Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55743 |
|---|---|
| ensemblid | ENSG00000072609.18 |
| hgncid | 20455 |
| symbol | CHFR |
| name | checkpoint with forkhead and ring finger domains |
| refseq_nuc | NM_001161346.2 |
| refseq_prot | NP_001154818.1 |
| ensembl_nuc | ENST00000450056.7 |
| ensembl_prot | ENSP00000398735.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 132832356 |
| end | 132887605 |
| strand | - |
| ver | v1.2 |
| region | chr12:132832356-132887605 |
| region5000 | chr12:132827356-132892605 |
| regionname0 | CHFR_chr12_132832356_132887605 |
| regionname5000 | CHFR_chr12_132827356_132892605 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 652 | 221 | 49 | 39 | 111 | 7 | 14 | 81 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002 | 0/0 | 652 | 89 | 17 | 21 | 33 | 5 | 13 | 24 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003 | 0/1 | 652 | 55 | 19 | 13 | 7 | 6 | 9 | 4 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004 | 0/0 | 652 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0005 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0006 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0007 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| 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 | 0/0 | 1959 | 152 | 33 | 26 | 84 | 3 | 6 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0002 | 0/0 | 1959 | 85 | 17 | 21 | 32 | 5 | 10 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0003 | 0/1 | 1959 | 53 | 17 | 13 | 7 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0004 | 0/0 | 1959 | 51 | 2 | 11 | 26 | 4 | 8 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0005 | 1/0 | 1959 | 15 | 14 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0006 | 0/0 | 1959 | 9 | 0 | 0 | 9 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0007 | 0/0 | 1959 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0008 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0009 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0010 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0011 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0012 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0013 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0014 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0015 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| c0016 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| 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 | 9308 | 30 | 0 | 10 | 4 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0002 | 0/0 | 9416 | 25 | 8 | 9 | 1 | 2 | 5 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0003 | 0/0 | 9308 | 23 | 0 | 4 | 15 | 1 | 3 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0004 | 0/0 | 9416 | 13 | 1 | 2 | 10 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0005 | 0/0 | 9416 | 13 | 0 | 3 | 10 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0006 | 0/0 | 9471 | 11 | 0 | 7 | 2 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0007 | 0/0 | 9308 | 8 | 1 | 2 | 0 | 2 | 3 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0008 | 0/0 | 9728 | 8 | 0 | 4 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0009 | 0/0 | 9273 | 7 | 7 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0010 | 0/0 | 9728 | 7 | 0 | 0 | 7 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0011 | 0/0 | 9763 | 7 | 0 | 0 | 7 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0012 | 0/0 | 9506 | 7 | 0 | 0 | 6 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0013 | 0/0 | 9308 | 6 | 5 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0014 | 0/0 | 9763 | 6 | 4 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0015 | 0/0 | 9728 | 6 | 0 | 1 | 4 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0016 | 0/0 | 9728 | 5 | 5 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0017 | 0/0 | 9308 | 4 | 0 | 3 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0018 | 0/0 | 9238 | 4 | 0 | 0 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0019 | 0/0 | 9308 | 4 | 3 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0020 | 0/0 | 9413 | 4 | 3 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0021 | 0/0 | 9235 | 4 | 4 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0022 | 0/0 | 9309 | 3 | 0 | 0 | 2 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0023 | 0/0 | 9273 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0024 | 0/0 | 9271 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0025 | 0/0 | 9798 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0026 | 0/0 | 9728 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0027 | 0/0 | 9763 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0028 | 0/0 | 9416 | 3 | 0 | 1 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0029 | 0/0 | 9417 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0030 | 0/0 | 9416 | 3 | 0 | 0 | 0 | 3 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0031 | 0/0 | 9416 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0032 | 0/0 | 9416 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0033 | 0/0 | 9471 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0034 | 0/0 | 9308 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0035 | 0/0 | 9273 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0036 | 0/0 | 9308 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0037 | 0/0 | 9308 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0038 | 1/0 | 9270 | 2 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0039 | 0/0 | 9270 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0040 | 0/0 | 9693 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0041 | 0/0 | 9728 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0042 | 0/0 | 9763 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0043 | 0/0 | 9728 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0044 | 0/0 | 9728 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0045 | 0/0 | 9381 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0046 | 0/0 | 9416 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0047 | 0/0 | 9416 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0048 | 0/0 | 9416 | 2 | 0 | 1 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0049 | 0/0 | 9451 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0050 | 0/0 | 9471 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0051 | 0/0 | 9401 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0052 | 0/0 | 9471 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0053 | 0/0 | 9471 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0054 | 0/0 | 9476 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0055 | 0/0 | 9616 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0056 | 0/0 | 9309 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0057 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0058 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0059 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0060 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0061 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0062 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0063 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0064 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0065 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0066 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0067 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0068 | 0/0 | 9413 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0069 | 0/0 | 9413 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0070 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0071 | 0/0 | 9273 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0072 | 0/0 | 9169 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0073 | 0/0 | 9274 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0074 | 0/0 | 9273 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0075 | 0/0 | 9270 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0076 | 0/0 | 9270 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0077 | 0/0 | 9270 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0078 | 0/0 | 9270 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0079 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0080 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0081 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0082 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0083 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0084 | 0/0 | 9728 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0085 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0086 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0087 | 0/0 | 9728 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0088 | 0/0 | 9729 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0089 | 0/0 | 9729 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0090 | 0/0 | 9728 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0091 | 0/0 | 9728 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0092 | 0/0 | 9729 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0093 | 0/0 | 9728 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0094 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0095 | 0/0 | 9728 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0096 | 0/0 | 9728 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0097 | 0/0 | 9728 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0098 | 0/0 | 9729 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0099 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0100 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0101 | 0/0 | 9764 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0102 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0103 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0104 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0105 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0106 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0107 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0108 | 0/0 | 9728 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0109 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0110 | 0/0 | 9729 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0111 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0112 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0113 | 0/0 | 9763 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0114 | 0/0 | 9764 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0115 | 0/0 | 9763 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0116 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0117 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0118 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0119 | 0/0 | 9273 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0120 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0121 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0122 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0123 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0124 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0125 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0126 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0127 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0128 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0129 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0130 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0131 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0132 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0133 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0134 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0135 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0136 | 0/0 | 9452 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0137 | 0/0 | 9346 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0138 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0139 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0140 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0141 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0142 | 0/0 | 9486 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0143 | 0/0 | 9471 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0144 | 0/0 | 9506 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0145 | 0/0 | 9541 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0146 | 0/0 | 9472 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0147 | 0/0 | 9471 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0148 | 0/0 | 9472 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0149 | 0/0 | 9472 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0150 | 0/0 | 9471 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0151 | 0/0 | 9408 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0152 | 0/0 | 9437 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| t0153 | 0/0 | 9436 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| 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 | 0/0 | 1959 | 152 | 33 | 26 | 84 | 3 | 6 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004 | 0/0 | 1959 | 51 | 2 | 11 | 26 | 4 | 8 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005 | 1/0 | 1959 | 15 | 14 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0010 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0015 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0016 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002 | 0/0 | 1959 | 85 | 17 | 21 | 32 | 5 | 10 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0007 | 0/0 | 1959 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0011 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0013 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003 | 0/1 | 1959 | 53 | 17 | 13 | 7 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0008 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006 | 0/0 | 1959 | 9 | 0 | 0 | 9 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0005c0009 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0006c0014 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0007c0012 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0006 | 0/0 | 11429 | 11 | 0 | 7 | 2 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0008 | 0/0 | 11686 | 8 | 0 | 4 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0009 | 0/0 | 11231 | 7 | 7 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0010 | 0/0 | 11686 | 7 | 0 | 0 | 7 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0011 | 0/0 | 11721 | 7 | 0 | 0 | 7 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0012 | 0/0 | 11464 | 7 | 0 | 0 | 6 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0014 | 0/0 | 11721 | 6 | 4 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0015 | 0/0 | 11686 | 6 | 0 | 1 | 4 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0016 | 0/0 | 11686 | 5 | 5 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0023 | 0/0 | 11231 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0025 | 0/0 | 11756 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0026 | 0/0 | 11686 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0027 | 0/0 | 11721 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0033 | 0/0 | 11429 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0040 | 0/0 | 11651 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0041 | 0/0 | 11686 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0042 | 0/0 | 11721 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0043 | 0/0 | 11686 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0044 | 0/0 | 11686 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0050 | 0/0 | 11429 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0051 | 0/0 | 11359 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0052 | 0/0 | 11429 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0053 | 0/0 | 11429 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0070 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0072 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0073 | 0/0 | 11232 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0074 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0079 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0080 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0081 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0082 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0083 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0084 | 0/0 | 11686 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0085 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0086 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0087 | 0/0 | 11686 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0088 | 0/0 | 11687 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0089 | 0/0 | 11687 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0090 | 0/0 | 11686 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0091 | 0/0 | 11686 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0092 | 0/0 | 11687 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0093 | 0/0 | 11686 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0094 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0095 | 0/0 | 11686 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0096 | 0/0 | 11686 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0097 | 0/0 | 11686 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0098 | 0/0 | 11687 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0099 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0100 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0101 | 0/0 | 11722 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0102 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0103 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0104 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0105 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0106 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0107 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0108 | 0/0 | 11686 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0109 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0110 | 0/0 | 11687 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0111 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0112 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0113 | 0/0 | 11721 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0114 | 0/0 | 11722 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0115 | 0/0 | 11721 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0116 | 0/0 | 11651 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0117 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0118 | 0/0 | 11686 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0119 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0143 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0144 | 0/0 | 11464 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0145 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0146 | 0/0 | 11430 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0147 | 0/0 | 11429 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0148 | 0/0 | 11430 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0149 | 0/0 | 11430 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0150 | 0/0 | 11429 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0151 | 0/0 | 11366 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0152 | 0/0 | 11395 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0001t0153 | 0/0 | 11394 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0003 | 0/0 | 11266 | 22 | 0 | 3 | 15 | 1 | 3 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0007 | 0/0 | 11266 | 8 | 1 | 2 | 0 | 2 | 3 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0017 | 0/0 | 11266 | 3 | 0 | 2 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0018 | 0/0 | 11196 | 4 | 0 | 0 | 4 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0022 | 0/0 | 11267 | 3 | 0 | 0 | 2 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0034 | 0/0 | 11266 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0035 | 0/0 | 11231 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0036 | 0/0 | 11266 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0056 | 0/0 | 11267 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0057 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0058 | 0/0 | 11267 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0059 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0004t0060 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0021 | 0/0 | 11193 | 4 | 4 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0024 | 0/0 | 11229 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0038 | 1/0 | 11228 | 2 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0039 | 0/0 | 11228 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0075 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0076 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0077 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0005t0078 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0010t0033 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0015t0003 | 0/0 | 11266 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0001c0016t0017 | 0/0 | 11266 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0002 | 0/0 | 11374 | 22 | 8 | 8 | 1 | 2 | 3 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0004 | 0/0 | 11374 | 13 | 1 | 2 | 10 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0005 | 0/0 | 11374 | 12 | 0 | 3 | 9 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0028 | 0/0 | 11374 | 3 | 0 | 1 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0029 | 0/0 | 11375 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0030 | 0/0 | 11374 | 3 | 0 | 0 | 0 | 3 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0045 | 0/0 | 11339 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0046 | 0/0 | 11374 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0047 | 0/0 | 11374 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0048 | 0/0 | 11374 | 2 | 0 | 1 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0049 | 0/0 | 11409 | 2 | 1 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0120 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0121 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0122 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0123 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0125 | 0/0 | 11375 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0126 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0127 | 0/0 | 11339 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0128 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0129 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0130 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0132 | 0/0 | 11374 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0133 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0136 | 0/0 | 11410 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0137 | 0/0 | 11304 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0138 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0139 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0140 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0141 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0002t0142 | 0/0 | 11444 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0007t0002 | 0/0 | 11374 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0011t0124 | 0/0 | 11374 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0002c0013t0005 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0001 | 0/1 | 11266 | 30 | 0 | 10 | 4 | 6 | 9 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0013 | 0/0 | 11266 | 6 | 5 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0019 | 0/0 | 11266 | 2 | 1 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0020 | 0/0 | 11371 | 4 | 3 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0037 | 0/0 | 11266 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0061 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0062 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0063 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0064 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0065 | 0/0 | 11266 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0066 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0067 | 0/0 | 11266 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0068 | 0/0 | 11371 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0003t0069 | 0/0 | 11371 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0003c0008t0019 | 0/0 | 11266 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006t0031 | 0/0 | 11374 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006t0032 | 0/0 | 11374 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006t0131 | 0/0 | 11374 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006t0134 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0004c0006t0135 | 0/0 | 11375 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0005c0009t0054 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0005c0009t0055 | 0/0 | 11574 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0006c0014t0002 | 0/0 | 11374 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| a0007c0012t0071 | 0/0 | 11231 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | copy fasta | chr12 | 132827356 | 132892605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0012g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0014g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0015g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0016g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0016g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0016g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0016g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0023g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0025g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0025g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0025g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0026g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0026g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0027g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0027g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0033g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0033g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0040g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0040g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0041g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0041g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0042g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0042g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0043g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0044g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0050g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0050g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0051g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0051g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0052g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0052g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0053g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0053g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0070g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0072g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0073g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0074g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0079g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0080g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0081g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0082g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0083g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0084g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0085g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0086g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0087g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0088g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0089g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0090g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0091g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0092g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0093g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0094g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0095g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0096g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0097g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0098g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0099g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0100g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0101g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0102g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0103g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0104g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0105g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0106g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0107g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0108g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0109g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0110g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0111g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0112g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0113g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0114g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0115g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0116g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0117g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0118g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0119g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0143g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0144g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0145g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0146g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0147g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0148g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0149g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0150g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0151g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0152g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0001t0153g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0007g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0017g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0017g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0018g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0018g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0018g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0018g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0022g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0022g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0022g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0034g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0034g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0035g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0035g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0036g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0036g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0056g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0057g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0058g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0059g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0004t0060g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0024g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0024g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0038g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0038g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0039g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0039g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0075g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0076g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0077g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0005t0078g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0010t0033g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0015t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0001c0016t0017g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0028g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0028g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0028g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0029g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0029g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0029g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0030g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0030g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0030g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0045g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0046g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0046g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0047g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0048g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0048g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0049g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0049g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0120g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0121g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0122g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0123g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0125g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0126g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0127g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0128g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0129g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0130g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0132g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0133g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0136g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0137g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0138g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0139g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0140g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0141g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0002t0142g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0007t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0011t0124g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0002c0013t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0013g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0019g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0019g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0020g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0020g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0020g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0020g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0037g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0037g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0061g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0062g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0063g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0064g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0065g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0066g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0067g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0068g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0003t0069g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0008t0019g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0003c0008t0019g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0031g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0031g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0031g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0032g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0032g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0032g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0131g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0134g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0004c0006t0135g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0005c0009t0054g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0005c0009t0055g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0006c0014t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| a0007c0012t0071g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0100 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00099 | hp2 | a0002 | c0002 | t0030 | g0101 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0356 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00140 | hp2 | a0001 | c0001 | t0050 | g0130 | EUR | GBR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00280 | hp1 | a0001 | c0004 | t0003 | g0226 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0317 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0300 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00323 | hp2 | a0001 | c0004 | t0007 | g0012 | EUR | FIN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00408 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00408 | hp2 | a0001 | c0001 | t0042 | g0276 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00423 | hp1 | a0001 | c0001 | t0109 | g0301 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00423 | hp2 | a0002 | c0002 | t0047 | g0010 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00438 | hp1 | a0001 | c0001 | t0051 | g0146 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0318 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00544 | hp1 | a0001 | c0004 | t0003 | g0191 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0197 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00558 | hp1 | a0001 | c0001 | t0105 | g0273 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00558 | hp2 | a0001 | c0001 | t0079 | g0245 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00597 | hp1 | a0001 | c0001 | t0083 | g0272 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00597 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0077 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00609 | hp2 | a0001 | c0001 | t0010 | g0258 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00642 | hp1 | a0002 | c0002 | t0005 | g0114 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00642 | hp2 | a0001 | c0001 | t0150 | g0144 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00673 | hp1 | a0002 | c0002 | t0005 | g0107 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0310 | EAS | CHS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00733 | hp1 | a0002 | c0002 | t0122 | g0058 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00733 | hp2 | a0006 | c0014 | t0002 | g0049 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00735 | hp1 | a0001 | c0004 | t0003 | g0204 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0315 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0053 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00741 | hp1 | a0002 | c0002 | t0125 | g0066 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG00741 | hp2 | a0001 | c0001 | t0110 | g0263 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01070 | hp2 | a0001 | c0004 | t0036 | g0206 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01071 | hp1 | a0001 | c0004 | t0036 | g0207 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0327 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01099 | hp1 | a0001 | c0015 | t0003 | g0205 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01099 | hp2 | a0002 | c0002 | t0028 | g0060 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01106 | hp1 | a0003 | c0003 | t0013 | g0027 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01106 | hp2 | a0001 | c0001 | t0153 | g0155 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01109 | hp1 | a0001 | c0004 | t0017 | g0222 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01109 | hp2 | a0002 | c0002 | t0049 | g0042 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01167 | hp1 | a0001 | c0001 | t0014 | g0279 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01167 | hp2 | a0002 | c0002 | t0005 | g0071 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01168 | hp1 | a0001 | c0004 | t0003 | g0199 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01169 | hp1 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01169 | hp2 | a0001 | c0004 | t0003 | g0198 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01175 | hp1 | a0001 | c0004 | t0035 | g0213 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01175 | hp2 | a0003 | c0003 | t0069 | g0323 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01192 | hp2 | a0002 | c0002 | t0121 | g0061 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01243 | hp1 | a0001 | c0004 | t0056 | g0211 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01243 | hp2 | a0001 | c0001 | t0084 | g0292 | AMR | PUR | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0139 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0343 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01256 | hp1 | a0001 | c0004 | t0007 | g0219 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0333 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01257 | hp2 | a0002 | c0002 | t0120 | g0091 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0332 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01258 | hp2 | a0001 | c0004 | t0007 | g0218 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0132 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0147 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01346 | hp1 | a0001 | c0016 | t0017 | g0223 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01346 | hp2 | a0001 | c0001 | t0146 | g0131 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01433 | hp1 | a0002 | c0002 | t0048 | g0040 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01433 | hp2 | a0001 | c0001 | t0147 | g0133 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0266 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0326 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01515 | hp1 | a0002 | c0002 | t0030 | g0103 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01515 | hp2 | a0001 | c0004 | t0007 | g0012 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0355 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01516 | hp2 | a0001 | c0001 | t0050 | g0136 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01517 | hp1 | a0002 | c0002 | t0030 | g0102 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0354 | EUR | IBS | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01884 | hp1 | a0001 | c0001 | t0151 | g0140 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01884 | hp2 | a0001 | c0005 | t0024 | g0175 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01891 | hp1 | a0001 | c0001 | t0023 | g0001 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01891 | hp2 | a0003 | c0003 | t0064 | g0028 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01934 | hp1 | a0001 | c0001 | t0089 | g0282 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01934 | hp2 | a0003 | c0003 | t0020 | g0322 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0342 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01943 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0294 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01952 | hp2 | a0002 | c0002 | t0004 | g0165 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01975 | hp2 | a0001 | c0001 | t0096 | g0293 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01978 | hp1 | a0001 | c0001 | t0008 | g0304 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01981 | hp1 | a0001 | c0001 | t0093 | g0284 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01981 | hp2 | a0001 | c0001 | t0148 | g0143 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02004 | hp1 | a0001 | c0001 | t0095 | g0295 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02004 | hp2 | a0001 | c0004 | t0017 | g0221 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02015 | hp1 | a0001 | c0001 | t0025 | g0242 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02015 | hp2 | a0002 | c0002 | t0140 | g0096 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02027 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02027 | hp2 | a0001 | c0001 | t0104 | g0309 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02040 | hp1 | a0001 | c0001 | t0051 | g0153 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02040 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0115 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02071 | hp1 | a0001 | c0001 | t0043 | g0017 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02071 | hp2 | a0001 | c0001 | t0025 | g0262 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02074 | hp1 | a0001 | c0001 | t0107 | g0241 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02074 | hp2 | a0002 | c0002 | t0045 | g0007 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02083 | hp1 | a0001 | c0001 | t0043 | g0017 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02083 | hp2 | a0001 | c0001 | t0010 | g0259 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02129 | hp1 | a0002 | c0002 | t0133 | g0041 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0337 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02132 | hp1 | a0003 | c0003 | t0019 | g0351 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02132 | hp2 | a0002 | c0002 | t0045 | g0007 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02145 | hp1 | a0002 | c0002 | t0132 | g0047 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02145 | hp2 | a0001 | c0005 | t0039 | g0180 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0331 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02155 | hp1 | a0002 | c0002 | t0005 | g0092 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02155 | hp2 | a0001 | c0001 | t0012 | g0123 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02165 | hp1 | a0001 | c0001 | t0094 | g0270 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02165 | hp2 | a0001 | c0001 | t0080 | g0237 | EAS | CDX | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02257 | hp1 | a0003 | c0003 | t0061 | g0020 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02257 | hp2 | a0002 | c0002 | t0029 | g0078 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02258 | hp1 | a0003 | c0003 | t0013 | g0021 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02280 | hp2 | a0001 | c0001 | t0087 | g0281 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02293 | hp1 | a0002 | c0002 | t0005 | g0008 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | PEL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02523 | hp1 | a0001 | c0001 | t0098 | g0296 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02523 | hp2 | a0001 | c0001 | t0143 | g0124 | EAS | KHV | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0328 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02602 | hp2 | a0002 | c0002 | t0123 | g0109 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02615 | hp1 | a0001 | c0001 | t0119 | g0035 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02615 | hp2 | a0002 | c0002 | t0137 | g0067 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02622 | hp1 | a0003 | c0003 | t0013 | g0026 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0250 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02630 | hp1 | a0001 | c0005 | t0078 | g0179 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02630 | hp2 | a0001 | c0001 | t0044 | g0018 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02647 | hp1 | a0001 | c0001 | t0092 | g0239 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02647 | hp2 | a0002 | c0002 | t0029 | g0097 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02698 | hp1 | a0002 | c0002 | t0048 | g0044 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0137 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02717 | hp1 | a0001 | c0001 | t0070 | g0178 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02717 | hp2 | a0001 | c0001 | t0044 | g0018 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02723 | hp1 | a0001 | c0001 | t0072 | g0352 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02723 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02735 | hp1 | a0001 | c0004 | t0007 | g0216 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0313 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02738 | hp1 | a0001 | c0004 | t0022 | g0203 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02738 | hp2 | a0001 | c0001 | t0053 | g0151 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02809 | hp1 | a0003 | c0003 | t0013 | g0024 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02809 | hp2 | a0003 | c0003 | t0020 | g0320 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02818 | hp1 | a0003 | c0003 | t0063 | g0345 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02818 | hp2 | a0001 | c0001 | t0090 | g0039 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02886 | hp1 | a0003 | c0003 | t0019 | g0346 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02886 | hp2 | a0001 | c0005 | t0024 | g0171 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0251 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02895 | hp2 | a0003 | c0008 | t0019 | g0350 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02896 | hp1 | a0001 | c0001 | t0091 | g0065 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02896 | hp2 | a0002 | c0002 | t0046 | g0082 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02897 | hp1 | a0002 | c0002 | t0046 | g0083 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02897 | hp2 | a0003 | c0008 | t0019 | g0349 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0004 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0094 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02965 | hp2 | a0001 | c0001 | t0097 | g0283 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02970 | hp1 | a0001 | c0005 | t0024 | g0174 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02976 | hp1 | a0003 | c0003 | t0065 | g0023 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02976 | hp2 | a0001 | c0005 | t0021 | g0182 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03017 | hp1 | a0002 | c0011 | t0124 | g0059 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0334 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03041 | hp1 | a0003 | c0003 | t0068 | g0321 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03041 | hp2 | a0003 | c0003 | t0013 | g0025 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03130 | hp1 | a0003 | c0003 | t0037 | g0347 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03139 | hp1 | a0001 | c0005 | t0077 | g0186 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03139 | hp2 | a0003 | c0003 | t0013 | g0022 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03195 | hp1 | a0005 | c0009 | t0055 | g0106 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03195 | hp2 | a0001 | c0005 | t0021 | g0185 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0280 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03225 | hp2 | a0003 | c0003 | t0062 | g0029 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03453 | hp1 | a0002 | c0002 | t0049 | g0043 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03453 | hp2 | a0001 | c0005 | t0021 | g0184 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03486 | hp1 | a0005 | c0009 | t0054 | g0118 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0314 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03490 | hp2 | a0001 | c0004 | t0007 | g0215 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03491 | hp1 | a0002 | c0002 | t0136 | g0085 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03491 | hp2 | a0001 | c0004 | t0007 | g0224 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03516 | hp1 | a0001 | c0005 | t0038 | g0177 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0278 | AFR | ESN | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03540 | hp1 | a0003 | c0003 | t0020 | g0319 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0335 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03669 | hp1 | a0002 | c0007 | t0002 | g0064 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03669 | hp2 | a0002 | c0002 | t0130 | g0095 | SAS | PJL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0104 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0330 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0125 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03831 | hp2 | a0002 | c0002 | t0028 | g0056 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03834 | hp1 | a0001 | c0001 | t0053 | g0141 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03834 | hp2 | a0002 | c0002 | t0028 | g0057 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0353 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0344 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03942 | hp2 | a0001 | c0004 | t0003 | g0011 | SAS | BEB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04115 | hp1 | a0001 | c0004 | t0058 | g0187 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04115 | hp2 | a0001 | c0001 | t0149 | g0142 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0316 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0011 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0126 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG04204 | hp2 | a0001 | c0004 | t0003 | g0202 | SAS | STU | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18522 | hp1 | a0001 | c0001 | t0074 | g0034 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18522 | hp2 | a0001 | c0001 | t0016 | g0234 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18747 | hp1 | a0002 | c0002 | t0005 | g0008 | EAS | CHB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18747 | hp2 | a0001 | c0001 | t0010 | g0277 | EAS | CHB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18906 | hp1 | a0003 | c0003 | t0020 | g0324 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18906 | hp2 | a0001 | c0001 | t0073 | g0032 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18939 | hp1 | a0002 | c0002 | t0005 | g0093 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18939 | hp2 | a0001 | c0004 | t0022 | g0193 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18942 | hp1 | a0001 | c0004 | t0018 | g0086 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18942 | hp2 | a0001 | c0004 | t0003 | g0189 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18943 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18943 | hp2 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0108 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18944 | hp2 | a0002 | c0002 | t0005 | g0088 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0325 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0225 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18947 | hp1 | a0001 | c0001 | t0027 | g0015 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18947 | hp2 | a0001 | c0004 | t0034 | g0196 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18948 | hp1 | a0002 | c0002 | t0005 | g0090 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18948 | hp2 | a0001 | c0001 | t0099 | g0238 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18950 | hp1 | a0002 | c0002 | t0126 | g0117 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0287 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18951 | hp1 | a0001 | c0010 | t0033 | g0128 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18951 | hp2 | a0001 | c0001 | t0010 | g0289 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18952 | hp1 | a0001 | c0001 | t0112 | g0233 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18952 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0256 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18954 | hp2 | a0004 | c0006 | t0032 | g0159 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18956 | hp1 | a0001 | c0004 | t0057 | g0214 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18956 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18959 | hp1 | a0001 | c0004 | t0059 | g0192 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18959 | hp2 | a0001 | c0001 | t0106 | g0291 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18960 | hp1 | a0002 | c0002 | t0005 | g0112 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18960 | hp2 | a0001 | c0001 | t0103 | g0274 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18962 | hp1 | a0004 | c0006 | t0031 | g0162 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18962 | hp2 | a0001 | c0001 | t0081 | g0252 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18963 | hp1 | a0001 | c0001 | t0033 | g0149 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18963 | hp2 | a0001 | c0001 | t0114 | g0288 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18967 | hp1 | a0001 | c0001 | t0027 | g0307 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18967 | hp2 | a0001 | c0004 | t0018 | g0209 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18968 | hp1 | a0004 | c0006 | t0031 | g0161 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18968 | hp2 | a0001 | c0001 | t0118 | g0268 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18969 | hp1 | a0001 | c0001 | t0100 | g0297 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18969 | hp2 | a0004 | c0006 | t0131 | g0158 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18970 | hp1 | a0001 | c0001 | t0011 | g0264 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18970 | hp2 | a0002 | c0002 | t0005 | g0099 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18973 | hp1 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18975 | hp1 | a0002 | c0002 | t0141 | g0084 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18975 | hp2 | a0001 | c0001 | t0026 | g0271 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18977 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18977 | hp2 | a0001 | c0004 | t0060 | g0230 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0228 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18979 | hp2 | a0001 | c0001 | t0088 | g0269 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18980 | hp1 | a0001 | c0001 | t0040 | g0253 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18980 | hp2 | a0002 | c0002 | t0138 | g0089 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18983 | hp1 | a0001 | c0001 | t0027 | g0015 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0248 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18984 | hp2 | a0001 | c0001 | t0052 | g0169 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18985 | hp1 | a0001 | c0001 | t0025 | g0255 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18985 | hp2 | a0001 | c0004 | t0022 | g0229 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18986 | hp1 | a0001 | c0004 | t0018 | g0208 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18986 | hp2 | a0001 | c0001 | t0116 | g0311 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18990 | hp1 | a0001 | c0001 | t0052 | g0170 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18990 | hp2 | a0002 | c0002 | t0127 | g0076 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18991 | hp1 | a0001 | c0004 | t0003 | g0188 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18991 | hp2 | a0001 | c0001 | t0117 | g0232 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18992 | hp1 | a0001 | c0001 | t0015 | g0235 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18992 | hp2 | a0001 | c0004 | t0003 | g0194 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18994 | hp1 | a0001 | c0001 | t0145 | g0312 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18994 | hp2 | a0001 | c0001 | t0085 | g0285 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0329 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18998 | hp2 | a0001 | c0001 | t0111 | g0260 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18999 | hp1 | a0001 | c0001 | t0041 | g0257 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA18999 | hp2 | a0002 | c0013 | t0005 | g0121 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19000 | hp1 | a0004 | c0006 | t0135 | g0164 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19000 | hp2 | a0001 | c0001 | t0101 | g0303 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19002 | hp1 | a0002 | c0002 | t0004 | g0111 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19002 | hp2 | a0001 | c0001 | t0041 | g0305 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19004 | hp1 | a0001 | c0004 | t0034 | g0195 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19004 | hp2 | a0003 | c0003 | t0067 | g0336 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19005 | hp2 | a0001 | c0001 | t0113 | g0261 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19006 | hp1 | a0001 | c0004 | t0003 | g0231 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19006 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0074 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19009 | hp2 | a0001 | c0001 | t0040 | g0265 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0227 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19012 | hp1 | a0001 | c0001 | t0015 | g0298 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19012 | hp2 | a0002 | c0002 | t0139 | g0063 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19043 | hp1 | a0001 | c0005 | t0076 | g0173 | AFR | LWK | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0004 | AFR | LWK | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19055 | hp1 | a0003 | c0003 | t0066 | g0338 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19055 | hp2 | a0004 | c0006 | t0134 | g0157 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19056 | hp1 | a0002 | c0002 | t0005 | g0087 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0290 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19057 | hp1 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19057 | hp2 | a0002 | c0002 | t0047 | g0010 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19058 | hp1 | a0001 | c0001 | t0015 | g0244 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19058 | hp2 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19060 | hp2 | a0001 | c0001 | t0115 | g0267 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19063 | hp1 | a0004 | c0006 | t0031 | g0163 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19063 | hp2 | a0001 | c0001 | t0144 | g0127 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19065 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19065 | hp2 | a0001 | c0001 | t0026 | g0016 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19066 | hp1 | a0001 | c0001 | t0011 | g0243 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19066 | hp2 | a0002 | c0002 | t0004 | g0070 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19077 | hp1 | a0001 | c0001 | t0102 | g0308 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19077 | hp2 | a0001 | c0004 | t0003 | g0201 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19083 | hp1 | a0001 | c0001 | t0026 | g0016 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19083 | hp2 | a0002 | c0002 | t0004 | g0110 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19084 | hp1 | a0004 | c0006 | t0032 | g0156 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19084 | hp2 | a0001 | c0004 | t0018 | g0212 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19086 | hp1 | a0001 | c0001 | t0033 | g0129 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0240 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19087 | hp1 | a0001 | c0001 | t0086 | g0299 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19088 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19088 | hp2 | a0001 | c0001 | t0082 | g0246 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19090 | hp1 | a0002 | c0002 | t0128 | g0051 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19090 | hp2 | a0001 | c0004 | t0003 | g0200 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19091 | hp1 | a0001 | c0001 | t0042 | g0275 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19091 | hp2 | a0004 | c0006 | t0032 | g0160 | EAS | JPT | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19240 | hp1 | a0003 | c0003 | t0037 | g0348 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA19240 | hp2 | a0002 | c0002 | t0142 | g0068 | AFR | YRI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | ASW | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20129 | hp2 | a0001 | c0001 | t0152 | g0154 | AFR | ASW | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0340 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0080 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0341 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20805 | hp2 | a0001 | c0004 | t0017 | g0220 | EUR | TSI | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20905 | hp1 | a0002 | c0002 | t0129 | g0119 | SAS | GIH | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20905 | hp2 | a0002 | c0007 | t0002 | g0069 | SAS | GIH | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01123 | hp1 | a0001 | c0001 | t0108 | g0254 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG01123 | hp2 | a0002 | c0002 | t0029 | g0167 | AMR | CLM | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0249 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0302 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG02559 | hp2 | a0001 | c0005 | t0021 | g0183 | AFR | ACB | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03471 | hp1 | a0007 | c0012 | t0071 | g0019 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG03471 | hp2 | a0001 | c0005 | t0075 | g0172 | AFR | MSL | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG06807 | hp1 | a0001 | c0004 | t0035 | g0210 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| HG06807 | hp2 | a0001 | c0005 | t0039 | g0181 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0075 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| NA20300 | hp2 | a0001 | c0004 | t0007 | g0217 | AFR | USA | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0339 | REF | REF | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0038 | g0176 | REF | REF | CHFR_chr12_132827356_132892605 | CHFR | chr12 | 132827356 | 132892605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132847076
|
C | T | 1 | a0003 | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
missense_variant | MODERATE | c.1702G>A | p.Val568Met | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/18 | 1773/11228 | 1702/1959 | 568/652 | chr12 | 132847076 | ||
| chr12:132851656
|
G | A | 3 | a0002a0004a0006 | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
missense_variant | MODERATE | c.1454C>T | p.Ala485Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1525/11228 | 1454/1959 | 485/652 | chr12 | 132851656 | ||
| chr12:132853460
|
G | A | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1343C>T | p.Ala448Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/18 | 1414/11228 | 1343/1959 | 448/652 | chr12 | 132853460 | ||
| chr12:132859207
|
C | T | 1 | a0004 | 9 | NA18954.hp2 NA18962.hp1 NA18968.hp1 others(6): Show |
missense_variant | MODERATE | c.772G>A | p.Gly258Arg | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/18 | 843/11228 | 772/1959 | 258/652 | chr12 | 132859207 | ||
| chr12:132861523
|
G | A | 1 | a0006 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.695C>T | p.Ser232Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/18 | 766/11228 | 695/1959 | 232/652 | chr12 | 132861523 | ||
| chr12:132861611
|
G | A | 1 | a0005 | 2 | HG03195.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.607C>T | p.Pro203Ser | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/18 | 678/11228 | 607/1959 | 203/652 | chr12 | 132861611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132847109
|
A | G | 3 | a0001c0004a0001c0015a0001c0016 | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
synonymous_variant | LOW | c.1669T>C | p.Leu557Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/18 | 1740/11228 | 1669/1959 | 557/652 | chr12 | 132847109 | ||
| chr12:132848657
|
G | A | 1 | a0001c0010 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.1560C>T | p.Cys520Cys | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/18 | 1631/11228 | 1560/1959 | 520/652 | chr12 | 132848657 | ||
| chr12:132851694
|
C | T | 1 | a0003c0008 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1416G>A | p.Leu472Leu | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1487/11228 | 1416/1959 | 472/652 | chr12 | 132851694 | ||
| chr12:132851733
|
G | A | 1 | a0002c0011 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1377C>T | p.Val459Val | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/18 | 1448/11228 | 1377/1959 | 459/652 | chr12 | 132851733 | ||
| chr12:132853522
|
C | T | 1 | a0002c0007 | 2 | HG03669.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1281G>A | p.Ala427Ala | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/18 | 1352/11228 | 1281/1959 | 427/652 | chr12 | 132853522 | ||
| chr12:132856587
|
T | C | 15 | a0001c0001a0001c0004a0001c0010others(12): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
synonymous_variant | LOW | c.1110A>G | p.Arg370Arg | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/18 | 1181/11228 | 1110/1959 | 370/652 | chr12 | 132856587 | ||
| chr12:132857472
|
G | A | 1 | a0002c0013 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.999C>T | p.Pro333Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/18 | 1070/11228 | 999/1959 | 333/652 | chr12 | 132857472 | ||
| chr12:132859130
|
T | G | 3 | a0001c0004a0001c0015a0001c0016 | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
synonymous_variant | LOW | c.849A>C | p.Pro283Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/18 | 920/11228 | 849/1959 | 283/652 | chr12 | 132859130 | ||
| chr12:132869644
|
T | C | 1 | a0001c0015 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.558A>G | p.Ala186Ala | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/18 | 629/11228 | 558/1959 | 186/652 | chr12 | 132869644 | ||
| chr12:132869761
|
G | C | 1 | a0001c0016 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.441C>G | p.Pro147Pro | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/18 | 512/11228 | 441/1959 | 147/652 | chr12 | 132869761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132832496
|
G | GA | 1 | a0001c0005t0024 | 3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9057dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 9057 | chr12 | 132832496 | |||||
| chr12:132832636
|
A | G | 1 | a0003c0003t0064 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8918T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8918 | chr12 | 132832636 | |||||
| chr12:132832810
|
G | A | 1 | a0001c0001t0052 | 2 | NA18984.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8744C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8744 | chr12 | 132832810 | |||||
| chr12:132832860
|
C | T | 1 | a0001c0001t0105 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8694G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8694 | chr12 | 132832860 | |||||
| chr12:132832998
|
G | A | 35 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(32): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*8556C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8556 | chr12 | 132832998 | |||||
| chr12:132833117
|
A | G | 2 | a0005c0009t0054a0005c0009t0055 | 2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8437T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8437 | chr12 | 132833117 | |||||
| chr12:132833153
|
C | T | 38 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(35): Show | 98 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*8401G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8401 | chr12 | 132833153 | |||||
| chr12:132833176
|
C | T | 26 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(23): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*8378G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8378 | chr12 | 132833176 | |||||
| chr12:132833304
|
G | A | 1 | a0001c0001t0107 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8250C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8250 | chr12 | 132833304 | |||||
| chr12:132833465
|
G | A | 1 | a0001c0001t0051 | 2 | HG00438.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8089C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8089 | chr12 | 132833465 | |||||
| chr12:132833549
|
C | T | 1 | a0002c0002t0133 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8005G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 8005 | chr12 | 132833549 | |||||
| chr12:132833830
|
G | A | 1 | a0001c0004t0060 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7724C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7724 | chr12 | 132833830 | |||||
| chr12:132833840
|
A | G | 151 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(148): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*7714T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7714 | chr12 | 132833840 | |||||
| chr12:132833849
|
T | C | 1 | a0003c0003t0068 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7705A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7705 | chr12 | 132833849 | |||||
| chr12:132833854
|
C | A | 21 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(18): Show | 42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*7700G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7700 | chr12 | 132833854 | |||||
| chr12:132834097
|
T | C | 1 | a0001c0001t0106 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7457A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7457 | chr12 | 132834097 | |||||
| chr12:132834174
|
C | G | 3 | a0003c0003t0001a0003c0003t0066a0003c0003t0067 | 32 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7380G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7380 | chr12 | 132834174 | |||||
| chr12:132834255
|
G | C | 1 | a0001c0001t0072 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7299C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7299 | chr12 | 132834255 | |||||
| chr12:132834267
|
G | A | 1 | a0002c0002t0121 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7287C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7287 | chr12 | 132834267 | |||||
| chr12:132834532
|
T | C | 14 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(11): Show | 49 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*7022A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 7022 | chr12 | 132834532 | |||||
| chr12:132834712
|
C | CT | 21 | a0001c0001t0073a0001c0001t0088a0001c0001t0089others(18): Show | 25 | HG00741.hp1 HG00741.hp2 HG01123.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*6841dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6841 | chr12 | 132834712 | |||||
| chr12:132834739
|
A | G | 151 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(148): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*6815T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6815 | chr12 | 132834739 | |||||
| chr12:132834779
|
G | A | 1 | a0001c0001t0147 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6775C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6775 | chr12 | 132834779 | |||||
| chr12:132834802
|
G | A | 1 | a0002c0002t0137 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6752C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6752 | chr12 | 132834802 | |||||
| chr12:132834889
|
G | T | 151 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(148): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*6665C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6665 | chr12 | 132834889 | |||||
| chr12:132834939
|
G | T | 1 | a0001c0001t0103 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6615C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6615 | chr12 | 132834939 | |||||
| chr12:132834959
|
C | T | 63 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(60): Show | 118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*6595G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6595 | chr12 | 132834959 | |||||
| chr12:132834963
|
C | T | 1 | a0001c0004t0060 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6591G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6591 | chr12 | 132834963 | |||||
| chr12:132835009
|
G | A | 1 | a0001c0005t0076 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6545C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6545 | chr12 | 132835009 | |||||
| chr12:132835174
|
C | T | 1 | a0001c0001t0023 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6380G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6380 | chr12 | 132835174 | |||||
| chr12:132835401
|
G | C | 151 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(148): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*6153C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6153 | chr12 | 132835401 | |||||
| chr12:132835536
|
C | G | 21 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(18): Show | 42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*6018G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 6018 | chr12 | 132835536 | |||||
| chr12:132835555
|
A | G | 3 | a0003c0003t0001a0003c0003t0066a0003c0003t0067 | 32 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5999T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5999 | chr12 | 132835555 | |||||
| chr12:132835585
|
G | A | 1 | a0001c0001t0148 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5969C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5969 | chr12 | 132835585 | |||||
| chr12:132835751
|
C | T | 27 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(24): Show | 102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5803G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5803 | chr12 | 132835751 | |||||
| chr12:132835779
|
G | A | 1 | a0001c0001t0072 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5775C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5775 | chr12 | 132835779 | |||||
| chr12:132835803
|
G | A | 1 | a0002c0002t0046 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5751C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5751 | chr12 | 132835803 | |||||
| chr12:132835828
|
CAGGCTCC others(28): Show |
C | 1 | a0001c0001t0051 | 2 | HG00438.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5691_*5725delATCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5691 | chr12 | 132835828 | |||||
| chr12:132835834
|
C | T | 1 | a0001c0001t0092 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5720G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5720 | chr12 | 132835834 | |||||
| chr12:132835842
|
A | G | 18 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(15): Show | 38 | HG00140.hp2 HG00642.hp2 HG01106.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5712T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5712 | chr12 | 132835842 | |||||
| chr12:132835842
|
AGCGCACG others(28): Show |
A | 1 | a0001c0004t0035 | 2 | HG01175.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5677_*5711delCGTG others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5677 | chr12 | 132835842 | |||||
| chr12:132835848
|
C | T | 1 | a0001c0001t0104 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5706G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5706 | chr12 | 132835848 | |||||
| chr12:132835852
|
C | A | 1 | a0001c0001t0100 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5702G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5702 | chr12 | 132835852 | |||||
| chr12:132835852
|
C | CCTCACAG others(63): Show |
1 | a0001c0001t0025 | 3 | HG02015.hp1 HG02071.hp2 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5701_*5702insTGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5701 | chr12 | 132835852 | |||||
| chr12:132835862
|
A | C | 8 | a0001c0001t0009a0001c0001t0023a0001c0001t0025others(5): Show | 18 | HG01891.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5692T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5692 | chr12 | 132835862 | |||||
| chr12:132835863
|
T | C | 9 | a0001c0001t0009a0001c0001t0023a0001c0001t0025others(6): Show | 19 | HG01891.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5691A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5691 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(28): Show |
29 | a0001c0001t0008a0001c0001t0010a0001c0001t0014others(26): Show | 61 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(28): Show |
2 | a0001c0001t0090a0001c0001t0097 | 2 | HG02818.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(63): Show |
1 | a0001c0001t0089 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(273): Show |
1 | a0001c0001t0091 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGGCA others(276): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(63): Show |
1 | a0002c0002t0142 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5690_*5691insGTCA others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835863
|
T | TAGGCTCC others(28): Show |
5 | a0001c0001t0043a0001c0001t0083a0001c0001t0104others(2): Show | 6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5656_*5690dupGGCA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5690 | chr12 | 132835863 | |||||
| chr12:132835877
|
G | A | 46 | a0001c0001t0009a0001c0001t0011a0001c0001t0027others(43): Show | 135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*5677C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5677 | chr12 | 132835877 | |||||
| chr12:132835883
|
C | G | 15 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(12): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5671G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5671 | chr12 | 132835883 | |||||
| chr12:132835887
|
A | C | 2 | a0002c0002t0129a0002c0002t0130 | 2 | HG03669.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5667T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5667 | chr12 | 132835887 | |||||
| chr12:132835897
|
C | A | 3 | a0001c0001t0051a0001c0001t0091a0001c0001t0094 | 4 | HG00438.hp1 HG02040.hp1 HG02165.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5657G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5657 | chr12 | 132835897 | |||||
| chr12:132835912
|
G | A | 5 | a0001c0004t0007a0001c0004t0018a0001c0004t0035others(2): Show | 17 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5642C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5642 | chr12 | 132835912 | |||||
| chr12:132835917
|
A | ACGGCACT others(29): Show |
1 | a0001c0001t0098 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5636_*5637insGTGC others(32): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5636 | chr12 | 132835917 | |||||
| chr12:132835932
|
A | ACAGGCTC others(28): Show |
1 | a0001c0001t0090 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5621_*5622insGCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5621 | chr12 | 132835932 | |||||
| chr12:132835932
|
A | ACAGGCTC others(98): Show |
1 | a0005c0009t0055 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5621_*5622insGCAC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5621 | chr12 | 132835932 | |||||
| chr12:132835932
|
A | C | 20 | a0001c0001t0027a0001c0001t0042a0001c0001t0051others(17): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5622T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5622 | chr12 | 132835932 | |||||
| chr12:132835962
|
C | CAGTGCCA others(28): Show |
1 | a0002c0002t0136 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5591_*5592insCTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5591 | chr12 | 132835962 | |||||
| chr12:132835962
|
C | G | 1 | a0002c0002t0127 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5592G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5592 | chr12 | 132835962 | |||||
| chr12:132835967
|
A | ACAGGCTC others(28): Show |
1 | a0002c0002t0049 | 2 | HG01109.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5586_*5587insGCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5586 | chr12 | 132835967 | |||||
| chr12:132835967
|
A | C | 69 | a0001c0001t0006a0001c0001t0009a0001c0001t0012others(66): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*5587T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5587 | chr12 | 132835967 | |||||
| chr12:132835997
|
G | C | 78 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*5557C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5557 | chr12 | 132835997 | |||||
| chr12:132835997
|
G | GAGTGCCA others(28): Show |
1 | a0002c0002t0137 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5522_*5556dupGTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5556 | chr12 | 132835997 | |||||
| chr12:132835997
|
GAGTGCCA others(28): Show |
G | 1 | a0001c0005t0021 | 4 | HG02559.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5522_*5556delGTGA others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5522 | chr12 | 132835997 | |||||
| chr12:132836002
|
C | A | 13 | a0001c0001t0011a0001c0001t0027a0001c0001t0042others(10): Show | 24 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5552G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5552 | chr12 | 132836002 | |||||
| chr12:132836037
|
C | A | 8 | a0001c0001t0027a0001c0001t0042a0001c0001t0101others(5): Show | 40 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5517G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5517 | chr12 | 132836037 | |||||
| chr12:132836054
|
C | T | 1 | a0001c0001t0109 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5500G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5500 | chr12 | 132836054 | |||||
| chr12:132836062
|
A | ACTCACAG others(28): Show |
13 | a0001c0001t0006a0001c0001t0033a0001c0001t0050others(10): Show | 26 | HG00140.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5491_*5492insGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5491 | chr12 | 132836062 | |||||
| chr12:132836062
|
A | C | 3 | a0001c0001t0051a0001c0001t0152a0001c0001t0153 | 4 | HG00438.hp1 HG01106.hp2 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5492T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5492 | chr12 | 132836062 | |||||
| chr12:132836067
|
C | G | 1 | a0002c0002t0129 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5487G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5487 | chr12 | 132836067 | |||||
| chr12:132836072
|
C | A | 79 | a0001c0001t0009a0001c0001t0023a0001c0001t0041others(76): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*5482G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5482 | chr12 | 132836072 | |||||
| chr12:132836072
|
C | CCAGGCTC others(28): Show |
13 | a0001c0001t0010a0001c0001t0040a0001c0001t0043others(10): Show | 21 | HG00558.hp1 HG00609.hp2 HG01243.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5481_*5482insTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5481 | chr12 | 132836072 | |||||
| chr12:132836072
|
C | CCAGGCTC others(378): Show |
4 | a0001c0001t0008a0001c0001t0093a0001c0001t0094others(1): Show | 11 | HG00741.hp2 HG01496.hp1 HG01928.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5481_*5482insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5481 | chr12 | 132836072 | |||||
| chr12:132836097
|
A | ACTCACAG others(378): Show |
1 | a0001c0001t0026 | 3 | NA18975.hp2 NA19065.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | |||||
| chr12:132836097
|
A | ACTCACAG others(378): Show |
2 | a0001c0001t0011a0001c0001t0114 | 8 | HG00597.hp2 NA18950.hp2 NA18963.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | |||||
| chr12:132836097
|
A | ACTCACAG others(343): Show |
2 | a0001c0001t0080a0001c0001t0099 | 2 | HG02165.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | |||||
| chr12:132836097
|
A | ACTCACAG others(378): Show |
1 | a0001c0001t0014 | 6 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5457insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5456 | chr12 | 132836097 | |||||
| chr12:132836097
|
A | C | 4 | a0001c0001t0012a0001c0001t0033a0001c0001t0091others(1): Show | 10 | HG02040.hp2 HG02155.hp2 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5457T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5457 | chr12 | 132836097 | |||||
| chr12:132836097
|
ACTCACAG others(133): Show |
A | 1 | a0001c0001t0072 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5317_*5456del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836097 | |||||
| chr12:132836107
|
C | A | 68 | a0001c0001t0008a0001c0001t0010a0001c0001t0011others(65): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*5447G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5447 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(413): Show |
1 | a0001c0001t0027 | 3 | NA18947.hp1 NA18967.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(413): Show |
2 | a0001c0001t0042a0001c0001t0115 | 3 | HG00408.hp2 NA19060.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0102 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(413): Show |
1 | a0001c0001t0101 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0103 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0116 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0092 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5446_*5447insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5446 | chr12 | 132836107 | |||||
| chr12:132836107
|
CCAGGCTC others(28): Show |
C | 4 | a0001c0001t0009a0001c0001t0073a0001c0001t0074others(1): Show | 10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5412_*5446delTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5412 | chr12 | 132836107 | |||||
| chr12:132836121
|
C | CGGCGCAC others(378): Show |
2 | a0001c0001t0112a0001c0001t0117 | 2 | NA18952.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5432_*5433insCTGC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5432 | chr12 | 132836121 | |||||
| chr12:132836121
|
C | CGGCGCAC others(378): Show |
8 | a0001c0001t0010a0001c0001t0015a0001c0001t0016others(5): Show | 17 | HG00323.hp1 HG00597.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5432_*5433insCTGC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5432 | chr12 | 132836121 | |||||
| chr12:132836132
|
A | ACTCACAG others(378): Show |
1 | a0001c0001t0113 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | |||||
| chr12:132836132
|
A | ACTCACAG others(413): Show |
1 | a0001c0001t0087 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | |||||
| chr12:132836132
|
A | ACTCACAG others(98): Show |
1 | a0001c0001t0145 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5421_*5422insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5421 | chr12 | 132836132 | |||||
| chr12:132836132
|
A | C | 18 | a0001c0001t0006a0001c0001t0033a0001c0001t0050others(15): Show | 32 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5422T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5422 | chr12 | 132836132 | |||||
| chr12:132836142
|
A | C | 40 | a0001c0001t0006a0001c0001t0010a0001c0001t0012others(37): Show | 70 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*5412T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5412 | chr12 | 132836142 | |||||
| chr12:132836156
|
C | CGGCGCAC others(343): Show |
1 | a0001c0001t0079 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5397_*5398insCTGC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5397 | chr12 | 132836156 | |||||
| chr12:132836156
|
C | CGGCGCAC others(98): Show |
1 | a0001c0001t0091 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5397_*5398insCTGC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5397 | chr12 | 132836156 | |||||
| chr12:132836156
|
C | G | 11 | a0001c0001t0014a0001c0001t0027a0001c0001t0042others(8): Show | 19 | HG00408.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5398G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5398 | chr12 | 132836156 | |||||
| chr12:132836167
|
A | C | 18 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(15): Show | 39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5387T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5387 | chr12 | 132836167 | |||||
| chr12:132836167
|
ACTCACAG others(63): Show |
A | 1 | a0001c0004t0018 | 4 | NA18942.hp1 NA18967.hp2 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5317_*5386delGGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836167 | |||||
| chr12:132836177
|
A | C | 27 | a0001c0001t0008a0001c0001t0010a0001c0001t0012others(24): Show | 54 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*5377T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5377 | chr12 | 132836177 | |||||
| chr12:132836177
|
A | CCAGGCTC others(28): Show |
1 | a0001c0001t0033 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5377_*5378insCACT others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5377 | chr12 | 132836177 | |||||
| chr12:132836202
|
A | C | 22 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(19): Show | 44 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5352T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5352 | chr12 | 132836202 | |||||
| chr12:132836202
|
ACTCACAG others(28): Show |
A | 2 | a0001c0001t0023a0007c0012t0071 | 4 | HG01891.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5317_*5351delGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836202 | |||||
| chr12:132836212
|
C | A | 82 | a0001c0001t0006a0001c0001t0011a0001c0001t0033others(79): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*5342G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5342 | chr12 | 132836212 | |||||
| chr12:132836212
|
C | CCAGGCTC others(63): Show |
2 | a0001c0001t0012a0001c0001t0144 | 8 | HG02040.hp2 HG02155.hp2 HG03831.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5341_*5342insTCAC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5341 | chr12 | 132836212 | |||||
| chr12:132836237
|
C | A | 123 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(120): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*5317G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5317 | chr12 | 132836237 | |||||
| chr12:132836242
|
C | G | 9 | a0001c0004t0003a0001c0004t0017a0001c0004t0022others(6): Show | 35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*5312G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5312 | chr12 | 132836242 | |||||
| chr12:132836247
|
C | A | 24 | a0001c0001t0006a0001c0001t0012a0001c0001t0025others(21): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*5307G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5307 | chr12 | 132836247 | |||||
| chr12:132836247
|
C | CCAGGCTC others(98): Show |
1 | a0005c0009t0054 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5306_*5307insTCAC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5306 | chr12 | 132836247 | |||||
| chr12:132836247
|
C | CCAGGCTC others(133): Show |
1 | a0005c0009t0055 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5306_*5307insTCAC others(136): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5306 | chr12 | 132836247 | |||||
| chr12:132836272
|
A | C | 51 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(48): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*5282T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5282 | chr12 | 132836272 | |||||
| chr12:132836282
|
C | A | 38 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(35): Show | 78 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5272G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5272 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(413): Show |
2 | a0001c0001t0025a0001c0001t0109 | 4 | HG00423.hp1 HG02015.hp1 HG02071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0095 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(413): Show |
1 | a0001c0001t0100 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(416): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0097 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(28): Show |
10 | a0001c0001t0014a0001c0001t0042a0001c0001t0079others(7): Show | 16 | HG00408.hp2 HG00558.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5237_*5271dupTCAC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(63): Show |
2 | a0001c0001t0011a0001c0001t0113 | 8 | HG00597.hp2 NA18950.hp2 NA18970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5202_*5271dupTCAC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0111 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0096 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
8 | a0001c0001t0010a0001c0001t0043a0001c0001t0044others(5): Show | 15 | HG00558.hp1 HG00609.hp2 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
2 | a0001c0001t0081a0001c0001t0118 | 2 | NA18962.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0041 | 2 | NA18999.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0090 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(378): Show |
1 | a0001c0001t0108 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(381): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836282
|
C | CCAGGCTC others(343): Show |
1 | a0001c0001t0089 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271_*5272insTCAC others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5271 | chr12 | 132836282 | |||||
| chr12:132836307
|
C | A | 5 | a0001c0001t0072a0004c0006t0032a0004c0006t0131others(2): Show | 7 | HG02723.hp1 NA18954.hp2 NA18969.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5247G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5247 | chr12 | 132836307 | |||||
| chr12:132836317
|
A | C | 4 | a0002c0002t0123a0002c0002t0129a0003c0003t0063others(1): Show | 4 | HG02602.hp2 HG02818.hp1 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5237T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5237 | chr12 | 132836317 | |||||
| chr12:132836342
|
C | A | 1 | a0001c0001t0016 | 5 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5212G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5212 | chr12 | 132836342 | |||||
| chr12:132836347
|
C | G | 1 | a0001c0001t0086 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5207G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5207 | chr12 | 132836347 | |||||
| chr12:132836357
|
C | CTCCCAGC others(343): Show |
1 | a0001c0001t0098 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5196_*5197insATGA others(346): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5196 | chr12 | 132836357 | |||||
| chr12:132836372
|
A | T | 2 | a0002c0002t0045a0002c0002t0127 | 3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5182T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5182 | chr12 | 132836372 | |||||
| chr12:132836401
|
C | G | 2 | a0002c0002t0045a0002c0002t0127 | 3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5153G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5153 | chr12 | 132836401 | |||||
| chr12:132836405
|
G | A | 3 | a0001c0001t0072a0002c0002t0123a0002c0011t0124 | 3 | HG02602.hp2 HG02723.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5149C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5149 | chr12 | 132836405 | |||||
| chr12:132836407
|
T | A | 58 | a0001c0001t0008a0001c0001t0010a0001c0001t0011others(55): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*5147A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5147 | chr12 | 132836407 | |||||
| chr12:132836410
|
G | GCCCTCAC others(64): Show |
1 | a0001c0001t0114 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5143_*5144insGCCG others(67): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5143 | chr12 | 132836410 | |||||
| chr12:132836412
|
C | A | 2 | a0002c0002t0045a0002c0002t0127 | 3 | HG02074.hp2 HG02132.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5142G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5142 | chr12 | 132836412 | |||||
| chr12:132836412
|
C | CCTCACAG others(28): Show |
2 | a0001c0001t0027a0001c0001t0115 | 4 | NA18947.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5107_*5141dupTGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | |||||
| chr12:132836412
|
C | CCTCACAG others(63): Show |
1 | a0004c0006t0131 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5072_*5141dupTGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | |||||
| chr12:132836412
|
C | CCTCACAG others(28): Show |
1 | a0002c0002t0138 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5141_*5142insTGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5141 | chr12 | 132836412 | |||||
| chr12:132836436
|
C | A | 1 | a0003c0003t0069 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5118G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5118 | chr12 | 132836436 | |||||
| chr12:132836436
|
C | G | 7 | a0002c0002t0004a0002c0002t0045a0002c0002t0047others(4): Show | 21 | HG00423.hp2 HG00609.hp1 HG01943.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5118G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5118 | chr12 | 132836436 | |||||
| chr12:132836447
|
A | C | 32 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(29): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*5107T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5107 | chr12 | 132836447 | |||||
| chr12:132836471
|
G | C | 3 | a0001c0001t0097a0003c0003t0062a0004c0006t0131 | 3 | HG02965.hp2 HG03225.hp2 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5083C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5083 | chr12 | 132836471 | |||||
| chr12:132836482
|
A | ACTCACAG others(98): Show |
12 | a0002c0002t0048a0002c0002t0049a0002c0002t0132others(9): Show | 21 | HG01109.hp2 HG01175.hp2 HG01433.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | ACTCACAG others(98): Show |
1 | a0002c0002t0125 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | ACTCACAG others(63): Show |
3 | a0002c0002t0045a0002c0002t0127a0002c0002t0138 | 4 | HG02074.hp2 HG02132.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(66): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | ACTCACAG others(28): Show |
1 | a0004c0006t0131 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(31): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | ACTCACAG others(98): Show |
1 | a0002c0002t0136 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | ACTCACAG others(98): Show |
23 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(20): Show | 76 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5071_*5072insGGCC others(101): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5071 | chr12 | 132836482 | |||||
| chr12:132836482
|
A | C | 5 | a0001c0001t0033a0001c0001t0144a0001c0001t0145others(2): Show | 6 | HG03225.hp2 NA18951.hp1 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5072T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5072 | chr12 | 132836482 | |||||
| chr12:132836506
|
C | CGGCGCAC others(308): Show |
1 | a0001c0001t0040 | 2 | NA18980.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5047_*5048insCTGC others(311): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5047 | chr12 | 132836506 | |||||
| chr12:132836506
|
C | G | 1 | a0003c0003t0062 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5048G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5048 | chr12 | 132836506 | |||||
| chr12:132836545
|
G | A | 32 | a0001c0001t0008a0001c0001t0010a0001c0001t0011others(29): Show | 60 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5009C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 5009 | chr12 | 132836545 | |||||
| chr12:132836563
|
C | G | 2 | a0001c0001t0044a0001c0001t0084 | 3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4991G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4991 | chr12 | 132836563 | |||||
| chr12:132836661
|
G | A | 1 | a0003c0003t0066 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4893C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4893 | chr12 | 132836661 | |||||
| chr12:132837038
|
G | A | 1 | a0002c0002t0047 | 2 | HG00423.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4516C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4516 | chr12 | 132837038 | |||||
| chr12:132837066
|
T | G | 2 | a0005c0009t0054a0005c0009t0055 | 2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4488A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4488 | chr12 | 132837066 | |||||
| chr12:132837087
|
G | T | 2 | a0002c0002t0125a0002c0002t0142 | 2 | HG00741.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4467C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4467 | chr12 | 132837087 | |||||
| chr12:132837094
|
C | G | 19 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(16): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4460G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4460 | chr12 | 132837094 | |||||
| chr12:132837468
|
T | C | 136 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(133): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*4086A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4086 | chr12 | 132837468 | |||||
| chr12:132837513
|
G | C | 1 | a0001c0001t0116 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4041C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4041 | chr12 | 132837513 | |||||
| chr12:132837543
|
A | G | 9 | a0003c0003t0013a0003c0003t0019a0003c0003t0037others(6): Show | 17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4011T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 4011 | chr12 | 132837543 | |||||
| chr12:132837647
|
G | A | 1 | a0007c0012t0071 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3907C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3907 | chr12 | 132837647 | |||||
| chr12:132837665
|
C | T | 21 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(18): Show | 42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3889G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3889 | chr12 | 132837665 | |||||
| chr12:132837697
|
T | C | 159 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(156): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*3857A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3857 | chr12 | 132837697 | |||||
| chr12:132837715
|
G | C | 2 | a0002c0002t0048a0002c0002t0049 | 4 | HG01109.hp2 HG01433.hp1 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3839C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3839 | chr12 | 132837715 | |||||
| chr12:132837718
|
G | T | 2 | a0005c0009t0054a0005c0009t0055 | 2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3836C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3836 | chr12 | 132837718 | |||||
| chr12:132837974
|
C | A | 15 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(12): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3580G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3580 | chr12 | 132837974 | |||||
| chr12:132837974
|
C | T | 1 | a0003c0003t0061 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3580G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3580 | chr12 | 132837974 | |||||
| chr12:132838129
|
C | T | 1 | a0001c0004t0058 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3425G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3425 | chr12 | 132838129 | |||||
| chr12:132838184
|
G | A | 2 | a0005c0009t0054a0005c0009t0055 | 2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3370C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3370 | chr12 | 132838184 | |||||
| chr12:132838283
|
C | T | 1 | a0001c0001t0083 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3271G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3271 | chr12 | 132838283 | |||||
| chr12:132838311
|
T | C | 1 | a0001c0005t0078 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3243A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3243 | chr12 | 132838311 | |||||
| chr12:132838321
|
C | T | 1 | a0001c0001t0023 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3233G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3233 | chr12 | 132838321 | |||||
| chr12:132838453
|
G | A | 1 | a0003c0003t0067 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3101C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3101 | chr12 | 132838453 | |||||
| chr12:132838470
|
C | T | 1 | a0001c0001t0082 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3084 | chr12 | 132838470 | |||||
| chr12:132838535
|
A | G | 13 | a0002c0002t0121a0003c0003t0001a0003c0003t0013others(10): Show | 50 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3019T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3019 | chr12 | 132838535 | |||||
| chr12:132838549
|
G | A | 2 | a0005c0009t0054a0005c0009t0055 | 2 | HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3005C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 3005 | chr12 | 132838549 | |||||
| chr12:132838856
|
G | A | 1 | a0001c0001t0072 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2698C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2698 | chr12 | 132838856 | |||||
| chr12:132838915
|
A | G | 1 | a0001c0001t0143 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2639 | chr12 | 132838915 | |||||
| chr12:132839152
|
G | A | 7 | a0001c0004t0003a0001c0004t0022a0001c0004t0034others(4): Show | 31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2402C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2402 | chr12 | 132839152 | |||||
| chr12:132839225
|
G | A | 7 | a0002c0002t0005a0002c0002t0120a0002c0002t0138others(4): Show | 18 | HG00642.hp1 HG00673.hp1 HG01167.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2329C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2329 | chr12 | 132839225 | |||||
| chr12:132839253
|
C | T | 2 | a0001c0001t0081a0007c0012t0071 | 2 | HG03471.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2301G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2301 | chr12 | 132839253 | |||||
| chr12:132839317
|
G | A | 1 | a0001c0001t0070 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2237 | chr12 | 132839317 | |||||
| chr12:132839357
|
C | A | 60 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(57): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2197 | chr12 | 132839357 | |||||
| chr12:132839539
|
C | T | 15 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(12): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2015G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 2015 | chr12 | 132839539 | |||||
| chr12:132839686
|
C | G | 1 | a0001c0004t0034 | 2 | NA18947.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1868G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1868 | chr12 | 132839686 | |||||
| chr12:132839877
|
T | C | 60 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(57): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1677 | chr12 | 132839877 | |||||
| chr12:132839928
|
T | C | 1 | a0001c0004t0036 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1626 | chr12 | 132839928 | |||||
| chr12:132839934
|
C | CGCCCCTG others(31): Show |
98 | a0001c0001t0006a0001c0001t0009a0001c0001t0012others(95): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*1619_*1620insAAGG others(34): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1619 | chr12 | 132839934 | |||||
| chr12:132839951
|
G | GGGACCTC others(31): Show |
54 | a0001c0001t0008a0001c0001t0010a0001c0001t0011others(51): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1602_*1603insGGAG others(34): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1602 | chr12 | 132839951 | |||||
| chr12:132840100
|
G | A | 1 | a0001c0001t0119 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1454 | chr12 | 132840100 | |||||
| chr12:132840132
|
A | G | 5 | a0002c0002t0028a0002c0002t0121a0002c0002t0122others(2): Show | 7 | HG00733.hp1 HG01099.hp2 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1422T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1422 | chr12 | 132840132 | |||||
| chr12:132840327
|
C | CA | 40 | a0001c0001t0072a0002c0002t0002a0002c0002t0004others(37): Show | 100 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1226dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1226 | chr12 | 132840327 | |||||
| chr12:132840492
|
T | C | 1 | a0001c0001t0044 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1062A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1062 | chr12 | 132840492 | |||||
| chr12:132840540
|
C | T | 2 | a0001c0001t0079a0001c0001t0080 | 2 | HG00558.hp2 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1014G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 1014 | chr12 | 132840540 | |||||
| chr12:132840628
|
T | C | 1 | a0001c0001t0149 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 926 | chr12 | 132840628 | |||||
| chr12:132840671
|
G | C | 1 | a0002c0002t0142 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*883C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 883 | chr12 | 132840671 | |||||
| chr12:132840699
|
T | C | 39 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(36): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 855 | chr12 | 132840699 | |||||
| chr12:132840705
|
T | TGGGGCTG others(119): Show |
1 | a0001c0001t0050 | 2 | HG00140.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*848_*849insGAGCCT others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 848 | chr12 | 132840705 | |||||
| chr12:132840725
|
C | CAAGGGAG others(119): Show |
1 | a0001c0001t0150 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | |||||
| chr12:132840725
|
C | CAAGGGAG others(119): Show |
16 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(13): Show | 36 | HG00438.hp1 HG01106.hp2 HG01168.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(120): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | |||||
| chr12:132840725
|
C | CAAGGGAG others(56): Show |
3 | a0001c0001t0151a0005c0009t0054a0005c0009t0055 | 3 | HG01884.hp1 HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*828_*829insCTGTGA others(57): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 828 | chr12 | 132840725 | |||||
| chr12:132840725
|
C | G | 1 | a0001c0001t0050 | 2 | HG00140.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 829 | chr12 | 132840725 | |||||
| chr12:132840776
|
C | T | 90 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(87): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 778 | chr12 | 132840776 | |||||
| chr12:132840838
|
G | A | 1 | a0001c0001t0117 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 716 | chr12 | 132840838 | |||||
| chr12:132840882
|
C | T | 1 | a0002c0002t0120 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 672 | chr12 | 132840882 | |||||
| chr12:132840883
|
G | A | 2 | a0001c0001t0073a0001c0001t0074 | 2 | NA18522.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*671C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 671 | chr12 | 132840883 | |||||
| chr12:132841203
|
A | G | 152 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(149): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 351 | chr12 | 132841203 | |||||
| chr12:132841216
|
T | C | 54 | a0001c0001t0008a0001c0001t0010a0001c0001t0011others(51): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*338A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 338 | chr12 | 132841216 | |||||
| chr12:132841280
|
G | A | 2 | a0001c0001t0152a0001c0001t0153 | 2 | HG01106.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 274 | chr12 | 132841280 | |||||
| chr12:132841322
|
C | T | 39 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(36): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 232 | chr12 | 132841322 | |||||
| chr12:132841323
|
G | A | 1 | a0001c0001t0118 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 231 | chr12 | 132841323 | |||||
| chr12:132841361
|
C | A | 1 | a0001c0001t0119 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 193 | chr12 | 132841361 | |||||
| chr12:132841396
|
T | TAA | 58 | a0001c0001t0006a0001c0001t0012a0001c0001t0033others(55): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*157dupTT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 157 | chr12 | 132841396 | |||||
| chr12:132841429
|
T | C | 1 | a0001c0001t0053 | 2 | HG02738.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 125 | chr12 | 132841429 | |||||
| chr12:132841483
|
C | T | 17 | a0001c0004t0003a0001c0004t0007a0001c0004t0017others(14): Show | 55 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*71G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 18/18 | 71 | chr12 | 132841483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132841634
|
T | C | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-38A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841634 | ||||||
| chr12:132841713
|
A | G | 11 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(8): Show | 14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1917-117T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841713 | ||||||
| chr12:132841810
|
A | G | 299 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(296): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1917-214T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841810 | ||||||
| chr12:132841814
|
G | A | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1917-218C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841814 | ||||||
| chr12:132841878
|
G | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1917-282C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841878 | ||||||
| chr12:132841883
|
G | A | 1 | a0003c0003t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1917-287C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841883 | ||||||
| chr12:132841885
|
T | C | 1 | a0001c0001t0098g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1917-289A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841885 | ||||||
| chr12:132841970
|
T | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1917-374A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132841970 | ||||||
| chr12:132842067
|
CCTCTATA | C | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1917-478_1917-472d others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842067 | ||||||
| chr12:132842095
|
C | T | 3 | a0003c0003t0019g0346a0003c0008t0019g0349a0003c0008t0019g0350 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1917-499G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842095 | ||||||
| chr12:132842108
|
CA | C | 142 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(139): Show | 156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1917-513delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842108 | ||||||
| chr12:132842108
|
CAA | C | 181 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(178): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1917-514_1917-513d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842108 | ||||||
| chr12:132842132
|
G | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1917-536C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842132 | ||||||
| chr12:132842365
|
C | T | 1 | a0001c0004t0003g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1916+646G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842365 | ||||||
| chr12:132842425
|
G | A | 1 | a0001c0001t0011g0248 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1916+586C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842425 | ||||||
| chr12:132842441
|
G | A | 1 | a0001c0001t0085g0285 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1916+570C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842441 | ||||||
| chr12:132842453
|
C | T | 1 | a0001c0004t0018g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1916+558G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842453 | ||||||
| chr12:132842454
|
A | G | 17 | a0001c0004t0007g0012a0001c0004t0007g0215a0001c0004t0007g0216others(14): Show | 18 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1916+557T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842454 | ||||||
| chr12:132842487
|
A | C | 1 | a0001c0001t0009g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1916+524T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842487 | ||||||
| chr12:132842507
|
C | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1916+504G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842507 | ||||||
| chr12:132842580
|
C | T | 1 | a0002c0002t0137g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1916+431G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842580 | ||||||
| chr12:132842710
|
G | A | 91 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(88): Show | 99 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1916+301C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842710 | ||||||
| chr12:132842832
|
G | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1916+179C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842832 | ||||||
| chr12:132842856
|
G | A | 1 | a0001c0004t0058g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1916+155C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 17/17 | chr12 | 132842856 | ||||||
| chr12:132843160
|
C | A | 1 | a0003c0003t0001g0325 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1844-77G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843160 | ||||||
| chr12:132843178
|
G | A | 1 | a0007c0012t0071g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1844-95C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843178 | ||||||
| chr12:132843222
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1844-139C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843222 | ||||||
| chr12:132843223
|
G | C | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1844-140C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843223 | ||||||
| chr12:132843252
|
A | G | 32 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(29): Show | 35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1844-169T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843252 | ||||||
| chr12:132843600
|
G | A | 1 | a0006c0014t0002g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1843+427C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843600 | ||||||
| chr12:132843688
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1843+339G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843688 | ||||||
| chr12:132843766
|
T | C | 1 | a0001c0001t0010g0236 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1843+261A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843766 | ||||||
| chr12:132843805
|
C | T | 1 | a0001c0001t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1843+222G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843805 | ||||||
| chr12:132843809
|
C | T | 14 | a0002c0002t0048g0040a0002c0002t0048g0044a0002c0002t0049g0042others(11): Show | 14 | HG01109.hp2 HG01433.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1843+218G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843809 | ||||||
| chr12:132843937
|
G | A | 1 | a0001c0001t0114g0288 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1843+90C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843937 | ||||||
| chr12:132843947
|
C | CA | 7 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0339others(4): Show | 7 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843+79dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843947 | ||||||
| chr12:132843947
|
CA | C | 49 | a0001c0001t0042g0275a0001c0001t0097g0283a0001c0004t0003g0003others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843+79delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 16/17 | chr12 | 132843947 | ||||||
| chr12:132844157
|
CCCAGCAA others(2): Show |
C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1736-32_1736-24del others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844157 | ||||||
| chr12:132844323
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1736-189G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844323 | ||||||
| chr12:132844452
|
T | TG | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-319_1736-318i others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844452 | ||||||
| chr12:132844456
|
T | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-322A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844456 | ||||||
| chr12:132844458
|
G | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-324C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844458 | ||||||
| chr12:132844459
|
T | C | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-325A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844459 | ||||||
| chr12:132844460
|
A | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-326T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844460 | ||||||
| chr12:132844468
|
T | G | 2 | a0001c0005t0075g0172a0001c0005t0076g0173 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1736-334A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844468 | ||||||
| chr12:132844474
|
C | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-340G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844474 | ||||||
| chr12:132844475
|
T | G | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-341A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844475 | ||||||
| chr12:132844486
|
G | A | 53 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(50): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1736-352C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844486 | ||||||
| chr12:132844491
|
A | G | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-357T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844491 | ||||||
| chr12:132844498
|
A | C | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-364T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844498 | ||||||
| chr12:132844506
|
G | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-372C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844506 | ||||||
| chr12:132844508
|
T | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-374A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844508 | ||||||
| chr12:132844512
|
C | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-378G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844512 | ||||||
| chr12:132844515
|
A | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-381T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844515 | ||||||
| chr12:132844519
|
C | CAG | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-386_1736-385i others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844519 | ||||||
| chr12:132844520
|
G | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-386C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844520 | ||||||
| chr12:132844527
|
A | G | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-393T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844527 | ||||||
| chr12:132844539
|
C | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-405G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844539 | ||||||
| chr12:132844547
|
G | A | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-413C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844547 | ||||||
| chr12:132844556
|
T | C | 1 | a0001c0004t0003g0194 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1736-422A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844556 | ||||||
| chr12:132844580
|
G | A | 1 | a0001c0005t0021g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1736-446C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844580 | ||||||
| chr12:132844618
|
G | A | 1 | a0002c0002t0048g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1736-484C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844618 | ||||||
| chr12:132844627
|
A | C | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1736-493T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844627 | ||||||
| chr12:132844755
|
C | T | 11 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(8): Show | 14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1736-621G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844755 | ||||||
| chr12:132844791
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1736-657G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844791 | ||||||
| chr12:132844813
|
A | G | 1 | a0001c0004t0003g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1736-679T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844813 | ||||||
| chr12:132844816
|
A | G | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1736-682T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844816 | ||||||
| chr12:132844923
|
A | G | 237 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(234): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1736-789T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844923 | ||||||
| chr12:132844929
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1736-795C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844929 | ||||||
| chr12:132844957
|
T | C | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1736-823A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132844957 | ||||||
| chr12:132845021
|
C | T | 2 | a0003c0003t0001g0052a0003c0003t0001g0053 | 2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1736-887G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845021 | ||||||
| chr12:132845050
|
A | G | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1736-916T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845050 | ||||||
| chr12:132845080
|
TTAAAA | T | 237 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(234): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1736-951_1736-947d others(7): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845080 | ||||||
| chr12:132845194
|
G | A | 1 | a0001c0001t0149g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1736-1060C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845194 | ||||||
| chr12:132845195
|
C | G | 1 | a0003c0003t0020g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1736-1061G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845195 | ||||||
| chr12:132845222
|
G | A | 1 | a0003c0003t0067g0336 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1736-1088C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845222 | ||||||
| chr12:132845252
|
G | A | 3 | a0002c0002t0002g0055a0002c0002t0002g0062a0002c0002t0002g0113 | 3 | HG00735.hp2 HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1736-1118C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845252 | ||||||
| chr12:132845464
|
A | T | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1736-1330T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845464 | ||||||
| chr12:132845465
|
A | T | 57 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1736-1331T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845465 | ||||||
| chr12:132845467
|
A | AT | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1736-1334_1736-133 others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845467 | ||||||
| chr12:132845467
|
A | T | 3 | a0001c0001t0089g0282a0001c0001t0090g0039a0001c0001t0091g0065 | 3 | HG01934.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1736-1333T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845467 | ||||||
| chr12:132845469
|
T | A | 330 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(327): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1736-1335A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845469 | ||||||
| chr12:132845477
|
T | A | 339 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(336): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1736-1343A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845477 | ||||||
| chr12:132845478
|
A | T | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1736-1344T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845478 | ||||||
| chr12:132845571
|
G | A | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1736-1437C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845571 | ||||||
| chr12:132845614
|
C | T | 1 | a0001c0001t0070g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1735+1429G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845614 | ||||||
| chr12:132845629
|
G | A | 145 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(142): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+1414C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845629 | ||||||
| chr12:132845781
|
G | GGGTGACT others(1): Show |
49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1735+1261_1735+126 others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845781 | ||||||
| chr12:132845808
|
C | T | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1735+1235G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845808 | ||||||
| chr12:132845817
|
G | C | 1 | a0002c0011t0124g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1735+1226C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132845817 | ||||||
| chr12:132846159
|
G | A | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1735+884C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846159 | ||||||
| chr12:132846220
|
T | C | 3 | a0001c0001t0025g0242a0001c0001t0025g0255a0001c0001t0025g0262 | 3 | HG02015.hp1 HG02071.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1735+823A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846220 | ||||||
| chr12:132846242
|
T | C | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1735+801A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846242 | ||||||
| chr12:132846263
|
C | CT | 9 | a0001c0001t0009g0037a0001c0004t0003g0225a0001c0004t0017g0221others(6): Show | 9 | HG02004.hp2 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735+779dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | ||||||
| chr12:132846263
|
C | CTT | 95 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(92): Show | 99 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1735+778_1735+779d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | ||||||
| chr12:132846263
|
C | CTTT | 8 | a0001c0001t0015g0244a0001c0001t0041g0305a0001c0001t0079g0245others(5): Show | 8 | HG00558.hp2 HG02132.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735+777_1735+779d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | ||||||
| chr12:132846263
|
C | CTTTT | 59 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(56): Show | 63 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1735+776_1735+779d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | ||||||
| chr12:132846263
|
CTT | C | 129 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(126): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1735+778_1735+779d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846263 | ||||||
| chr12:132846292
|
T | C | 1 | a0001c0001t0074g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1735+751A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846292 | ||||||
| chr12:132846294
|
G | A | 50 | a0001c0001t0008g0266a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1735+749C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846294 | ||||||
| chr12:132846301
|
C | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1735+742G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846301 | ||||||
| chr12:132846302
|
C | G | 239 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1735+741G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846302 | ||||||
| chr12:132846380
|
A | G | 144 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(141): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+663T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846380 | ||||||
| chr12:132846408
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1735+635C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846408 | ||||||
| chr12:132846411
|
C | T | 1 | a0001c0001t0107g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1735+632G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846411 | ||||||
| chr12:132846412
|
G | A | 146 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(143): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1735+631C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846412 | ||||||
| chr12:132846414
|
C | T | 144 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(141): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+629G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846414 | ||||||
| chr12:132846419
|
C | T | 144 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(141): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1735+624G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846419 | ||||||
| chr12:132846476
|
T | C | 237 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(234): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1735+567A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846476 | ||||||
| chr12:132846479
|
CCAGGATG others(18): Show |
C | 1 | a0001c0001t0144g0127 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1735+539_1735+563d others(27): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846479 | ||||||
| chr12:132846512
|
C | T | 5 | a0002c0002t0028g0056a0002c0002t0028g0057a0002c0002t0028g0060others(2): Show | 5 | HG01099.hp2 HG02602.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735+531G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846512 | ||||||
| chr12:132846516
|
C | A | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1735+527G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846516 | ||||||
| chr12:132846548
|
GC | G | 37 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1735+494delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846548 | ||||||
| chr12:132846618
|
C | T | 1 | a0001c0001t0070g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1735+425G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846618 | ||||||
| chr12:132846920
|
A | G | 7 | a0002c0002t0005g0008a0002c0002t0005g0071a0002c0002t0005g0087others(4): Show | 8 | HG00642.hp1 HG01167.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1735+123T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846920 | ||||||
| chr12:132846993
|
C | T | 2 | a0001c0001t0112g0233a0001c0001t0117g0232 | 2 | NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1735+50G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 15/17 | chr12 | 132846993 | ||||||
| chr12:132847280
|
G | A | 341 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(338): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1648-150C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847280 | ||||||
| chr12:132847298
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1648-168C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847298 | ||||||
| chr12:132847593
|
G | A | 1 | a0001c0001t0006g0134 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1648-463C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847593 | ||||||
| chr12:132847917
|
CATGCAGA others(87): Show |
C | 1 | a0001c0005t0038g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1647+74_1647+167de others(95): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847917 | ||||||
| chr12:132847962
|
C | T | 1 | a0001c0004t0007g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1647+123G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 14/17 | chr12 | 132847962 | ||||||
| chr12:132848317
|
T | C | 1 | a0002c0002t0002g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1577-162A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/17 | chr12 | 132848317 | ||||||
| chr12:132848361
|
T | C | 1 | a0001c0001t0089g0282 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1577-206A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 13/17 | chr12 | 132848361 | ||||||
| chr12:132848761
|
C | T | 2 | a0002c0002t0002g0050a0002c0002t0002g0072 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1493-37G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132848761 | ||||||
| chr12:132848857
|
C | T | 1 | a0001c0001t0006g0137 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1493-133G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132848857 | ||||||
| chr12:132849124
|
A | G | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1493-400T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849124 | ||||||
| chr12:132849187
|
G | C | 1 | a0002c0002t0138g0089 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1493-463C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849187 | ||||||
| chr12:132849363
|
G | A | 58 | a0001c0005t0024g0171a0001c0005t0024g0174a0001c0005t0024g0175others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1493-639C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849363 | ||||||
| chr12:132849375
|
G | A | 1 | a0002c0002t0125g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1493-651C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849375 | ||||||
| chr12:132849376
|
T | C | 1 | a0002c0002t0125g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1493-652A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849376 | ||||||
| chr12:132849380
|
G | A | 1 | a0001c0004t0018g0086 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1493-656C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849380 | ||||||
| chr12:132849512
|
C | T | 1 | a0002c0002t0129g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1493-788G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849512 | ||||||
| chr12:132849526
|
C | T | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1493-802G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849526 | ||||||
| chr12:132849578
|
C | A | 1 | a0002c0002t0127g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1493-854G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849578 | ||||||
| chr12:132849599
|
C | CT | 60 | a0001c0001t0012g0125a0001c0004t0003g0200a0001c0004t0003g0228others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1493-876dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849599 | ||||||
| chr12:132849638
|
T | G | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1493-914A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849638 | ||||||
| chr12:132849651
|
A | C | 2 | a0003c0003t0001g0332a0003c0003t0001g0333 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1493-927T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849651 | ||||||
| chr12:132849832
|
C | T | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1493-1108G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849832 | ||||||
| chr12:132849897
|
T | C | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1493-1173A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132849897 | ||||||
| chr12:132850015
|
G | A | 2 | a0003c0003t0037g0347a0003c0003t0037g0348 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1493-1291C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850015 | ||||||
| chr12:132850054
|
C | T | 2 | a0001c0001t0152g0154a0001c0001t0153g0155 | 2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1493-1330G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850054 | ||||||
| chr12:132850144
|
G | A | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1493-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850144 | ||||||
| chr12:132850266
|
TATA | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1492+1349_1492+135 others(7): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850266 | ||||||
| chr12:132850333
|
G | A | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492+1285C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850333 | ||||||
| chr12:132850359
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1492+1259G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850359 | ||||||
| chr12:132850480
|
T | C | 1 | a0001c0004t0060g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1492+1138A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850480 | ||||||
| chr12:132850496
|
G | A | 10 | a0002c0002t0133g0041a0004c0006t0031g0161a0004c0006t0031g0162others(7): Show | 10 | HG02129.hp1 NA18954.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492+1122C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850496 | ||||||
| chr12:132850519
|
G | A | 1 | a0001c0001t0070g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1492+1099C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850519 | ||||||
| chr12:132850525
|
C | T | 5 | a0001c0001t0043g0017a0001c0001t0083g0272a0001c0001t0104g0309others(2): Show | 6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1492+1093G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850525 | ||||||
| chr12:132850563
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1492+1055C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850563 | ||||||
| chr12:132850759
|
C | T | 7 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0339others(4): Show | 7 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492+859G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850759 | ||||||
| chr12:132850964
|
C | CAT | 9 | a0001c0001t0070g0178a0001c0005t0077g0186a0003c0003t0001g0315others(6): Show | 9 | HG00738.hp1 HG01255.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492+652_1492+653d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
C | CATAT | 10 | a0001c0005t0021g0182a0001c0005t0021g0183a0001c0005t0021g0185others(7): Show | 10 | HG02132.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492+650_1492+653d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
C | CATATATA others(1): Show |
3 | a0001c0005t0021g0184a0001c0005t0078g0179a0003c0003t0001g0344 | 3 | HG02630.hp1 HG03453.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1492+646_1492+653d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
C | CATATATA others(3): Show |
1 | a0001c0005t0075g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1492+644_1492+653d others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
C | CATATATA others(5): Show |
1 | a0001c0005t0024g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1492+642_1492+653d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
C | CATATATA others(17): Show |
2 | a0001c0005t0024g0174a0001c0005t0076g0173 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1492+630_1492+653d others(26): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CAT | C | 49 | a0001c0004t0003g0191a0001c0004t0007g0012a0001c0004t0007g0217others(46): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1492+652_1492+653d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATAT | C | 57 | a0001c0001t0084g0292a0001c0004t0003g0194a0001c0004t0007g0215others(54): Show | 61 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1492+650_1492+653d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATATAT | C | 12 | a0001c0001t0089g0282a0001c0001t0090g0039a0001c0001t0091g0065others(9): Show | 12 | HG00544.hp2 HG00733.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1492+648_1492+653d others(8): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATATATA others(1): Show |
C | 37 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(34): Show | 40 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1492+646_1492+653d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATATATA others(3): Show |
C | 36 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(33): Show | 42 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1492+644_1492+653d others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATATATA others(5): Show |
C | 79 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(76): Show | 84 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1492+642_1492+653d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132850964
|
CATATATA others(7): Show |
C | 40 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(37): Show | 42 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1492+640_1492+653d others(16): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132850964 | ||||||
| chr12:132851022
|
C | T | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492+596G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851022 | ||||||
| chr12:132851025
|
C | T | 2 | a0001c0001t0083g0272a0001c0001t0105g0273 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1492+593G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851025 | ||||||
| chr12:132851029
|
C | T | 1 | a0001c0001t0148g0143 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1492+589G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851029 | ||||||
| chr12:132851446
|
G | A | 90 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(87): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1492+172C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851446 | ||||||
| chr12:132851545
|
C | T | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1492+73G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851545 | ||||||
| chr12:132851595
|
C | T | 3 | a0001c0001t0006g0135a0001c0001t0006g0139a0001c0001t0006g0147 | 3 | HG01255.hp1 HG01261.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1492+23G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 12/17 | chr12 | 132851595 | ||||||
| chr12:132851770
|
G | A | 1 | a0002c0002t0141g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1373-33C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851770 | ||||||
| chr12:132851840
|
G | C | 1 | a0001c0001t0106g0291 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1373-103C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851840 | ||||||
| chr12:132851880
|
G | A | 355 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(352): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1373-143C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851880 | ||||||
| chr12:132851904
|
G | A | 1 | a0001c0001t0006g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1373-167C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851904 | ||||||
| chr12:132851908
|
A | T | 7 | a0001c0005t0021g0182a0001c0005t0021g0183a0001c0005t0021g0184others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-171T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132851908 | ||||||
| chr12:132852006
|
CAG | C | 90 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(87): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1373-271_1373-270d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852006 | ||||||
| chr12:132852132
|
T | C | 2 | a0001c0001t0051g0146a0001c0001t0051g0153 | 2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1373-395A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852132 | ||||||
| chr12:132852147
|
AT | A | 95 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(92): Show | 103 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1373-411delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852147 | ||||||
| chr12:132852268
|
A | G | 10 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-531T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852268 | ||||||
| chr12:132852382
|
G | A | 1 | a0003c0003t0061g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1373-645C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852382 | ||||||
| chr12:132852458
|
A | AG | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1373-722dupC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852458 | ||||||
| chr12:132852489
|
G | A | 1 | a0001c0001t0151g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1373-752C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852489 | ||||||
| chr12:132852519
|
T | TG | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1373-783dupC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852519 | ||||||
| chr12:132852692
|
T | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1372+739A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852692 | ||||||
| chr12:132852763
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1372+668C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852763 | ||||||
| chr12:132852815
|
G | A | 1 | a0002c0002t0142g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1372+616C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132852815 | ||||||
| chr12:132853017
|
T | C | 1 | a0002c0002t0132g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1372+414A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853017 | ||||||
| chr12:132853048
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1372+383G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853048 | ||||||
| chr12:132853049
|
G | A | 3 | a0004c0006t0031g0161a0004c0006t0031g0162a0004c0006t0031g0163 | 3 | NA18962.hp1 NA18968.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1372+382C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 11/17 | chr12 | 132853049 | ||||||
| chr12:132853619
|
T | C | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1230-46A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853619 | ||||||
| chr12:132853706
|
G | A | 1 | a0001c0001t0107g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1230-133C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853706 | ||||||
| chr12:132853762
|
G | A | 2 | a0001c0004t0003g0226a0001c0004t0003g0227 | 2 | HG00280.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230-189C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853762 | ||||||
| chr12:132853831
|
G | C | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1230-258C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853831 | ||||||
| chr12:132853904
|
G | A | 1 | a0001c0001t0010g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1230-331C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853904 | ||||||
| chr12:132853919
|
C | T | 6 | a0003c0003t0020g0319a0003c0003t0020g0320a0003c0003t0020g0322others(3): Show | 6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-346G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853919 | ||||||
| chr12:132853924
|
A | T | 1 | a0001c0001t0090g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1230-351T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853924 | ||||||
| chr12:132853951
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1230-378C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853951 | ||||||
| chr12:132853957
|
C | T | 2 | a0001c0001t0051g0146a0001c0001t0051g0153 | 2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1230-384G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132853957 | ||||||
| chr12:132854010
|
C | T | 189 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1230-437G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854010 | ||||||
| chr12:132854159
|
G | A | 1 | a0003c0003t0001g0329 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1230-586C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854159 | ||||||
| chr12:132854202
|
T | A | 17 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.1230-629A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854202 | ||||||
| chr12:132854248
|
TCTC | T | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230-678_1230-676d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854248 | ||||||
| chr12:132854398
|
G | A | 6 | a0001c0001t0015g0294a0001c0001t0015g0298a0001c0001t0015g0300others(3): Show | 6 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-825C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854398 | ||||||
| chr12:132854409
|
G | C | 90 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(87): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1230-836C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854409 | ||||||
| chr12:132854770
|
C | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1230-1197G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854770 | ||||||
| chr12:132854812
|
C | T | 9 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(6): Show | 10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230-1239G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854812 | ||||||
| chr12:132854871
|
G | A | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1230-1298C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854871 | ||||||
| chr12:132854982
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1230-1409G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132854982 | ||||||
| chr12:132855118
|
C | T | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1229+1350G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855118 | ||||||
| chr12:132855233
|
C | A | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+1235G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855233 | ||||||
| chr12:132855242
|
GA | G | 140 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(137): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1229+1225delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855242 | ||||||
| chr12:132855273
|
T | A | 1 | a0001c0001t0149g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1229+1195A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855273 | ||||||
| chr12:132855393
|
G | A | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+1075C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855393 | ||||||
| chr12:132855416
|
C | A | 1 | a0001c0001t0015g0235 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1229+1052G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855416 | ||||||
| chr12:132855491
|
C | T | 1 | a0001c0004t0034g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1229+977G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855491 | ||||||
| chr12:132855501
|
C | A | 1 | a0001c0004t0003g0194 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1229+967G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855501 | ||||||
| chr12:132855510
|
C | CA | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1229+957dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855510 | ||||||
| chr12:132855537
|
T | C | 1 | a0003c0003t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1229+931A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855537 | ||||||
| chr12:132855560
|
G | A | 2 | a0001c0001t0053g0141a0001c0001t0053g0151 | 2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1229+908C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855560 | ||||||
| chr12:132855622
|
G | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1229+846C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855622 | ||||||
| chr12:132855688
|
T | G | 1 | a0001c0001t0112g0233 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1229+780A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855688 | ||||||
| chr12:132855853
|
GT | G | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0189others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1229+614delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855853 | ||||||
| chr12:132855914
|
C | T | 1 | a0001c0001t0092g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1229+554G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855914 | ||||||
| chr12:132855999
|
C | T | 5 | a0002c0002t0002g0104a0002c0002t0002g0105a0002c0002t0030g0101others(2): Show | 5 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1229+469G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132855999 | ||||||
| chr12:132856067
|
A | T | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1229+401T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856067 | ||||||
| chr12:132856158
|
C | T | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1229+310G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856158 | ||||||
| chr12:132856186
|
C | A | 1 | a0001c0001t0006g0137 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1229+282G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856186 | ||||||
| chr12:132856267
|
C | T | 1 | a0001c0001t0079g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1229+201G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856267 | ||||||
| chr12:132856406
|
G | A | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1229+62C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 10/17 | chr12 | 132856406 | ||||||
| chr12:132856651
|
C | T | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1067-21G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856651 | ||||||
| chr12:132856654
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1067-24G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856654 | ||||||
| chr12:132856662
|
G | A | 2 | a0002c0002t0129g0119a0002c0002t0130g0095 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1067-32C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856662 | ||||||
| chr12:132856714
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1067-84G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856714 | ||||||
| chr12:132856877
|
C | T | 3 | a0001c0001t0026g0016a0001c0001t0026g0271a0001c0001t0094g0270 | 4 | HG02165.hp1 NA18975.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-247G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856877 | ||||||
| chr12:132856905
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1067-275C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856905 | ||||||
| chr12:132856976
|
C | A | 11 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(8): Show | 14 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1067-346G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856976 | ||||||
| chr12:132856989
|
G | A | 1 | a0001c0001t0105g0273 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1067-359C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132856989 | ||||||
| chr12:132857005
|
GCCCTCAC others(26): Show |
G | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1066+367_1067-376d others(35): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857005 | ||||||
| chr12:132857018
|
T | C | 286 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(283): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1066+387A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857018 | ||||||
| chr12:132857045
|
C | T | 1 | a0001c0001t0053g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1066+360G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857045 | ||||||
| chr12:132857071
|
A | G | 1 | a0002c0002t0002g0122 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066+334T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857071 | ||||||
| chr12:132857107
|
C | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1066+298G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857107 | ||||||
| chr12:132857112
|
G | A | 1 | a0001c0004t0018g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1066+293C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857112 | ||||||
| chr12:132857118
|
G | T | 3 | a0001c0005t0024g0171a0001c0005t0024g0174a0001c0005t0024g0175 | 3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1066+287C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857118 | ||||||
| chr12:132857120
|
G | A | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1066+285C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857120 | ||||||
| chr12:132857144
|
C | T | 7 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0339others(4): Show | 7 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066+261G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857144 | ||||||
| chr12:132857145
|
G | A | 2 | a0001c0001t0150g0144a0001c0001t0151g0140 | 2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1066+260C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857145 | ||||||
| chr12:132857279
|
G | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1066+126C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857279 | ||||||
| chr12:132857332
|
C | A | 1 | a0001c0001t0006g0150 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1066+73G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 9/17 | chr12 | 132857332 | ||||||
| chr12:132857630
|
A | G | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.912-71T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857630 | ||||||
| chr12:132857917
|
A | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.912-358T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857917 | ||||||
| chr12:132857967
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.912-408G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132857967 | ||||||
| chr12:132858220
|
T | C | 189 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.912-661A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858220 | ||||||
| chr12:132858600
|
C | T | 50 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(47): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.911+468G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858600 | ||||||
| chr12:132858718
|
C | T | 2 | a0001c0005t0075g0172a0001c0005t0076g0173 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.911+350G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858718 | ||||||
| chr12:132858725
|
T | TA | 37 | a0001c0004t0003g0003a0001c0004t0003g0188a0001c0004t0003g0191others(34): Show | 39 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.911+342dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | ||||||
| chr12:132858725
|
T | TAA | 14 | a0001c0004t0003g0011a0001c0004t0003g0189a0001c0004t0003g0200others(11): Show | 15 | HG00280.hp1 HG03942.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.911+341_911+342dup others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | ||||||
| chr12:132858725
|
TA | T | 106 | a0001c0001t0006g0126a0001c0001t0006g0135a0001c0001t0006g0138others(103): Show | 114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.911+342delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | ||||||
| chr12:132858725
|
TAA | T | 53 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0137others(50): Show | 57 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.911+341_911+342del others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | ||||||
| chr12:132858725
|
TAAA | T | 36 | a0001c0001t0006g0145a0001c0001t0152g0154a0001c0001t0153g0155others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.911+340_911+342del others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858725 | ||||||
| chr12:132858744
|
A | G | 1 | a0001c0001t0079g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.911+324T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858744 | ||||||
| chr12:132858778
|
T | TA | 7 | a0003c0003t0019g0346a0003c0003t0037g0347a0003c0003t0037g0348others(4): Show | 7 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.911+289dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858778 | ||||||
| chr12:132858816
|
C | T | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.911+252G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858816 | ||||||
| chr12:132858859
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.911+209C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858859 | ||||||
| chr12:132858863
|
A | G | 339 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(336): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.911+205T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858863 | ||||||
| chr12:132858920
|
CCACCCAC others(2): Show |
C | 3 | a0002c0002t0048g0040a0002c0002t0049g0042a0002c0002t0049g0043 | 3 | HG01109.hp2 HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.911+139_911+147del others(9): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858920 | ||||||
| chr12:132858948
|
C | T | 28 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(25): Show | 31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.911+120G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132858948 | ||||||
| chr12:132859009
|
C | T | 57 | a0001c0001t0152g0154a0001c0001t0153g0155a0003c0003t0001g0052others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.911+59G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859009 | ||||||
| chr12:132859012
|
G | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.911+56C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859012 | ||||||
| chr12:132859052
|
G | A | 4 | a0001c0001t0089g0282a0001c0001t0090g0039a0001c0001t0091g0065others(1): Show | 4 | HG01934.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.911+16C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 8/17 | chr12 | 132859052 | ||||||
| chr12:132859275
|
C | T | 7 | a0002c0002t0002g0079a0002c0002t0002g0080a0002c0002t0002g0081others(4): Show | 7 | HG00733.hp2 HG03491.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-48G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859275 | ||||||
| chr12:132859410
|
G | C | 3 | a0001c0005t0024g0171a0001c0005t0024g0174a0001c0005t0024g0175 | 3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-183C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859410 | ||||||
| chr12:132859463
|
T | A | 3 | a0002c0002t0004g0070a0002c0002t0004g0077a0002c0002t0004g0108 | 3 | HG00609.hp1 NA18944.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.752-236A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859463 | ||||||
| chr12:132859638
|
C | A | 1 | a0001c0001t0090g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.752-411G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859638 | ||||||
| chr12:132859809
|
A | C | 1 | a0001c0001t0090g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.752-582T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859809 | ||||||
| chr12:132859913
|
C | T | 36 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(33): Show | 38 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.752-686G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859913 | ||||||
| chr12:132859938
|
G | A | 1 | a0001c0004t0018g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.752-711C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132859938 | ||||||
| chr12:132860280
|
CT | C | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.752-1054delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860280 | ||||||
| chr12:132860288
|
A | G | 11 | a0001c0001t0010g0236a0001c0001t0010g0258a0001c0001t0010g0289others(8): Show | 11 | HG00609.hp2 HG00673.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.752-1061T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860288 | ||||||
| chr12:132860365
|
AAGT | A | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.751+1099_751+1101d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860365 | ||||||
| chr12:132860378
|
G | A | 1 | a0001c0005t0039g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.751+1089C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860378 | ||||||
| chr12:132860494
|
C | T | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.751+973G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860494 | ||||||
| chr12:132860654
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.751+813C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860654 | ||||||
| chr12:132860875
|
T | A | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.751+592A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860875 | ||||||
| chr12:132860903
|
C | G | 1 | a0001c0001t0053g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.751+564G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132860903 | ||||||
| chr12:132861104
|
G | C | 1 | a0001c0016t0017g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.751+363C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861104 | ||||||
| chr12:132861133
|
C | T | 1 | a0003c0003t0001g0344 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.751+334G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861133 | ||||||
| chr12:132861344
|
C | T | 1 | a0002c0002t0123g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+123G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861344 | ||||||
| chr12:132861393
|
G | A | 1 | a0001c0001t0097g0283 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751+74C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861393 | ||||||
| chr12:132861395
|
A | C | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.751+72T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 7/17 | chr12 | 132861395 | ||||||
| chr12:132861688
|
C | G | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-54G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861688 | ||||||
| chr12:132861691
|
T | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-57A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861691 | ||||||
| chr12:132861910
|
C | T | 5 | a0001c0001t0012g0002a0001c0001t0012g0123a0001c0001t0012g0125others(2): Show | 7 | HG02040.hp2 HG02155.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-276G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861910 | ||||||
| chr12:132861940
|
C | T | 1 | a0001c0001t0118g0268 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.584-306G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861940 | ||||||
| chr12:132861995
|
G | A | 1 | a0001c0001t0011g0264 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.584-361C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132861995 | ||||||
| chr12:132862136
|
G | T | 1 | a0003c0003t0063g0345 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.584-502C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862136 | ||||||
| chr12:132862250
|
G | A | 1 | a0001c0001t0008g0304 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.584-616C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862250 | ||||||
| chr12:132862262
|
C | T | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-628G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862262 | ||||||
| chr12:132862399
|
C | A | 2 | a0001c0001t0152g0154a0001c0001t0153g0155 | 2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.584-765G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862399 | ||||||
| chr12:132862408
|
C | T | 1 | a0001c0001t0145g0312 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.584-774G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862408 | ||||||
| chr12:132862416
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-782C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862416 | ||||||
| chr12:132862529
|
G | A | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.584-895C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862529 | ||||||
| chr12:132862680
|
C | G | 25 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.584-1046G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862680 | ||||||
| chr12:132862754
|
G | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.584-1120C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862754 | ||||||
| chr12:132862833
|
G | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-1199C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862833 | ||||||
| chr12:132862860
|
A | G | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.584-1226T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862860 | ||||||
| chr12:132862895
|
T | C | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.584-1261A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862895 | ||||||
| chr12:132862958
|
G | A | 3 | a0001c0001t0089g0282a0001c0001t0090g0039a0001c0001t0091g0065 | 3 | HG01934.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.584-1324C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862958 | ||||||
| chr12:132862998
|
G | A | 3 | a0001c0001t0149g0142a0001c0001t0150g0144a0001c0001t0151g0140 | 3 | HG00642.hp2 HG01884.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.584-1364C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132862998 | ||||||
| chr12:132863010
|
C | T | 2 | a0001c0001t0152g0154a0001c0001t0153g0155 | 2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.584-1376G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863010 | ||||||
| chr12:132863054
|
G | A | 17 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.584-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863054 | ||||||
| chr12:132863188
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-1554C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863188 | ||||||
| chr12:132863192
|
G | A | 1 | a0001c0004t0007g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.584-1558C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863192 | ||||||
| chr12:132863209
|
TA | T | 11 | a0001c0001t0008g0240a0001c0001t0008g0256a0001c0001t0016g0234others(8): Show | 11 | HG00280.hp2 HG01517.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.584-1576delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863209 | ||||||
| chr12:132863453
|
G | A | 3 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0341 | 3 | HG00738.hp2 HG01069.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.584-1819C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863453 | ||||||
| chr12:132863460
|
G | A | 1 | a0007c0012t0071g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.584-1826C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863460 | ||||||
| chr12:132863594
|
T | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-1960A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863594 | ||||||
| chr12:132863602
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.584-1968C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863602 | ||||||
| chr12:132863701
|
G | A | 4 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(1): Show | 4 | HG00738.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-2067C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863701 | ||||||
| chr12:132863718
|
G | A | 1 | a0001c0001t0006g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.584-2084C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863718 | ||||||
| chr12:132863912
|
C | T | 1 | a0002c0002t0049g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.584-2278G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132863912 | ||||||
| chr12:132864094
|
T | C | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-2460A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864094 | ||||||
| chr12:132864101
|
A | C | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.584-2467T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864101 | ||||||
| chr12:132864115
|
T | G | 9 | a0001c0004t0007g0012a0001c0004t0007g0217a0001c0004t0007g0218others(6): Show | 10 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-2481A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864115 | ||||||
| chr12:132864176
|
G | GA | 92 | a0001c0001t0012g0123a0001c0001t0086g0299a0002c0002t0002g0009others(89): Show | 97 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.584-2543dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864176 | ||||||
| chr12:132864188
|
C | A | 189 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.584-2554G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864188 | ||||||
| chr12:132864199
|
G | T | 1 | a0001c0001t0053g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.584-2565C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864199 | ||||||
| chr12:132864244
|
C | T | 2 | a0001c0004t0007g0218a0001c0004t0007g0219 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.584-2610G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864244 | ||||||
| chr12:132864329
|
C | T | 1 | a0001c0004t0057g0214 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.584-2695G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864329 | ||||||
| chr12:132864343
|
G | A | 1 | a0001c0001t0098g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.584-2709C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864343 | ||||||
| chr12:132864353
|
G | A | 1 | a0001c0001t0009g0005 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.584-2719C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864353 | ||||||
| chr12:132864374
|
A | C | 1 | a0001c0001t0070g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.584-2740T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864374 | ||||||
| chr12:132864436
|
TTG | T | 4 | a0001c0001t0033g0129a0001c0001t0033g0149a0001c0001t0144g0127others(1): Show | 4 | NA18951.hp1 NA18963.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-2804_584-2803d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864436 | ||||||
| chr12:132864467
|
TAGA | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.584-2836_584-2834d others(5): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864467 | ||||||
| chr12:132864540
|
G | C | 2 | a0003c0008t0019g0349a0003c0008t0019g0350 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.584-2906C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864540 | ||||||
| chr12:132864733
|
A | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-3099T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864733 | ||||||
| chr12:132864792
|
G | T | 6 | a0001c0004t0007g0012a0001c0004t0035g0210a0001c0004t0035g0213others(3): Show | 7 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-3158C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864792 | ||||||
| chr12:132864830
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.584-3196C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864830 | ||||||
| chr12:132864844
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.584-3210C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864844 | ||||||
| chr12:132864866
|
T | C | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-3232A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864866 | ||||||
| chr12:132864938
|
G | A | 1 | a0001c0001t0040g0265 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.584-3304C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132864938 | ||||||
| chr12:132865101
|
C | T | 341 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(338): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.584-3467G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865101 | ||||||
| chr12:132865194
|
C | T | 28 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(25): Show | 31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.584-3560G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865194 | ||||||
| chr12:132865294
|
G | A | 1 | a0002c0002t0128g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.584-3660C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865294 | ||||||
| chr12:132865387
|
G | T | 1 | a0001c0001t0016g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.584-3753C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865387 | ||||||
| chr12:132865497
|
T | C | 346 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(343): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.584-3863A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865497 | ||||||
| chr12:132865498
|
G | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584-3864C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865498 | ||||||
| chr12:132865518
|
G | A | 2 | a0002c0002t0002g0050a0002c0002t0002g0072 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.584-3884C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865518 | ||||||
| chr12:132865652
|
TC | T | 67 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(64): Show | 75 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.583+3966delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865652 | ||||||
| chr12:132865653
|
C | CT | 40 | a0001c0001t0006g0126a0001c0001t0012g0125a0001c0001t0051g0146others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.583+3965dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | ||||||
| chr12:132865653
|
C | T | 20 | a0001c0001t0008g0304a0001c0001t0011g0287a0001c0001t0014g0278others(17): Show | 20 | HG00423.hp1 HG01123.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+3966G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | ||||||
| chr12:132865653
|
CT | C | 136 | a0001c0001t0050g0136a0001c0001t0072g0352a0001c0001t0151g0140others(133): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.583+3965delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | ||||||
| chr12:132865653
|
CTT | C | 12 | a0001c0001t0009g0005a0001c0001t0009g0031a0001c0001t0009g0033others(9): Show | 15 | HG01167.hp2 HG01168.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.583+3964_583+3965d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865653 | ||||||
| chr12:132865658
|
T | G | 3 | a0001c0001t0027g0015a0001c0001t0027g0307a0001c0001t0115g0267 | 4 | NA18947.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+3961A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865658 | ||||||
| chr12:132865747
|
C | T | 1 | a0004c0006t0134g0157 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.583+3872G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132865747 | ||||||
| chr12:132866001
|
T | G | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+3618A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866001 | ||||||
| chr12:132866070
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.583+3549G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866070 | ||||||
| chr12:132866237
|
C | T | 4 | a0003c0003t0001g0339a0003c0003t0001g0340a0003c0003t0001g0342others(1): Show | 4 | HG01255.hp2 HG01943.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+3382G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866237 | ||||||
| chr12:132866253
|
C | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+3366G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866253 | ||||||
| chr12:132866254
|
G | A | 2 | a0001c0004t0007g0218a0001c0004t0007g0219 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.583+3365C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866254 | ||||||
| chr12:132866300
|
C | T | 10 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+3319G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866300 | ||||||
| chr12:132866317
|
G | A | 1 | a0002c0002t0004g0120 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.583+3302C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866317 | ||||||
| chr12:132866419
|
A | C | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.583+3200T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866419 | ||||||
| chr12:132866493
|
T | G | 1 | a0001c0001t0149g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.583+3126A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866493 | ||||||
| chr12:132866564
|
C | T | 17 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.583+3055G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866564 | ||||||
| chr12:132866577
|
T | TGTTACAA others(11): Show |
7 | a0001c0001t0072g0352a0001c0004t0017g0220a0001c0004t0017g0221others(4): Show | 7 | HG01109.hp1 HG01346.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+3024_583+3041d others(20): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866577 | ||||||
| chr12:132866577
|
TGTTACAA others(11): Show |
T | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.583+3024_583+3041d others(20): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866577 | ||||||
| chr12:132866626
|
C | G | 1 | a0001c0001t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.583+2993G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866626 | ||||||
| chr12:132866627
|
G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.583+2992C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866627 | ||||||
| chr12:132866697
|
C | T | 1 | a0001c0004t0003g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.583+2922G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866697 | ||||||
| chr12:132866907
|
G | A | 33 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.583+2712C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866907 | ||||||
| chr12:132866932
|
G | T | 60 | a0001c0001t0012g0002a0001c0001t0012g0123a0001c0001t0012g0125others(57): Show | 62 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.583+2687C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866932 | ||||||
| chr12:132866991
|
G | A | 1 | a0001c0001t0025g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.583+2628C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132866991 | ||||||
| chr12:132867120
|
C | G | 6 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(3): Show | 7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+2499G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867120 | ||||||
| chr12:132867182
|
G | A | 1 | a0003c0003t0013g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.583+2437C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867182 | ||||||
| chr12:132867205
|
C | A | 1 | a0001c0001t0033g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.583+2414G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867205 | ||||||
| chr12:132867289
|
G | T | 239 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.583+2330C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867289 | ||||||
| chr12:132867329
|
A | G | 1 | a0001c0001t0103g0274 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.583+2290T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867329 | ||||||
| chr12:132867403
|
T | C | 1 | a0003c0003t0019g0346 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583+2216A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867403 | ||||||
| chr12:132867442
|
A | C | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.583+2177T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867442 | ||||||
| chr12:132867730
|
C | T | 1 | a0001c0001t0097g0283 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.583+1889G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867730 | ||||||
| chr12:132867733
|
G | A | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.583+1886C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867733 | ||||||
| chr12:132867824
|
A | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.583+1795T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867824 | ||||||
| chr12:132867848
|
C | T | 4 | a0001c0004t0003g0198a0001c0004t0003g0199a0001c0004t0003g0202others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+1771G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867848 | ||||||
| chr12:132867872
|
C | G | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.583+1747G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867872 | ||||||
| chr12:132867957
|
AT | A | 49 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.583+1661delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867957 | ||||||
| chr12:132867958
|
T | TA | 32 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(29): Show | 35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.583+1660_583+1661i others(3): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867958 | ||||||
| chr12:132867959
|
T | A | 290 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(287): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.583+1660A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867959 | ||||||
| chr12:132867969
|
T | A | 51 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.583+1650A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867969 | ||||||
| chr12:132867969
|
TA | T | 4 | a0003c0003t0001g0330a0003c0003t0001g0334a0003c0003t0001g0335others(1): Show | 4 | HG02976.hp1 HG03017.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+1649delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132867969 | ||||||
| chr12:132868021
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.583+1598G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868021 | ||||||
| chr12:132868220
|
G | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+1399C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868220 | ||||||
| chr12:132868262
|
G | C | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.583+1357C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868262 | ||||||
| chr12:132868266
|
A | G | 189 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.583+1353T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868266 | ||||||
| chr12:132868270
|
C | T | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.583+1349G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868270 | ||||||
| chr12:132868351
|
G | A | 2 | a0001c0001t0026g0016a0001c0001t0026g0271 | 3 | NA18975.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.583+1268C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868351 | ||||||
| chr12:132868367
|
G | A | 1 | a0001c0001t0100g0297 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.583+1252C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868367 | ||||||
| chr12:132868388
|
C | CTGAGGCA others(5): Show |
3 | a0002c0002t0048g0040a0002c0002t0049g0042a0002c0002t0049g0043 | 3 | HG01109.hp2 HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.583+1219_583+1230d others(14): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868388 | ||||||
| chr12:132868406
|
G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.583+1213C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868406 | ||||||
| chr12:132868424
|
C | T | 1 | a0001c0001t0109g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.583+1195G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868424 | ||||||
| chr12:132868464
|
C | T | 239 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(236): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.583+1155G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868464 | ||||||
| chr12:132868479
|
G | C | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.583+1140C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868479 | ||||||
| chr12:132868521
|
C | CA | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.583+1097dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868521 | ||||||
| chr12:132868573
|
G | GGGAGGCT others(175): Show |
187 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(184): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.583+1045_583+1046i others(184): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868573 | ||||||
| chr12:132868581
|
G | A | 3 | a0001c0001t0014g0004a0001c0001t0014g0279a0001c0001t0014g0280 | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+1038C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868581 | ||||||
| chr12:132868656
|
A | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+963T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868656 | ||||||
| chr12:132868663
|
G | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0279a0001c0001t0014g0280 | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.583+956C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868663 | ||||||
| chr12:132868675
|
G | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+944C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868675 | ||||||
| chr12:132868681
|
A | AAACAAAC others(172): Show |
2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+937_583+938ins others(179): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868681 | ||||||
| chr12:132868683
|
A | C | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.583+936T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868683 | ||||||
| chr12:132868806
|
ATGGGGCC others(305): Show |
A | 90 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(87): Show | 98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.583+501_583+812del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868806 | ||||||
| chr12:132868812
|
CCGAGGGG others(227): Show |
C | 2 | a0001c0004t0017g0221a0001c0004t0017g0222 | 2 | HG01109.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.583+573_583+806del | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868812 | ||||||
| chr12:132868837
|
G | A | 3 | a0001c0001t0009g0033a0001c0001t0009g0036a0001c0001t0119g0035 | 3 | HG02486.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.583+782C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868837 | ||||||
| chr12:132868841
|
G | A | 1 | a0002c0002t0002g0122 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.583+778C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868841 | ||||||
| chr12:132868868
|
T | C | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+751A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868868 | ||||||
| chr12:132868907
|
T | C | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+712A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868907 | ||||||
| chr12:132868917
|
CTGCTGGT others(32): Show |
C | 1 | a0001c0004t0003g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.583+663_583+701del others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868917 | ||||||
| chr12:132868923
|
G | C | 1 | a0001c0001t0074g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+696C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868923 | ||||||
| chr12:132868929
|
C | T | 1 | a0001c0001t0074g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+690G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868929 | ||||||
| chr12:132868948
|
GGGAGTGA others(71): Show |
G | 1 | a0001c0001t0074g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+593_583+670del others(78): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868948 | ||||||
| chr12:132868956
|
T | C | 48 | a0001c0001t0070g0178a0001c0001t0072g0352a0001c0004t0003g0003others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.583+663A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868956 | ||||||
| chr12:132868961
|
G | C | 9 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(6): Show | 10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+658C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868961 | ||||||
| chr12:132868988
|
G | A | 7 | a0002c0002t0002g0055a0002c0002t0028g0056a0002c0002t0028g0057others(4): Show | 7 | HG00733.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.583+631C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132868988 | ||||||
| chr12:132869008
|
T | C | 1 | a0001c0004t0003g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.583+611A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869008 | ||||||
| chr12:132869040
|
C | G | 1 | a0001c0001t0074g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+579G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869040 | ||||||
| chr12:132869046
|
T | TCGAGGGG others(32): Show |
126 | a0001c0001t0072g0352a0002c0002t0002g0009a0002c0002t0002g0045others(123): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.583+534_583+572dup others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869046 | ||||||
| chr12:132869046
|
TCGAGGGG others(32): Show |
T | 12 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(9): Show | 15 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+534_583+572del others(39): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869046 | ||||||
| chr12:132869124
|
C | T | 9 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(6): Show | 10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+495G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869124 | ||||||
| chr12:132869151
|
C | T | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+468G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869151 | ||||||
| chr12:132869163
|
C | CCGAGGGG others(344): Show |
2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+455_583+456ins others(351): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869163 | ||||||
| chr12:132869164
|
C | T | 1 | a0001c0001t0026g0016 | 2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.583+455G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869164 | ||||||
| chr12:132869260
|
T | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+359A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869260 | ||||||
| chr12:132869266
|
C | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.583+353G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869266 | ||||||
| chr12:132869570
|
A | G | 1 | a0001c0001t0119g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.583+49T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 6/17 | chr12 | 132869570 | ||||||
| chr12:132869827
|
G | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0279a0001c0001t0014g0280 | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-29C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132869827 | ||||||
| chr12:132869852
|
C | T | 1 | a0001c0001t0087g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.404-54G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132869852 | ||||||
| chr12:132870075
|
G | A | 4 | a0001c0005t0024g0171a0001c0005t0024g0174a0001c0005t0024g0175others(1): Show | 4 | HG01106.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-277C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870075 | ||||||
| chr12:132870081
|
G | A | 11 | a0002c0002t0048g0044a0002c0002t0133g0041a0004c0006t0031g0161others(8): Show | 11 | HG02129.hp1 HG02698.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-283C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870081 | ||||||
| chr12:132870099
|
T | G | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.404-301A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870099 | ||||||
| chr12:132870123
|
C | T | 1 | a0003c0003t0001g0329 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.404-325G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870123 | ||||||
| chr12:132870236
|
C | T | 101 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(98): Show | 112 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.404-438G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870236 | ||||||
| chr12:132870256
|
G | T | 1 | a0001c0001t0081g0252 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.404-458C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870256 | ||||||
| chr12:132870257
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.404-459G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870257 | ||||||
| chr12:132870276
|
C | T | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.403+448G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870276 | ||||||
| chr12:132870293
|
A | G | 1 | a0002c0002t0030g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.403+431T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870293 | ||||||
| chr12:132870354
|
A | AAAAC | 51 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.403+366_403+369dup others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870354 | ||||||
| chr12:132870530
|
T | C | 1 | a0003c0003t0001g0355 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+194A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870530 | ||||||
| chr12:132870531
|
C | CA | 36 | a0001c0001t0015g0294a0001c0001t0042g0276a0001c0001t0088g0269others(33): Show | 39 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.403+192dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | ||||||
| chr12:132870531
|
C | T | 1 | a0003c0003t0001g0355 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+193G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | ||||||
| chr12:132870531
|
CA | C | 99 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(96): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.403+192delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870531 | ||||||
| chr12:132870532
|
A | C | 1 | a0003c0003t0001g0355 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403+192T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870532 | ||||||
| chr12:132870552
|
T | A | 5 | a0001c0001t0043g0017a0001c0001t0083g0272a0001c0001t0104g0309others(2): Show | 6 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+172A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870552 | ||||||
| chr12:132870570
|
G | T | 6 | a0003c0003t0019g0346a0003c0003t0037g0347a0003c0003t0037g0348others(3): Show | 6 | HG02818.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+154C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870570 | ||||||
| chr12:132870609
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.403+115C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870609 | ||||||
| chr12:132870638
|
T | C | 55 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.403+86A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870638 | ||||||
| chr12:132870652
|
T | C | 3 | a0001c0004t0003g0198a0001c0004t0003g0199a0001c0004t0003g0202 | 3 | HG01168.hp1 HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.403+72A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870652 | ||||||
| chr12:132870656
|
T | C | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.403+68A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 5/17 | chr12 | 132870656 | ||||||
| chr12:132871102
|
C | T | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.344-319G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871102 | ||||||
| chr12:132871218
|
G | A | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.344-435C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871218 | ||||||
| chr12:132871223
|
G | A | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.344-440C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871223 | ||||||
| chr12:132871269
|
C | T | 237 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(234): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.344-486G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871269 | ||||||
| chr12:132871308
|
C | T | 94 | a0002c0002t0002g0009a0002c0002t0002g0045a0002c0002t0002g0046others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.344-525G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871308 | ||||||
| chr12:132871351
|
C | T | 1 | a0003c0003t0001g0329 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.344-568G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871351 | ||||||
| chr12:132871408
|
C | T | 1 | a0003c0003t0001g0315 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.344-625G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871408 | ||||||
| chr12:132871413
|
T | C | 1 | a0002c0002t0136g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.344-630A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871413 | ||||||
| chr12:132871415
|
G | C | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.344-632C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871415 | ||||||
| chr12:132871428
|
C | G | 189 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.344-645G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871428 | ||||||
| chr12:132871429
|
G | A | 1 | a0001c0004t0003g0200 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.344-646C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871429 | ||||||
| chr12:132871600
|
C | T | 1 | a0003c0003t0020g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343+685G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871600 | ||||||
| chr12:132871628
|
C | T | 37 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(34): Show | 39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.343+657G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871628 | ||||||
| chr12:132871630
|
G | T | 4 | a0002c0002t0005g0087a0002c0002t0005g0088a0002c0002t0005g0090others(1): Show | 4 | NA18944.hp2 NA18948.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+655C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871630 | ||||||
| chr12:132871665
|
A | G | 341 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(338): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.343+620T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871665 | ||||||
| chr12:132871744
|
C | T | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.343+541G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871744 | ||||||
| chr12:132871805
|
G | A | 47 | a0001c0001t0072g0352a0001c0004t0003g0003a0001c0004t0003g0011others(44): Show | 51 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.343+480C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871805 | ||||||
| chr12:132871915
|
T | C | 1 | a0003c0003t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.343+370A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871915 | ||||||
| chr12:132871935
|
A | G | 4 | a0001c0001t0016g0251a0003c0003t0019g0346a0003c0008t0019g0349others(1): Show | 4 | HG02886.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+350T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871935 | ||||||
| chr12:132871967
|
G | C | 225 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(222): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.343+318C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132871967 | ||||||
| chr12:132872192
|
T | C | 1 | a0001c0001t0006g0137 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.343+93A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872192 | ||||||
| chr12:132872217
|
C | T | 1 | a0005c0009t0055g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.343+68G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872217 | ||||||
| chr12:132872226
|
A | G | 5 | a0001c0001t0014g0278a0001c0001t0016g0249a0001c0001t0016g0250others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+59T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872226 | ||||||
| chr12:132872229
|
G | A | 66 | a0001c0001t0006g0150a0001c0001t0006g0152a0001c0001t0026g0016others(63): Show | 72 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.343+56C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872229 | ||||||
| chr12:132872237
|
G | A | 3 | a0002c0002t0028g0056a0002c0002t0028g0057a0002c0002t0028g0060 | 3 | HG01099.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.343+48C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 4/17 | chr12 | 132872237 | ||||||
| chr12:132872432
|
A | G | 1 | a0001c0005t0024g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234-38T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872432 | ||||||
| chr12:132872577
|
G | A | 1 | a0002c0002t0004g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.234-183C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872577 | ||||||
| chr12:132872591
|
G | A | 77 | a0001c0001t0014g0004a0001c0001t0014g0279a0001c0001t0014g0280others(74): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.234-197C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872591 | ||||||
| chr12:132872781
|
C | A | 52 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-387G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872781 | ||||||
| chr12:132872863
|
G | A | 87 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(84): Show | 93 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-469C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132872863 | ||||||
| chr12:132873035
|
T | A | 1 | a0001c0005t0075g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234-641A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873035 | ||||||
| chr12:132873063
|
A | G | 1 | a0002c0002t0125g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234-669T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873063 | ||||||
| chr12:132873251
|
A | C | 50 | a0001c0001t0015g0300a0001c0001t0086g0299a0001c0004t0003g0003others(47): Show | 54 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.234-857T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873251 | ||||||
| chr12:132873358
|
G | A | 1 | a0003c0003t0019g0351 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.234-964C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873358 | ||||||
| chr12:132873443
|
G | C | 89 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(86): Show | 97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.234-1049C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873443 | ||||||
| chr12:132873448
|
G | A | 75 | a0001c0004t0018g0086a0002c0002t0002g0009a0002c0002t0002g0045others(72): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.234-1054C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873448 | ||||||
| chr12:132873459
|
C | T | 3 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0061g0020 | 3 | HG02257.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.234-1065G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873459 | ||||||
| chr12:132873506
|
TGCTGGAC others(83): Show |
T | 128 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(125): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.234-1202_234-1113d others(92): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873506 | ||||||
| chr12:132873558
|
G | A | 95 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(92): Show | 100 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-1164C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873558 | ||||||
| chr12:132873612
|
T | C | 8 | a0002c0002t0002g0048a0002c0002t0002g0100a0002c0002t0002g0104others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-1218A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873612 | ||||||
| chr12:132873620
|
CCTGCTCC others(82): Show |
C | 1 | a0001c0001t0106g0291 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.234-1315_234-1227d others(91): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873620 | ||||||
| chr12:132873634
|
C | T | 4 | a0001c0001t0011g0243a0001c0001t0011g0248a0001c0001t0011g0287others(1): Show | 4 | NA18950.hp2 NA18983.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1240G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873634 | ||||||
| chr12:132873648
|
G | A | 1 | a0002c0002t0048g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234-1254C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873648 | ||||||
| chr12:132873744
|
T | C | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.234-1350A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873744 | ||||||
| chr12:132873745
|
G | A | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.234-1351C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873745 | ||||||
| chr12:132873795
|
G | A | 10 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.234-1401C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132873795 | ||||||
| chr12:132874048
|
C | T | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.234-1654G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874048 | ||||||
| chr12:132874336
|
G | A | 1 | a0001c0005t0077g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234-1942C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874336 | ||||||
| chr12:132874366
|
T | G | 1 | a0001c0001t0119g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234-1972A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874366 | ||||||
| chr12:132874511
|
C | T | 1 | a0001c0001t0015g0247 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.234-2117G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874511 | ||||||
| chr12:132874552
|
C | T | 3 | a0001c0005t0024g0171a0001c0005t0024g0174a0001c0005t0024g0175 | 3 | HG01884.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.234-2158G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874552 | ||||||
| chr12:132874583
|
G | A | 1 | a0002c0002t0139g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.234-2189C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874583 | ||||||
| chr12:132874601
|
AGAACAGG others(46): Show |
A | 84 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(81): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-2260_234-2208d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874601 | ||||||
| chr12:132874691
|
G | A | 32 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(29): Show | 35 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.234-2297C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874691 | ||||||
| chr12:132874857
|
C | G | 2 | a0001c0001t0010g0236a0001c0001t0010g0289 | 2 | NA18943.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.234-2463G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874857 | ||||||
| chr12:132874901
|
GCGGGGAA others(46): Show |
G | 1 | a0001c0001t0103g0274 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.234-2560_234-2508d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874901 | ||||||
| chr12:132874954
|
A | G | 41 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(38): Show | 43 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-2560T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874954 | ||||||
| chr12:132874955
|
C | T | 41 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(38): Show | 43 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-2561G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874955 | ||||||
| chr12:132874958
|
G | GGAAGCCA others(46): Show |
1 | a0002c0002t0002g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.233+2544_234-2565d others(55): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132874958 | ||||||
| chr12:132875006
|
C | T | 1 | a0002c0002t0132g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+2549G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875006 | ||||||
| chr12:132875033
|
C | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233+2522G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875033 | ||||||
| chr12:132875081
|
G | T | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.233+2474C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875081 | ||||||
| chr12:132875098
|
G | A | 10 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+2457C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875098 | ||||||
| chr12:132875305
|
C | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233+2250G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875305 | ||||||
| chr12:132875382
|
T | G | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.233+2173A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875382 | ||||||
| chr12:132875483
|
C | T | 49 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(46): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.233+2072G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875483 | ||||||
| chr12:132875489
|
G | A | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.233+2066C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875489 | ||||||
| chr12:132875670
|
C | T | 4 | a0001c0001t0015g0244a0001c0001t0079g0245a0001c0001t0080g0237others(1): Show | 4 | HG00558.hp2 HG02165.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1885G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875670 | ||||||
| chr12:132875897
|
G | A | 97 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(94): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.233+1658C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132875897 | ||||||
| chr12:132876173
|
C | CA | 107 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(104): Show | 118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.233+1381dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876173 | ||||||
| chr12:132876182
|
A | G | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.233+1373T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876182 | ||||||
| chr12:132876251
|
T | C | 1 | a0001c0001t0006g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.233+1304A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876251 | ||||||
| chr12:132876367
|
T | C | 1 | a0004c0006t0135g0164 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.233+1188A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876367 | ||||||
| chr12:132876749
|
T | C | 1 | a0003c0003t0001g0342 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.233+806A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876749 | ||||||
| chr12:132876763
|
A | G | 2 | a0002c0007t0002g0064a0002c0007t0002g0069 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.233+792T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876763 | ||||||
| chr12:132876951
|
C | G | 1 | a0001c0001t0091g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233+604G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876951 | ||||||
| chr12:132876952
|
G | A | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.233+603C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876952 | ||||||
| chr12:132876955
|
C | A | 1 | a0001c0005t0038g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.233+600G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876955 | ||||||
| chr12:132876955
|
C | T | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.233+600G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132876955 | ||||||
| chr12:132877090
|
C | T | 6 | a0003c0003t0020g0319a0003c0003t0020g0320a0003c0003t0020g0322others(3): Show | 6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+465G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877090 | ||||||
| chr12:132877302
|
G | A | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233+253C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877302 | ||||||
| chr12:132877303
|
G | A | 1 | a0003c0003t0066g0338 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.233+252C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877303 | ||||||
| chr12:132877321
|
G | C | 1 | a0001c0001t0006g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.233+234C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877321 | ||||||
| chr12:132877362
|
T | C | 2 | a0001c0001t0150g0144a0001c0001t0151g0140 | 2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.233+193A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 3/17 | chr12 | 132877362 | ||||||
| chr12:132877708
|
C | T | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.134-54G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877708 | ||||||
| chr12:132877768
|
TA | T | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.134-115delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877768 | ||||||
| chr12:132877769
|
A | T | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-115T>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877769 | ||||||
| chr12:132877804
|
A | G | 3 | a0001c0001t0011g0243a0001c0001t0011g0287a0001c0001t0011g0290 | 3 | NA18950.hp2 NA19056.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.134-150T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877804 | ||||||
| chr12:132877833
|
C | T | 1 | a0001c0005t0075g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134-179G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877833 | ||||||
| chr12:132877834
|
GC | G | 15 | a0001c0001t0090g0039a0002c0002t0048g0040a0002c0002t0048g0044others(12): Show | 15 | HG01109.hp2 HG01433.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-181delG | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877834 | ||||||
| chr12:132877924
|
T | G | 1 | a0001c0001t0070g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.134-270A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877924 | ||||||
| chr12:132877966
|
C | G | 1 | a0001c0001t0009g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.134-312G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877966 | ||||||
| chr12:132877981
|
T | G | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.134-327A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877981 | ||||||
| chr12:132877992
|
C | T | 1 | a0003c0003t0001g0327 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.134-338G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132877992 | ||||||
| chr12:132878068
|
C | T | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-414G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878068 | ||||||
| chr12:132878097
|
C | T | 6 | a0003c0003t0020g0319a0003c0003t0020g0320a0003c0003t0020g0322others(3): Show | 6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-443G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878097 | ||||||
| chr12:132878338
|
G | A | 5 | a0004c0006t0032g0156a0004c0006t0032g0159a0004c0006t0032g0160others(2): Show | 5 | NA18954.hp2 NA18969.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-684C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878338 | ||||||
| chr12:132878384
|
G | A | 77 | a0001c0004t0018g0086a0002c0002t0002g0009a0002c0002t0002g0045others(74): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.134-730C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878384 | ||||||
| chr12:132878448
|
G | A | 1 | a0001c0004t0003g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.134-794C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878448 | ||||||
| chr12:132878473
|
T | TA | 6 | a0001c0001t0042g0275a0001c0001t0042g0276a0001c0001t0102g0308others(3): Show | 6 | HG00408.hp2 HG02602.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-820dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878473 | ||||||
| chr12:132878473
|
TA | T | 50 | a0001c0001t0015g0300a0001c0001t0025g0242a0001c0004t0003g0003others(47): Show | 54 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-820delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878473 | ||||||
| chr12:132878479
|
A | G | 1 | a0001c0001t0091g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-825T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878479 | ||||||
| chr12:132878583
|
A | G | 341 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(338): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.134-929T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878583 | ||||||
| chr12:132878595
|
A | G | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.134-941T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878595 | ||||||
| chr12:132878616
|
G | A | 38 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.134-962C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878616 | ||||||
| chr12:132878642
|
A | G | 1 | a0002c0002t0004g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-988T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878642 | ||||||
| chr12:132878686
|
G | C | 1 | a0001c0001t0072g0352 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.134-1032C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878686 | ||||||
| chr12:132878692
|
G | A | 97 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(94): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1038C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878692 | ||||||
| chr12:132878711
|
T | C | 2 | a0001c0001t0044g0018a0001c0001t0084g0292 | 3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-1057A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878711 | ||||||
| chr12:132878745
|
G | A | 97 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(94): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1091C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878745 | ||||||
| chr12:132878832
|
A | G | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1178T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878832 | ||||||
| chr12:132878832
|
AG | A | 28 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(25): Show | 30 | HG00140.hp2 HG01168.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.134-1179delC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878832 | ||||||
| chr12:132878833
|
G | A | 12 | a0001c0001t0006g0152a0001c0001t0051g0146a0001c0001t0053g0141others(9): Show | 12 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1179C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878833 | ||||||
| chr12:132878833
|
G | GA | 44 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.134-1180dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878833 | ||||||
| chr12:132878884
|
C | T | 1 | a0001c0004t0058g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.134-1230G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878884 | ||||||
| chr12:132878902
|
G | A | 1 | a0001c0004t0018g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.134-1248C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878902 | ||||||
| chr12:132878998
|
T | G | 1 | a0001c0001t0084g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-1344A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878998 | ||||||
| chr12:132878999
|
G | T | 1 | a0002c0007t0002g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.134-1345C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132878999 | ||||||
| chr12:132879005
|
G | T | 97 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(94): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1351C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879005 | ||||||
| chr12:132879009
|
G | T | 2 | a0002c0007t0002g0064a0004c0006t0031g0161 | 2 | HG03669.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.134-1355C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879009 | ||||||
| chr12:132879009
|
GT | G | 199 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(196): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.134-1356delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879009 | ||||||
| chr12:132879010
|
T | G | 2 | a0002c0007t0002g0064a0004c0006t0031g0161 | 2 | HG03669.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.134-1356A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879010 | ||||||
| chr12:132879011
|
T | G | 4 | a0003c0003t0001g0318a0003c0003t0001g0325a0003c0003t0001g0337others(1): Show | 4 | HG00438.hp2 HG02129.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1357A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879011 | ||||||
| chr12:132879070
|
T | A | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1416A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879070 | ||||||
| chr12:132879074
|
G | A | 1 | a0001c0004t0003g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.134-1420C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879074 | ||||||
| chr12:132879153
|
C | T | 1 | a0004c0006t0032g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.134-1499G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879153 | ||||||
| chr12:132879275
|
T | A | 1 | a0001c0001t0012g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.134-1621A>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879275 | ||||||
| chr12:132879275
|
T | G | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.134-1621A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879275 | ||||||
| chr12:132879297
|
C | G | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.134-1643G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879297 | ||||||
| chr12:132879353
|
T | C | 1 | a0001c0001t0006g0145 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.134-1699A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879353 | ||||||
| chr12:132879370
|
T | C | 2 | a0005c0009t0054g0118a0005c0009t0055g0106 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1716A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879370 | ||||||
| chr12:132879380
|
T | G | 1 | a0001c0001t0117g0232 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.134-1726A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879380 | ||||||
| chr12:132879395
|
C | CT | 14 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(11): Show | 15 | HG00735.hp2 HG01070.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-1742dupA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879395 | ||||||
| chr12:132879431
|
C | T | 6 | a0001c0001t0015g0294a0001c0001t0015g0298a0001c0001t0015g0300others(3): Show | 6 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-1777G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879431 | ||||||
| chr12:132879459
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-1805G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879459 | ||||||
| chr12:132879460
|
A | G | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.134-1806T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879460 | ||||||
| chr12:132879484
|
G | A | 1 | a0001c0001t0010g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.134-1830C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879484 | ||||||
| chr12:132879627
|
G | A | 1 | a0001c0001t0023g0001 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.134-1973C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879627 | ||||||
| chr12:132879636
|
G | A | 97 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(94): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1982C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879636 | ||||||
| chr12:132879641
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.134-1987C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879641 | ||||||
| chr12:132879892
|
A | G | 78 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(75): Show | 83 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.134-2238T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132879892 | ||||||
| chr12:132880147
|
T | G | 1 | a0003c0003t0063g0345 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.134-2493A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880147 | ||||||
| chr12:132880182
|
A | C | 1 | a0003c0003t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.134-2528T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880182 | ||||||
| chr12:132880246
|
C | G | 7 | a0002c0002t0002g0055a0002c0002t0028g0056a0002c0002t0028g0057others(4): Show | 7 | HG00733.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-2592G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880246 | ||||||
| chr12:132880431
|
G | T | 2 | a0001c0005t0075g0172a0001c0005t0076g0173 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-2777C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880431 | ||||||
| chr12:132880518
|
C | T | 1 | a0002c0002t0004g0054 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-2864G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880518 | ||||||
| chr12:132880526
|
C | T | 96 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(93): Show | 101 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.134-2872G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880526 | ||||||
| chr12:132880548
|
C | T | 1 | a0001c0004t0018g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.134-2894G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880548 | ||||||
| chr12:132880595
|
T | C | 1 | a0001c0001t0093g0284 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-2941A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880595 | ||||||
| chr12:132880615
|
G | A | 1 | a0001c0001t0008g0240 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.134-2961C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880615 | ||||||
| chr12:132880616
|
C | T | 1 | a0001c0001t0008g0240 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.134-2962G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880616 | ||||||
| chr12:132880663
|
AAG | A | 102 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(99): Show | 113 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.134-3011_134-3010d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880663 | ||||||
| chr12:132880664
|
AG | A | 5 | a0001c0001t0008g0286a0001c0001t0085g0285a0001c0001t0086g0299others(2): Show | 5 | HG02257.hp1 NA18952.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-3011delC | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880664 | ||||||
| chr12:132880709
|
G | C | 99 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(96): Show | 104 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.134-3055C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880709 | ||||||
| chr12:132880783
|
G | A | 45 | a0003c0003t0001g0052a0003c0003t0001g0053a0003c0003t0001g0313others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.134-3129C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880783 | ||||||
| chr12:132880834
|
G | A | 7 | a0001c0005t0021g0182a0001c0005t0021g0183a0001c0005t0021g0184others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-3180C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880834 | ||||||
| chr12:132880922
|
G | A | 101 | a0001c0001t0051g0146a0001c0001t0051g0153a0001c0001t0090g0039others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-3268C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880922 | ||||||
| chr12:132880930
|
A | G | 1 | a0003c0003t0061g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.134-3276T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880930 | ||||||
| chr12:132880979
|
A | G | 1 | a0001c0004t0018g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.134-3325T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132880979 | ||||||
| chr12:132881025
|
G | T | 3 | a0001c0004t0003g0226a0001c0004t0003g0227a0001c0004t0060g0230 | 3 | HG00280.hp1 NA18977.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.134-3371C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881025 | ||||||
| chr12:132881035
|
G | A | 88 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(85): Show | 96 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.134-3381C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881035 | ||||||
| chr12:132881056
|
C | G | 2 | a0001c0004t0036g0206a0001c0004t0036g0207 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.134-3402G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881056 | ||||||
| chr12:132881058
|
G | C | 1 | a0002c0002t0004g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-3404C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881058 | ||||||
| chr12:132881065
|
G | A | 44 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(41): Show | 47 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.134-3411C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881065 | ||||||
| chr12:132881111
|
A | G | 1 | a0001c0001t0080g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.134-3457T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881111 | ||||||
| chr12:132881196
|
T | G | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-3542A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881196 | ||||||
| chr12:132881257
|
C | CA | 149 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(146): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.134-3604dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881257 | ||||||
| chr12:132881568
|
C | G | 36 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.134-3914G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881568 | ||||||
| chr12:132881589
|
C | T | 28 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(25): Show | 31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-3935G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881589 | ||||||
| chr12:132881596
|
G | A | 6 | a0004c0006t0032g0156a0004c0006t0032g0159a0004c0006t0032g0160others(3): Show | 6 | NA18954.hp2 NA18969.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-3942C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881596 | ||||||
| chr12:132881724
|
C | T | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-4070G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881724 | ||||||
| chr12:132881725
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.134-4071C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881725 | ||||||
| chr12:132881731
|
G | A | 1 | a0002c0002t0129g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.134-4077C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881731 | ||||||
| chr12:132881792
|
C | T | 109 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(106): Show | 120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.134-4138G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881792 | ||||||
| chr12:132881800
|
G | A | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.134-4146C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881800 | ||||||
| chr12:132881831
|
G | A | 1 | a0002c0002t0002g0122 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.134-4177C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881831 | ||||||
| chr12:132881867
|
CA | C | 56 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(53): Show | 59 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.134-4214delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881867 | ||||||
| chr12:132881867
|
CAA | C | 272 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.134-4215_134-4214d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881867 | ||||||
| chr12:132881940
|
G | A | 1 | a0001c0001t0051g0153 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.134-4286C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132881940 | ||||||
| chr12:132882070
|
G | C | 2 | a0001c0001t0044g0018a0001c0001t0084g0292 | 3 | HG01243.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-4416C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882070 | ||||||
| chr12:132882432
|
C | T | 1 | a0001c0001t0090g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+4764G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882432 | ||||||
| chr12:132882609
|
C | T | 10 | a0003c0003t0013g0021a0003c0003t0013g0022a0003c0003t0013g0024others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+4587G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882609 | ||||||
| chr12:132882638
|
A | G | 1 | a0001c0005t0077g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.133+4558T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882638 | ||||||
| chr12:132882653
|
C | T | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+4543G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882653 | ||||||
| chr12:132882684
|
C | T | 43 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.133+4512G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882684 | ||||||
| chr12:132882701
|
A | G | 1 | a0001c0001t0090g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+4495T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882701 | ||||||
| chr12:132882706
|
GT | G | 181 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(178): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.133+4489delA | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882706 | ||||||
| chr12:132882759
|
G | T | 43 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.133+4437C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882759 | ||||||
| chr12:132882929
|
T | C | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+4267A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882929 | ||||||
| chr12:132882976
|
A | G | 6 | a0003c0003t0020g0319a0003c0003t0020g0320a0003c0003t0020g0322others(3): Show | 6 | HG01175.hp2 HG01934.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+4220T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132882976 | ||||||
| chr12:132883092
|
T | C | 1 | a0003c0003t0001g0343 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.133+4104A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883092 | ||||||
| chr12:132883155
|
C | T | 1 | a0003c0003t0001g0339 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.133+4041G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883155 | ||||||
| chr12:132883387
|
T | C | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+3809A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883387 | ||||||
| chr12:132883407
|
T | C | 341 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(338): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.133+3789A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883407 | ||||||
| chr12:132883422
|
G | A | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3774C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883422 | ||||||
| chr12:132883426
|
C | CA | 10 | a0001c0001t0015g0298a0001c0001t0070g0178a0001c0001t0072g0352others(7): Show | 10 | HG00642.hp1 HG00735.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+3769dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883426 | ||||||
| chr12:132883426
|
C | CAA | 37 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(34): Show | 39 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.133+3768_133+3769d others(4): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883426 | ||||||
| chr12:132883446
|
C | T | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.133+3750G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883446 | ||||||
| chr12:132883563
|
A | G | 1 | a0001c0001t0015g0235 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.133+3633T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883563 | ||||||
| chr12:132883595
|
C | T | 1 | a0002c0002t0002g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133+3601G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883595 | ||||||
| chr12:132883626
|
T | C | 109 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(106): Show | 120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+3570A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883626 | ||||||
| chr12:132883649
|
C | G | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3547G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883649 | ||||||
| chr12:132883830
|
T | C | 39 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(36): Show | 41 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+3366A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883830 | ||||||
| chr12:132883866
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.133+3330C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883866 | ||||||
| chr12:132883883
|
C | G | 1 | a0002c0002t0129g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.133+3313G>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883883 | ||||||
| chr12:132883917
|
A | C | 38 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(35): Show | 40 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.133+3279T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132883917 | ||||||
| chr12:132884312
|
G | T | 1 | a0006c0014t0002g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.133+2884C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884312 | ||||||
| chr12:132884313
|
G | C | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+2883C>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884313 | ||||||
| chr12:132884415
|
C | CA | 135 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(132): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.133+2780dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884415 | ||||||
| chr12:132884670
|
T | G | 1 | a0001c0001t0010g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133+2526A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884670 | ||||||
| chr12:132884929
|
T | C | 2 | a0001c0001t0152g0154a0001c0001t0153g0155 | 2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.133+2267A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884929 | ||||||
| chr12:132884973
|
A | C | 1 | a0003c0003t0001g0318 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.133+2223T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884973 | ||||||
| chr12:132884981
|
G | A | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+2215C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132884981 | ||||||
| chr12:132885148
|
G | A | 2 | a0002c0002t0047g0010a0002c0002t0126g0117 | 3 | HG00423.hp2 NA18950.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.133+2048C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885148 | ||||||
| chr12:132885265
|
G | A | 1 | a0005c0009t0054g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133+1931C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885265 | ||||||
| chr12:132885366
|
G | A | 1 | a0001c0005t0077g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.133+1830C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885366 | ||||||
| chr12:132885419
|
T | TATAA | 95 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(92): Show | 103 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.133+1773_133+1776d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | ||||||
| chr12:132885419
|
T | TATAAATA others(1): Show |
6 | a0001c0001t0015g0300a0001c0001t0086g0299a0002c0002t0002g0122others(3): Show | 6 | HG00323.hp1 NA18984.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+1769_133+1776d others(10): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | ||||||
| chr12:132885419
|
TATAA | T | 112 | a0001c0001t0016g0234a0001c0001t0090g0039a0001c0004t0003g0003others(109): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.133+1773_133+1776d others(6): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885419 | ||||||
| chr12:132885436
|
A | G | 1 | a0001c0005t0024g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+1760T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885436 | ||||||
| chr12:132885454
|
A | C | 1 | a0001c0004t0003g0231 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.133+1742T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885454 | ||||||
| chr12:132885596
|
G | A | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+1600C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885596 | ||||||
| chr12:132885743
|
C | A | 109 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(106): Show | 120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+1453G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885743 | ||||||
| chr12:132885776
|
G | T | 1 | a0001c0004t0058g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.133+1420C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885776 | ||||||
| chr12:132885778
|
T | C | 1 | a0003c0003t0066g0338 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.133+1418A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885778 | ||||||
| chr12:132885861
|
T | C | 3 | a0001c0004t0003g0228a0001c0004t0003g0231a0001c0004t0022g0229 | 3 | NA18979.hp1 NA18985.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.133+1335A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132885861 | ||||||
| chr12:132886141
|
A | G | 340 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(337): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.133+1055T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886141 | ||||||
| chr12:132886173
|
A | C | 109 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(106): Show | 120 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133+1023T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886173 | ||||||
| chr12:132886182
|
C | T | 1 | a0003c0003t0001g0317 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.133+1014G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886182 | ||||||
| chr12:132886309
|
TCAAAAAA others(5): Show |
T | 2 | a0001c0001t0112g0233a0001c0001t0117g0232 | 2 | NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.133+875_133+886del others(12): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886309 | ||||||
| chr12:132886339
|
C | A | 11 | a0001c0001t0010g0038a0003c0003t0013g0021a0003c0003t0013g0022others(8): Show | 11 | HG01106.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.133+857G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886339 | ||||||
| chr12:132886341
|
A | C | 1 | a0001c0001t0010g0038 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+855T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886341 | ||||||
| chr12:132886342
|
G | A | 1 | a0001c0001t0010g0038 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+854C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886342 | ||||||
| chr12:132886347
|
A | C | 101 | a0001c0001t0090g0039a0001c0001t0091g0065a0001c0004t0018g0086others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.133+849T>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886347 | ||||||
| chr12:132886360
|
G | A | 1 | a0001c0001t0109g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.133+836C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886360 | ||||||
| chr12:132886374
|
C | CA | 9 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(6): Show | 10 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+821dupT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | ||||||
| chr12:132886374
|
CA | C | 146 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.133+821delT | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | ||||||
| chr12:132886374
|
CAA | C | 161 | a0001c0001t0006g0126a0001c0001t0006g0132a0001c0001t0006g0134others(158): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.133+820_133+821del others(2): Show |
CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886374 | ||||||
| chr12:132886500
|
C | A | 48 | a0001c0004t0003g0003a0001c0004t0003g0011a0001c0004t0003g0188others(45): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+696G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886500 | ||||||
| chr12:132886557
|
T | G | 88 | a0001c0001t0008g0013a0001c0001t0008g0240a0001c0001t0008g0256others(85): Show | 96 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.133+639A>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886557 | ||||||
| chr12:132886584
|
G | T | 1 | a0001c0001t0010g0038 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+612C>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886584 | ||||||
| chr12:132886661
|
T | C | 1 | a0001c0001t0116g0311 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.133+535A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886661 | ||||||
| chr12:132886817
|
T | C | 1 | a0001c0001t0145g0312 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.133+379A>G | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886817 | ||||||
| chr12:132886923
|
A | G | 57 | a0001c0001t0009g0005a0001c0001t0009g0030a0001c0001t0009g0031others(54): Show | 60 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.133+273T>C | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132886923 | ||||||
| chr12:132887189
|
C | T | 4 | a0003c0003t0001g0313a0003c0003t0001g0314a0003c0003t0001g0315others(1): Show | 4 | HG00738.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.133+7G>A | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 2/17 | chr12 | 132887189 | ||||||
| chr12:132887383
|
G | A | 44 | a0001c0001t0072g0352a0003c0003t0001g0313a0003c0003t0001g0314others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.-12-43C>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 1/17 | chr12 | 132887383 | ||||||
| chr12:132887529
|
C | A | 4 | a0003c0003t0001g0353a0003c0003t0001g0354a0003c0003t0001g0355others(1): Show | 4 | HG00140.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+18G>T | CHFR | ENSG00000072609.18 | transcript | ENST00000450056.7 | protein_coding | 1/17 | chr12 | 132887529 |