Search by Gene
| geneid | 56947 |
|---|---|
| ensemblid | ENSG00000168958.21 |
| hgncid | 24858 |
| symbol | MFF |
| name | mitochondrial fission factor |
| refseq_nuc | NM_001277062.2 |
| refseq_prot | NP_001263991.1 |
| ensembl_nuc | ENST00000304593.14 |
| ensembl_prot | ENSP00000304898.10 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 227325251 |
| end | 227357833 |
| strand | + |
| ver | v1.2 |
| region | chr2:227325251-227357833 |
| region5000 | chr2:227320251-227362833 |
| regionname0 | MFF_chr2_227325251_227357833 |
| regionname5000 | MFF_chr2_227320251_227362833 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 291 | 405 | 96 | 56 | 199 | 14 | 38 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0002 | 0/0 | 291 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 876 | 305 | 65 | 41 | 155 | 9 | 33 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| c0002 | 0/0 | 876 | 63 | 22 | 8 | 27 | 5 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| c0003 | 0/0 | 876 | 33 | 8 | 7 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| c0004 | 0/0 | 876 | 4 | 1 | 0 | 1 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| c0005 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1046 | 141 | 21 | 20 | 79 | 5 | 15 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0002 | 0/0 | 1046 | 90 | 12 | 17 | 43 | 4 | 14 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0003 | 0/0 | 1046 | 45 | 5 | 6 | 28 | 5 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0004 | 0/0 | 1046 | 32 | 7 | 7 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0005 | 0/0 | 1046 | 28 | 9 | 1 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0006 | 0/0 | 1046 | 13 | 13 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0007 | 1/0 | 1046 | 12 | 11 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0008 | 0/0 | 1046 | 11 | 11 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0009 | 0/0 | 1046 | 7 | 0 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0010 | 0/0 | 1046 | 5 | 3 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0011 | 0/0 | 1046 | 4 | 1 | 0 | 1 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0012 | 0/0 | 1046 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0013 | 0/0 | 1049 | 3 | 0 | 2 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0014 | 0/0 | 1046 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0015 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0016 | 0/0 | 1046 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0017 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0018 | 0/0 | 1046 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0019 | 0/0 | 1046 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0020 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0021 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0022 | 0/0 | 1046 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0023 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| t0024 | 0/0 | 1046 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 30 | 2 | 8 | 17 | 0 | 3 | MFF_chr2_227320251_227362833 | MFF |
| g0002 | 0/0 | 25 | 0 | 6 | 16 | 1 | 2 | MFF_chr2_227320251_227362833 | MFF |
| g0003 | 0/0 | 22 | 1 | 4 | 13 | 2 | 2 | MFF_chr2_227320251_227362833 | MFF |
| g0004 | 0/0 | 15 | 0 | 0 | 12 | 3 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0005 | 0/0 | 9 | 2 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0006 | 0/0 | 9 | 2 | 4 | 2 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0011 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF |
| g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0015 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0026 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0045 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 305 | 65 | 41 | 155 | 9 | 33 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 63 | 22 | 8 | 27 | 5 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 33 | 8 | 7 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0002c0005 | a0002 | c0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 141 | 21 | 20 | 79 | 5 | 15 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 88 | 10 | 17 | 43 | 4 | 14 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 28 | 9 | 1 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 13 | 13 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 1/0 | 12 | 11 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 44 | 5 | 6 | 27 | 5 | 1 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002t0010 | a0001 | c0002 | t0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0002t0016 | a0001 | c0002 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 32 | 7 | 7 | 16 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0003t0018 | a0001 | c0003 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0001c0004t0011 | a0001 | c0004 | t0011 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| a0002c0005t0003 | a0002 | c0005 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 30 | 2 | 8 | 17 | 0 | 3 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 22 | 1 | 4 | 13 | 2 | 2 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 19 | 0 | 5 | 11 | 1 | 2 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0007 | a0001 | c0001 | t0002 | g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0034 | a0001 | c0001 | t0002 | g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0035 | a0001 | c0001 | t0002 | g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0005 | a0001 | c0001 | t0005 | g0005 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0013 | a0001 | c0001 | t0005 | g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0018 | a0001 | c0001 | t0005 | g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0032 | a0001 | c0001 | t0005 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0053 | a0001 | c0001 | t0005 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0054 | a0001 | c0001 | t0005 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0055 | a0001 | c0001 | t0005 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0056 | a0001 | c0001 | t0005 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0057 | a0001 | c0001 | t0005 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0058 | a0001 | c0001 | t0005 | g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0059 | a0001 | c0001 | t0005 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0060 | a0001 | c0001 | t0005 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0061 | a0001 | c0001 | t0005 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0062 | a0001 | c0001 | t0005 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0005g0063 | a0001 | c0001 | t0005 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0012 | a0001 | c0001 | t0006 | g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0104 | a0001 | c0001 | t0006 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0106 | a0001 | c0001 | t0006 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0107 | a0001 | c0001 | t0006 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0108 | a0001 | c0001 | t0006 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0109 | a0001 | c0001 | t0006 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0110 | a0001 | c0001 | t0006 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0111 | a0001 | c0001 | t0006 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0006g0172 | a0001 | c0001 | t0006 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0017 | a0001 | c0001 | t0007 | g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0046 | a0001 | c0001 | t0007 | g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0047 | a0001 | c0001 | t0007 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0207 | a0001 | c0001 | t0007 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0208 | a0001 | c0001 | t0007 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0209 | a0001 | c0001 | t0007 | g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0007g0214 | a0001 | c0001 | t0007 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0009g0002 | a0001 | c0001 | t0009 | g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0009g0010 | a0001 | c0001 | t0009 | g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0012g0020 | a0001 | c0001 | t0012 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0012g0075 | a0001 | c0001 | t0012 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0013g0002 | a0001 | c0001 | t0013 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0013g0010 | a0001 | c0001 | t0013 | g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0013g0066 | a0001 | c0001 | t0013 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0014g0005 | a0001 | c0001 | t0014 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0015g0134 | a0001 | c0001 | t0015 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0017g0087 | a0001 | c0001 | t0017 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0019g0067 | a0001 | c0001 | t0019 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0020g0164 | a0001 | c0001 | t0020 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0021g0131 | a0001 | c0001 | t0021 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0022g0161 | a0001 | c0001 | t0022 | g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0023g0084 | a0001 | c0001 | t0023 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0001t0024g0070 | a0001 | c0001 | t0024 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0002g0126 | a0001 | c0002 | t0002 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0002g0128 | a0001 | c0002 | t0002 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0004 | a0001 | c0002 | t0003 | g0004 | 0/0 | 15 | 0 | 0 | 12 | 3 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0030 | a0001 | c0002 | t0003 | g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0043 | a0001 | c0002 | t0003 | g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0045 | a0001 | c0002 | t0003 | g0045 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0127 | a0001 | c0002 | t0003 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0175 | a0001 | c0002 | t0003 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0176 | a0001 | c0002 | t0003 | g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0177 | a0001 | c0002 | t0003 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0178 | a0001 | c0002 | t0003 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0179 | a0001 | c0002 | t0003 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0180 | a0001 | c0002 | t0003 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0181 | a0001 | c0002 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0184 | a0001 | c0002 | t0003 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0185 | a0001 | c0002 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0186 | a0001 | c0002 | t0003 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0187 | a0001 | c0002 | t0003 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0188 | a0001 | c0002 | t0003 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0189 | a0001 | c0002 | t0003 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0190 | a0001 | c0002 | t0003 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0191 | a0001 | c0002 | t0003 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0192 | a0001 | c0002 | t0003 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0193 | a0001 | c0002 | t0003 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0194 | a0001 | c0002 | t0003 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0195 | a0001 | c0002 | t0003 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0196 | a0001 | c0002 | t0003 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0003g0198 | a0001 | c0002 | t0003 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0014 | a0001 | c0002 | t0008 | g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0031 | a0001 | c0002 | t0008 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0049 | a0001 | c0002 | t0008 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0174 | a0001 | c0002 | t0008 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0200 | a0001 | c0002 | t0008 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0202 | a0001 | c0002 | t0008 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0008g0203 | a0001 | c0002 | t0008 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0010g0044 | a0001 | c0002 | t0010 | g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0010g0182 | a0001 | c0002 | t0010 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0010g0183 | a0001 | c0002 | t0010 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0010g0199 | a0001 | c0002 | t0010 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0002t0016g0201 | a0001 | c0002 | t0016 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0006 | a0001 | c0003 | t0004 | g0006 | 0/0 | 9 | 2 | 4 | 2 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0025 | a0001 | c0003 | t0004 | g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0036 | a0001 | c0003 | t0004 | g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0037 | a0001 | c0003 | t0004 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0050 | a0001 | c0003 | t0004 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0112 | a0001 | c0003 | t0004 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0114 | a0001 | c0003 | t0004 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0115 | a0001 | c0003 | t0004 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0116 | a0001 | c0003 | t0004 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0117 | a0001 | c0003 | t0004 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0118 | a0001 | c0003 | t0004 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0119 | a0001 | c0003 | t0004 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0120 | a0001 | c0003 | t0004 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0121 | a0001 | c0003 | t0004 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0122 | a0001 | c0003 | t0004 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0123 | a0001 | c0003 | t0004 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0124 | a0001 | c0003 | t0004 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0125 | a0001 | c0003 | t0004 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0173 | a0001 | c0003 | t0004 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0004g0206 | a0001 | c0003 | t0004 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0003t0018g0113 | a0001 | c0003 | t0018 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0004t0011g0210 | a0001 | c0004 | t0011 | g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0004t0011g0211 | a0001 | c0004 | t0011 | g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0004t0011g0212 | a0001 | c0004 | t0011 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0001c0004t0011g0213 | a0001 | c0004 | t0011 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| a0002c0005t0003g0197 | a0002 | c0005 | t0003 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFF_chr2_227320251_227362833 | MFF |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0196 | EUR | GBR | MFF_chr2_227320251_227362833 | MFF |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | MFF_chr2_227320251_227362833 | MFF |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | MFF_chr2_227320251_227362833 | MFF |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | MFF_chr2_227320251_227362833 | MFF |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MFF_chr2_227320251_227362833 | MFF |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | FIN | MFF_chr2_227320251_227362833 | MFF |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00423 | hp1 | a0001 | c0003 | t0004 | g0119 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00558 | hp2 | a0001 | c0003 | t0004 | g0206 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00639 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | CHS | MFF_chr2_227320251_227362833 | MFF |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG00738 | hp1 | a0001 | c0003 | t0004 | g0118 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0190 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0125 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01106 | hp1 | a0001 | c0002 | t0010 | g0044 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01109 | hp2 | a0001 | c0002 | t0010 | g0044 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0192 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01169 | hp2 | a0001 | c0003 | t0004 | g0006 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0178 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0176 | AMR | PUR | MFF_chr2_227320251_227362833 | MFF |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01361 | hp1 | a0001 | c0003 | t0004 | g0123 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0010 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01433 | hp1 | a0001 | c0001 | t0022 | g0161 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0177 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | MFF_chr2_227320251_227362833 | MFF |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0045 | EUR | IBS | MFF_chr2_227320251_227362833 | MFF |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | MFF_chr2_227320251_227362833 | MFF |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | MFF_chr2_227320251_227362833 | MFF |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | MFF_chr2_227320251_227362833 | MFF |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG01891 | hp2 | a0001 | c0002 | t0008 | g0049 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01975 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG02015 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02055 | hp1 | a0001 | c0002 | t0010 | g0182 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02074 | hp1 | a0001 | c0003 | t0004 | g0006 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02074 | hp2 | a0001 | c0001 | t0024 | g0070 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02080 | hp1 | a0002 | c0005 | t0003 | g0197 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02080 | hp2 | a0001 | c0003 | t0004 | g0124 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02083 | hp1 | a0001 | c0003 | t0004 | g0006 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02129 | hp2 | a0001 | c0004 | t0011 | g0213 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0116 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MFF_chr2_227320251_227362833 | MFF |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | MFF_chr2_227320251_227362833 | MFF |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | CDX | MFF_chr2_227320251_227362833 | MFF |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | MFF_chr2_227320251_227362833 | MFF |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | MFF_chr2_227320251_227362833 | MFF |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02257 | hp2 | a0001 | c0002 | t0008 | g0014 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFF_chr2_227320251_227362833 | MFF |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02280 | hp2 | a0001 | c0002 | t0016 | g0201 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0117 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02572 | hp1 | a0001 | c0002 | t0008 | g0014 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02647 | hp1 | a0001 | c0002 | t0008 | g0031 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0066 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0127 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02698 | hp2 | a0001 | c0004 | t0011 | g0211 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG02809 | hp1 | a0001 | c0002 | t0008 | g0014 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02818 | hp1 | a0001 | c0002 | t0008 | g0014 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02886 | hp1 | a0001 | c0004 | t0011 | g0212 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0188 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0186 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0173 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0199 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0189 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0037 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0202 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03453 | hp1 | a0001 | c0002 | t0008 | g0174 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03491 | hp2 | a0001 | c0003 | t0004 | g0006 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | MFF_chr2_227320251_227362833 | MFF |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | GWD | MFF_chr2_227320251_227362833 | MFF |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | MFF_chr2_227320251_227362833 | MFF |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04184 | hp1 | a0001 | c0001 | t0019 | g0067 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MFF_chr2_227320251_227362833 | MFF |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04204 | hp1 | a0001 | c0003 | t0004 | g0122 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0058 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | MFF_chr2_227320251_227362833 | MFF |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0200 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | CHB | MFF_chr2_227320251_227362833 | MFF |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MFF_chr2_227320251_227362833 | MFF |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | MFF_chr2_227320251_227362833 | MFF |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MFF_chr2_227320251_227362833 | MFF |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA18906 | hp2 | a0001 | c0003 | t0018 | g0113 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18942 | hp1 | a0001 | c0003 | t0004 | g0120 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18943 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18945 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18946 | hp2 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18948 | hp2 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18949 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18963 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18969 | hp1 | a0001 | c0001 | t0023 | g0084 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18972 | hp2 | a0001 | c0001 | t0020 | g0164 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18990 | hp2 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19000 | hp1 | a0001 | c0001 | t0021 | g0131 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0115 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19001 | hp2 | a0001 | c0001 | t0015 | g0134 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19005 | hp2 | a0001 | c0003 | t0004 | g0114 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0050 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19055 | hp2 | a0001 | c0003 | t0004 | g0121 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19056 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19062 | hp1 | a0001 | c0001 | t0017 | g0087 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19065 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19077 | hp1 | a0001 | c0003 | t0004 | g0112 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19078 | hp1 | a0001 | c0003 | t0004 | g0025 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19081 | hp2 | a0001 | c0003 | t0004 | g0036 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19084 | hp1 | a0001 | c0003 | t0004 | g0036 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | YRI | MFF_chr2_227320251_227362833 | MFF |
| NA20129 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | ASW | MFF_chr2_227320251_227362833 | MFF |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | MFF_chr2_227320251_227362833 | MFF |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MFF_chr2_227320251_227362833 | MFF |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | MFF_chr2_227320251_227362833 | MFF |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | TSI | MFF_chr2_227320251_227362833 | MFF |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | TSI | MFF_chr2_227320251_227362833 | MFF |
| NA20905 | hp1 | a0001 | c0004 | t0011 | g0210 | SAS | GIH | MFF_chr2_227320251_227362833 | MFF |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | GIH | MFF_chr2_227320251_227362833 | MFF |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0031 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0195 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG02559 | hp2 | a0001 | c0002 | t0008 | g0203 | AFR | ACB | MFF_chr2_227320251_227362833 | MFF |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | MFF_chr2_227320251_227362833 | MFF |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | USA | MFF_chr2_227320251_227362833 | MFF |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | USA | MFF_chr2_227320251_227362833 | MFF |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MFF_chr2_227320251_227362833 | MFF |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | USA | MFF_chr2_227320251_227362833 | MFF |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | USA | MFF_chr2_227320251_227362833 | MFF |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | MFF_chr2_227320251_227362833 | MFF |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0026 | REF | REF | MFF_chr2_227320251_227362833 | MFF |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0209 | REF | REF | MFF_chr2_227320251_227362833 | MFF |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227347251
|
C | T | 1 | a0002 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.466C>T | p.Arg156Trp | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/9 | 795/1921 | 466/876 | 156/291 | chr2 | 227347251 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227332522
|
G | A | 1 | a0001c0003 | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
synonymous_variant | LOW | c.285G>A | p.Thr95Thr | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/9 | 614/1921 | 285/876 | 95/291 | chr2 | 227332522 | ||
| chr2:227352544
|
C | A | 1 | a0001c0004 | 4 | HG02129.hp2 HG02698.hp2 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.630C>A | p.Ala210Ala | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/9 | 959/1921 | 630/876 | 210/291 | chr2 | 227352544 | ||
| chr2:227357009
|
A | G | 2 | a0001c0002a0002c0005 | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
synonymous_variant | LOW | c.768A>G | p.Leu256Leu | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 1097/1921 | 768/876 | 256/291 | chr2 | 227357009 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227325269
|
C | A | 2 | a0001c0002t0003a0002c0005t0003 | 45 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-311C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | 5397 | chr2 | 227325269 | |||||
| chr2:227325274
|
C | T | 1 | a0001c0001t0024 | 1 | HG02074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-306C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | chr2 | 227325274 | ||||||
| chr2:227325285
|
C | G | 1 | a0001c0001t0009 | 7 | NA18945.hp2 NA18949.hp1 NA18952.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-295C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | 5381 | chr2 | 227325285 | |||||
| chr2:227325286
|
C | G | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | 298 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
5_prime_UTR_variant | MODIFIER | c.-294C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | 5380 | chr2 | 227325286 | |||||
| chr2:227325310
|
C | T | 1 | a0001c0002t0010 | 5 | HG01106.hp1 HG01109.hp2 HG02055.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-270C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | chr2 | 227325310 | ||||||
| chr2:227325349
|
A | G | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
5_prime_UTR_variant | MODIFIER | c.-231A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | 5317 | chr2 | 227325349 | |||||
| chr2:227325413
|
C | G | 1 | a0001c0001t0023 | 1 | NA18969.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-167C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/9 | chr2 | 227325413 | ||||||
| chr2:227328717
|
G | A | 1 | a0001c0001t0014 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/9 | 1949 | chr2 | 227328717 | |||||
| chr2:227357220
|
C | A | 1 | a0001c0001t0017 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 103 | chr2 | 227357220 | |||||
| chr2:227357246
|
G | C | 2 | a0001c0001t0005a0001c0001t0014 | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 129 | chr2 | 227357246 | |||||
| chr2:227357282
|
A | C | 1 | a0001c0004t0011 | 4 | HG02129.hp2 HG02698.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 165 | chr2 | 227357282 | |||||
| chr2:227357323
|
T | A | 1 | a0001c0001t0017 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 206 | chr2 | 227357323 | |||||
| chr2:227357425
|
C | T | 1 | a0001c0002t0016 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 308 | chr2 | 227357425 | |||||
| chr2:227357493
|
A | C | 1 | a0001c0001t0012 | 4 | HG02015.hp1 NA18943.hp2 NA18944.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 376 | chr2 | 227357493 | |||||
| chr2:227357535
|
T | TTTA | 1 | a0001c0001t0013 | 3 | HG01192.hp2 HG01361.hp2 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*419_*420insTAT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 420 | INFO_REALIGN_3_PRIME | chr2 | 227357535 | ||||
| chr2:227357555
|
G | A | 2 | a0001c0003t0004a0001c0003t0018 | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*438G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 438 | chr2 | 227357555 | |||||
| chr2:227357577
|
C | G | 5 | a0001c0001t0001a0001c0001t0015a0001c0001t0020others(2): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*460C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 460 | chr2 | 227357577 | |||||
| chr2:227357637
|
C | T | 1 | a0001c0001t0022 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 520 | chr2 | 227357637 | |||||
| chr2:227357764
|
C | G | 1 | a0001c0001t0020 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 647 | chr2 | 227357764 | |||||
| chr2:227357764
|
C | T | 2 | a0001c0001t0019a0001c0001t0021 | 2 | HG04184.hp1 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*647C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 647 | chr2 | 227357764 | |||||
| chr2:227357765
|
G | A | 1 | a0001c0001t0006 | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*648G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 648 | chr2 | 227357765 | |||||
| chr2:227357781
|
A | G | 1 | a0001c0003t0018 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 9/9 | 664 | chr2 | 227357781 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227325435
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
splice_region_variant&intron_variant | LOW | c.-153+8T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325435 | ||||||
| chr2:227325450
|
C | T | 1 | a0001c0003t0004g0206 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-153+23C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325450 | ||||||
| chr2:227325502
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-153+75C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325502 | ||||||
| chr2:227325534
|
GC | G | 35 | a0001c0002t0003g0004a0001c0002t0003g0030a0001c0002t0003g0043others(32): Show | 54 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.-153+114delC | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227325534 | |||||
| chr2:227325640
|
G | A | 1 | a0001c0001t0005g0018 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-153+213G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325640 | ||||||
| chr2:227325651
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-153+224T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325651 | ||||||
| chr2:227325722
|
G | T | 1 | a0001c0001t0007g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-153+295G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325722 | ||||||
| chr2:227325729
|
T | A | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-153+302T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227325729 | ||||||
| chr2:227326080
|
GACCTTCC others(26): Show |
G | 1 | a0001c0003t0004g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-153+655_-153+687d others(35): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227326080 | |||||
| chr2:227326226
|
G | GA | 8 | a0001c0001t0001g0051a0001c0001t0007g0017a0001c0001t0007g0046others(5): Show | 13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-153+813dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227326226 | |||||
| chr2:227326226
|
GA | G | 6 | a0001c0002t0008g0202a0001c0002t0008g0203a0001c0004t0011g0210others(3): Show | 6 | HG02129.hp2 HG02559.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153+813delA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227326226 | |||||
| chr2:227326328
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-153+901G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326328 | ||||||
| chr2:227326472
|
A | C | 1 | a0001c0001t0006g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-153+1045A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326472 | ||||||
| chr2:227326479
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-153+1052G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326479 | ||||||
| chr2:227326486
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.-153+1059A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326486 | ||||||
| chr2:227326619
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-153+1192T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326619 | ||||||
| chr2:227326620
|
T | G | 1 | a0001c0001t0001g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-153+1193T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326620 | ||||||
| chr2:227326699
|
C | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0010others(53): Show | 106 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-153+1272C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326699 | ||||||
| chr2:227326932
|
T | C | 1 | a0001c0001t0013g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-153+1505T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227326932 | ||||||
| chr2:227327143
|
T | C | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-152-1535T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327143 | ||||||
| chr2:227327188
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-152-1490C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327188 | ||||||
| chr2:227327202
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-152-1476A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327202 | ||||||
| chr2:227327250
|
A | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-152-1428A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327250 | ||||||
| chr2:227327429
|
G | GA | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-152-1241dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227327429 | |||||
| chr2:227327507
|
A | AAGT | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-152-1171_-152-117 others(7): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327507 | ||||||
| chr2:227327551
|
T | G | 2 | a0001c0001t0005g0053a0001c0001t0005g0054 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-152-1127T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327551 | ||||||
| chr2:227327572
|
C | G | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.-152-1106C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327572 | ||||||
| chr2:227327585
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-152-1093A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327585 | ||||||
| chr2:227327757
|
G | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(61): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-152-921G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227327757 | ||||||
| chr2:227328035
|
A | G | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-152-643A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328035 | ||||||
| chr2:227328092
|
C | G | 1 | a0001c0002t0008g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-152-586C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328092 | ||||||
| chr2:227328092
|
C | T | 1 | a0001c0001t0007g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-152-586C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328092 | ||||||
| chr2:227328143
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-152-535A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328143 | ||||||
| chr2:227328169
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 297 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-152-509G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328169 | ||||||
| chr2:227328295
|
C | CA | 8 | a0001c0001t0005g0055a0001c0001t0007g0017a0001c0001t0007g0046others(5): Show | 12 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-152-358dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227328295 | |||||
| chr2:227328295
|
CA | C | 12 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0032others(9): Show | 26 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-152-358delA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227328295 | |||||
| chr2:227328313
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-152-365A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328313 | ||||||
| chr2:227328318
|
AAAC | A | 17 | a0001c0001t0001g0170a0001c0002t0003g0045a0001c0003t0004g0006others(14): Show | 30 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-152-359_-152-357d others(5): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328318 | ||||||
| chr2:227328319
|
AAC | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(66): Show | 132 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-152-358_-152-357d others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328319 | ||||||
| chr2:227328320
|
AC | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0015others(80): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-152-356delC | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227328320 | |||||
| chr2:227328321
|
C | A | 18 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(15): Show | 22 | HG01106.hp2 HG01358.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.-152-357C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328321 | ||||||
| chr2:227328330
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(61): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-152-348T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328330 | ||||||
| chr2:227328336
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(211): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.-152-342T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328336 | ||||||
| chr2:227328364
|
C | CAT | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-152-306_-152-305d others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 227328364 | |||||
| chr2:227328648
|
T | G | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-30T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 1/8 | chr2 | 227328648 | ||||||
| chr2:227329127
|
ATTTGAAG others(12): Show |
A | 4 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+350_-41+368del others(19): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 227329127 | |||||
| chr2:227329141
|
C | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0132others(5): Show | 14 | NA18747.hp2 NA18951.hp1 NA18959.hp1 others(11): Show |
intron_variant | MODIFIER | c.-41+352C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227329141 | ||||||
| chr2:227329764
|
A | T | 57 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(54): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-40-862A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227329764 | ||||||
| chr2:227329765
|
G | T | 57 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(54): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-40-861G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227329765 | ||||||
| chr2:227329854
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.-40-772G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227329854 | ||||||
| chr2:227329923
|
T | TA | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(146): Show | 281 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.-40-692dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 227329923 | |||||
| chr2:227329923
|
T | TAA | 58 | a0001c0001t0001g0105a0001c0001t0001g0152a0001c0001t0002g0002others(55): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-40-693_-40-692dup others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 227329923 | |||||
| chr2:227329937
|
C | T | 57 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(54): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-40-689C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227329937 | ||||||
| chr2:227330318
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-40-308G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227330318 | ||||||
| chr2:227330332
|
G | A | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40-294G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227330332 | ||||||
| chr2:227330335
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-291G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227330335 | ||||||
| chr2:227330338
|
AGTATGTG others(1): Show |
A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.-40-277_-40-270del others(8): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 227330338 | |||||
| chr2:227330547
|
G | A | 1 | a0001c0002t0003g0043 | 2 | HG01255.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-40-79G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 2/8 | chr2 | 227330547 | ||||||
| chr2:227330876
|
G | A | 1 | a0001c0001t0019g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.181+30G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227330876 | ||||||
| chr2:227330927
|
T | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0068a0001c0001t0002g0074others(1): Show | 7 | HG01981.hp1 HG02273.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+81T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227330927 | ||||||
| chr2:227331046
|
A | T | 4 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+200A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331046 | ||||||
| chr2:227331047
|
C | T | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.181+201C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331047 | ||||||
| chr2:227331209
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181+363A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331209 | ||||||
| chr2:227331251
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.181+405C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331251 | ||||||
| chr2:227331290
|
C | T | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.181+444C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331290 | ||||||
| chr2:227331490
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.181+644T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331490 | ||||||
| chr2:227331650
|
C | T | 1 | a0001c0001t0007g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.182-769C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331650 | ||||||
| chr2:227331698
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.182-721C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331698 | ||||||
| chr2:227331855
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0025a0001c0003t0004g0036others(18): Show | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.182-564A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331855 | ||||||
| chr2:227331871
|
G | C | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.182-548G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331871 | ||||||
| chr2:227331949
|
C | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0033a0001c0001t0002g0069others(6): Show | 19 | HG02015.hp1 HG02074.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.182-470C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331949 | ||||||
| chr2:227331958
|
C | CAT | 15 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(12): Show | 17 | HG00438.hp2 HG01074.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.182-460_182-459dup others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331958 | |||||
| chr2:227331959
|
A | ATAT | 30 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0010others(27): Show | 71 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.182-459_182-458ins others(3): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATATT | 16 | a0001c0001t0002g0011a0001c0001t0002g0024a0001c0001t0002g0068others(13): Show | 22 | HG00673.hp1 HG01106.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.182-459_182-458ins others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATATTT | 3 | a0001c0001t0002g0033a0001c0001t0002g0098a0001c0001t0007g0017 | 7 | HG02451.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-459_182-458ins others(5): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATATTTTT others(9): Show |
1 | a0001c0001t0007g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.182-459_182-458ins others(16): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATTTTTTT others(3): Show |
3 | a0001c0002t0010g0044a0001c0002t0010g0182a0001c0004t0011g0210 | 4 | HG01106.hp1 HG01109.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-439_182-430dup others(10): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATTTTTTT others(4): Show |
2 | a0001c0004t0011g0211a0001c0004t0011g0213 | 2 | HG02129.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.182-440_182-430dup others(11): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATTTTTTT others(5): Show |
2 | a0001c0002t0008g0200a0001c0004t0011g0212 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.182-441_182-430dup others(12): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
A | ATTTTTTT others(6): Show |
3 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0016g0201 | 3 | HG02280.hp2 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.182-442_182-430dup others(13): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
AT | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0153others(5): Show | 11 | HG03453.hp2 HG03516.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.182-430delT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATT | A | 8 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(5): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-431_182-430del others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTT | A | 12 | a0001c0003t0004g0006a0001c0003t0004g0037a0001c0003t0004g0050others(9): Show | 21 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.182-433_182-430del others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTTTT | A | 8 | a0001c0001t0005g0054a0001c0001t0005g0057a0001c0001t0005g0058others(5): Show | 12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-435_182-430del others(6): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTTTTT | A | 11 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(8): Show | 24 | HG00609.hp2 HG00639.hp2 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.182-436_182-430del others(7): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.182-440_182-430del others(11): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0003t0004g0025a0001c0003t0004g0036a0001c0003t0004g0112others(1): Show | 7 | HG00558.hp2 NA18948.hp2 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-441_182-430del others(12): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331959
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0003t0004g0116 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.182-442_182-430del others(13): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227331959 | |||||
| chr2:227331960
|
T | TA | 31 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0015others(28): Show | 65 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.182-459_182-458ins others(1): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331960 | ||||||
| chr2:227331961
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(41): Show | 99 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.182-458T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331961 | ||||||
| chr2:227331962
|
T | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0153others(5): Show | 11 | HG03453.hp2 HG03516.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.182-457T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331962 | ||||||
| chr2:227331963
|
T | A | 8 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(5): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-456T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331963 | ||||||
| chr2:227331964
|
T | A | 3 | a0001c0003t0004g0115a0001c0003t0004g0123a0001c0003t0004g0124 | 3 | HG01361.hp1 HG02080.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.182-455T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331964 | ||||||
| chr2:227331965
|
T | A | 12 | a0001c0003t0004g0006a0001c0003t0004g0037a0001c0003t0004g0050others(9): Show | 21 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.182-454T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331965 | ||||||
| chr2:227331966
|
T | A | 2 | a0001c0002t0008g0174a0001c0003t0004g0125 | 2 | HG01099.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.182-453T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331966 | ||||||
| chr2:227331967
|
T | A | 3 | a0001c0002t0008g0014a0001c0002t0008g0031a0001c0002t0008g0049 | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-452T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331967 | ||||||
| chr2:227331970
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.182-449T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331970 | ||||||
| chr2:227331972
|
T | A | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.182-447T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331972 | ||||||
| chr2:227331973
|
T | A | 4 | a0001c0003t0004g0025a0001c0003t0004g0036a0001c0003t0004g0112others(1): Show | 7 | HG00558.hp2 NA18948.hp2 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-446T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331973 | ||||||
| chr2:227331974
|
T | A | 1 | a0001c0003t0004g0116 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.182-445T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331974 | ||||||
| chr2:227331995
|
G | A | 18 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(15): Show | 32 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.182-424G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227331995 | ||||||
| chr2:227332003
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.182-416G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332003 | ||||||
| chr2:227332017
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.182-402G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332017 | ||||||
| chr2:227332057
|
C | T | 2 | a0001c0003t0004g0037a0001c0003t0004g0173 | 3 | HG02965.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.182-362C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332057 | ||||||
| chr2:227332121
|
G | A | 4 | a0001c0004t0011g0210a0001c0004t0011g0211a0001c0004t0011g0212others(1): Show | 4 | HG02129.hp2 HG02698.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-298G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332121 | ||||||
| chr2:227332133
|
G | T | 2 | a0001c0002t0003g0193a0001c0002t0003g0198 | 2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.182-286G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332133 | ||||||
| chr2:227332148
|
A | AT | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.182-266dupT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 227332148 | |||||
| chr2:227332252
|
G | A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.182-167G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332252 | ||||||
| chr2:227332334
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0075 | 4 | HG02015.hp1 NA18943.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-85G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 3/8 | chr2 | 227332334 | ||||||
| chr2:227332652
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.351+64A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332652 | ||||||
| chr2:227332657
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.351+69G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332657 | ||||||
| chr2:227332750
|
A | G | 1 | a0001c0002t0003g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.351+162A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332750 | ||||||
| chr2:227332772
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.351+184A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332772 | ||||||
| chr2:227332874
|
G | T | 2 | a0001c0002t0008g0014a0001c0002t0008g0031 | 6 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+286G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332874 | ||||||
| chr2:227332985
|
C | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.351+397C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227332985 | ||||||
| chr2:227333010
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.351+422G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333010 | ||||||
| chr2:227333134
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.351+546G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333134 | ||||||
| chr2:227333156
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.351+568G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333156 | ||||||
| chr2:227333230
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0025a0001c0003t0004g0036others(18): Show | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.351+642A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333230 | ||||||
| chr2:227333249
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+661G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333249 | ||||||
| chr2:227333343
|
A | G | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.351+755A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333343 | ||||||
| chr2:227333644
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.351+1056C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333644 | ||||||
| chr2:227333733
|
G | A | 2 | a0001c0002t0008g0014a0001c0002t0008g0031 | 6 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+1145G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333733 | ||||||
| chr2:227333770
|
T | C | 1 | a0001c0002t0003g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.351+1182T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333770 | ||||||
| chr2:227333886
|
A | G | 17 | a0001c0003t0004g0006a0001c0003t0004g0025a0001c0003t0004g0036others(14): Show | 28 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.351+1298A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333886 | ||||||
| chr2:227333890
|
C | A | 1 | a0001c0003t0004g0117 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.351+1302C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333890 | ||||||
| chr2:227333929
|
C | T | 1 | a0001c0004t0011g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.351+1341C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333929 | ||||||
| chr2:227333930
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0025a0001c0003t0004g0036others(18): Show | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.351+1342G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333930 | ||||||
| chr2:227333971
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1383G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227333971 | ||||||
| chr2:227334017
|
T | G | 1 | a0001c0001t0021g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.351+1429T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334017 | ||||||
| chr2:227334057
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.351+1469A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334057 | ||||||
| chr2:227334143
|
C | G | 1 | a0001c0001t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.351+1555C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334143 | ||||||
| chr2:227334304
|
C | T | 1 | a0001c0001t0002g0023 | 3 | HG00735.hp2 HG01255.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.351+1716C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334304 | ||||||
| chr2:227334331
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.351+1743T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334331 | ||||||
| chr2:227334333
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.351+1745A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334333 | ||||||
| chr2:227334385
|
G | A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.351+1797G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334385 | ||||||
| chr2:227334742
|
C | T | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.351+2154C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334742 | ||||||
| chr2:227334752
|
G | A | 1 | a0001c0002t0003g0186 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.351+2164G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334752 | ||||||
| chr2:227334785
|
A | G | 2 | a0001c0003t0004g0117a0001c0003t0004g0122 | 2 | HG02451.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.351+2197A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334785 | ||||||
| chr2:227334892
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.351+2304G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334892 | ||||||
| chr2:227334896
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.351+2308C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227334896 | ||||||
| chr2:227335043
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(61): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.351+2455C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335043 | ||||||
| chr2:227335060
|
A | G | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+2472A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335060 | ||||||
| chr2:227335063
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.351+2475C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335063 | ||||||
| chr2:227335075
|
G | A | 1 | a0001c0003t0004g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+2487G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335075 | ||||||
| chr2:227335149
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.351+2561A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335149 | ||||||
| chr2:227335160
|
ACT | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0136others(1): Show | 7 | HG00438.hp1 HG02155.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2575_351+2576d others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227335160 | |||||
| chr2:227335171
|
C | CA | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(90): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.351+2599dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227335171 | |||||
| chr2:227335171
|
C | CAA | 90 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0149others(87): Show | 159 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.351+2598_351+2599d others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227335171 | |||||
| chr2:227335171
|
C | CAAA | 21 | a0001c0001t0002g0083a0001c0001t0002g0091a0001c0001t0002g0092others(18): Show | 38 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.351+2597_351+2599d others(5): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227335171 | |||||
| chr2:227335324
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+2736C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335324 | ||||||
| chr2:227335345
|
G | A | 2 | a0001c0002t0003g0176a0001c0002t0003g0177 | 2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.351+2757G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335345 | ||||||
| chr2:227335418
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.351+2830C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335418 | ||||||
| chr2:227335419
|
G | A | 1 | a0001c0003t0004g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.351+2831G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335419 | ||||||
| chr2:227335674
|
G | A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.351+3086G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335674 | ||||||
| chr2:227335889
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 12 | HG01978.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+3301A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227335889 | ||||||
| chr2:227336029
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.351+3441A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336029 | ||||||
| chr2:227336130
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+3542A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336130 | ||||||
| chr2:227336480
|
G | A | 8 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(5): Show | 9 | HG01106.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-3812G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336480 | ||||||
| chr2:227336540
|
A | G | 1 | a0002c0005t0003g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.352-3752A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336540 | ||||||
| chr2:227336586
|
T | G | 1 | a0001c0001t0001g0029 | 3 | NA18946.hp1 NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.352-3706T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336586 | ||||||
| chr2:227336613
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.352-3679C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336613 | ||||||
| chr2:227336614
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.352-3678C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336614 | ||||||
| chr2:227336615
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.352-3677A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336615 | ||||||
| chr2:227336616
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.352-3676C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336616 | ||||||
| chr2:227336637
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.352-3655A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336637 | ||||||
| chr2:227336660
|
A | G | 1 | a0001c0001t0006g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352-3632A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336660 | ||||||
| chr2:227336741
|
T | C | 1 | a0001c0004t0011g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.352-3551T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336741 | ||||||
| chr2:227336801
|
G | A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-3491G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336801 | ||||||
| chr2:227336830
|
C | T | 57 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(54): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.352-3462C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336830 | ||||||
| chr2:227336906
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-3386C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227336906 | ||||||
| chr2:227337137
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.352-3155A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337137 | ||||||
| chr2:227337291
|
G | A | 10 | a0001c0001t0002g0048a0001c0001t0006g0012a0001c0001t0006g0104others(7): Show | 14 | HG01071.hp1 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.352-3001G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337291 | ||||||
| chr2:227337314
|
C | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(211): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.352-2978C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337314 | ||||||
| chr2:227337589
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.352-2703A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337589 | ||||||
| chr2:227337614
|
T | TA | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.352-2678_352-2677i others(3): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337614 | ||||||
| chr2:227337624
|
CT | C | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.352-2667delT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337624 | ||||||
| chr2:227337696
|
C | T | 1 | a0001c0001t0005g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.352-2596C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337696 | ||||||
| chr2:227337722
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.352-2570C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227337722 | ||||||
| chr2:227338004
|
A | G | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.352-2288A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338004 | ||||||
| chr2:227338044
|
GA | G | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.352-2235delA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227338044 | |||||
| chr2:227338075
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-2217A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338075 | ||||||
| chr2:227338089
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.352-2203C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338089 | ||||||
| chr2:227338202
|
T | C | 1 | a0001c0001t0007g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.352-2090T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338202 | ||||||
| chr2:227338238
|
A | G | 1 | a0001c0002t0003g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.352-2054A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338238 | ||||||
| chr2:227338261
|
C | T | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-2031C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338261 | ||||||
| chr2:227338360
|
ACT | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(184): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.352-1929_352-1928d others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227338360 | |||||
| chr2:227338363
|
C | G | 2 | a0001c0002t0003g0178a0001c0002t0003g0187 | 2 | HG01243.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.352-1929C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338363 | ||||||
| chr2:227338365
|
G | C | 2 | a0001c0002t0003g0178a0001c0002t0003g0187 | 2 | HG01243.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.352-1927G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338365 | ||||||
| chr2:227338368
|
T | A | 2 | a0001c0002t0003g0178a0001c0002t0003g0187 | 2 | HG01243.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.352-1924T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338368 | ||||||
| chr2:227338369
|
C | A | 2 | a0001c0002t0003g0178a0001c0002t0003g0187 | 2 | HG01243.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.352-1923C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338369 | ||||||
| chr2:227338369
|
C | CA | 38 | a0001c0001t0002g0019a0001c0001t0002g0068a0001c0001t0002g0074others(35): Show | 59 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.352-1909dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227338369 | |||||
| chr2:227338373
|
A | AG | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-1919_352-1918i others(3): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338373 | ||||||
| chr2:227338380
|
A | G | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-1912A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338380 | ||||||
| chr2:227338426
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(61): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.352-1866G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338426 | ||||||
| chr2:227338430
|
C | G | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-1862C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338430 | ||||||
| chr2:227338554
|
G | A | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-1738G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338554 | ||||||
| chr2:227338628
|
G | A | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.352-1664G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338628 | ||||||
| chr2:227338780
|
A | G | 1 | a0001c0001t0005g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.352-1512A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338780 | ||||||
| chr2:227338844
|
C | A | 1 | a0001c0001t0002g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.352-1448C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338844 | ||||||
| chr2:227338844
|
C | CA | 62 | a0001c0001t0001g0038a0001c0001t0001g0105a0001c0001t0001g0133others(59): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.352-1437dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227338844 | |||||
| chr2:227338905
|
T | G | 18 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(15): Show | 35 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.352-1387T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338905 | ||||||
| chr2:227338923
|
T | C | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-1369T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227338923 | ||||||
| chr2:227339064
|
C | T | 2 | a0001c0001t0005g0058a0001c0001t0005g0063 | 2 | HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.352-1228C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339064 | ||||||
| chr2:227339117
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.352-1175A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339117 | ||||||
| chr2:227339179
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.352-1113A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339179 | ||||||
| chr2:227339201
|
C | CA | 38 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0002t0002g0126others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.352-1076dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227339201 | |||||
| chr2:227339201
|
CA | C | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.352-1076delA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227339201 | |||||
| chr2:227339216
|
A | T | 1 | a0001c0001t0015g0134 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.352-1076A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339216 | ||||||
| chr2:227339521
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.352-771G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339521 | ||||||
| chr2:227339551
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 284 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.352-741C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339551 | ||||||
| chr2:227339636
|
G | A | 1 | a0001c0001t0002g0021 | 3 | HG02965.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.352-656G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339636 | ||||||
| chr2:227339645
|
T | C | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-647T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227339645 | ||||||
| chr2:227340091
|
G | GGT | 43 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(40): Show | 67 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.352-184_352-183dup others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 227340091 | |||||
| chr2:227340181
|
G | A | 1 | a0001c0001t0005g0013 | 4 | HG00609.hp2 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-111G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227340181 | ||||||
| chr2:227340213
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.352-79C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227340213 | ||||||
| chr2:227340266
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.352-26C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 4/8 | chr2 | 227340266 | ||||||
| chr2:227340719
|
C | T | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.440+339C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340719 | ||||||
| chr2:227340727
|
C | T | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.440+347C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340727 | ||||||
| chr2:227340759
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.440+379T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340759 | ||||||
| chr2:227340791
|
A | G | 1 | a0001c0002t0010g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.440+411A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340791 | ||||||
| chr2:227340837
|
G | A | 1 | a0001c0002t0003g0043 | 2 | HG01255.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.440+457G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340837 | ||||||
| chr2:227340947
|
T | A | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.440+567T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340947 | ||||||
| chr2:227340985
|
A | G | 1 | a0001c0001t0002g0035 | 2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.440+605A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227340985 | ||||||
| chr2:227341001
|
CATT | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.440+623_440+625del others(3): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227341001 | |||||
| chr2:227341126
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.440+746A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341126 | ||||||
| chr2:227341140
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(211): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.440+760A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341140 | ||||||
| chr2:227341267
|
T | C | 1 | a0001c0001t0022g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.440+887T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341267 | ||||||
| chr2:227341289
|
GT | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(199): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.440+921delT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227341289 | |||||
| chr2:227341539
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.440+1159C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341539 | ||||||
| chr2:227341541
|
A | G | 27 | a0001c0002t0003g0004a0001c0002t0003g0030a0001c0002t0003g0043others(24): Show | 45 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.440+1161A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341541 | ||||||
| chr2:227341634
|
T | C | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.440+1254T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341634 | ||||||
| chr2:227341688
|
G | A | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.440+1308G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341688 | ||||||
| chr2:227341733
|
G | A | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.440+1353G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341733 | ||||||
| chr2:227341801
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 297 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.440+1421T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341801 | ||||||
| chr2:227341851
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.440+1471A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341851 | ||||||
| chr2:227341903
|
G | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.440+1523G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341903 | ||||||
| chr2:227341996
|
T | A | 1 | a0001c0003t0004g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.440+1616T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227341996 | ||||||
| chr2:227342063
|
T | C | 1 | a0001c0002t0003g0187 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.440+1683T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342063 | ||||||
| chr2:227342168
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0142 | 4 | HG00408.hp1 NA18939.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+1788G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342168 | ||||||
| chr2:227342177
|
T | C | 4 | a0001c0004t0011g0210a0001c0004t0011g0211a0001c0004t0011g0212others(1): Show | 4 | HG02129.hp2 HG02698.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+1797T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342177 | ||||||
| chr2:227342183
|
T | G | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.440+1803T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342183 | ||||||
| chr2:227342254
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.440+1874G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342254 | ||||||
| chr2:227342378
|
T | C | 2 | a0001c0003t0004g0036a0001c0003t0004g0112 | 3 | NA19077.hp1 NA19081.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.440+1998T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342378 | ||||||
| chr2:227342429
|
T | A | 1 | a0001c0003t0004g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.440+2049T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342429 | ||||||
| chr2:227342531
|
C | T | 1 | a0001c0003t0004g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.440+2151C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342531 | ||||||
| chr2:227342619
|
G | A | 1 | a0001c0001t0023g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.440+2239G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342619 | ||||||
| chr2:227342855
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440+2475T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342855 | ||||||
| chr2:227342909
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(147): Show | 295 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.440+2529G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342909 | ||||||
| chr2:227342909
|
G | T | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.440+2529G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227342909 | ||||||
| chr2:227343060
|
C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.440+2680C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343060 | ||||||
| chr2:227343084
|
A | G | 1 | a0001c0004t0011g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.440+2704A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343084 | ||||||
| chr2:227343126
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.440+2746T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343126 | ||||||
| chr2:227343168
|
A | AT | 38 | a0001c0001t0001g0165a0001c0001t0015g0134a0001c0002t0002g0126others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.440+2801dupT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227343168 | |||||
| chr2:227343189
|
G | A | 3 | a0001c0002t0008g0014a0001c0002t0008g0031a0001c0002t0008g0049 | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+2809G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343189 | ||||||
| chr2:227343572
|
T | C | 1 | a0001c0001t0006g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.440+3192T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343572 | ||||||
| chr2:227343680
|
C | T | 2 | a0001c0002t0003g0176a0001c0002t0003g0177 | 2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.440+3300C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343680 | ||||||
| chr2:227343746
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.440+3366T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343746 | ||||||
| chr2:227343811
|
G | A | 1 | a0001c0003t0004g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.441-3415G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227343811 | ||||||
| chr2:227344538
|
T | TA | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 57 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.441-2682dupA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227344538 | |||||
| chr2:227344546
|
A | G | 11 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0174others(8): Show | 12 | HG01106.hp1 HG01109.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.441-2680A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344546 | ||||||
| chr2:227344630
|
G | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(149): Show | 298 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.441-2596G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344630 | ||||||
| chr2:227344682
|
A | T | 4 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-2544A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344682 | ||||||
| chr2:227344725
|
TA | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(206): Show | 391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.441-2489delA | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227344725 | |||||
| chr2:227344744
|
C | T | 1 | a0001c0004t0011g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.441-2482C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344744 | ||||||
| chr2:227344756
|
T | TGC | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.441-2470_441-2469i others(4): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344756 | ||||||
| chr2:227344847
|
C | A | 4 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-2379C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344847 | ||||||
| chr2:227344890
|
T | C | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.441-2336T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227344890 | ||||||
| chr2:227345087
|
C | T | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.441-2139C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345087 | ||||||
| chr2:227345125
|
A | G | 3 | a0001c0002t0008g0014a0001c0002t0008g0031a0001c0002t0008g0049 | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-2101A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345125 | ||||||
| chr2:227345419
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(211): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.441-1807A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345419 | ||||||
| chr2:227345648
|
A | G | 19 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(16): Show | 36 | HG00609.hp2 HG00639.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.441-1578A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345648 | ||||||
| chr2:227345666
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(211): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.441-1560A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345666 | ||||||
| chr2:227345783
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.441-1443A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345783 | ||||||
| chr2:227345810
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.441-1416G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345810 | ||||||
| chr2:227345916
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.441-1310C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345916 | ||||||
| chr2:227345924
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0075 | 4 | HG02015.hp1 NA18943.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-1302G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345924 | ||||||
| chr2:227345953
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.441-1273A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227345953 | ||||||
| chr2:227346184
|
C | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(29): Show | 72 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.441-1042C>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346184 | ||||||
| chr2:227346309
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0162others(1): Show | 7 | NA18969.hp2 NA18970.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-917G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346309 | ||||||
| chr2:227346358
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.441-868T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346358 | ||||||
| chr2:227346359
|
G | A | 1 | a0001c0001t0020g0164 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.441-867G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346359 | ||||||
| chr2:227346396
|
A | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0163 | 4 | NA18969.hp2 NA18988.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-830A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346396 | ||||||
| chr2:227346745
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.441-481C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346745 | ||||||
| chr2:227346754
|
T | C | 56 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(53): Show | 106 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.441-472T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346754 | ||||||
| chr2:227346771
|
G | A | 1 | a0001c0002t0003g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441-455G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346771 | ||||||
| chr2:227346775
|
TCA | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.441-447_441-446del others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 227346775 | |||||
| chr2:227346857
|
G | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0033a0001c0001t0002g0069others(6): Show | 19 | HG02015.hp1 HG02074.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-369G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346857 | ||||||
| chr2:227346864
|
G | A | 1 | a0001c0002t0003g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.441-362G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227346864 | ||||||
| chr2:227347064
|
A | G | 1 | a0001c0001t0020g0164 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.441-162A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227347064 | ||||||
| chr2:227347187
|
G | A | 1 | a0001c0001t0005g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.441-39G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 5/8 | chr2 | 227347187 | ||||||
| chr2:227347696
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.599+312A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227347696 | ||||||
| chr2:227347825
|
CT | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0137 | 3 | HG00280.hp1 HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.599+447delT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227347825 | |||||
| chr2:227347849
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0167 | 2 | NA18990.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.599+465G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227347849 | ||||||
| chr2:227347850
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.599+466G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227347850 | ||||||
| chr2:227347993
|
A | AT | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.599+616dupT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227347993 | |||||
| chr2:227348082
|
G | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(61): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.599+698G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348082 | ||||||
| chr2:227348172
|
A | AATCATGA others(8): Show |
1 | a0001c0001t0001g0165 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.599+790_599+791ins others(15): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227348172 | |||||
| chr2:227348236
|
T | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 297 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.599+852T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348236 | ||||||
| chr2:227348344
|
G | A | 11 | a0001c0001t0002g0022a0001c0001t0002g0083a0001c0001t0002g0085others(8): Show | 13 | HG00408.hp2 HG01081.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.599+960G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348344 | ||||||
| chr2:227348493
|
G | T | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.599+1109G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348493 | ||||||
| chr2:227348591
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(189): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.599+1207C>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348591 | ||||||
| chr2:227348894
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(189): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.599+1510C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348894 | ||||||
| chr2:227348903
|
A | G | 2 | a0001c0002t0003g0186a0001c0002t0003g0195 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.599+1519A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227348903 | ||||||
| chr2:227349087
|
G | C | 4 | a0001c0004t0011g0210a0001c0004t0011g0211a0001c0004t0011g0212others(1): Show | 4 | HG02129.hp2 HG02698.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+1703G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349087 | ||||||
| chr2:227349122
|
G | A | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.599+1738G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349122 | ||||||
| chr2:227349368
|
A | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.599+1984A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349368 | ||||||
| chr2:227349566
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.599+2182G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349566 | ||||||
| chr2:227349599
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0042 | 8 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.599+2215A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349599 | ||||||
| chr2:227349619
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.599+2235A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349619 | ||||||
| chr2:227349826
|
C | T | 57 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(54): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.599+2442C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349826 | ||||||
| chr2:227349954
|
A | T | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.600-2560A>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227349954 | ||||||
| chr2:227350000
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.600-2514A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350000 | ||||||
| chr2:227350297
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.600-2217G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350297 | ||||||
| chr2:227350298
|
G | A | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.600-2216G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350298 | ||||||
| chr2:227350437
|
G | A | 2 | a0001c0002t0003g0186a0001c0002t0003g0195 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.600-2077G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350437 | ||||||
| chr2:227350748
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0098 | 4 | HG02615.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-1766G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350748 | ||||||
| chr2:227350870
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.600-1644A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350870 | ||||||
| chr2:227350913
|
A | G | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.600-1601A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350913 | ||||||
| chr2:227350936
|
T | A | 3 | a0001c0002t0003g0178a0001c0002t0003g0188a0001c0002t0003g0189 | 3 | HG01243.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600-1578T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350936 | ||||||
| chr2:227350995
|
G | A | 1 | a0001c0001t0023g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.600-1519G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350995 | ||||||
| chr2:227350995
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.600-1519G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227350995 | ||||||
| chr2:227351207
|
A | G | 2 | a0001c0002t0003g0187a0001c0002t0003g0191 | 2 | NA19078.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.600-1307A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351207 | ||||||
| chr2:227351277
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0025a0001c0003t0004g0036others(18): Show | 33 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.600-1237A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351277 | ||||||
| chr2:227351364
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.600-1150T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351364 | ||||||
| chr2:227351409
|
TGTA | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(189): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.600-1102_600-1100d others(5): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227351409 | |||||
| chr2:227351501
|
CT | C | 22 | a0001c0002t0003g0004a0001c0002t0003g0030a0001c0002t0003g0043others(19): Show | 40 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.600-1011delT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227351501 | |||||
| chr2:227351604
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(189): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.600-910C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351604 | ||||||
| chr2:227351697
|
C | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0104a0001c0001t0006g0106others(6): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.600-817C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351697 | ||||||
| chr2:227351698
|
G | A | 2 | a0001c0003t0004g0117a0001c0003t0004g0122 | 2 | HG02451.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.600-816G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351698 | ||||||
| chr2:227351900
|
G | A | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.600-614G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351900 | ||||||
| chr2:227351909
|
T | C | 3 | a0001c0002t0003g0178a0001c0002t0003g0188a0001c0002t0003g0189 | 3 | HG01243.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600-605T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227351909 | ||||||
| chr2:227352012
|
G | A | 14 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0014others(11): Show | 19 | HG01106.hp1 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.600-502G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352012 | ||||||
| chr2:227352024
|
G | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0001g0141others(1): Show | 6 | HG00408.hp1 NA18939.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.600-490G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352024 | ||||||
| chr2:227352074
|
T | C | 4 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0008g0200others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-440T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352074 | ||||||
| chr2:227352102
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.600-412G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352102 | ||||||
| chr2:227352112
|
C | T | 3 | a0001c0003t0004g0120a0001c0003t0004g0121a0001c0003t0004g0124 | 3 | HG02080.hp2 NA18942.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.600-402C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352112 | ||||||
| chr2:227352157
|
A | AT | 38 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(35): Show | 61 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.600-347dupT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 227352157 | |||||
| chr2:227352276
|
G | A | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.600-238G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 6/8 | chr2 | 227352276 | ||||||
| chr2:227352612
|
T | A | 1 | a0001c0002t0003g0176 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.659+39T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227352612 | ||||||
| chr2:227352745
|
A | G | 1 | a0001c0001t0006g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.659+172A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227352745 | ||||||
| chr2:227353181
|
G | C | 1 | a0001c0002t0008g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.659+608G>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227353181 | ||||||
| chr2:227353535
|
T | G | 1 | a0001c0002t0003g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.659+962T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227353535 | ||||||
| chr2:227353760
|
C | T | 2 | a0001c0001t0001g0103a0001c0002t0008g0203 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.659+1187C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227353760 | ||||||
| chr2:227354188
|
T | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0132others(3): Show | 12 | NA18747.hp2 NA18951.hp1 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.660-1489T>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227354188 | ||||||
| chr2:227354551
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.660-1126A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227354551 | ||||||
| chr2:227354608
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0169 | 3 | HG01978.hp1 HG02683.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.660-1069T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227354608 | ||||||
| chr2:227354657
|
G | A | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.660-1020G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227354657 | ||||||
| chr2:227354704
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.660-973T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227354704 | ||||||
| chr2:227354713
|
A | AT | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.660-960dupT | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 227354713 | |||||
| chr2:227354754
|
ATT | A | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.660-920_660-919del others(2): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 227354754 | |||||
| chr2:227355059
|
G | A | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.660-618G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355059 | ||||||
| chr2:227355288
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.660-389A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355288 | ||||||
| chr2:227355298
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0042 | 8 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-379A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355298 | ||||||
| chr2:227355386
|
A | G | 2 | a0001c0002t0008g0202a0001c0002t0008g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.660-291A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355386 | ||||||
| chr2:227355428
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(1): Show | 9 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.660-249T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355428 | ||||||
| chr2:227355445
|
C | T | 67 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(64): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.660-232C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355445 | ||||||
| chr2:227355511
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(23): Show | 44 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(41): Show |
intron_variant | MODIFIER | c.660-166T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355511 | ||||||
| chr2:227355571
|
A | G | 1 | a0001c0003t0018g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.660-106A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355571 | ||||||
| chr2:227355572
|
A | G | 67 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(64): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.660-105A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355572 | ||||||
| chr2:227355617
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0046a0001c0001t0007g0047others(2): Show | 10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.660-60G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 7/8 | chr2 | 227355617 | ||||||
| chr2:227355785
|
A | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0202a0001c0002t0008g0203 | 3 | HG02559.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.744+24A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227355785 | ||||||
| chr2:227355793
|
C | T | 1 | a0001c0001t0007g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744+32C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227355793 | ||||||
| chr2:227355812
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(62): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.744+51T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227355812 | ||||||
| chr2:227355987
|
CAAA | C | 41 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0003g0004others(38): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.744+227_744+229del others(3): Show |
MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227355987 | ||||||
| chr2:227356053
|
T | C | 154 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0007others(151): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.744+292T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356053 | ||||||
| chr2:227356122
|
A | G | 127 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0010others(124): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.744+361A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356122 | ||||||
| chr2:227356141
|
C | T | 67 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(64): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.744+380C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356141 | ||||||
| chr2:227356200
|
T | C | 4 | a0001c0002t0010g0044a0001c0002t0010g0182a0001c0002t0010g0183others(1): Show | 5 | HG01106.hp1 HG01109.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+439T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356200 | ||||||
| chr2:227356212
|
G | A | 2 | a0001c0002t0003g0186a0001c0002t0003g0195 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.744+451G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356212 | ||||||
| chr2:227356287
|
G | T | 1 | a0001c0002t0003g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.744+526G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356287 | ||||||
| chr2:227356404
|
G | A | 2 | a0001c0003t0004g0037a0001c0003t0004g0173 | 3 | HG02965.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.745-582G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356404 | ||||||
| chr2:227356432
|
C | T | 1 | a0001c0003t0004g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.745-554C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356432 | ||||||
| chr2:227356549
|
G | A | 1 | a0001c0003t0004g0116 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.745-437G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356549 | ||||||
| chr2:227356564
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.745-422A>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356564 | ||||||
| chr2:227356597
|
T | C | 1 | a0001c0001t0021g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.745-389T>C | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356597 | ||||||
| chr2:227356600
|
G | A | 16 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0018others(13): Show | 29 | HG00609.hp2 HG00639.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.745-386G>A | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356600 | ||||||
| chr2:227356616
|
G | T | 1 | a0001c0001t0005g0032 | 2 | NA18955.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.745-370G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356616 | ||||||
| chr2:227356813
|
A | G | 1 | a0001c0001t0005g0032 | 2 | NA18955.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.745-173A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356813 | ||||||
| chr2:227356931
|
C | T | 1 | a0001c0002t0003g0190 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.745-55C>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356931 | ||||||
| chr2:227356951
|
A | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0080a0001c0001t0002g0088others(1): Show | 5 | NA19009.hp1 NA19077.hp2 NA19080.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-35A>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356951 | ||||||
| chr2:227356970
|
T | G | 1 | a0001c0001t0017g0087 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.745-16T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356970 | ||||||
| chr2:227356973
|
G | T | 1 | a0001c0001t0017g0087 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.745-13G>T | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356973 | ||||||
| chr2:227356974
|
T | G | 1 | a0001c0001t0017g0087 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.745-12T>G | MFF | ENSG00000168958.21 | transcript | ENST00000304593.14 | protein_coding | 8/8 | chr2 | 227356974 |