| geneid | 401138 |
|---|---|
| ensemblid | ENSG00000187689.10 |
| hgncid | 33188 |
| symbol | AMTN |
| name | amelotin |
| refseq_nuc | NM_212557.4 |
| refseq_prot | NP_997722.1 |
| ensembl_nuc | ENST00000339336.9 |
| ensembl_prot | ENSP00000341013.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70518569 |
| end | 70532743 |
| strand | + |
| ver | v1.2 |
| region | chr4:70518569-70532743 |
| region5000 | chr4:70513569-70537743 |
| regionname0 | AMTN_chr4_70518569_70532743 |
| regionname5000 | AMTN_chr4_70513569_70537743 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 209 | 314 | 82 | 62 | 129 | 11 | 28 | 100 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0002 | 0/0 | 209 | 67 | 2 | 7 | 44 | 3 | 11 | 36 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0003 | 0/0 | 209 | 58 | 0 | 5 | 47 | 1 | 5 | 36 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0004 | 0/0 | 209 | 8 | 6 | 1 | 0 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0005 | 0/0 | 209 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0006 | 0/0 | 209 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0007 | 0/0 | 209 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0008 | 0/0 | 209 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0009 | 0/0 | 209 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0010 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0011 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 630 | 193 | 63 | 25 | 82 | 8 | 14 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0002 | 0/1 | 630 | 121 | 19 | 37 | 47 | 3 | 14 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0003 | 0/0 | 630 | 67 | 2 | 7 | 44 | 3 | 11 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0004 | 0/0 | 630 | 57 | 0 | 5 | 46 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0005 | 0/0 | 630 | 8 | 6 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0006 | 0/0 | 630 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0007 | 0/0 | 630 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0008 | 0/0 | 630 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0009 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0010 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0011 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0012 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| c0013 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 380 | 364 | 77 | 66 | 167 | 12 | 41 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| t0002 | 1/0 | 380 | 75 | 2 | 9 | 55 | 4 | 4 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| t0003 | 0/0 | 380 | 15 | 13 | 2 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| t0004 | 0/0 | 380 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| t0005 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| t0006 | 0/0 | 380 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 75 | 7 | 29 | 28 | 3 | 7 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0002 | 0/0 | 38 | 7 | 7 | 15 | 3 | 6 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0003 | 0/0 | 27 | 0 | 0 | 26 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0004 | 0/0 | 19 | 1 | 1 | 14 | 0 | 3 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0005 | 0/0 | 19 | 0 | 1 | 17 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0006 | 0/0 | 12 | 9 | 3 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0007 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0008 | 0/0 | 9 | 2 | 0 | 7 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0009 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0010 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0011 | 0/0 | 6 | 3 | 2 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0014 | 0/0 | 6 | 2 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0015 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0018 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0019 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0021 | 1/0 | 4 | 0 | 1 | 0 | 2 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0026 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0032 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0034 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0035 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0036 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0037 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 630 | 193 | 63 | 25 | 82 | 8 | 14 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0002 | 0/1 | 630 | 121 | 19 | 37 | 47 | 3 | 14 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0002c0003 | 0/0 | 630 | 67 | 2 | 7 | 44 | 3 | 11 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0003c0004 | 0/0 | 630 | 57 | 0 | 5 | 46 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0003c0009 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0004c0005 | 0/0 | 630 | 8 | 6 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0005c0006 | 0/0 | 630 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0006c0007 | 0/0 | 630 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0007c0008 | 0/0 | 630 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0008c0012 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0009c0010 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0010c0011 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0011c0013 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1009 | 105 | 47 | 14 | 29 | 4 | 11 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0001t0002 | 1/0 | 1009 | 71 | 1 | 9 | 53 | 4 | 3 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0001t0003 | 0/0 | 1009 | 15 | 13 | 2 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0001t0004 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0002t0001 | 0/1 | 1009 | 120 | 19 | 36 | 47 | 3 | 14 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0001c0002t0006 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0002c0003t0001 | 0/0 | 1009 | 66 | 2 | 7 | 44 | 3 | 10 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0002c0003t0005 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0003c0004t0001 | 0/0 | 1009 | 57 | 0 | 5 | 46 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0003c0009t0001 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0004c0005t0001 | 0/0 | 1009 | 7 | 6 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0004c0005t0002 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0005c0006t0001 | 0/0 | 1009 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0006c0007t0002 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0007c0008t0001 | 0/0 | 1009 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0008c0012t0001 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0009c0010t0001 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0010c0011t0002 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| a0011c0013t0001 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | copy fasta | chr4 | 70513569 | 70537743 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 36 | 6 | 6 | 15 | 3 | 6 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0006 | 0/0 | 12 | 9 | 3 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0037 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0005 | 0/0 | 18 | 0 | 1 | 16 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0007 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0021 | 1/0 | 4 | 0 | 1 | 0 | 2 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0032 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0036 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0001 | 0/1 | 74 | 7 | 28 | 28 | 3 | 7 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0011 | 0/0 | 6 | 3 | 2 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0015 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0004 | 0/0 | 18 | 1 | 1 | 14 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0008 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0019 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0003 | 0/0 | 26 | 0 | 0 | 25 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0009 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0034 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0035 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0005c0006t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0005c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0006c0007t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0006c0007t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0007c0008t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0008c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0009c0010t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0010c0011t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0011c0013t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00099 | hp2 | a0003 | c0004 | t0001 | g0034 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0026 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00438 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00544 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00621 | hp1 | a0003 | c0009 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00642 | hp2 | a0003 | c0004 | t0001 | g0050 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00673 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0083 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00735 | hp1 | a0008 | c0012 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0123 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0049 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0079 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01192 | hp1 | a0004 | c0005 | t0001 | g0035 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01243 | hp1 | a0005 | c0006 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01358 | hp2 | a0009 | c0010 | t0001 | g0068 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0019 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0082 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01981 | hp2 | a0001 | c0002 | t0006 | g0070 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02055 | hp2 | a0010 | c0011 | t0002 | g0116 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02083 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02155 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02165 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0014 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02717 | hp1 | a0004 | c0005 | t0001 | g0035 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0019 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0042 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02818 | hp2 | a0005 | c0006 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02922 | hp1 | a0004 | c0005 | t0001 | g0051 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02922 | hp2 | a0011 | c0013 | t0001 | g0008 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0043 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03669 | hp2 | a0004 | c0005 | t0002 | g0117 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03688 | hp2 | a0003 | c0004 | t0001 | g0050 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0121 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03831 | hp1 | a0003 | c0004 | t0001 | g0009 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0078 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0042 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0026 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0003 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04199 | hp1 | a0002 | c0003 | t0005 | g0004 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0076 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04228 | hp2 | a0007 | c0008 | t0001 | g0045 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18941 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18946 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18951 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18956 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18957 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18961 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18961 | hp2 | a0006 | c0007 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18962 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18963 | hp2 | a0003 | c0004 | t0001 | g0126 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18965 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18973 | hp2 | a0006 | c0007 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18974 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18975 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18977 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18982 | hp1 | a0003 | c0004 | t0001 | g0127 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18986 | hp2 | a0003 | c0004 | t0001 | g0103 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18992 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18995 | hp1 | a0003 | c0004 | t0001 | g0120 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19000 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19005 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19007 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19012 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19059 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19062 | hp2 | a0003 | c0004 | t0001 | g0130 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19064 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19065 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19068 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19075 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19076 | hp2 | a0003 | c0004 | t0001 | g0102 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19080 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19086 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0128 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0051 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | ASW | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20805 | hp1 | a0007 | c0008 | t0001 | g0045 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20905 | hp1 | a0003 | c0004 | t0001 | g0049 | SAS | GIH | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | GIH | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0129 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0001 | REF | REF | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0021 | REF | REF | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518820
|
C | T | 1 | a0002 | 67 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(64): Show |
missense_variant | MODERATE | c.43C>T | p.Arg15Trp | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 144/1009 | 43/630 | 15/209 | chr4 | 70518820 | ||
| chr4:70518829
|
C | T | 1 | a0011 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.52C>T | p.Pro18Ser | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 153/1009 | 52/630 | 18/209 | chr4 | 70518829 | ||
| chr4:70522834
|
A | G | 2 | a0003a0007 | 60 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
missense_variant | MODERATE | c.134A>G | p.Asn45Ser | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/9 | 235/1009 | 134/630 | 45/209 | chr4 | 70522834 | ||
| chr4:70523868
|
G | T | 1 | a0008 | 1 | HG00735.hp1 | missense_variant&splice_region_variant | MODERATE | c.139G>T | p.Val47Phe | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/9 | 240/1009 | 139/630 | 47/209 | chr4 | 70523868 | ||
| chr4:70523877
|
T | C | 1 | a0004 | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
missense_variant | MODERATE | c.148T>C | p.Ser50Pro | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/9 | 249/1009 | 148/630 | 50/209 | chr4 | 70523877 | ||
| chr4:70524930
|
G | A | 1 | a0009 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.263G>A | p.Gly88Glu | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/9 | 364/1009 | 263/630 | 88/209 | chr4 | 70524930 | ||
| chr4:70528753
|
G | A | 1 | a0007 | 2 | HG04228.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.325G>A | p.Ala109Thr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/9 | 426/1009 | 325/630 | 109/209 | chr4 | 70528753 | ||
| chr4:70531066
|
C | T | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.385C>T | p.His129Tyr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 486/1009 | 385/630 | 129/209 | chr4 | 70531066 | ||
| chr4:70531193
|
G | A | 1 | a0006 | 2 | NA18961.hp2 NA18973.hp2 |
missense_variant | MODERATE | c.512G>A | p.Arg171His | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 613/1009 | 512/630 | 171/209 | chr4 | 70531193 | ||
| chr4:70531211
|
G | T | 1 | a0005 | 3 | HG01243.hp1 HG02615.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.530G>T | p.Gly177Val | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 631/1009 | 530/630 | 177/209 | chr4 | 70531211 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518789
|
G | A | 1 | a0003c0009 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.12G>A | p.Thr4Thr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 113/1009 | 12/630 | 4/209 | chr4 | 70518789 | ||
| chr4:70531272
|
C | T | 3 | a0001c0002a0008c0012a0009c0010 | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
synonymous_variant | LOW | c.591C>T | p.Ile197Ile | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 692/1009 | 591/630 | 197/209 | chr4 | 70531272 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518570
|
T | C | 1 | a0001c0001t0003 | 15 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/9 | chr4 | 70518570 | ||||||
| chr4:70518615
|
G | A | 1 | a0002c0003t0005 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/9 | 163 | chr4 | 70518615 | |||||
| chr4:70518771
|
C | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | chr4 | 70518771 | ||||||
| chr4:70532504
|
G | T | 1 | a0001c0001t0004 | 2 | HG02258.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*39G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 9/9 | 39 | chr4 | 70532504 | |||||
| chr4:70532622
|
A | C | 1 | a0001c0002t0006 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 9/9 | 157 | chr4 | 70532622 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518739
|
A | AGTAACAC others(6): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0038others(2): Show | 10 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-15-21_-15-9dupAAC others(10): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 70518739 | |||||
| chr4:70518862
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.54+31G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518862 | ||||||
| chr4:70518896
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.54+65C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518896 | ||||||
| chr4:70518922
|
GCT | G | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.54+94_54+95delCT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70518922 | |||||
| chr4:70518975
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.54+144A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518975 | ||||||
| chr4:70519014
|
A | G | 1 | a0003c0004t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.54+183A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519014 | ||||||
| chr4:70519063
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.54+232A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519063 | ||||||
| chr4:70519078
|
G | A | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.54+247G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519078 | ||||||
| chr4:70519123
|
G | T | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.54+292G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519123 | ||||||
| chr4:70519190
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.54+359G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519190 | ||||||
| chr4:70519217
|
G | A | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+386G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519217 | ||||||
| chr4:70519284
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+453T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519284 | ||||||
| chr4:70519319
|
A | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+488A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519319 | ||||||
| chr4:70519345
|
T | C | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+514T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519345 | ||||||
| chr4:70519380
|
C | T | 1 | a0001c0001t0002g0036 | 3 | HG00323.hp1 HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.54+549C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519380 | ||||||
| chr4:70519409
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.54+578G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519409 | ||||||
| chr4:70519438
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0004g0086a0001c0001t0004g0087 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.54+607T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519438 | ||||||
| chr4:70519450
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+619T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519450 | ||||||
| chr4:70519473
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+642A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519473 | ||||||
| chr4:70519512
|
TAAAA | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+682_54+685delAA others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519512 | ||||||
| chr4:70519572
|
C | A | 1 | a0007c0008t0001g0045 | 2 | HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.54+741C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519572 | ||||||
| chr4:70519617
|
T | C | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+786T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519617 | ||||||
| chr4:70519698
|
A | AT | 12 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 17 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+877dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519698 | |||||
| chr4:70519699
|
T | TTTTTTTA | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(58): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.54+874_54+875insAT others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519699 | |||||
| chr4:70519711
|
CT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.54+889delT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519711 | |||||
| chr4:70519730
|
A | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+899A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519730 | ||||||
| chr4:70519872
|
G | A | 1 | a0001c0002t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.54+1041G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519872 | ||||||
| chr4:70519913
|
C | CGT | 26 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0002t0001g0001others(23): Show | 113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.54+1101_54+1102dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | |||||
| chr4:70519913
|
C | CGTGT | 3 | a0001c0002t0001g0015a0001c0002t0001g0041a0001c0002t0001g0071 | 8 | HG00558.hp1 HG01175.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1099_54+1102dup others(4): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | |||||
| chr4:70519913
|
CGT | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+1101_54+1102del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | |||||
| chr4:70519932
|
GTC | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 22 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+1103_54+1104del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519932 | |||||
| chr4:70519934
|
C | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.54+1103C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519934 | ||||||
| chr4:70520010
|
AT | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+1186delT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70520010 | |||||
| chr4:70520075
|
T | TAC | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.54+1245_54+1246ins others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70520075 | |||||
| chr4:70520137
|
T | C | 3 | a0003c0004t0001g0016a0003c0004t0001g0102a0003c0004t0001g0103 | 7 | NA18941.hp2 NA18946.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+1306T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520137 | ||||||
| chr4:70520145
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.54+1314T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520145 | ||||||
| chr4:70520183
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.54+1352C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520183 | ||||||
| chr4:70520257
|
GAGGCGAC others(7): Show |
G | 1 | a0003c0004t0001g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.54+1427_54+1440del others(14): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520257 | ||||||
| chr4:70520261
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+1430C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520261 | ||||||
| chr4:70520311
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54+1480C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520311 | ||||||
| chr4:70520311
|
C | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(64): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.54+1480C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520311 | ||||||
| chr4:70520352
|
G | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(125): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.54+1521G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520352 | ||||||
| chr4:70520374
|
A | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+1543A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520374 | ||||||
| chr4:70520458
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+1627C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520458 | ||||||
| chr4:70520531
|
A | T | 1 | a0003c0004t0001g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.54+1700A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520531 | ||||||
| chr4:70520560
|
C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.54+1729C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520560 | ||||||
| chr4:70520684
|
A | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.54+1853A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520684 | ||||||
| chr4:70520687
|
A | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0144 | 3 | NA18941.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.54+1856A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520687 | ||||||
| chr4:70520946
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1809C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520946 | ||||||
| chr4:70521001
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1754A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521001 | ||||||
| chr4:70521119
|
C | T | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0018others(20): Show | 108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.55-1636C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521119 | ||||||
| chr4:70521142
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1613G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521142 | ||||||
| chr4:70521151
|
G | C | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-1604G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521151 | ||||||
| chr4:70521153
|
C | T | 3 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0093 | 8 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-1602C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521153 | ||||||
| chr4:70521173
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1582G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521173 | ||||||
| chr4:70521205
|
A | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.55-1550A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521205 | ||||||
| chr4:70521211
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1544C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521211 | ||||||
| chr4:70521255
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1500C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521255 | ||||||
| chr4:70521302
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.55-1453C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521302 | ||||||
| chr4:70521320
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1435C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521320 | ||||||
| chr4:70521344
|
C | T | 1 | a0001c0001t0001g0030 | 3 | HG02630.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.55-1411C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521344 | ||||||
| chr4:70521378
|
TA | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(68): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.55-1361delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521378 | |||||
| chr4:70521415
|
G | GAA | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1333_55-1332dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521415 | |||||
| chr4:70521470
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1285C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521470 | ||||||
| chr4:70521519
|
G | A | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.55-1236G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521519 | ||||||
| chr4:70521525
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.55-1230G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521525 | ||||||
| chr4:70521604
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.55-1151G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521604 | ||||||
| chr4:70521640
|
C | CT | 10 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0036others(7): Show | 35 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.55-1079dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTT | 10 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0124others(7): Show | 22 | HG00408.hp2 HG00609.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-1080_55-1079dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTT | 5 | a0001c0001t0001g0125a0001c0001t0002g0032a0001c0001t0002g0099others(2): Show | 7 | HG01952.hp2 HG02055.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1081_55-1079dup others(3): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTTTT | 8 | a0002c0003t0001g0008a0002c0003t0001g0012a0002c0003t0001g0026others(5): Show | 24 | HG00323.hp2 HG01192.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-1083_55-1079dup others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTTTTT | 8 | a0002c0003t0001g0004a0002c0003t0001g0027a0002c0003t0001g0043others(5): Show | 29 | HG00642.hp1 HG01255.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.55-1084_55-1079dup others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTTTTTT | 6 | a0001c0001t0001g0010a0002c0003t0001g0010a0002c0003t0001g0079others(3): Show | 11 | HG01109.hp2 HG01261.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1085_55-1079dup others(7): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTTTTTT others(3): Show |
2 | a0002c0003t0001g0019a0002c0003t0001g0085 | 5 | HG01517.hp2 HG02027.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-1088_55-1079dup others(10): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | CTTTTTTT others(4): Show |
1 | a0002c0003t0001g0083 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.55-1089_55-1079dup others(11): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
C | T | 1 | a0001c0001t0002g0033 | 3 | NA18948.hp1 NA18985.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.55-1115C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521640 | ||||||
| chr4:70521640
|
CTT | C | 6 | a0001c0001t0001g0104a0003c0004t0001g0009a0003c0004t0001g0049others(3): Show | 16 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.55-1080_55-1079del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTT | C | 11 | a0003c0004t0001g0003a0003c0004t0001g0016a0003c0004t0001g0034others(8): Show | 43 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.55-1081_55-1079del others(3): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(4): Show | 15 | HG02074.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-1083_55-1079del others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTT | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(25): Show | 88 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.55-1084_55-1079del others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT | C | 7 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 10 | HG01346.hp2 HG01934.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-1085_55-1079del others(7): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0047 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.55-1089_55-1079del others(11): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0088a0001c0001t0004g0086 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.55-1093_55-1079del others(15): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1094_55-1079del others(16): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT others(10): Show |
C | 4 | a0001c0002t0001g0018a0001c0002t0001g0069a0001c0002t0006g0070others(1): Show | 7 | HG00423.hp1 HG01981.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1095_55-1079del others(17): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521640
|
CTTTTTTT others(11): Show |
C | 25 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(22): Show | 117 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.55-1096_55-1079del others(18): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | |||||
| chr4:70521643
|
T | C | 1 | a0003c0004t0001g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.55-1112T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521643 | ||||||
| chr4:70521644
|
T | C | 5 | a0003c0004t0001g0009a0003c0004t0001g0049a0003c0004t0001g0050others(2): Show | 15 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.55-1111T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521644 | ||||||
| chr4:70521645
|
T | C | 12 | a0003c0004t0001g0003a0003c0004t0001g0016a0003c0004t0001g0034others(9): Show | 44 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.55-1110T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521645 | ||||||
| chr4:70521646
|
T | C | 6 | a0003c0004t0001g0009a0003c0004t0001g0049a0003c0004t0001g0050others(3): Show | 16 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.55-1109T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521646 | ||||||
| chr4:70521647
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0053others(13): Show | 54 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.55-1108T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521647 | ||||||
| chr4:70521648
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 64 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.55-1107T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521648 | ||||||
| chr4:70521649
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.55-1106T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521649 | ||||||
| chr4:70521713
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.55-1042G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521713 | ||||||
| chr4:70521733
|
C | G | 5 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0128others(2): Show | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-1022C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521733 | ||||||
| chr4:70521772
|
A | T | 1 | a0003c0004t0001g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.55-983A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521772 | ||||||
| chr4:70521823
|
T | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(34): Show | 148 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.55-932T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521823 | ||||||
| chr4:70521863
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(34): Show | 148 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.55-892G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521863 | ||||||
| chr4:70521867
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55-888G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521867 | ||||||
| chr4:70521936
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55-819C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521936 | ||||||
| chr4:70522009
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-746G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522009 | ||||||
| chr4:70522032
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-723T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522032 | ||||||
| chr4:70522045
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55-710A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522045 | ||||||
| chr4:70522121
|
G | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(36): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-634G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522121 | ||||||
| chr4:70522189
|
C | T | 1 | a0009c0010t0001g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.55-566C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522189 | ||||||
| chr4:70522200
|
GA | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(36): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-548delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70522200 | |||||
| chr4:70522326
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.55-429C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522326 | ||||||
| chr4:70522327
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0093 | 8 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-428G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522327 | ||||||
| chr4:70522333
|
G | GC | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(36): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-421dupC | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70522333 | |||||
| chr4:70522347
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.55-408A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522347 | ||||||
| chr4:70522412
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.55-343A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522412 | ||||||
| chr4:70522512
|
A | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.55-243A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522512 | ||||||
| chr4:70522519
|
C | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.55-236C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522519 | ||||||
| chr4:70522545
|
C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-210C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522545 | ||||||
| chr4:70522662
|
A | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-93A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522662 | ||||||
| chr4:70522677
|
T | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.55-78T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522677 | ||||||
| chr4:70522856
|
TGGAACAT others(23): Show |
T | 1 | a0002c0003t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138+46_138+75delTA others(28): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 70522856 | |||||
| chr4:70522872
|
C | T | 2 | a0001c0001t0004g0086a0001c0001t0004g0087 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.138+34C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522872 | ||||||
| chr4:70522924
|
C | T | 1 | a0002c0003t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138+86C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522924 | ||||||
| chr4:70522949
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+111C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522949 | ||||||
| chr4:70522969
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+131G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522969 | ||||||
| chr4:70522989
|
G | A | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.138+151G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522989 | ||||||
| chr4:70523132
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.138+294C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523132 | ||||||
| chr4:70523205
|
A | T | 18 | a0003c0004t0001g0003a0003c0004t0001g0009a0003c0004t0001g0016others(15): Show | 60 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.138+367A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523205 | ||||||
| chr4:70523241
|
T | G | 1 | a0001c0002t0001g0039 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.138+403T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523241 | ||||||
| chr4:70523476
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.139-392C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523476 | ||||||
| chr4:70523513
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.139-355C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523513 | ||||||
| chr4:70523514
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.139-354G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523514 | ||||||
| chr4:70523548
|
C | A | 5 | a0001c0002t0001g0060a0003c0004t0001g0120a0003c0004t0001g0122others(2): Show | 5 | HG01358.hp2 HG01433.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-320C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523548 | ||||||
| chr4:70523629
|
C | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.139-239C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523629 | ||||||
| chr4:70523665
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-203G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523665 | ||||||
| chr4:70523780
|
C | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(36): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.139-88C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523780 | ||||||
| chr4:70523940
|
G | C | 1 | a0001c0002t0001g0058 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.204+7G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70523940 | ||||||
| chr4:70523952
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(36): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.204+19T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70523952 | ||||||
| chr4:70524059
|
C | T | 5 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0128others(2): Show | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+126C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524059 | ||||||
| chr4:70524077
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+144G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524077 | ||||||
| chr4:70524148
|
T | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(61): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.204+215T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524148 | ||||||
| chr4:70524199
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+266C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524199 | ||||||
| chr4:70524220
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(124): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.204+287T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524220 | ||||||
| chr4:70524352
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.204+419G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524352 | ||||||
| chr4:70524431
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-441T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524431 | ||||||
| chr4:70524463
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.205-409C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524463 | ||||||
| chr4:70524467
|
A | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-405A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524467 | ||||||
| chr4:70524499
|
T | A | 1 | a0001c0001t0004g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.205-373T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524499 | ||||||
| chr4:70524604
|
C | G | 1 | a0002c0003t0001g0027 | 3 | HG00642.hp1 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.205-268C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524604 | ||||||
| chr4:70524658
|
GAA | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.205-211_205-210del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 70524658 | |||||
| chr4:70524684
|
C | T | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.205-188C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524684 | ||||||
| chr4:70524754
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.205-118G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524754 | ||||||
| chr4:70524814
|
T | G | 1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.205-58T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524814 | ||||||
| chr4:70524865
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.205-7C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524865 | ||||||
| chr4:70525064
|
A | G | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.294+103A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525064 | ||||||
| chr4:70525078
|
C | A | 41 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(38): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.294+117C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525078 | ||||||
| chr4:70525105
|
A | G | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+144A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525105 | ||||||
| chr4:70525174
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(126): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.294+213T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525174 | ||||||
| chr4:70525343
|
G | A | 4 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0128others(1): Show | 7 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+382G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525343 | ||||||
| chr4:70525388
|
C | T | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+427C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525388 | ||||||
| chr4:70525389
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.294+428G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525389 | ||||||
| chr4:70525471
|
A | T | 1 | a0004c0005t0001g0128 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.294+510A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525471 | ||||||
| chr4:70525760
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.294+799C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525760 | ||||||
| chr4:70525760
|
C | T | 1 | a0001c0002t0001g0011 | 6 | HG00738.hp1 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+799C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525760 | ||||||
| chr4:70525769
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.294+808G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525769 | ||||||
| chr4:70525939
|
T | C | 3 | a0003c0004t0001g0034a0003c0004t0001g0049a0003c0004t0001g0050 | 7 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+978T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525939 | ||||||
| chr4:70525941
|
C | T | 1 | a0004c0005t0001g0128 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.294+980C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525941 | ||||||
| chr4:70526164
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+1203C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526164 | ||||||
| chr4:70526182
|
A | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+1221A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526182 | ||||||
| chr4:70526340
|
A | C | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.294+1379A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526340 | ||||||
| chr4:70526360
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.294+1399T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526360 | ||||||
| chr4:70526436
|
A | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+1475A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526436 | ||||||
| chr4:70526491
|
T | A | 4 | a0002c0003t0001g0026a0002c0003t0001g0042a0002c0003t0001g0043others(1): Show | 8 | HG00323.hp2 HG01261.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+1530T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526491 | ||||||
| chr4:70526544
|
A | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.294+1583A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526544 | ||||||
| chr4:70526588
|
C | T | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.294+1627C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526588 | ||||||
| chr4:70526800
|
C | G | 1 | a0010c0011t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.294+1839C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526800 | ||||||
| chr4:70526886
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.295-1837C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526886 | ||||||
| chr4:70527019
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0072 | 2 | HG03927.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.295-1704G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527019 | ||||||
| chr4:70527229
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.295-1494A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527229 | ||||||
| chr4:70527233
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.295-1490G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527233 | ||||||
| chr4:70527266
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295-1457C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527266 | ||||||
| chr4:70527277
|
GA | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0056 | 5 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1440delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 70527277 | |||||
| chr4:70527284
|
G | T | 4 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0128others(1): Show | 7 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-1439G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527284 | ||||||
| chr4:70527465
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.295-1258C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527465 | ||||||
| chr4:70527560
|
C | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.295-1163C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527560 | ||||||
| chr4:70527713
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-1010C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527713 | ||||||
| chr4:70527727
|
T | C | 2 | a0001c0002t0001g0040a0001c0002t0001g0071 | 3 | HG00558.hp1 NA18971.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.295-996T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527727 | ||||||
| chr4:70527757
|
G | T | 1 | a0001c0001t0003g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.295-966G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527757 | ||||||
| chr4:70527871
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-852T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527871 | ||||||
| chr4:70527875
|
A | G | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.295-848A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527875 | ||||||
| chr4:70528023
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.295-700T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528023 | ||||||
| chr4:70528041
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(59): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.295-682C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528041 | ||||||
| chr4:70528072
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.295-651T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528072 | ||||||
| chr4:70528151
|
A | AT | 5 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0137others(2): Show | 8 | HG02074.hp2 HG02083.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-563dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 70528151 | |||||
| chr4:70528158
|
T | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0069 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.295-565T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528158 | ||||||
| chr4:70528226
|
C | T | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.295-497C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528226 | ||||||
| chr4:70528227
|
T | TC | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.295-496_295-495ins others(1): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528227 | ||||||
| chr4:70528303
|
A | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-420A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528303 | ||||||
| chr4:70528467
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-256G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528467 | ||||||
| chr4:70528616
|
C | T | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.295-107C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528616 | ||||||
| chr4:70528646
|
T | A | 1 | a0001c0001t0002g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.295-77T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528646 | ||||||
| chr4:70528682
|
C | G | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.295-41C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528682 | ||||||
| chr4:70528771
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.330+13C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70528771 | ||||||
| chr4:70528948
|
A | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.330+190A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70528948 | ||||||
| chr4:70529022
|
G | A | 1 | a0002c0003t0001g0079 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.331-162G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529022 | ||||||
| chr4:70529042
|
T | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.331-142T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529042 | ||||||
| chr4:70529068
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.331-116A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529068 | ||||||
| chr4:70529256
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0004g0086a0001c0001t0004g0087 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.357+46A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529256 | ||||||
| chr4:70529313
|
T | C | 1 | a0003c0004t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.357+103T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529313 | ||||||
| chr4:70529432
|
G | A | 1 | a0002c0003t0001g0077 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.357+222G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529432 | ||||||
| chr4:70529473
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.357+263C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529473 | ||||||
| chr4:70529528
|
A | G | 1 | a0003c0004t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+318A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529528 | ||||||
| chr4:70529571
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357+361G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529571 | ||||||
| chr4:70529633
|
G | A | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.357+423G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529633 | ||||||
| chr4:70529722
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+512T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529722 | ||||||
| chr4:70529725
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.357+515G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529725 | ||||||
| chr4:70529772
|
T | C | 1 | a0001c0001t0002g0047 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.357+562T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529772 | ||||||
| chr4:70529775
|
T | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+565T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529775 | ||||||
| chr4:70529778
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+568C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529778 | ||||||
| chr4:70529805
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+595G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529805 | ||||||
| chr4:70529827
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.357+617A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529827 | ||||||
| chr4:70529854
|
T | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0018others(20): Show | 108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.357+644T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529854 | ||||||
| chr4:70529991
|
T | TA | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+782dupA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70529991 | |||||
| chr4:70530003
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(72): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.357+793T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530003 | ||||||
| chr4:70530203
|
C | T | 1 | a0002c0003t0001g0082 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.358-836C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530203 | ||||||
| chr4:70530221
|
GCA | G | 52 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0104others(49): Show | 186 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.358-793_358-792del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | |||||
| chr4:70530221
|
GCACA | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 119 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.358-795_358-792del others(4): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | |||||
| chr4:70530221
|
GCACACA | G | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.358-797_358-792del others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | |||||
| chr4:70530256
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0073 | 4 | NA18947.hp1 NA18985.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-783A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530256 | ||||||
| chr4:70530318
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0004g0086a0001c0001t0004g0087 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.358-721G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530318 | ||||||
| chr4:70530371
|
G | A | 1 | a0004c0005t0001g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.358-668G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530371 | ||||||
| chr4:70530381
|
G | T | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.358-658G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530381 | ||||||
| chr4:70530492
|
A | G | 3 | a0002c0003t0001g0012a0002c0003t0001g0044a0002c0003t0001g0081 | 9 | HG02080.hp2 NA18943.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.358-547A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530492 | ||||||
| chr4:70530596
|
T | C | 1 | a0003c0004t0001g0049 | 2 | HG00741.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.358-443T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530596 | ||||||
| chr4:70530642
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358-397T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530642 | ||||||
| chr4:70530649
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(153): Show | 453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
intron_variant | MODIFIER | c.358-390A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530649 | ||||||
| chr4:70531349
|
G | T | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.619+49G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531349 | ||||||
| chr4:70531478
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0114 | 3 | NA18964.hp1 NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.619+178C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531478 | ||||||
| chr4:70531598
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.619+298C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531598 | ||||||
| chr4:70531640
|
T | A | 1 | a0001c0002t0001g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.619+340T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531640 | ||||||
| chr4:70531647
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.619+347G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531647 | ||||||
| chr4:70531656
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0089others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.619+356C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531656 | ||||||
| chr4:70531763
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0056 | 5 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+463C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531763 | ||||||
| chr4:70531796
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0111a0001c0001t0002g0113 | 8 | HG00408.hp2 HG02523.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.619+496G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531796 | ||||||
| chr4:70531876
|
G | A | 2 | a0001c0001t0004g0086a0001c0001t0004g0087 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.619+576G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531876 | ||||||
| chr4:70531978
|
A | T | 1 | a0002c0003t0001g0080 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.620-477A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531978 | ||||||
| chr4:70531981
|
A | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-474A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531981 | ||||||
| chr4:70532064
|
A | G | 2 | a0001c0001t0004g0086a0001c0001t0004g0087 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.620-391A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532064 | ||||||
| chr4:70532146
|
C | A | 13 | a0001c0001t0001g0088a0001c0001t0003g0020a0001c0001t0003g0028others(10): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.620-309C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532146 | ||||||
| chr4:70532181
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.620-274G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532181 | ||||||
| chr4:70532225
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.620-230G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532225 | ||||||
| chr4:70532240
|
C | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(64): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.620-215C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532240 | ||||||
| chr4:70532347
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.620-108G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532347 | ||||||
| chr4:70532355
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.620-100T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532355 | ||||||
| chr4:70532384
|
T | G | 1 | a0002c0003t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.620-71T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532384 | ||||||
| chr4:70532438
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.620-17G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532438 |