001t0001g0312others(13): Show | 16 | HG02109.hp2 HG02155.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | ||||||
| chr4:109753216
|
T | TTATATAA others(46): Show |
1 | a0001c0001t0003g0347 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.905-714_905-713ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | ||||||
| chr4:109753216
|
T | TTATATAA others(93): Show |
2 | a0002c0003t0001g0316a0002c0003t0001g0317 | 2 | NA18952.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.905-714_905-713ins others(100): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | ||||||
| chr4:109753216
|
T | TTATATAA others(61): Show |
19 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0165others(16): Show | 19 | HG00280.hp2 HG00639.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(68): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | ||||||
| chr4:109753217
|
A | AAC | 63 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(60): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-715_905-714ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | ||||||
| chr4:109753217
|
A | C | 21 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0165others(18): Show | 21 | HG00280.hp2 HG00639.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.905-714T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | ||||||
| chr4:109753217
|
A | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.905-714T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | ||||||
| chr4:109753219
|
T | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-716A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753219 | ||||||
| chr4:109753219
|
T | TATAA | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.905-717_905-716ins others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753219 | ||||||
| chr4:109753223
|
T | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.905-720A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753223 | ||||||
| chr4:109753224
|
T | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.905-721A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753224 | ||||||
| chr4:109753225
|
T | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-722A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753225 | ||||||
| chr4:109753226
|
AT | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-724delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753226 | ||||||
| chr4:109753227
|
T | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-724A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753227 | ||||||
| chr4:109753228
|
A | AATATATA others(21): Show |
1 | a0001c0002t0001g0273 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.905-726_905-725ins others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | ||||||
| chr4:109753228
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.905-726_905-725ins others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | ||||||
| chr4:109753228
|
A | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.905-725T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | ||||||
| chr4:109753231
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-728T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753231 | ||||||
| chr4:109753232
|
T | TTTA | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-730_905-729ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753232 | ||||||
| chr4:109753233
|
A | AAATAAAT others(24): Show |
2 | a0003c0004t0001g0020a0003c0004t0002g0029 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.905-761_905-731dup others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753233 | ||||||
| chr4:109753233
|
A | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-730T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753233 | ||||||
| chr4:109753234
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-731T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753234 | ||||||
| chr4:109753235
|
A | T | 1 | a0001c0002t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.905-732T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753235 | ||||||
| chr4:109753236
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-733A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753236 | ||||||
| chr4:109753238
|
A | T | 12 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(9): Show | 12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-735T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753238 | ||||||
| chr4:109753245
|
A | C | 6 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(3): Show | 6 | HG00280.hp1 NA18983.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-742T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753245 | ||||||
| chr4:109753247
|
A | T | 8 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(5): Show | 8 | HG00280.hp1 HG01081.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-744T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753247 | ||||||
| chr4:109753248
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-745T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753248 | ||||||
| chr4:109753249
|
T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.905-746A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753249 | ||||||
| chr4:109753249
|
T | TATATATT others(4): Show |
1 | a0001c0008t0001g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-747_905-746ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753249 | ||||||
| chr4:109753250
|
AT | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-748delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753250 | ||||||
| chr4:109753251
|
T | TAA | 8 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(5): Show | 8 | HG00280.hp1 HG01081.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-749_905-748ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753251 | ||||||
| chr4:109753254
|
A | T | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-751T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753254 | ||||||
| chr4:109753255
|
T | A | 11 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-752A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753255 | ||||||
| chr4:109753256
|
T | A | 12 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(9): Show | 12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-753A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753256 | ||||||
| chr4:109753259
|
T | A | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-756A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753259 | ||||||
| chr4:109753260
|
T | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0160a0001c0001t0001g0218others(22): Show | 25 | HG00735.hp1 HG00738.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.905-757A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753260 | ||||||
| chr4:109753260
|
TA | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-758delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753260 | ||||||
| chr4:109753264
|
T | TA | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.905-762dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753264 | ||||||
| chr4:109753264
|
T | TATTTATT others(5): Show |
68 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(65): Show | 68 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.905-762_905-761ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753264 | ||||||
| chr4:109753265
|
A | ATTTATTA others(1): Show |
24 | a0001c0001t0001g0017a0001c0001t0001g0160a0001c0001t0001g0218others(21): Show | 24 | HG00735.hp1 HG00738.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.905-763_905-762ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753265 | ||||||
| chr4:109753267
|
T | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-764A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753267 | ||||||
| chr4:109753269
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-766T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753269 | ||||||
| chr4:109753278
|
AAT | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-777_905-776del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753278 | ||||||
| chr4:109753279
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-787_905-777dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753279 | ||||||
| chr4:109753280
|
T | C | 24 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0161others(21): Show | 24 | HG00280.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.905-777A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753280 | ||||||
| chr4:109753283
|
ATATTTAT others(5): Show |
A | 1 | a0003c0004t0001g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.905-792_905-781del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753283 | ||||||
| chr4:109753291
|
T | A | 71 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(68): Show | 71 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.905-788A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753291 | ||||||
| chr4:109753293
|
TATA | T | 21 | a0001c0001t0001g0160a0001c0001t0001g0248a0001c0001t0001g0252others(18): Show | 21 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.905-793_905-791del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753293 | ||||||
| chr4:109753295
|
T | TA | 103 | a0001c0001t0001g0018a0001c0001t0001g0187a0001c0001t0001g0194others(100): Show | 104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-793dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | ||||||
| chr4:109753295
|
T | TAAATAAA others(9): Show |
2 | a0001c0001t0003g0148a0002c0003t0001g0259 | 2 | HG03195.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.905-793_905-792ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | ||||||
| chr4:109753295
|
T | TATTTATA others(5): Show |
1 | a0003c0004t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.905-793_905-792ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | ||||||
| chr4:109753295
|
T | TATTTATT others(5): Show |
104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(101): Show | 106 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.905-793_905-792ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | ||||||
| chr4:109753296
|
A | AAATAAAT others(123): Show |
12 | a0001c0001t0001g0098a0001c0001t0001g0312a0001c0001t0001g0319others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(130): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | ||||||
| chr4:109753296
|
A | AAATATTT others(44): Show |
1 | a0001c0001t0001g0017 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.905-794_905-793ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | ||||||
| chr4:109753296
|
A | ATTTATTA others(1): Show |
70 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(67): Show | 70 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | ||||||
| chr4:109753296
|
A | ATTTATTA others(44): Show |
20 | a0001c0001t0001g0004a0001c0001t0001g0270a0001c0001t0001g0286others(17): Show | 21 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | ||||||
| chr4:109753310
|
A | AATAAATA others(93): Show |
1 | a0002c0003t0001g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.905-808_905-807ins others(100): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753310 | ||||||
| chr4:109753310
|
A | ACATATAT others(4): Show |
1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905-808_905-807ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753310 | ||||||
| chr4:109753311
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905-808A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | ||||||
| chr4:109753311
|
T | C | 4 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0003g0148others(1): Show | 4 | HG03195.hp1 NA18950.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-808A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | ||||||
| chr4:109753311
|
T | TATATATT others(4): Show |
103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(100): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.905-809_905-808ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | ||||||
| chr4:109753311
|
T | TATATATT others(126): Show |
1 | a0002c0003t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.905-809_905-808ins others(133): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | ||||||
| chr4:109753322
|
T | A | 1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-819A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753322 | ||||||
| chr4:109753324
|
T | TATA | 3 | a0003c0004t0001g0149a0003c0004t0001g0150a0003c0004t0001g0304 | 3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905-824_905-822dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753324
|
T | TATAA | 85 | a0001c0001t0003g0148a0001c0002t0001g0001a0001c0002t0001g0008others(82): Show | 86 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.905-825_905-822dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753324
|
T | TATAAATA others(87): Show |
2 | a0001c0001t0001g0018a0002c0003t0001g0314 | 2 | HG03486.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.905-822_905-821ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753324
|
T | TATATTTA others(7): Show |
2 | a0001c0002t0001g0057a0001c0002t0001g0086 | 2 | NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.905-822_905-821ins others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753324
|
T | TATATTTA others(8): Show |
7 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0201others(4): Show | 7 | HG00280.hp1 HG01081.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.905-822_905-821ins others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753324
|
T | TATATTTA others(50): Show |
7 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(4): Show | 7 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.905-822_905-821ins others(57): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | ||||||
| chr4:109753328
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-825T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753328 | ||||||
| chr4:109753329
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-826T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753329 | ||||||
| chr4:109753338
|
A | ATATATAT others(4): Show |
69 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0036others(66): Show | 70 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-846_905-836dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753338 | ||||||
| chr4:109753339
|
T | TATATATT others(4): Show |
1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-837_905-836ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753339 | ||||||
| chr4:109753341
|
T | A | 1 | a0001c0002t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-838A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753341 | ||||||
| chr4:109753350
|
T | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0187a0001c0001t0001g0194others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-847A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753350 | ||||||
| chr4:109753352
|
TATA | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.905-852_905-850del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753352 | ||||||
| chr4:109753354
|
T | TA | 8 | a0001c0002t0001g0054a0001c0002t0001g0136a0001c0002t0001g0175others(5): Show | 8 | HG01975.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-852dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | ||||||
| chr4:109753354
|
T | TAAATAAA others(9): Show |
1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-852_905-851ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | ||||||
| chr4:109753354
|
T | TATTTATT others(5): Show |
3 | a0001c0001t0003g0148a0001c0002t0001g0022a0001c0002t0001g0035 | 3 | HG02886.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.905-852_905-851ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | ||||||
| chr4:109753355
|
A | AAATAAAT others(123): Show |
3 | a0001c0002t0001g0119a0001c0002t0001g0126a0001c0002t0001g0217 | 3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.905-853_905-852ins others(130): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | ||||||
| chr4:109753355
|
A | AAATATTT others(16): Show |
1 | a0002c0003t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.905-853_905-852ins others(23): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | ||||||
| chr4:109753355
|
A | AAATATTT others(44): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(1): Show | 4 | HG02723.hp2 HG03098.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-853_905-852ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | ||||||
| chr4:109753355
|
A | ATTTATTA others(1): Show |
9 | a0001c0001t0001g0018a0001c0001t0001g0187a0001c0001t0001g0194others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-853_905-852ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | ||||||
| chr4:109753355
|
A | ATTTATTA others(44): Show |
1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-853_905-852ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | ||||||
| chr4:109753356
|
A | T | 9 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-853T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753356 | ||||||
| chr4:109753358
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.905-855T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753358 | ||||||
| chr4:109753359
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-856T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753359 | ||||||
| chr4:109753370
|
T | C | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-867A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753370 | ||||||
| chr4:109753370
|
T | TATATATT others(4): Show |
1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-868_905-867ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753370 | ||||||
| chr4:109753381
|
T | A | 69 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0036others(66): Show | 70 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-878A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753381 | ||||||
| chr4:109753383
|
T | TATA | 5 | a0001c0001t0001g0160a0001c0001t0001g0248a0001c0001t0001g0252others(2): Show | 5 | NA18959.hp2 NA18982.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-883_905-881dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | ||||||
| chr4:109753383
|
T | TATAA | 8 | a0001c0002t0001g0054a0001c0002t0001g0120a0001c0002t0001g0136others(5): Show | 8 | HG01975.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-884_905-881dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | ||||||
| chr4:109753383
|
T | TATATTTA others(7): Show |
71 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(68): Show | 72 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.905-881_905-880ins others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | ||||||
| chr4:109753387
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-884T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753387 | ||||||
| chr4:109753388
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-885T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753388 | ||||||
| chr4:109753397
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-905_905-895dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753397 | ||||||
| chr4:109753401
|
A | G | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-898T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753401 | ||||||
| chr4:109753404
|
TTTA | T | 5 | a0001c0002t0001g0086a0001c0006t0005g0041a0001c0006t0005g0042others(2): Show | 5 | HG02647.hp1 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-904_905-902del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753404 | ||||||
| chr4:109753404
|
TTTATTAT others(7): Show |
T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-915_905-902del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753404 | ||||||
| chr4:109753405
|
T | TTATTATA others(8): Show |
2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-917_905-903dup others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753405 | ||||||
| chr4:109753411
|
TATAA | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(118): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.905-912_905-909del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753411 | ||||||
| chr4:109753412
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.905-909T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753412 | ||||||
| chr4:109753413
|
TA | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(182): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.905-911delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753413 | ||||||
| chr4:109753415
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-912T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753415 | ||||||
| chr4:109753416
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-913T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753416 | ||||||
| chr4:109753418
|
A | ATTAT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-916_905-915ins others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753418 | ||||||
| chr4:109753418
|
A | ATTTAT | 18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-916_905-915ins others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753418 | ||||||
| chr4:109753419
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-916T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753419 | ||||||
| chr4:109753424
|
T | A | 18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-921A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753424 | ||||||
| chr4:109753424
|
T | G | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-921A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753424 | ||||||
| chr4:109753428
|
A | AAT | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(188): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.905-927_905-926dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753428 | ||||||
| chr4:109753428
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-925T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753428 | ||||||
| chr4:109753429
|
A | ATTT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-927_905-926ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753429 | ||||||
| chr4:109753429
|
A | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0002t0002g0012others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-926T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753429 | ||||||
| chr4:109753433
|
ATT | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG02257.hp2 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-932_905-931del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753433 | ||||||
| chr4:109753434
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-931A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753434 | ||||||
| chr4:109753435
|
T | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-932A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753435 | ||||||
| chr4:109753435
|
T | TATA | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-933_905-932ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753435 | ||||||
| chr4:109753436
|
T | A | 18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-933A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753436 | ||||||
| chr4:109753438
|
T | TA | 18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-936_905-935ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753438 | ||||||
| chr4:109753439
|
T | A | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-936A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753439 | ||||||
| chr4:109753440
|
A | T | 18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-937T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753440 | ||||||
| chr4:109753441
|
TATA | T | 84 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.905-941_905-939del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753441 | ||||||
| chr4:109753443
|
T | TA | 3 | a0001c0002t0001g0054a0001c0002t0001g0136a0010c0013t0001g0297 | 3 | HG01975.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-941dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753443 | ||||||
| chr4:109753443
|
T | TAAATAAA others(9): Show |
1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-941_905-940ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753443 | ||||||
| chr4:109753446
|
T | G | 1 | a0001c0002t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905-943A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753446 | ||||||
| chr4:109753447
|
A | G | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-944T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753447 | ||||||
| chr4:109753448
|
A | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0312a0001c0001t0001g0319others(23): Show | 26 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-945T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753448 | ||||||
| chr4:109753449
|
A | T | 1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-946T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753449 | ||||||
| chr4:109753452
|
T | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-949A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753452 | ||||||
| chr4:109753452
|
T | TTTA | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-952_905-950dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753452 | ||||||
| chr4:109753453
|
T | A | 1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-950A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753453 | ||||||
| chr4:109753453
|
T | TTA | 62 | a0001c0001t0001g0004a0001c0001t0001g0286a0001c0001t0001g0287others(59): Show | 63 | HG00099.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.905-952_905-951dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753453 | ||||||
| chr4:109753455
|
A | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-952T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753455 | ||||||
| chr4:109753456
|
T | TA | 87 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(84): Show | 88 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.905-954dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753456 | ||||||
| chr4:109753457
|
A | AATATATA others(5): Show |
2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-955_905-954ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753457 | ||||||
| chr4:109753457
|
AT | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(99): Show | 104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-955delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753457 | ||||||
| chr4:109753459
|
A | AT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-957dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753459 | ||||||
| chr4:109753460
|
T | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-957A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753460 | ||||||
| chr4:109753462
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-959A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753462 | ||||||
| chr4:109753463
|
A | T | 1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-960T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753463 | ||||||
| chr4:109753464
|
T | TA | 5 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(2): Show | 5 | HG02809.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-962_905-961ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753464 | ||||||
| chr4:109753464
|
T | TTTATTAT others(114): Show |
1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-962_905-961ins others(121): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753464 | ||||||
| chr4:109753465
|
T | A | 3 | a0001c0001t0001g0018a0001c0002t0002g0012a0002c0003t0001g0259 | 3 | HG02257.hp2 HG03486.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.905-962A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753465 | ||||||
| chr4:109753467
|
A | AT | 4 | a0001c0001t0001g0218a0001c0002t0001g0119a0001c0002t0001g0126others(1): Show | 4 | HG00738.hp2 HG01074.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-965dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753467 | ||||||
| chr4:109753467
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-964T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753467 | ||||||
| chr4:109753468
|
TATTAATA others(4): Show |
T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(106): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.905-976_905-966del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753468 | ||||||
| chr4:109753469
|
AT | A | 76 | a0001c0001t0001g0018a0001c0002t0001g0001a0001c0002t0001g0008others(73): Show | 77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-967delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753469 | ||||||
| chr4:109753470
|
T | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-967A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753470 | ||||||
| chr4:109753470
|
T | TA | 4 | a0001c0001t0001g0218a0001c0002t0001g0119a0001c0002t0001g0126others(1): Show | 4 | HG00738.hp2 HG01074.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-968_905-967ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753470 | ||||||
| chr4:109753471
|
T | A | 6 | a0001c0002t0001g0054a0001c0002t0001g0057a0001c0002t0001g0120others(3): Show | 6 | HG01975.hp1 HG02280.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-968A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753471 | ||||||
| chr4:109753472
|
A | AT | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-970_905-969ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753472 | ||||||
| chr4:109753472
|
A | T | 3 | a0001c0001t0001g0280a0001c0002t0001g0057a0001c0002t0001g0120 | 3 | HG01167.hp1 NA19043.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.905-969T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753472 | ||||||
| chr4:109753475
|
A | G | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-972T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753475 | ||||||
| chr4:109753476
|
A | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0312a0001c0001t0001g0319others(23): Show | 26 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-973T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753476 | ||||||
| chr4:109753477
|
A | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-974T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753477 | ||||||
| chr4:109753479
|
A | AAT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-977_905-976ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753479 | ||||||
| chr4:109753479
|
A | T | 1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-976T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753479 | ||||||
| chr4:109753481
|
T | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.905-978A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | ||||||
| chr4:109753481
|
T | G | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-978A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | ||||||
| chr4:109753481
|
T | TA | 20 | a0001c0001t0001g0312a0001c0001t0001g0319a0001c0001t0003g0148others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-979_905-978ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | ||||||
| chr4:109753481
|
T | TTATAATA others(9): Show |
3 | a0001c0002t0001g0119a0001c0002t0001g0126a0001c0002t0001g0217 | 3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.905-979_905-978ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | ||||||
| chr4:109753485
|
A | T | 5 | a0001c0001t0001g0018a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-982T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753485 | ||||||
| chr4:109753486
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-983T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753486 | ||||||
| chr4:109753489
|
A | T | 198 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.905-986T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753489 | ||||||
| chr4:109753490
|
A | ATT | 73 | a0001c0001t0001g0218a0001c0002t0001g0001a0001c0002t0001g0008others(70): Show | 74 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.905-988_905-987ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753490 | ||||||
| chr4:109753493
|
TTTATAAT others(7): Show |
T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1004_905-991de others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753493 | ||||||
| chr4:109753494
|
T | TA | 76 | a0001c0001t0001g0218a0001c0002t0001g0001a0001c0002t0001g0008others(73): Show | 77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-992_905-991ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753494 | ||||||
| chr4:109753496
|
A | C | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-993T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753496 | ||||||
| chr4:109753497
|
TA | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.905-995delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753497 | ||||||
| chr4:109753498
|
A | AT | 12 | a0001c0001t0001g0151a0001c0001t0001g0174a0001c0001t0001g0275others(9): Show | 12 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-996_905-995ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753498 | ||||||
| chr4:109753498
|
A | T | 4 | a0001c0002t0001g0120a0001c0002t0003g0296a0002c0003t0001g0259others(1): Show | 4 | HG01975.hp1 HG02809.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-995T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753498 | ||||||
| chr4:109753499
|
A | G | 1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-996T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753499 | ||||||
| chr4:109753499
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-996T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753499 | ||||||
| chr4:109753500
|
T | TAA | 73 | a0001c0001t0001g0218a0001c0002t0001g0001a0001c0002t0001g0008others(70): Show | 74 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.905-998_905-997ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753500 | ||||||
| chr4:109753501
|
A | G | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-998T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753501 | ||||||
| chr4:109753503
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0250 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.905-1000T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753503 | ||||||
| chr4:109753503
|
AT | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1001delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753503 | ||||||
| chr4:109753504
|
T | A | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1001A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753504 | ||||||
| chr4:109753505
|
T | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(103): Show | 108 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.905-1002A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753505 | ||||||
| chr4:109753506
|
T | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1003A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753506 | ||||||
| chr4:109753506
|
TA | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 107 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.905-1004delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753506 | ||||||
| chr4:109753507
|
A | ATATATAT | 68 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(65): Show | 69 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.905-1005_905-1004i others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753507 | ||||||
| chr4:109753507
|
A | ATGTATAT | 4 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0081others(1): Show | 4 | NA18956.hp2 NA18969.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1005_905-1004i others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753507 | ||||||
| chr4:109753509
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1006A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753509 | ||||||
| chr4:109753510
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1007T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753510 | ||||||
| chr4:109753512
|
A | C | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1009T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753512 | ||||||
| chr4:109753513
|
TA | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0187a0001c0001t0001g0194others(10): Show | 13 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-1011delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753513 | ||||||
| chr4:109753514
|
A | AAATAAAT others(184): Show |
1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1012_905-1011i others(193): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | ||||||
| chr4:109753514
|
A | AATAAATA others(18): Show |
1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-1012_905-1011i others(27): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | ||||||
| chr4:109753514
|
A | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.905-1011T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | ||||||
| chr4:109753515
|
A | AATATTTA others(73): Show |
2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-1013_905-1012i others(82): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | ||||||
| chr4:109753515
|
A | ATAAATAT others(19): Show |
18 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0306others(15): Show | 18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-1013_905-1012i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | ||||||
| chr4:109753515
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1012T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | ||||||
| chr4:109753516
|
A | G | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1013T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753516 | ||||||
| chr4:109753516
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1013T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753516 | ||||||
| chr4:109753518
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1015T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753518 | ||||||
| chr4:109753519
|
A | T | 6 | a0001c0002t0001g0120a0001c0002t0001g0175a0001c0002t0001g0176others(3): Show | 6 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1016T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753519 | ||||||
| chr4:109753520
|
A | T | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1017T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753520 | ||||||
| chr4:109753521
|
T | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1018A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753521 | ||||||
| chr4:109753522
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1019T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753522 | ||||||
| chr4:109753524
|
T | A | 3 | a0001c0002t0001g0054a0001c0002t0001g0136a0002c0003t0001g0259 | 3 | HG02280.hp2 HG03540.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.905-1021A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753524 | ||||||
| chr4:109753524
|
T | TA | 4 | a0001c0002t0001g0120a0001c0002t0001g0175a0001c0002t0001g0176others(1): Show | 4 | HG02976.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1022_905-1021i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753524 | ||||||
| chr4:109753526
|
A | C | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1023T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753526 | ||||||
| chr4:109753527
|
TA | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1025delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753527 | ||||||
| chr4:109753529
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1026T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753529 | ||||||
| chr4:109753530
|
TAAATATT others(4): Show |
T | 4 | a0001c0006t0005g0041a0001c0006t0005g0042a0001c0008t0001g0293others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1038_905-1028d others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753530 | ||||||
| chr4:109753531
|
A | G | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1028T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753531 | ||||||
| chr4:109753532
|
A | T | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.905-1029T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753532 | ||||||
| chr4:109753535
|
A | AAT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1033_905-1032i others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753535 | ||||||
| chr4:109753539
|
A | C | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1036T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753539 | ||||||
| chr4:109753541
|
A | AT | 3 | a0001c0002t0001g0054a0001c0002t0001g0120a0001c0002t0001g0136 | 3 | HG02280.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1039_905-1038i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753541 | ||||||
| chr4:109753541
|
A | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(106): Show | 110 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.905-1038T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753541 | ||||||
| chr4:109753542
|
A | T | 12 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(9): Show | 12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-1039T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753542 | ||||||
| chr4:109753543
|
T | TA | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1041dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753543 | ||||||
| chr4:109753544
|
A | G | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1041T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753544 | ||||||
| chr4:109753546
|
ATT | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1045_905-1044d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753546 | ||||||
| chr4:109753547
|
T | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1044A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753547 | ||||||
| chr4:109753548
|
T | A | 12 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(9): Show | 12 | HG00280.hp1 HG01081.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.905-1045A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753548 | ||||||
| chr4:109753549
|
T | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1046A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753549 | ||||||
| chr4:109753549
|
TA | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0120a0001c0002t0001g0136 | 3 | HG02280.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1047delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753549 | ||||||
| chr4:109753552
|
TA | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1050delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753552 | ||||||
| chr4:109753553
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1050T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753553 | ||||||
| chr4:109753554
|
T | TA | 22 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(19): Show | 22 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.905-1052dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753554 | ||||||
| chr4:109753554
|
TATAAATA | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1058_905-1052d others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753554 | ||||||
| chr4:109753555
|
A | C | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1052T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753555 | ||||||
| chr4:109753556
|
TA | T | 11 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.905-1054delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753556 | ||||||
| chr4:109753557
|
A | AAATATTT others(163): Show |
1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-1055_905-1054i others(172): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753557 | ||||||
| chr4:109753557
|
A | T | 4 | a0001c0001t0001g0018a0001c0002t0001g0054a0001c0002t0001g0120others(1): Show | 4 | HG02280.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1054T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753557 | ||||||
| chr4:109753558
|
A | ATGT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1056_905-1055i others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753558 | ||||||
| chr4:109753558
|
A | T | 23 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1055T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753558 | ||||||
| chr4:109753559
|
A | G | 23 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1056T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753559 | ||||||
| chr4:109753559
|
A | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1056T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753559 | ||||||
| chr4:109753562
|
A | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(30): Show | 33 | HG00280.hp1 HG00639.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.905-1059T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753562 | ||||||
| chr4:109753563
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1060T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753563 | ||||||
| chr4:109753564
|
T | A | 23 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1061A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753564 | ||||||
| chr4:109753565
|
A | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(23): Show | 26 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.905-1062T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753565 | ||||||
| chr4:109753567
|
T | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1064A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753567 | ||||||
| chr4:109753567
|
T | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1064A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753567 | ||||||
| chr4:109753569
|
A | C | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1066T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753569 | ||||||
| chr4:109753571
|
A | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1068T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753571 | ||||||
| chr4:109753571
|
AAT | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1070_905-1069d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753571 | ||||||
| chr4:109753572
|
A | T | 23 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1069T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753572 | ||||||
| chr4:109753573
|
T | TATATATT others(4): Show |
5 | a0001c0001t0001g0018a0001c0002t0001g0054a0001c0002t0001g0120others(2): Show | 5 | HG02280.hp2 HG02809.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-1071_905-1070i others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753573 | ||||||
| chr4:109753573
|
TATA | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1073_905-1071d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753573 | ||||||
| chr4:109753574
|
A | G | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1071T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753574 | ||||||
| chr4:109753576
|
A | AT | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1074dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753576 | ||||||
| chr4:109753576
|
ATATTTAT others(40): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.905-1120_905-1074d others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753576 | ||||||
| chr4:109753578
|
A | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1075T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753578 | ||||||
| chr4:109753579
|
T | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1076A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753579 | ||||||
| chr4:109753580
|
T | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1077A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | ||||||
| chr4:109753580
|
T | C | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1077A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | ||||||
| chr4:109753580
|
T | TATA | 11 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(8): Show | 11 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-1078_905-1077i others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | ||||||
| chr4:109753580
|
T | TATATAAT others(18): Show |
10 | a0001c0001t0001g0270a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1078_905-1077i others(27): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | ||||||
| chr4:109753580
|
T | TATATAAT others(40): Show |
1 | a0001c0002t0001g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1078_905-1077i others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | ||||||
| chr4:109753583
|
T | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1080A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753583 | ||||||
| chr4:109753584
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1081A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753584 | ||||||
| chr4:109753585
|
A | G | 14 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1082T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753585 | ||||||
| chr4:109753585
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1082T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753585 | ||||||
| chr4:109753589
|
AAATAAAT | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1093_905-1087d others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753589 | ||||||
| chr4:109753590
|
A | AT | 10 | a0001c0001t0001g0270a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1088_905-1087i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753590 | ||||||
| chr4:109753590
|
A | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(100): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.905-1087T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753590 | ||||||
| chr4:109753591
|
A | G | 10 | a0001c0001t0001g0270a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1088T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753591 | ||||||
| chr4:109753591
|
A | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.905-1088T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753591 | ||||||
| chr4:109753593
|
A | G | 1 | a0001c0002t0001g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1090T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | ||||||
| chr4:109753593
|
A | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1090T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | ||||||
| chr4:109753593
|
AAATAT | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(99): Show | 104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-1095_905-1091d others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | ||||||
| chr4:109753594
|
A | T | 27 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(24): Show | 27 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.905-1091T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753594 | ||||||
| chr4:109753595
|
A | G | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1092T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753595 | ||||||
| chr4:109753596
|
T | A | 10 | a0001c0001t0001g0270a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1093A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753596 | ||||||
| chr4:109753597
|
A | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 97 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.905-1094T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753597 | ||||||
| chr4:109753599
|
T | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1096A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | ||||||
| chr4:109753599
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.905-1096A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | ||||||
| chr4:109753599
|
T | TA | 15 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-1097_905-1096i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | ||||||
| chr4:109753601
|
A | C | 4 | a0001c0002t0001g0123a0001c0002t0001g0132a0001c0002t0002g0012others(1): Show | 4 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1098T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753601 | ||||||
| chr4:109753604
|
A | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(23): Show | 26 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.905-1101T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753604 | ||||||
| chr4:109753606
|
A | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(84): Show | 88 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.905-1103T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753606 | ||||||
| chr4:109753608
|
A | C | 6 | a0001c0001t0001g0015a0001c0002t0001g0055a0001c0002t0001g0124others(3): Show | 6 | HG01070.hp2 HG01978.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1105T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753608 | ||||||
| chr4:109753608
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(99): Show | 104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-1105T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753608 | ||||||
| chr4:109753610
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.905-1107T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753610 | ||||||
| chr4:109753611
|
T | A | 101 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(98): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.905-1108A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753611 | ||||||
| chr4:109753611
|
T | TA | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(99): Show | 104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-1109_905-1108i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753611 | ||||||
| chr4:109753612
|
T | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(100): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.905-1109A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | ||||||
| chr4:109753612
|
T | TATATAAT others(6): Show |
1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1110_905-1109i others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | ||||||
| chr4:109753612
|
T | TATCTAAT others(6): Show |
11 | a0001c0001t0001g0270a0001c0001t0001g0328a0001c0001t0001g0330others(8): Show | 11 | HG02027.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-1110_905-1109i others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | ||||||
| chr4:109753612
|
T | TGTATAA | 13 | a0001c0001t0001g0015a0001c0001t0001g0167a0001c0001t0001g0184others(10): Show | 13 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-1110_905-1109i others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | ||||||
| chr4:109753612
|
T | TGTATAAT others(86): Show |
1 | a0001c0001t0001g0333 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.905-1110_905-1109i others(95): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | ||||||
| chr4:109753613
|
TA | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(84): Show | 88 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.905-1111delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753613 | ||||||
| chr4:109753614
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.905-1111T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753614 | ||||||
| chr4:109753616
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1113A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753616 | ||||||
| chr4:109753619
|
A | AT | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.905-1117dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753619 | ||||||
| chr4:109753623
|
T | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.905-1120A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753623 | ||||||
| chr4:109753630
|
A | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(77): Show | 81 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.905-1127T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753630 | ||||||
| chr4:109753631
|
A | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.905-1128T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753631 | ||||||
| chr4:109753632
|
T | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.905-1129A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753632 | ||||||
| chr4:109753632
|
T | TATGTATA others(80): Show |
1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1130_905-1129i others(89): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753632 | ||||||
| chr4:109753635
|
G | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1132C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753635 | ||||||
| chr4:109753643
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1140A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753643 | ||||||
| chr4:109753645
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1142T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753645 | ||||||
| chr4:109753655
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1152A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753655 | ||||||
| chr4:109753657
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1154T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753657 | ||||||
| chr4:109753659
|
A | ATAATGTA others(51): Show |
1 | a0001c0001t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-1157_905-1156i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753659
|
A | ATAATGTA others(80): Show |
1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-1157_905-1156i others(89): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753659
|
A | ATAATGTA others(109): Show |
1 | a0001c0002t0001g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.905-1157_905-1156i others(118): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753659
|
A | ATAATGTA others(167): Show |
5 | a0001c0002t0001g0173a0001c0002t0001g0271a0001c0002t0001g0272others(2): Show | 5 | NA18959.hp2 NA18960.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-1157_905-1156i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753659
|
A | ATAATGTA others(167): Show |
1 | a0001c0002t0001g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.905-1157_905-1156i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753659
|
A | C | 135 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.905-1156T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | ||||||
| chr4:109753663
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1160A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753663 | ||||||
| chr4:109753664
|
G | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1161C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753664 | ||||||
| chr4:109753669
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1166T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753669 | ||||||
| chr4:109753681
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1178T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753681 | ||||||
| chr4:109753688
|
A | ATAATGTA others(51): Show |
1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1186_905-1185i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753688
|
A | ATAATGTA others(196): Show |
4 | a0004c0005t0001g0101a0004c0005t0001g0102a0004c0005t0001g0103others(1): Show | 4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1186_905-1185i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753688
|
A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0022a0001c0002t0001g0035 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.905-1186_905-1185i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753688
|
A | ATAATGTA others(167): Show |
7 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0074others(4): Show | 8 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-1186_905-1185i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753688
|
A | ATAATGTA others(196): Show |
1 | a0001c0002t0001g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.905-1186_905-1185i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753688
|
A | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.905-1185T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | ||||||
| chr4:109753689
|
T | A | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1186A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753689 | ||||||
| chr4:109753690
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1187T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753690 | ||||||
| chr4:109753692
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1189A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753692 | ||||||
| chr4:109753700
|
T | C | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1197A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753700 | ||||||
| chr4:109753713
|
T | TTATCTAA others(225): Show |
1 | a0001c0002t0001g0086 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-1211_905-1210i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753713 | ||||||
| chr4:109753717
|
A | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.905-1214T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753717 | ||||||
| chr4:109753717
|
ATAATGTA others(22): Show |
A | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.905-1243_905-1215d others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753717 | ||||||
| chr4:109753721
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1218A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753721 | ||||||
| chr4:109753729
|
T | C | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1226A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753729 | ||||||
| chr4:109753742
|
T | A | 18 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0067others(15): Show | 19 | HG00558.hp1 HG00733.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1239A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753742 | ||||||
| chr4:109753746
|
C | A | 2 | a0001c0002t0001g0083a0003c0004t0001g0304 | 2 | HG03579.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.905-1243G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753746 | ||||||
| chr4:109753750
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1247A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753750 | ||||||
| chr4:109753758
|
T | C | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1255A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753758 | ||||||
| chr4:109753775
|
C | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG00735.hp1 HG01123.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1272G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753775 | ||||||
| chr4:109753787
|
T | C | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1284A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753787 | ||||||
| chr4:109753804
|
C | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.905-1301G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753804 | ||||||
| chr4:109753816
|
T | C | 3 | a0003c0004t0001g0149a0003c0004t0001g0150a0003c0004t0001g0304 | 3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905-1313A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753816 | ||||||
| chr4:109753816
|
TTTATATT others(22): Show |
T | 23 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(20): Show | 23 | HG00673.hp1 HG00735.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.905-1342_905-1314d others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753816 | ||||||
| chr4:109753825
|
T | C | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.905-1322A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753825 | ||||||
| chr4:109753833
|
A | ATAATGTA others(195): Show |
1 | a0001c0002t0001g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.905-1331_905-1330i others(204): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | ATAATGTA others(196): Show |
42 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0039others(39): Show | 42 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.905-1331_905-1330i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0142a0001c0002t0001g0145 | 2 | NA18966.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | ATAATGTA others(196): Show |
1 | a0001c0002t0001g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.905-1331_905-1330i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | ATAATGTA others(22): Show |
2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | ATAATGTA others(109): Show |
2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(118): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753833
|
A | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0156others(74): Show | 79 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.905-1330T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | ||||||
| chr4:109753845
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.905-1342G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753845 | ||||||
| chr4:109753857
|
A | AATATCTA others(195): Show |
1 | a0001c0002t0001g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.905-1355_905-1354i others(204): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753857 | ||||||
| chr4:109753858
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.905-1355A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753858 | ||||||
| chr4:109753862
|
A | ATAATGTA others(225): Show |
3 | a0001c0002t0001g0065a0001c0002t0001g0066a0006c0014t0001g0064 | 3 | HG01069.hp2 HG01106.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | ||||||
| chr4:109753862
|
A | ATAATGTA others(225): Show |
1 | a0001c0002t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | ||||||
| chr4:109753862
|
A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0083a0001c0002t0001g0090 | 2 | NA18950.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | ||||||
| chr4:109753862
|
A | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.905-1359T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | ||||||
| chr4:109753874
|
T | C | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.905-1371A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753874 | ||||||
| chr4:109753891
|
A | C | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(303): Show | 309 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.905-1388T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753891 | ||||||
| chr4:109753895
|
T | TGTATAAT others(51): Show |
1 | a0001c0002t0001g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.905-1393_905-1392i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753895 | ||||||
| chr4:109753920
|
C | A | 3 | a0002c0003t0001g0316a0003c0004t0001g0149a0003c0004t0001g0150 | 3 | HG00738.hp1 HG02886.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.905-1417G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753920 | ||||||
| chr4:109753935
|
A | ATATTATA others(138): Show |
2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-1433_905-1432i others(147): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753935 | ||||||
| chr4:109753984
|
T | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(12): Show | 16 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.905-1481A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753984 | ||||||
| chr4:109754038
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.905-1535G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754038 | ||||||
| chr4:109754069
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.905-1566G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754069 | ||||||
| chr4:109754086
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1583G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754086 | ||||||
| chr4:109754109
|
G | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1606C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754109 | ||||||
| chr4:109754200
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.905-1697A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754200 | ||||||
| chr4:109754209
|
C | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1706G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754209 | ||||||
| chr4:109754217
|
C | T | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-1714G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754217 | ||||||
| chr4:109754229
|
G | A | 12 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.905-1726C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754229 | ||||||
| chr4:109754412
|
T | TA | 105 | a0001c0001t0001g0202a0001c0001t0001g0319a0001c0001t0001g0327others(102): Show | 106 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.905-1910dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | ||||||
| chr4:109754412
|
T | TAA | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.905-1911_905-1910d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | ||||||
| chr4:109754412
|
T | TAAA | 6 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0001g0276others(3): Show | 6 | HG00438.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1912_905-1910d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | ||||||
| chr4:109754427
|
G | A | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1924C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754427 | ||||||
| chr4:109754429
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1926T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754429 | ||||||
| chr4:109754434
|
C | CT | 86 | a0001c0001t0001g0174a0001c0001t0001g0256a0001c0001t0001g0275others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.905-1932dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754434 | ||||||
| chr4:109754434
|
CT | C | 6 | a0001c0001t0001g0159a0001c0001t0001g0186a0001c0001t0001g0223others(3): Show | 6 | HG02109.hp2 HG02155.hp2 NA19043.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1932delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754434 | ||||||
| chr4:109754583
|
G | C | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-2080C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754583 | ||||||
| chr4:109754621
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-2118G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754621 | ||||||
| chr4:109754630
|
G | GCAATCCT others(15): Show |
1 | a0001c0001t0001g0209 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.905-2149_905-2128d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754630 | ||||||
| chr4:109754699
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905-2196G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754699 | ||||||
| chr4:109754762
|
G | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.905-2259C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754762 | ||||||
| chr4:109754986
|
C | A | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(344): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.905-2483G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754986 | ||||||
| chr4:109755287
|
A | G | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.904+2476T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755287 | ||||||
| chr4:109755317
|
G | A | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+2446C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755317 | ||||||
| chr4:109755502
|
T | C | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+2261A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755502 | ||||||
| chr4:109755607
|
G | C | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.904+2156C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755607 | ||||||
| chr4:109755898
|
A | G | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+1865T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755898 | ||||||
| chr4:109755965
|
C | G | 1 | a0001c0002t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904+1798G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755965 | ||||||
| chr4:109756071
|
A | G | 1 | a0003c0004t0001g0152 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.904+1692T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756071 | ||||||
| chr4:109756206
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.904+1557C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756206 | ||||||
| chr4:109756253
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+1510C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756253 | ||||||
| chr4:109756278
|
C | A | 1 | a0002c0003t0001g0309 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+1485G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756278 | ||||||
| chr4:109756289
|
G | A | 1 | a0002c0003t0001g0309 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+1474C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756289 | ||||||
| chr4:109756310
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1453T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756310 | ||||||
| chr4:109756317
|
G | GA | 349 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(346): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.904+1445dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756317 | ||||||
| chr4:109756374
|
C | T | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+1389G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756374 | ||||||
| chr4:109756387
|
GGAA | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.904+1373_904+1375d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756387 | ||||||
| chr4:109756401
|
A | T | 1 | a0001c0002t0001g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.904+1362T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756401 | ||||||
| chr4:109756440
|
AAGG | A | 76 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(73): Show | 77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.904+1320_904+1322d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756440 | ||||||
| chr4:109756573
|
C | G | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.904+1190G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756573 | ||||||
| chr4:109756752
|
C | A | 6 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0291others(3): Show | 6 | HG02165.hp2 HG02698.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+1011G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756752 | ||||||
| chr4:109756769
|
G | T | 1 | a0001c0001t0001g0349 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.904+994C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756769 | ||||||
| chr4:109756837
|
CTACAAGA others(5): Show |
C | 1 | a0001c0002t0001g0040 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.904+914_904+925del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756837 | ||||||
| chr4:109756875
|
AGAAAGAA others(6): Show |
A | 1 | a0001c0001t0001g0159 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.904+875_904+887del others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756875 | ||||||
| chr4:109756880
|
GAAAGAAA others(7): Show |
G | 1 | a0001c0002t0001g0137 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.904+869_904+882del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756880 | ||||||
| chr4:109756885
|
A | G | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+878T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756885 | ||||||
| chr4:109756888
|
G | A | 19 | a0001c0001t0001g0312a0001c0001t0001g0319a0002c0003t0001g0259others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+875C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAA | 18 | a0001c0001t0001g0151a0001c0001t0001g0203a0001c0001t0001g0221others(15): Show | 18 | HG00323.hp2 HG00733.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.904+871_904+874dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0003g0148 | 3 | HG02723.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.904+868_904+874dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(1): Show |
14 | a0001c0001t0001g0220a0001c0001t0001g0289a0001c0001t0001g0292others(11): Show | 14 | HG00099.hp1 HG00735.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.904+867_904+874dup others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0146a0001c0001t0001g0256a0001c0002t0001g0044others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+863_904+874dup others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(9): Show |
7 | a0001c0001t0001g0165a0001c0002t0001g0035a0001c0002t0001g0075others(4): Show | 7 | HG00558.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.904+859_904+874dup others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(13): Show |
3 | a0001c0002t0001g0084a0001c0002t0001g0107a0004c0005t0001g0101 | 3 | HG02148.hp1 NA18941.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.904+855_904+874dup others(20): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(17): Show |
1 | a0004c0005t0001g0109 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.904+851_904+874dup others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(4): Show |
1 | a0001c0001t0001g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.904+874_904+875ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(8): Show |
1 | a0001c0001t0001g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(12): Show |
1 | a0001c0001t0001g0017 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(19): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
G | GGAAAGAA others(24): Show |
1 | a0001c0001t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAA | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0154a0001c0001t0001g0155others(39): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.904+871_904+874del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(1): Show |
G | 41 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0157others(38): Show | 41 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.904+867_904+874del others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(5): Show |
G | 42 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(39): Show | 42 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.904+863_904+874del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(9): Show |
G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0161others(28): Show | 33 | HG00099.hp2 HG01168.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.904+859_904+874del others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(13): Show |
G | 35 | a0001c0001t0001g0009a0001c0001t0001g0156a0001c0001t0001g0232others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+855_904+874del others(20): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(17): Show |
G | 22 | a0001c0001t0001g0171a0001c0001t0001g0185a0001c0001t0001g0188others(19): Show | 22 | HG01070.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.904+851_904+874del others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(21): Show |
G | 3 | a0001c0001t0001g0216a0001c0002t0001g0122a0001c0002t0002g0027 | 3 | HG03453.hp1 HG03491.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.904+847_904+874del others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(25): Show |
G | 6 | a0001c0001t0001g0214a0001c0002t0001g0083a0001c0002t0001g0090others(3): Show | 6 | HG01255.hp2 HG01346.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+843_904+874del others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756888
|
GGAAAGAA others(37): Show |
G | 2 | a0001c0002t0001g0052a0001c0002t0001g0130 | 2 | NA18970.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.904+831_904+874del others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | ||||||
| chr4:109756889
|
GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.904+860_904+873del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756889 | ||||||
| chr4:109756889
|
GAAAGAAA others(10): Show |
G | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.904+857_904+873del others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756889 | ||||||
| chr4:109756898
|
A | G | 1 | a0003c0004t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.904+865T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756898 | ||||||
| chr4:109756906
|
A | G | 1 | a0003c0004t0001g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.904+857T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756906 | ||||||
| chr4:109756918
|
A | AAAGAAAG others(87): Show |
1 | a0002c0003t0001g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.904+844_904+845ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756918 | ||||||
| chr4:109756918
|
A | AAAGAAAG others(98): Show |
1 | a0002c0003t0001g0307 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904+844_904+845ins others(105): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756918 | ||||||
| chr4:109756922
|
A | AAAGAAAG others(100): Show |
1 | a0002c0003t0001g0311 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.904+840_904+841ins others(107): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756922 | ||||||
| chr4:109756922
|
A | AAAGAAAG others(96): Show |
1 | a0002c0003t0001g0314 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.904+840_904+841ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756922 | ||||||
| chr4:109756926
|
A | AAAGAAAG others(90): Show |
1 | a0002c0003t0001g0310 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.904+836_904+837ins others(97): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756926 | ||||||
| chr4:109756930
|
A | AAAGAAAG others(96): Show |
1 | a0001c0001t0001g0319 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904+832_904+833ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756930 | ||||||
| chr4:109756930
|
A | AAAGAAAG others(100): Show |
1 | a0001c0001t0001g0312 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.904+832_904+833ins others(107): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756930 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(112): Show |
1 | a0002c0003t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(119): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(107): Show |
1 | a0002c0003t0001g0306 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(114): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(96): Show |
1 | a0002c0003t0001g0320 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(88): Show |
1 | a0002c0003t0001g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(95): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(80): Show |
1 | a0002c0003t0001g0325 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(87): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(84): Show |
1 | a0002c0003t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(91): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(75): Show |
1 | a0002c0003t0001g0318 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(82): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(76): Show |
1 | a0002c0003t0001g0317 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(83): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756934
|
A | AAAGAAAG others(80): Show |
1 | a0002c0003t0001g0316 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(87): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | ||||||
| chr4:109756938
|
A | AAAGAAAG others(72): Show |
1 | a0002c0003t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.904+824_904+825ins others(79): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756938 | ||||||
| chr4:109756942
|
A | AAAGAAAG others(76): Show |
1 | a0002c0003t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.904+820_904+821ins others(83): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756942 | ||||||
| chr4:109756949
|
G | GGAAGGAA others(91): Show |
1 | a0002c0003t0001g0309 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+813_904+814ins others(98): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756949 | ||||||
| chr4:109756955
|
AAGAAAGA others(15): Show |
A | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.904+786_904+807del others(22): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756955 | ||||||
| chr4:109756961
|
G | T | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.904+802C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756961 | ||||||
| chr4:109756965
|
G | T | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.904+798C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756965 | ||||||
| chr4:109756967
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.904+786_904+795del others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756967 | ||||||
| chr4:109756969
|
G | T | 3 | a0001c0002t0002g0024a0001c0002t0002g0025a0001c0002t0002g0027 | 3 | HG01255.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.904+794C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756969 | ||||||
| chr4:109756970
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0323a0001c0001t0002g0346 | 3 | HG02615.hp2 HG02738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.904+793T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756970 | ||||||
| chr4:109756973
|
G | T | 16 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0153others(13): Show | 16 | HG01255.hp2 HG01515.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.904+790C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756973 | ||||||
| chr4:109756977
|
G | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(74): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.904+786C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756977 | ||||||
| chr4:109756978
|
A | T | 2 | a0001c0001t0001g0196a0003c0004t0001g0149 | 2 | HG00544.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.904+785T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756978 | ||||||
| chr4:109756979
|
A | AAGAAAGA others(19): Show |
1 | a0004c0005t0001g0103 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.904+783_904+784ins others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756979 | ||||||
| chr4:109757195
|
AT | A | 6 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(3): Show | 6 | HG00738.hp1 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+567delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757195 | ||||||
| chr4:109757275
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+488G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757275 | ||||||
| chr4:109757276
|
C | CA | 74 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(71): Show | 75 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.904+486dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757276 | ||||||
| chr4:109757420
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.904+343G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757420 | ||||||
| chr4:109757663
|
CA | C | 137 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0010others(134): Show | 138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.904+99delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757663 | ||||||
| chr4:109757790
|
A | G | 10 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0038others(7): Show | 11 | HG00558.hp1 HG00733.hp1 HG01167.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.884-7T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757790 | ||||||
| chr4:109757801
|
A | C | 1 | a0001c0001t0001g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-18T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757801 | ||||||
| chr4:109757823
|
T | TTTTAA | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(331): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.884-41_884-40insTT others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757823 | ||||||
| chr4:109757827
|
G | T | 1 | a0001c0001t0001g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-44C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757827 | ||||||
| chr4:109757829
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-46T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757829 | ||||||
| chr4:109757846
|
G | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.884-63C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757846 | ||||||
| chr4:109758043
|
C | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884-260G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758043 | ||||||
| chr4:109758060
|
T | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.884-277A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758060 | ||||||
| chr4:109758113
|
C | T | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.884-330G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758113 | ||||||
| chr4:109758222
|
T | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.884-439A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758222 | ||||||
| chr4:109758300
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.884-517G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758300 | ||||||
| chr4:109758814
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.884-1031G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758814 | ||||||
| chr4:109758836
|
T | C | 21 | a0001c0001t0001g0187a0001c0001t0001g0312a0001c0001t0001g0313others(18): Show | 21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.884-1053A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758836 | ||||||
| chr4:109758861
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.884-1078C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758861 | ||||||
| chr4:109758891
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.884-1108C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758891 | ||||||
| chr4:109758968
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.884-1185G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758968 | ||||||
| chr4:109759222
|
C | A | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.883+1048G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759222 | ||||||
| chr4:109759253
|
TA | T | 81 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(78): Show | 82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.883+1016delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759253 | ||||||
| chr4:109759265
|
A | AT | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.883+1004_883+1005i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759265 | ||||||
| chr4:109759265
|
A | T | 168 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(165): Show | 169 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.883+1005T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759265 | ||||||
| chr4:109759476
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.883+794T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759476 | ||||||
| chr4:109759515
|
A | G | 340 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(337): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.883+755T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759515 | ||||||
| chr4:109759515
|
A | T | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883+755T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759515 | ||||||
| chr4:109759642
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.883+628G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759642 | ||||||
| chr4:109759837
|
T | C | 342 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.883+433A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759837 | ||||||
| chr4:109759936
|
T | TACAA | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.883+330_883+333dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759936 | ||||||
| chr4:109759965
|
G | A | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.883+305C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759965 | ||||||
| chr4:109759980
|
T | G | 10 | a0001c0002t0001g0061a0001c0002t0001g0065a0001c0002t0001g0066others(7): Show | 10 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.883+290A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759980 | ||||||
| chr4:109759984
|
A | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.883+286T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759984 | ||||||
| chr4:109759992
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.883+278C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759992 | ||||||
| chr4:109760101
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883+169C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109760101 | ||||||
| chr4:109760462
|
C | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.772+61G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 5/12 | chr4 | 109760462 | ||||||
| chr4:109760727
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.659-91T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760727 | ||||||
| chr4:109760903
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0058 | 3 | HG02897.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.659-267G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760903 | ||||||
| chr4:109760984
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.659-348C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760984 | ||||||
| chr4:109761331
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.658+186A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109761331 | ||||||
| chr4:109761448
|
T | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.658+69A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109761448 | ||||||
| chr4:109761720
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.483-28C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761720 | ||||||
| chr4:109761797
|
A | G | 74 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0022others(71): Show | 75 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.483-105T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761797 | ||||||
| chr4:109761927
|
C | T | 2 | a0001c0002t0001g0048a0001c0002t0001g0117 | 2 | HG00673.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.483-235G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761927 | ||||||
| chr4:109761982
|
G | C | 1 | a0001c0002t0001g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483-290C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761982 | ||||||
| chr4:109761982
|
G | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.483-290C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761982 | ||||||
| chr4:109762189
|
T | TAAA | 11 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0223others(8): Show | 11 | HG02004.hp1 HG02109.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.483-500_483-498dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | ||||||
| chr4:109762189
|
T | TAAAA | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.483-501_483-498dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | ||||||
| chr4:109762189
|
T | TAAAAA | 35 | a0001c0001t0001g0058a0001c0001t0001g0153a0001c0001t0001g0159others(32): Show | 35 | HG00673.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.483-502_483-498dup others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | ||||||
| chr4:109762189
|
T | TAAAAAA | 50 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.483-503_483-498dup others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | ||||||
| chr4:109762189
|
T | TAAAAAAA | 10 | a0001c0001t0001g0174a0001c0001t0001g0276a0001c0002t0001g0051others(7): Show | 10 | HG01243.hp2 HG02027.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-504_483-498dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | ||||||
| chr4:109762224
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483-532A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762224 | ||||||
| chr4:109762298
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.483-606C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762298 | ||||||
| chr4:109762323
|
G | A | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.483-631C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762323 | ||||||
| chr4:109762338
|
A | C | 1 | a0003c0004t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.483-646T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762338 | ||||||
| chr4:109762389
|
G | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-697C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762389 | ||||||
| chr4:109762390
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.483-698C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762390 | ||||||
| chr4:109762394
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.483-702G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762394 | ||||||
| chr4:109762498
|
T | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.483-806A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762498 | ||||||
| chr4:109762517
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.483-825G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762517 | ||||||
| chr4:109762591
|
T | C | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.483-899A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762591 | ||||||
| chr4:109762656
|
T | C | 4 | a0003c0004t0001g0013a0003c0004t0001g0014a0003c0004t0001g0021others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-964A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762656 | ||||||
| chr4:109762656
|
T | G | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.483-964A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762656 | ||||||
| chr4:109763029
|
T | C | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.483-1337A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763029 | ||||||
| chr4:109763067
|
G | T | 14 | a0001c0001t0001g0098a0001c0001t0001g0270a0001c0001t0001g0339others(11): Show | 14 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-1375C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763067 | ||||||
| chr4:109763154
|
T | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.482+1383A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763154 | ||||||
| chr4:109763194
|
C | G | 3 | a0002c0003t0001g0259a0002c0003t0001g0306a0002c0003t0001g0315 | 3 | HG02027.hp2 NA18950.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.482+1343G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763194 | ||||||
| chr4:109763220
|
G | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1317C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763220 | ||||||
| chr4:109763239
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1298A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763239 | ||||||
| chr4:109763421
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0270a0001c0001t0002g0346 | 3 | HG02615.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482+1116T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763421 | ||||||
| chr4:109763575
|
G | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482+962C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763575 | ||||||
| chr4:109763588
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.482+949A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763588 | ||||||
| chr4:109763631
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.482+906T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763631 | ||||||
| chr4:109763714
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.482+823C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763714 | ||||||
| chr4:109763892
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+645T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763892 | ||||||
| chr4:109763940
|
C | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.482+597G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763940 | ||||||
| chr4:109763946
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+591G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763946 | ||||||
| chr4:109764190
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.482+347T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764190 | ||||||
| chr4:109764523
|
A | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+14T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764523 | ||||||
| chr4:109764531
|
G | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0270a0001c0001t0001g0339others(14): Show | 17 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.482+6C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764531 | ||||||
| chr4:109764531
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0058 | 3 | HG02897.hp2 NA19030.hp2 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.482+6C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764531 | ||||||
| chr4:109764806
|
C | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.329-116G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764806 | ||||||
| chr4:109764845
|
A | G | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.329-155T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764845 | ||||||
| chr4:109764898
|
A | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.329-208T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764898 | ||||||
| chr4:109764923
|
A | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.329-233T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764923 | ||||||
| chr4:109764928
|
A | G | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.329-238T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764928 | ||||||
| chr4:109764954
|
C | G | 1 | a0001c0002t0002g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.329-264G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764954 | ||||||
| chr4:109765013
|
A | T | 2 | a0001c0002t0002g0023a0001c0002t0002g0024 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.329-323T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765013 | ||||||
| chr4:109765040
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-350G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765040 | ||||||
| chr4:109765151
|
T | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-461A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765151 | ||||||
| chr4:109765257
|
T | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.329-567A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765257 | ||||||
| chr4:109765620
|
C | G | 137 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0010others(134): Show | 138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.329-930G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765620 | ||||||
| chr4:109765703
|
G | A | 1 | a0001c0002t0001g0139 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.328+851C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765703 | ||||||
| chr4:109765776
|
TG | T | 139 | a0001c0001t0003g0337a0001c0001t0003g0338a0001c0002t0001g0001others(136): Show | 140 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.328+777delC | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765776 | ||||||
| chr4:109765803
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.328+751C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765803 | ||||||
| chr4:109765839
|
C | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.328+715G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765839 | ||||||
| chr4:109765893
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.328+661G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765893 | ||||||
| chr4:109766016
|
G | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.328+538C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766016 | ||||||
| chr4:109766113
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+441C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766113 | ||||||
| chr4:109766356
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.328+198G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766356 | ||||||
| chr4:109766872
|
C | T | 1 | a0001c0001t0001g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-48G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766872 | ||||||
| chr4:109766911
|
G | T | 1 | a0001c0002t0001g0047 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.58-87C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766911 | ||||||
| chr4:109766963
|
C | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-139G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766963 | ||||||
| chr4:109766976
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-152C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766976 | ||||||
| chr4:109767005
|
A | T | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-181T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767005 | ||||||
| chr4:109767169
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-345T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767169 | ||||||
| chr4:109767206
|
A | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-382T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767206 | ||||||
| chr4:109767270
|
A | C | 10 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-446T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767270 | ||||||
| chr4:109767334
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-510C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767334 | ||||||
| chr4:109767348
|
C | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-524G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767348 | ||||||
| chr4:109767419
|
T | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-595A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767419 | ||||||
| chr4:109767463
|
T | G | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-639A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767463 | ||||||
| chr4:109767476
|
T | C | 2 | a0001c0002t0001g0045a0001c0002t0001g0112 | 2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.58-652A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767476 | ||||||
| chr4:109767480
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-656G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767480 | ||||||
| chr4:109767486
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-662A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767486 | ||||||
| chr4:109767556
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-732C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767556 | ||||||
| chr4:109767608
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.58-784G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767608 | ||||||
| chr4:109767609
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-785C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767609 | ||||||
| chr4:109767611
|
T | A | 2 | a0001c0001t0001g0146a0001c0001t0003g0148 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58-787A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767611 | ||||||
| chr4:109767656
|
C | A | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-832G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767656 | ||||||
| chr4:109767659
|
T | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-835A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767659 | ||||||
| chr4:109767771
|
C | T | 63 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(60): Show | 63 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.58-947G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767771 | ||||||
| chr4:109767918
|
G | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-1094C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767918 | ||||||
| chr4:109767931
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.58-1107T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767931 | ||||||
| chr4:109767967
|
T | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-1143A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767967 | ||||||
| chr4:109767988
|
T | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-1164A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767988 | ||||||
| chr4:109768100
|
G | A | 1 | a0001c0001t0003g0348 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-1276C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768100 | ||||||
| chr4:109768188
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0002g0346 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-1364G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768188 | ||||||
| chr4:109768201
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1377C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768201 | ||||||
| chr4:109768278
|
C | CA | 44 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0036others(41): Show | 44 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.58-1455dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | ||||||
| chr4:109768278
|
CA | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 21 | HG00735.hp2 HG01081.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-1455delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | ||||||
| chr4:109768278
|
CAA | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.58-1456_58-1455del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | ||||||
| chr4:109768318
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.58-1494C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768318 | ||||||
| chr4:109768334
|
T | TA | 10 | a0001c0001t0001g0146a0001c0001t0001g0209a0001c0001t0001g0229others(7): Show | 10 | HG00639.hp2 HG01891.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-1511dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | ||||||
| chr4:109768334
|
T | TAA | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-1512_58-1511dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | ||||||
| chr4:109768334
|
T | TAAA | 63 | a0001c0001t0001g0098a0001c0002t0001g0001a0001c0002t0001g0008others(60): Show | 64 | HG00558.hp1 HG00733.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-1513_58-1511dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | ||||||
| chr4:109768334
|
TA | T | 12 | a0001c0001t0001g0164a0001c0001t0001g0183a0001c0001t0001g0187others(9): Show | 12 | HG00673.hp2 HG01168.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1511delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | ||||||
| chr4:109768401
|
T | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.58-1577A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768401 | ||||||
| chr4:109768440
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-1616G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768440 | ||||||
| chr4:109768455
|
C | T | 2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-1631G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768455 | ||||||
| chr4:109768478
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-1654T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768478 | ||||||
| chr4:109768583
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0003g0148 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58-1759T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768583 | ||||||
| chr4:109768614
|
C | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-1790G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768614 | ||||||
| chr4:109768633
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58-1809G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768633 | ||||||
| chr4:109768645
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58-1821G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768645 | ||||||
| chr4:109768718
|
C | T | 1 | a0001c0002t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.58-1894G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768718 | ||||||
| chr4:109768739
|
T | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-1915A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768739 | ||||||
| chr4:109768781
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1957A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768781 | ||||||
| chr4:109768845
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.58-2021T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768845 | ||||||
| chr4:109768893
|
T | TAC | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.58-2071_58-2070dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768893 | ||||||
| chr4:109768972
|
C | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.58-2148G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768972 | ||||||
| chr4:109768978
|
C | T | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-2154G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768978 | ||||||
| chr4:109768979
|
G | A | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-2155C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768979 | ||||||
| chr4:109769099
|
T | G | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.58-2275A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769099 | ||||||
| chr4:109769181
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-2357A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769181 | ||||||
| chr4:109769430
|
C | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.58-2606G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769430 | ||||||
| chr4:109769480
|
T | A | 83 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(80): Show | 83 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.58-2656A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769480 | ||||||
| chr4:109769503
|
A | T | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 83 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.58-2679T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769503 | ||||||
| chr4:109769529
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.58-2705G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769529 | ||||||
| chr4:109769584
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-2760C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769584 | ||||||
| chr4:109769778
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.58-2954G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769778 | ||||||
| chr4:109769862
|
A | G | 13 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0299others(10): Show | 13 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-3038T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769862 | ||||||
| chr4:109769880
|
C | T | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-3056G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769880 | ||||||
| chr4:109769960
|
G | A | 1 | a0009c0011t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-3136C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769960 | ||||||
| chr4:109770011
|
C | A | 2 | a0001c0002t0001g0036a0001c0002t0001g0073 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.58-3187G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770011 | ||||||
| chr4:109770067
|
C | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-3243G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770067 | ||||||
| chr4:109770095
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-3271G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770095 | ||||||
| chr4:109770349
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-3525G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770349 | ||||||
| chr4:109770502
|
GC | G | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-3679delG | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770502 | ||||||
| chr4:109770507
|
G | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-3683C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770507 | ||||||
| chr4:109770515
|
C | G | 1 | a0001c0001t0001g0313 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.58-3691G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770515 | ||||||
| chr4:109770556
|
TA | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.58-3733delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770556 | ||||||
| chr4:109770590
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0140 | 2 | HG01975.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.58-3766A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770590 | ||||||
| chr4:109770633
|
G | GA | 52 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 53 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.58-3810dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770633 | ||||||
| chr4:109770633
|
GA | G | 23 | a0001c0001t0001g0099a0001c0001t0001g0163a0001c0001t0001g0188others(20): Show | 23 | HG00735.hp2 HG01081.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.58-3810delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770633 | ||||||
| chr4:109770827
|
G | T | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4003C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770827 | ||||||
| chr4:109770860
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-4036T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770860 | ||||||
| chr4:109770879
|
C | T | 1 | a0001c0001t0001g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-4055G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770879 | ||||||
| chr4:109770902
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-4078C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770902 | ||||||
| chr4:109771075
|
G | A | 100 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(97): Show | 101 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.58-4251C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771075 | ||||||
| chr4:109771098
|
G | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-4274C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771098 | ||||||
| chr4:109771112
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-4288G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771112 | ||||||
| chr4:109771284
|
T | G | 2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-4460A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771284 | ||||||
| chr4:109771354
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58-4530G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771354 | ||||||
| chr4:109771400
|
T | TA | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-4577dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771400 | ||||||
| chr4:109771522
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.58-4698A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771522 | ||||||
| chr4:109771541
|
C | T | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-4717G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771541 | ||||||
| chr4:109771550
|
C | CA | 29 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 29 | HG00544.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4727dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771550 | ||||||
| chr4:109771550
|
C | CAA | 37 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(34): Show | 37 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-4728_58-4727dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771550 | ||||||
| chr4:109771596
|
C | A | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-4772G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771596 | ||||||
| chr4:109771714
|
C | CA | 41 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0166others(38): Show | 41 | HG00438.hp1 HG00741.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-4891dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771714
|
C | CAA | 90 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0100others(87): Show | 91 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.58-4892_58-4891dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771714
|
C | CAAA | 33 | a0001c0002t0001g0008a0001c0002t0001g0039a0001c0002t0001g0049others(30): Show | 33 | HG01069.hp2 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.58-4893_58-4891dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771714
|
C | CAAAA | 6 | a0001c0001t0001g0098a0001c0002t0001g0036a0001c0002t0001g0037others(3): Show | 6 | HG00733.hp1 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-4894_58-4891dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771714
|
CA | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00323.hp2 HG00738.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-4891delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771714
|
CAAA | C | 11 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(8): Show | 11 | HG01433.hp1 HG01928.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-4893_58-4891del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | ||||||
| chr4:109771845
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096 | 3 | HG01069.hp1 HG01071.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.58-5021T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771845 | ||||||
| chr4:109771935
|
T | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.58-5111A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771935 | ||||||
| chr4:109772279
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-5455C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772279 | ||||||
| chr4:109772294
|
T | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 64 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-5470A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772294 | ||||||
| chr4:109772379
|
G | A | 55 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-5555C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772379 | ||||||
| chr4:109772391
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-5567G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772391 | ||||||
| chr4:109772413
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.58-5589C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772413 | ||||||
| chr4:109772580
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58-5756G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772580 | ||||||
| chr4:109772581
|
G | GT | 138 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 139 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.58-5758dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772581 | ||||||
| chr4:109772653
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5829T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772653 | ||||||
| chr4:109772667
|
C | A | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-5843G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772667 | ||||||
| chr4:109772784
|
A | G | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-5960T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772784 | ||||||
| chr4:109772823
|
A | G | 50 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-5999T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772823 | ||||||
| chr4:109773213
|
C | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG00738.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-6389G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773213 | ||||||
| chr4:109773253
|
C | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-6429G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773253 | ||||||
| chr4:109773265
|
C | T | 1 | a0001c0002t0001g0010 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-6441G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773265 | ||||||
| chr4:109773300
|
G | A | 1 | a0001c0002t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.58-6476C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773300 | ||||||
| chr4:109773384
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.58-6560G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773384 | ||||||
| chr4:109773385
|
G | A | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-6561C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773385 | ||||||
| chr4:109773415
|
C | A | 2 | a0001c0002t0001g0052a0001c0002t0001g0130 | 2 | NA18970.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.58-6591G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773415 | ||||||
| chr4:109773465
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 64 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-6641C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773465 | ||||||
| chr4:109773473
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-6649C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773473 | ||||||
| chr4:109773493
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-6669G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773493 | ||||||
| chr4:109773597
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58-6773A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773597 | ||||||
| chr4:109773608
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-6784G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773608 | ||||||
| chr4:109773638
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.58-6814A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773638 | ||||||
| chr4:109773650
|
T | C | 2 | a0001c0001t0001g0336a0001c0001t0002g0329 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58-6826A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773650 | ||||||
| chr4:109773666
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-6842A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773666 | ||||||
| chr4:109773811
|
C | T | 164 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(161): Show | 165 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.58-6987G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773811 | ||||||
| chr4:109774100
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-7276A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774100 | ||||||
| chr4:109774205
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58-7381A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774205 | ||||||
| chr4:109774404
|
GAGCA | G | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-7584_58-7581del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774404 | ||||||
| chr4:109774434
|
G | A | 99 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(96): Show | 100 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.58-7610C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774434 | ||||||
| chr4:109774558
|
G | A | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-7734C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774558 | ||||||
| chr4:109774595
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-7771C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774595 | ||||||
| chr4:109774664
|
C | A | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-7840G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774664 | ||||||
| chr4:109774783
|
A | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-7959T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774783 | ||||||
| chr4:109774913
|
T | C | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.58-8089A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774913 | ||||||
| chr4:109775016
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.58-8192T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775016 | ||||||
| chr4:109775063
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-8239A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775063 | ||||||
| chr4:109775069
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-8245G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775069 | ||||||
| chr4:109775102
|
G | A | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-8278C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775102 | ||||||
| chr4:109775110
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.58-8286G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775110 | ||||||
| chr4:109775112
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58-8288C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775112 | ||||||
| chr4:109775183
|
C | G | 50 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-8359G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775183 | ||||||
| chr4:109775213
|
G | A | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.58-8389C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775213 | ||||||
| chr4:109775333
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58-8509C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775333 | ||||||
| chr4:109775394
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-8570G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775394 | ||||||
| chr4:109775619
|
A | G | 2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-8795T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775619 | ||||||
| chr4:109775755
|
T | C | 156 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(153): Show | 157 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.58-8931A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775755 | ||||||
| chr4:109775776
|
G | A | 1 | a0001c0002t0001g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.58-8952C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775776 | ||||||
| chr4:109775820
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-8996A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775820 | ||||||
| chr4:109775860
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.58-9036A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775860 | ||||||
| chr4:109775889
|
C | G | 135 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(132): Show | 136 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.58-9065G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775889 | ||||||
| chr4:109775993
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9169T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775993 | ||||||
| chr4:109776071
|
G | A | 50 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(47): Show | 50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-9247C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776071 | ||||||
| chr4:109776166
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.58-9342T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776166 | ||||||
| chr4:109776288
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9464C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776288 | ||||||
| chr4:109776313
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-9489A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776313 | ||||||
| chr4:109776316
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.58-9492A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776316 | ||||||
| chr4:109776366
|
G | C | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-9542C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776366 | ||||||
| chr4:109776402
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.58-9578G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776402 | ||||||
| chr4:109776413
|
G | A | 1 | a0001c0002t0001g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.58-9589C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776413 | ||||||
| chr4:109776470
|
T | C | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-9646A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776470 | ||||||
| chr4:109776499
|
A | G | 179 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(176): Show | 180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-9675T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776499 | ||||||
| chr4:109776631
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9807C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776631 | ||||||
| chr4:109776767
|
G | A | 22 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.58-9943C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776767 | ||||||
| chr4:109776801
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58-9977C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776801 | ||||||
| chr4:109776853
|
T | C | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-10029A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776853 | ||||||
| chr4:109776972
|
A | G | 179 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(176): Show | 180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-10148T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776972 | ||||||
| chr4:109777039
|
C | G | 1 | a0001c0001t0001g0229 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.58-10215G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777039 | ||||||
| chr4:109777068
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-10244G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777068 | ||||||
| chr4:109777130
|
C | A | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-10306G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777130 | ||||||
| chr4:109777130
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.58-10306G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777130 | ||||||
| chr4:109777185
|
A | T | 1 | a0003c0004t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-10361T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777185 | ||||||
| chr4:109777249
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-10425G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777249 | ||||||
| chr4:109777293
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-10469A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777293 | ||||||
| chr4:109777336
|
T | C | 1 | a0001c0001t0001g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-10512A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777336 | ||||||
| chr4:109777340
|
G | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58-10516C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777340 | ||||||
| chr4:109777342
|
A | G | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-10518T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777342 | ||||||
| chr4:109777360
|
C | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-10536G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777360 | ||||||
| chr4:109777388
|
T | C | 156 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(153): Show | 157 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.58-10564A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777388 | ||||||
| chr4:109777419
|
C | T | 135 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(132): Show | 136 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.58-10595G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777419 | ||||||
| chr4:109777450
|
T | C | 179 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(176): Show | 180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-10626A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777450 | ||||||
| chr4:109777522
|
C | CAATAATA others(2): Show |
12 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-10699_58-10698i others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777522 | ||||||
| chr4:109777530
|
A | T | 12 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-10706T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777530 | ||||||
| chr4:109777691
|
A | G | 24 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(21): Show | 24 | HG00673.hp1 HG00735.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.58-10867T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777691 | ||||||
| chr4:109777708
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-10884G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777708 | ||||||
| chr4:109777853
|
G | A | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-11029C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777853 | ||||||
| chr4:109777873
|
C | T | 179 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(176): Show | 180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-11049G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777873 | ||||||
| chr4:109777874
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11050C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777874 | ||||||
| chr4:109777934
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.58-11110A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777934 | ||||||
| chr4:109777942
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.58-11118T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777942 | ||||||
| chr4:109778001
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.58-11177T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778001 | ||||||
| chr4:109778036
|
A | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0195 | 2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.58-11212T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778036 | ||||||
| chr4:109778047
|
A | T | 13 | a0001c0001t0001g0270a0001c0001t0001g0339a0001c0001t0001g0340others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-11223T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778047 | ||||||
| chr4:109778081
|
G | C | 1 | a0001c0002t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.58-11257C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778081 | ||||||
| chr4:109778103
|
G | C | 1 | a0002c0003t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58-11279C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778103 | ||||||
| chr4:109778195
|
A | C | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-11371T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778195 | ||||||
| chr4:109778274
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11450A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778274 | ||||||
| chr4:109778275
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11451C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778275 | ||||||
| chr4:109778332
|
A | T | 4 | a0001c0002t0001g0045a0001c0002t0001g0112a0001c0002t0001g0131others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-11508T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778332 | ||||||
| chr4:109778683
|
A | G | 165 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(162): Show | 166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-11859T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778683 | ||||||
| chr4:109778784
|
T | C | 342 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.58-11960A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778784 | ||||||
| chr4:109778816
|
G | T | 2 | a0001c0001t0001g0336a0001c0001t0002g0329 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58-11992C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778816 | ||||||
| chr4:109778977
|
G | A | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-12153C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778977 | ||||||
| chr4:109779085
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.58-12261G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779085 | ||||||
| chr4:109779129
|
A | C | 165 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(162): Show | 166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-12305T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779129 | ||||||
| chr4:109779151
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-12327T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779151 | ||||||
| chr4:109779169
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.58-12345T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779169 | ||||||
| chr4:109779182
|
T | G | 165 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(162): Show | 166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-12358A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779182 | ||||||
| chr4:109779218
|
G | T | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-12394C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779218 | ||||||
| chr4:109779344
|
C | T | 30 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.58-12520G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779344 | ||||||
| chr4:109779371
|
C | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-12547G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779371 | ||||||
| chr4:109779693
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-12869T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779693 | ||||||
| chr4:109779699
|
A | G | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-12875T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779699 | ||||||
| chr4:109779724
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-12900G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779724 | ||||||
| chr4:109779778
|
A | G | 144 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(141): Show | 145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.58-12954T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779778 | ||||||
| chr4:109779799
|
C | T | 8 | a0001c0002t0001g0036a0001c0002t0001g0068a0001c0002t0001g0071others(5): Show | 8 | HG01074.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-12975G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779799 | ||||||
| chr4:109779805
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-12981T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779805 | ||||||
| chr4:109779828
|
T | C | 165 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(162): Show | 166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-13004A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779828 | ||||||
| chr4:109779911
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-13087C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779911 | ||||||
| chr4:109779923
|
G | A | 1 | a0001c0002t0001g0115 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.58-13099C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779923 | ||||||
| chr4:109779924
|
C | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0108a0011c0009t0001g0106 | 3 | HG01175.hp2 HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-13100G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779924 | ||||||
| chr4:109779954
|
TCCTTATA others(15): Show |
T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-13152_58-13131d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779954 | ||||||
| chr4:109780022
|
G | A | 1 | a0010c0013t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-13198C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780022 | ||||||
| chr4:109780165
|
G | C | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.58-13341C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780165 | ||||||
| chr4:109780252
|
C | T | 1 | a0003c0004t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58-13428G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780252 | ||||||
| chr4:109780331
|
T | G | 188 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(185): Show | 189 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.58-13507A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780331 | ||||||
| chr4:109780333
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02559.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-13509C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780333 | ||||||
| chr4:109780500
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-13676C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780500 | ||||||
| chr4:109780625
|
G | C | 2 | a0001c0008t0001g0293a0001c0008t0002g0269 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-13801C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780625 | ||||||
| chr4:109780631
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-13807C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780631 | ||||||
| chr4:109780824
|
T | A | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.58-14000A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780824 | ||||||
| chr4:109780969
|
G | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-14145C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780969 | ||||||
| chr4:109781049
|
T | C | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-14225A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781049 | ||||||
| chr4:109781085
|
A | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-14261T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781085 | ||||||
| chr4:109781238
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-14414A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781238 | ||||||
| chr4:109781354
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0002g0346 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-14530G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781354 | ||||||
| chr4:109781369
|
G | A | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-14545C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781369 | ||||||
| chr4:109781380
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-14556T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781380 | ||||||
| chr4:109781500
|
A | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-14676T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781500 | ||||||
| chr4:109781795
|
A | T | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-14971T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781795 | ||||||
| chr4:109781819
|
G | A | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-14995C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781819 | ||||||
| chr4:109781879
|
CACA | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0211a0001c0001t0001g0212others(8): Show | 11 | HG00639.hp2 HG01074.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-15058_58-15056d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781879 | ||||||
| chr4:109781904
|
A | G | 16 | a0001c0001t0001g0270a0001c0001t0001g0339a0001c0001t0001g0340others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-15080T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781904 | ||||||
| chr4:109781907
|
G | A | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.58-15083C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781907 | ||||||
| chr4:109782092
|
A | T | 56 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(53): Show | 56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-15268T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782092 | ||||||
| chr4:109782116
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-15292G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782116 | ||||||
| chr4:109782209
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-15385G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782209 | ||||||
| chr4:109782406
|
A | G | 1 | a0001c0001t0001g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-15582T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782406 | ||||||
| chr4:109782431
|
C | CA | 68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(65): Show | 68 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.58-15608dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | ||||||
| chr4:109782431
|
C | CAA | 126 | a0001c0001t0001g0004a0001c0001t0001g0085a0001c0001t0001g0099others(123): Show | 128 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.58-15609_58-15608d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | ||||||
| chr4:109782431
|
C | CAAA | 13 | a0001c0001t0001g0098a0001c0001t0001g0155a0001c0001t0001g0183others(10): Show | 13 | HG01175.hp1 HG01975.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-15610_58-15608d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | ||||||
| chr4:109782431
|
C | CAAAA | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.58-15611_58-15608d others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | ||||||
| chr4:109782446
|
T | A | 1 | a0001c0002t0001g0087 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-15622A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782446 | ||||||
| chr4:109782597
|
C | T | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-15773G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782597 | ||||||
| chr4:109782741
|
G | A | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-15917C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782741 | ||||||
| chr4:109782936
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0195 | 2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.58-16112G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782936 | ||||||
| chr4:109782976
|
T | C | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-16152A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782976 | ||||||
| chr4:109783201
|
C | A | 1 | a0006c0014t0001g0064 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.58-16377G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783201 | ||||||
| chr4:109783277
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58-16453G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783277 | ||||||
| chr4:109783372
|
T | C | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.58-16548A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783372 | ||||||
| chr4:109783411
|
A | G | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-16587T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783411 | ||||||
| chr4:109783811
|
T | TAATATAT others(3): Show |
19 | a0001c0002t0001g0011a0001c0002t0001g0051a0001c0002t0001g0052others(16): Show | 19 | HG00558.hp2 HG01070.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(5): Show |
12 | a0001c0002t0001g0043a0001c0002t0001g0044a0001c0002t0001g0048others(9): Show | 12 | HG00609.hp2 HG00673.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(7): Show |
4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0055others(1): Show | 4 | HG00609.hp1 HG01978.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(9): Show |
1 | a0001c0002t0001g0115 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(15): Show |
1 | a0001c0002t0001g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(17): Show |
2 | a0001c0002t0002g0024a0001c0002t0002g0026 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(19): Show |
1 | a0001c0002t0002g0023 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(23): Show |
2 | a0001c0002t0001g0136a0009c0011t0001g0113 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(25): Show |
1 | a0001c0002t0003g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(34): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(27): Show |
2 | a0001c0002t0001g0054a0001c0002t0002g0025 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(33): Show |
2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(42): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(35): Show |
1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(37): Show |
1 | a0001c0002t0001g0112 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(39): Show |
1 | a0001c0006t0005g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(48): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783811
|
T | TAATATAT others(41): Show |
1 | a0001c0002t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(50): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | ||||||
| chr4:109783812
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58-16988C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GAGATATT others(3): Show |
16 | a0001c0001t0001g0313a0001c0001t0001g0319a0002c0003t0001g0259others(13): Show | 16 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GAGATATT others(5): Show |
2 | a0001c0001t0001g0312a0002c0003t0001g0324 | 2 | HG03831.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GAGATATT others(9): Show |
2 | a0002c0003t0001g0310a0002c0003t0001g0311 | 2 | NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GAT | 25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 25 | HG00544.hp1 HG01109.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.58-16990_58-16989d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(1): Show |
3 | a0001c0002t0001g0040a0001c0002t0001g0104a0001c0002t0001g0105 | 3 | HG02004.hp1 HG02258.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.58-16996_58-16989d others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(5): Show |
1 | a0001c0002t0001g0180 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.58-17000_58-16989d others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(7): Show |
4 | a0004c0005t0001g0101a0004c0005t0001g0102a0004c0005t0001g0103others(1): Show | 4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-17002_58-16989d others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(9): Show |
2 | a0001c0002t0001g0073a0010c0013t0001g0297 | 2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.58-17004_58-16989d others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(15): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.58-17010_58-16989d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(17): Show |
1 | a0001c0002t0001g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(19): Show |
1 | a0001c0002t0001g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(27): Show |
3 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0004g0007 | 3 | HG01070.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(29): Show |
7 | a0001c0001t0001g0098a0001c0002t0001g0008a0001c0002t0001g0060others(4): Show | 7 | HG01071.hp1 HG01071.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(38): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(31): Show |
7 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(40): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(33): Show |
9 | a0001c0001t0001g0110a0001c0002t0001g0063a0001c0002t0001g0066others(6): Show | 9 | HG01069.hp2 HG01081.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(42): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(35): Show |
11 | a0001c0002t0001g0001a0001c0002t0001g0035a0001c0002t0001g0059others(8): Show | 12 | HG00733.hp1 HG01167.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(37): Show |
10 | a0001c0001t0001g0085a0001c0002t0001g0037a0001c0002t0001g0086others(7): Show | 10 | HG01123.hp2 HG01257.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(39): Show |
12 | a0001c0002t0001g0061a0001c0002t0001g0068a0001c0002t0001g0081others(9): Show | 12 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(48): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(41): Show |
6 | a0001c0002t0001g0057a0001c0002t0001g0077a0001c0002t0001g0078others(3): Show | 6 | NA18747.hp1 NA18984.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(50): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(43): Show |
1 | a0001c0002t0001g0076 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(52): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(49): Show |
2 | a0001c0002t0001g0074a0001c0002t0001g0075 | 2 | HG00558.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(58): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | GATATATA others(51): Show |
1 | a0001c0002t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
G | T | 55 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(52): Show | 55 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-16988C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
GAT | G | 7 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-16990_58-16989d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783812
|
GATAT | G | 5 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG02559.hp2 HG03195.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-16992_58-16989d others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | ||||||
| chr4:109783975
|
G | A | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-17151C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783975 | ||||||
| chr4:109784084
|
G | A | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-17260C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784084 | ||||||
| chr4:109784093
|
T | G | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-17269A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784093 | ||||||
| chr4:109784095
|
G | T | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-17271C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784095 | ||||||
| chr4:109784148
|
T | A | 1 | a0003c0004t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.58-17324A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784148 | ||||||
| chr4:109784472
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+17443T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784472 | ||||||
| chr4:109784893
|
GA | G | 189 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(186): Show | 190 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.57+17021delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784893 | ||||||
| chr4:109784993
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.57+16922C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784993 | ||||||
| chr4:109785016
|
C | A | 1 | a0002c0003t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+16899G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785016 | ||||||
| chr4:109785021
|
G | A | 7 | a0001c0001t0001g0146a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG06807.hp1 NA18961.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+16894C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785021 | ||||||
| chr4:109785052
|
C | A | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16863G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785052 | ||||||
| chr4:109785091
|
A | C | 165 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(162): Show | 166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.57+16824T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785091 | ||||||
| chr4:109785108
|
A | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+16807T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785108 | ||||||
| chr4:109785183
|
G | A | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16732C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785183 | ||||||
| chr4:109785296
|
G | A | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16619C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785296 | ||||||
| chr4:109785328
|
T | C | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.57+16587A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785328 | ||||||
| chr4:109785375
|
T | C | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+16540A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785375 | ||||||
| chr4:109785480
|
T | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 23 | HG00735.hp2 HG01261.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+16435A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785480 | ||||||
| chr4:109786051
|
A | C | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+15864T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786051 | ||||||
| chr4:109786077
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+15838T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786077 | ||||||
| chr4:109786082
|
G | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+15833C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786082 | ||||||
| chr4:109786223
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.57+15692C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786223 | ||||||
| chr4:109786225
|
T | C | 21 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(18): Show | 21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+15690A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786225 | ||||||
| chr4:109786239
|
C | T | 1 | a0001c0002t0001g0271 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.57+15676G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786239 | ||||||
| chr4:109786277
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0205 | 2 | NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.57+15638G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786277 | ||||||
| chr4:109786385
|
T | G | 9 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+15530A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786385 | ||||||
| chr4:109786390
|
C | CT | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+15524dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786390 | ||||||
| chr4:109786413
|
C | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+15502G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786413 | ||||||
| chr4:109786518
|
C | A | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+15397G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786518 | ||||||
| chr4:109786583
|
C | A | 100 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(97): Show | 101 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.57+15332G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786583 | ||||||
| chr4:109786610
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+15305C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786610 | ||||||
| chr4:109786694
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.57+15221C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786694 | ||||||
| chr4:109786727
|
A | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | NA18956.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+15188T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786727 | ||||||
| chr4:109786823
|
A | G | 21 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(18): Show | 21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+15092T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786823 | ||||||
| chr4:109786869
|
T | C | 79 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(76): Show | 80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.57+15046A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786869 | ||||||
| chr4:109786977
|
G | A | 9 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+14938C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786977 | ||||||
| chr4:109787127
|
C | A | 1 | a0001c0002t0001g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+14788G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787127 | ||||||
| chr4:109787147
|
T | G | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+14768A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787147 | ||||||
| chr4:109787250
|
T | C | 99 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(96): Show | 100 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.57+14665A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787250 | ||||||
| chr4:109787264
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.57+14651C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787264 | ||||||
| chr4:109787304
|
C | T | 1 | a0002c0003t0001g0309 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.57+14611G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787304 | ||||||
| chr4:109787361
|
A | C | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+14554T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787361 | ||||||
| chr4:109787417
|
G | A | 103 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(100): Show | 104 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.57+14498C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787417 | ||||||
| chr4:109787474
|
C | T | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+14441G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787474 | ||||||
| chr4:109787480
|
A | G | 112 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(109): Show | 112 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.57+14435T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787480 | ||||||
| chr4:109787514
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+14401T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787514 | ||||||
| chr4:109787588
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.57+14327C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787588 | ||||||
| chr4:109787595
|
T | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0108a0011c0009t0001g0106 | 3 | HG01175.hp2 HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+14320A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787595 | ||||||
| chr4:109787720
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+14195T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787720 | ||||||
| chr4:109787796
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+14119T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787796 | ||||||
| chr4:109787865
|
T | A | 7 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+14050A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787865 | ||||||
| chr4:109787892
|
G | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+14023C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787892 | ||||||
| chr4:109788006
|
A | G | 8 | a0001c0002t0001g0036a0001c0002t0001g0068a0001c0002t0001g0071others(5): Show | 8 | HG01074.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+13909T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788006 | ||||||
| chr4:109788044
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.57+13871A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788044 | ||||||
| chr4:109788137
|
A | G | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+13778T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788137 | ||||||
| chr4:109788376
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.57+13539C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788376 | ||||||
| chr4:109788501
|
C | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+13414G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788501 | ||||||
| chr4:109788517
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+13398A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788517 | ||||||
| chr4:109788718
|
G | T | 1 | a0002c0003t0001g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.57+13197C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788718 | ||||||
| chr4:109788723
|
G | A | 81 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(78): Show | 82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.57+13192C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788723 | ||||||
| chr4:109788861
|
G | C | 1 | a0001c0001t0001g0323 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.57+13054C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788861 | ||||||
| chr4:109788878
|
C | T | 80 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+13037G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788878 | ||||||
| chr4:109788890
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.57+13025G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788890 | ||||||
| chr4:109788951
|
A | G | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(322): Show | 328 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.57+12964T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788951 | ||||||
| chr4:109789020
|
G | T | 81 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(78): Show | 82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.57+12895C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789020 | ||||||
| chr4:109789038
|
C | A | 5 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0053others(2): Show | 5 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+12877G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789038 | ||||||
| chr4:109789042
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.57+12873A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789042 | ||||||
| chr4:109789134
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+12781T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789134 | ||||||
| chr4:109789160
|
A | G | 80 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+12755T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789160 | ||||||
| chr4:109789249
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+12666T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789249 | ||||||
| chr4:109789386
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+12529T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789386 | ||||||
| chr4:109789423
|
A | G | 3 | a0001c0001t0001g0270a0001c0008t0001g0293a0001c0008t0002g0269 | 3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+12492T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789423 | ||||||
| chr4:109789441
|
G | GAC | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+12472_57+12473d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789441 | ||||||
| chr4:109789461
|
G | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+12454C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789461 | ||||||
| chr4:109789552
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.57+12363T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789552 | ||||||
| chr4:109789568
|
T | C | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+12347A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789568 | ||||||
| chr4:109789830
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+12085C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789830 | ||||||
| chr4:109789925
|
G | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+11990C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789925 | ||||||
| chr4:109789938
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.57+11977C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789938 | ||||||
| chr4:109790007
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11908A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790007 | ||||||
| chr4:109790256
|
G | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+11659C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790256 | ||||||
| chr4:109790467
|
T | C | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+11448A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790467 | ||||||
| chr4:109790512
|
G | C | 1 | a0001c0002t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.57+11403C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790512 | ||||||
| chr4:109790531
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11384G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790531 | ||||||
| chr4:109790741
|
C | T | 2 | a0001c0002t0001g0022a0001c0002t0001g0035 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.57+11174G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790741 | ||||||
| chr4:109790791
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11124C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790791 | ||||||
| chr4:109790837
|
C | G | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+11078G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790837 | ||||||
| chr4:109790910
|
T | C | 1 | a0001c0002t0001g0040 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.57+11005A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790910 | ||||||
| chr4:109790952
|
A | G | 2 | a0001c0001t0001g0169a0002c0003t0001g0259 | 2 | NA18950.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.57+10963T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790952 | ||||||
| chr4:109791166
|
T | C | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+10749A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791166 | ||||||
| chr4:109791203
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+10712C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791203 | ||||||
| chr4:109791432
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.57+10483C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791432 | ||||||
| chr4:109791729
|
T | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+10186A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791729 | ||||||
| chr4:109791738
|
A | T | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+10177T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791738 | ||||||
| chr4:109791927
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.57+9988C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791927 | ||||||
| chr4:109792069
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.57+9846A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792069 | ||||||
| chr4:109792091
|
C | T | 80 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+9824G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792091 | ||||||
| chr4:109792119
|
C | A | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.57+9796G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792119 | ||||||
| chr4:109792327
|
T | C | 191 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(188): Show | 192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+9588A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792327 | ||||||
| chr4:109792376
|
G | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+9539C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792376 | ||||||
| chr4:109792447
|
A | C | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+9468T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792447 | ||||||
| chr4:109792523
|
C | T | 80 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+9392G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792523 | ||||||
| chr4:109792545
|
A | G | 2 | a0001c0002t0001g0045a0001c0002t0001g0112 | 2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.57+9370T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792545 | ||||||
| chr4:109792592
|
C | G | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+9323G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792592 | ||||||
| chr4:109792697
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+9218G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792697 | ||||||
| chr4:109792728
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0136 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57+9187A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792728 | ||||||
| chr4:109792747
|
C | T | 2 | a0001c0002t0001g0044a0001c0002t0001g0111 | 2 | NA18939.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.57+9168G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792747 | ||||||
| chr4:109792748
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+9167C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792748 | ||||||
| chr4:109792755
|
G | C | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+9160C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792755 | ||||||
| chr4:109792782
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+9133T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792782 | ||||||
| chr4:109792783
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+9132C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792783 | ||||||
| chr4:109792789
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+9126G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792789 | ||||||
| chr4:109792808
|
A | G | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+9107T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792808 | ||||||
| chr4:109792865
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+9050G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792865 | ||||||
| chr4:109792907
|
T | G | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+9008A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792907 | ||||||
| chr4:109792912
|
C | A | 1 | a0003c0004t0001g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.57+9003G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792912 | ||||||
| chr4:109792941
|
T | A | 3 | a0003c0004t0001g0013a0003c0004t0001g0014a0003c0004t0001g0021 | 3 | HG02055.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.57+8974A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792941 | ||||||
| chr4:109793147
|
C | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0258a0001c0001t0001g0270others(2): Show | 5 | HG00280.hp1 HG01081.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+8768G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793147 | ||||||
| chr4:109793203
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+8712A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793203 | ||||||
| chr4:109793251
|
C | T | 3 | a0001c0001t0001g0270a0001c0008t0001g0293a0001c0008t0002g0269 | 3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+8664G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793251 | ||||||
| chr4:109793293
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.57+8622A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793293 | ||||||
| chr4:109793370
|
G | A | 1 | a0004c0005t0001g0109 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.57+8545C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793370 | ||||||
| chr4:109793581
|
G | A | 12 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(9): Show | 12 | HG02004.hp2 NA18942.hp2 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+8334C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793581 | ||||||
| chr4:109793656
|
T | C | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+8259A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793656 | ||||||
| chr4:109793748
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+8167G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793748 | ||||||
| chr4:109793854
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+8061A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793854 | ||||||
| chr4:109793994
|
C | T | 4 | a0001c0002t0001g0061a0001c0002t0001g0065a0001c0002t0001g0066others(1): Show | 4 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+7921G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793994 | ||||||
| chr4:109794033
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+7882G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794033 | ||||||
| chr4:109794063
|
C | T | 1 | a0001c0002t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+7852G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794063 | ||||||
| chr4:109794129
|
T | A | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+7786A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794129 | ||||||
| chr4:109794237
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+7678A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794237 | ||||||
| chr4:109794303
|
G | T | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+7612C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794303 | ||||||
| chr4:109794317
|
C | T | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+7598G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794317 | ||||||
| chr4:109794535
|
T | C | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+7380A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794535 | ||||||
| chr4:109794786
|
C | G | 1 | a0001c0001t0001g0344 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+7129G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794786 | ||||||
| chr4:109794889
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(21): Show | 25 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+7026C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794889 | ||||||
| chr4:109794892
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+7023A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794892 | ||||||
| chr4:109794896
|
A | C | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+7019T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794896 | ||||||
| chr4:109794914
|
C | G | 1 | a0001c0002t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.57+7001G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794914 | ||||||
| chr4:109795016
|
C | T | 1 | a0007c0010t0001g0062 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.57+6899G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795016 | ||||||
| chr4:109795135
|
G | A | 1 | a0002c0003t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+6780C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795135 | ||||||
| chr4:109795204
|
A | T | 80 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+6711T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795204 | ||||||
| chr4:109795236
|
C | A | 1 | a0001c0002t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+6679G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795236 | ||||||
| chr4:109795251
|
C | T | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+6664G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795251 | ||||||
| chr4:109795252
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.57+6663C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795252 | ||||||
| chr4:109795311
|
G | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6604C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795311 | ||||||
| chr4:109795323
|
C | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0282others(11): Show | 15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+6592G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795323 | ||||||
| chr4:109795341
|
C | T | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6574G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795341 | ||||||
| chr4:109795362
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.57+6553A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795362 | ||||||
| chr4:109795447
|
T | C | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6468A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795447 | ||||||
| chr4:109795488
|
C | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6427G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795488 | ||||||
| chr4:109795604
|
C | T | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6311G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795604 | ||||||
| chr4:109795731
|
T | C | 87 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(84): Show | 87 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+6184A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795731 | ||||||
| chr4:109795742
|
T | A | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6173A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795742 | ||||||
| chr4:109795751
|
C | T | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+6164G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795751 | ||||||
| chr4:109795862
|
C | A | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6053G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795862 | ||||||
| chr4:109796003
|
C | T | 2 | a0003c0004t0001g0152a0003c0004t0001g0304 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+5912G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796003 | ||||||
| chr4:109796087
|
G | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5828C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796087 | ||||||
| chr4:109796216
|
A | C | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+5699T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796216 | ||||||
| chr4:109796222
|
A | C | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.57+5693T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796222 | ||||||
| chr4:109796235
|
G | A | 3 | a0001c0002t0001g0056a0001c0002t0001g0137a0002c0003t0001g0325 | 3 | HG02056.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.57+5680C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796235 | ||||||
| chr4:109796422
|
C | T | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+5493G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796422 | ||||||
| chr4:109796495
|
G | A | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+5420C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796495 | ||||||
| chr4:109796547
|
T | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5368A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796547 | ||||||
| chr4:109796551
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+5364G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796551 | ||||||
| chr4:109796682
|
T | C | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5233A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796682 | ||||||
| chr4:109796749
|
A | C | 1 | a0001c0002t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+5166T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796749 | ||||||
| chr4:109796812
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+5103T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796812 | ||||||
| chr4:109797088
|
T | C | 67 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(64): Show | 67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+4827A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797088 | ||||||
| chr4:109797156
|
C | A | 191 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(188): Show | 192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+4759G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797156 | ||||||
| chr4:109797299
|
C | T | 78 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+4616G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797299 | ||||||
| chr4:109797538
|
A | G | 2 | a0003c0004t0001g0149a0003c0004t0001g0150 | 2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+4377T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797538 | ||||||
| chr4:109797544
|
G | A | 87 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(84): Show | 87 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+4371C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797544 | ||||||
| chr4:109797561
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+4354T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797561 | ||||||
| chr4:109797568
|
GAC | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4345_57+4346del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797568 | ||||||
| chr4:109797574
|
T | C | 191 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(188): Show | 192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+4341A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797574 | ||||||
| chr4:109797708
|
A | C | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4207T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797708 | ||||||
| chr4:109797728
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+4187A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797728 | ||||||
| chr4:109797765
|
A | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4150T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797765 | ||||||
| chr4:109797786
|
G | A | 9 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+4129C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797786 | ||||||
| chr4:109797916
|
A | C | 1 | a0001c0001t0001g0328 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.57+3999T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797916 | ||||||
| chr4:109797930
|
A | C | 1 | a0001c0002t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.57+3985T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797930 | ||||||
| chr4:109798008
|
A | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3907T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798008 | ||||||
| chr4:109798198
|
G | A | 1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.57+3717C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798198 | ||||||
| chr4:109798217
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+3698T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798217 | ||||||
| chr4:109798303
|
C | T | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3612G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798303 | ||||||
| chr4:109798378
|
T | C | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3537A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798378 | ||||||
| chr4:109798471
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+3444A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798471 | ||||||
| chr4:109798508
|
G | GT | 20 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0183others(17): Show | 21 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.57+3406dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | ||||||
| chr4:109798508
|
G | GTT | 13 | a0001c0001t0001g0286a0001c0001t0001g0339a0001c0001t0001g0340others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+3405_57+3406dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | ||||||
| chr4:109798508
|
GT | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3406delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | ||||||
| chr4:109798519
|
T | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3396A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798519 | ||||||
| chr4:109798520
|
T | A | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.57+3395A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | ||||||
| chr4:109798520
|
T | TA | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(102): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.57+3394dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | ||||||
| chr4:109798520
|
T | TTA | 86 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0099others(83): Show | 87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.57+3394_57+3395ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | ||||||
| chr4:109798521
|
A | T | 7 | a0001c0001t0001g0151a0001c0001t0001g0282a0001c0001t0001g0283others(4): Show | 7 | HG00438.hp1 HG02109.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+3394T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798521 | ||||||
| chr4:109798789
|
CA | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+3125delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798789 | ||||||
| chr4:109798879
|
A | G | 51 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0043others(48): Show | 51 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.57+3036T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798879 | ||||||
| chr4:109798881
|
AGGAG | A | 110 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3030_57+3033del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798881 | ||||||
| chr4:109798916
|
C | T | 2 | a0001c0002t0002g0023a0001c0002t0002g0024 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+2999G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798916 | ||||||
| chr4:109799137
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.57+2778A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799137 | ||||||
| chr4:109799365
|
A | G | 68 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(65): Show | 68 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.57+2550T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799365 | ||||||
| chr4:109799432
|
C | A | 209 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(206): Show | 211 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.57+2483G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799432 | ||||||
| chr4:109799432
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+2483G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799432 | ||||||
| chr4:109799824
|
A | C | 2 | a0001c0006t0005g0041a0001c0006t0005g0042 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.57+2091T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799824 | ||||||
| chr4:109799830
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+2085A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799830 | ||||||
| chr4:109799835
|
T | A | 93 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(90): Show | 93 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.57+2080A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799835 | ||||||
| chr4:109799902
|
G | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.57+2013C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799902 | ||||||
| chr4:109799929
|
T | G | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.57+1986A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799929 | ||||||
| chr4:109800048
|
A | ATTTTTGG | 3 | a0001c0002t0002g0012a0003c0004t0001g0149a0003c0004t0001g0150 | 3 | HG00738.hp1 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.57+1860_57+1866dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800048 | ||||||
| chr4:109800055
|
G | GTT | 20 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(17): Show | 20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+1858_57+1859dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800055 | ||||||
| chr4:109800056
|
T | TTTTTGG | 29 | a0001c0001t0001g0146a0001c0001t0001g0277a0001c0001t0001g0298others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.57+1853_57+1858dup others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800056 | ||||||
| chr4:109800094
|
G | A | 2 | a0003c0004t0001g0152a0003c0004t0001g0304 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+1821C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800094 | ||||||
| chr4:109800293
|
C | CATAATTA others(16): Show |
8 | a0001c0001t0001g0277a0001c0001t0001g0299a0001c0001t0001g0300others(5): Show | 8 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1621_57+1622ins others(23): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800293 | ||||||
| chr4:109800321
|
G | GT | 9 | a0001c0001t0001g0339a0001c0002t0001g0022a0001c0002t0002g0023others(6): Show | 9 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+1593dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800321
|
G | GTT | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1592_57+1593dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800321
|
GT | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(208): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.57+1593delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800321
|
GTT | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0278others(40): Show | 44 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.57+1592_57+1593del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800321
|
GTTT | G | 10 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG01515.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+1591_57+1593del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800321
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+1579_57+1593del others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | ||||||
| chr4:109800378
|
C | G | 1 | a0003c0004t0001g0152 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+1537G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800378 | ||||||
| chr4:109800752
|
T | C | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+1163A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800752 | ||||||
| chr4:109800753
|
T | A | 1 | a0001c0002t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.57+1162A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800753 | ||||||
| chr4:109800755
|
A | G | 2 | a0001c0001t0003g0337a0001c0001t0003g0338 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.57+1160T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800755 | ||||||
| chr4:109800756
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+1159A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800756 | ||||||
| chr4:109800780
|
CAT | C | 22 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+1133_57+1134del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800780 | ||||||
| chr4:109800868
|
T | G | 1 | a0001c0001t0001g0326 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.57+1047A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800868 | ||||||
| chr4:109800920
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.57+995G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800920 | ||||||
| chr4:109801224
|
A | C | 1 | a0001c0002t0002g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.57+691T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801224 | ||||||
| chr4:109801349
|
G | A | 10 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(7): Show | 10 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+566C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801349 | ||||||
| chr4:109801590
|
C | T | 16 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(13): Show | 16 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+325G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801590 | ||||||
| chr4:109801730
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.57+185A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801730 | ||||||
| chr4:109801755
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.57+160T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801755 | ||||||
| chr4:109801861
|
T | C | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.57+54A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801861 | ||||||
| chr4:109801906
|
A | G | 1 | a0001c0002t0001g0008 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.57+9T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801906 |