| geneid | 175 |
|---|---|
| ensemblid | ENSG00000038002.9 |
| hgncid | 318 |
| symbol | AGA |
| name | aspartylglucosaminidase |
| refseq_nuc | NM_000027.4 |
| refseq_prot | NP_000018.2 |
| ensembl_nuc | ENST00000264595.7 |
| ensembl_prot | ENSP00000264595.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 177430774 |
| end | 177442437 |
| strand | - |
| ver | v1.2 |
| region | chr4:177430774-177442437 |
| region5000 | chr4:177425774-177447437 |
| regionname0 | AGA_chr4_177430774_177442437 |
| regionname5000 | AGA_chr4_177425774_177447437 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 346 | 407 | 67 | 73 | 204 | 16 | 46 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0002 | 1/0 | 346 | 25 | 22 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0003 | 0/0 | 346 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0004 | 0/0 | 346 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0005 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0006 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0007 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1041 | 404 | 65 | 72 | 204 | 16 | 46 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0002 | 1/0 | 1041 | 25 | 22 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0003 | 0/0 | 1041 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0004 | 0/0 | 1041 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0005 | 0/0 | 1041 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0006 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0007 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0008 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| c0009 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 997 | 217 | 70 | 28 | 89 | 8 | 21 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0002 | 0/1 | 997 | 193 | 22 | 48 | 90 | 8 | 24 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0003 | 0/0 | 997 | 13 | 0 | 0 | 12 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0004 | 0/0 | 997 | 11 | 0 | 0 | 11 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0005 | 0/0 | 997 | 3 | 0 | 1 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0006 | 0/0 | 997 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0007 | 0/0 | 997 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0008 | 0/0 | 997 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| t0009 | 0/0 | 997 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 41 | 0 | 9 | 22 | 1 | 9 | AGA_chr4_177425774_177447437 | AGA |
| g0002 | 0/0 | 36 | 0 | 5 | 26 | 3 | 2 | AGA_chr4_177425774_177447437 | AGA |
| g0003 | 0/0 | 29 | 0 | 0 | 28 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0004 | 0/0 | 14 | 1 | 6 | 3 | 0 | 4 | AGA_chr4_177425774_177447437 | AGA |
| g0005 | 0/0 | 12 | 5 | 3 | 0 | 2 | 2 | AGA_chr4_177425774_177447437 | AGA |
| g0006 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0007 | 0/0 | 9 | 2 | 4 | 2 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0008 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0009 | 0/1 | 8 | 0 | 1 | 1 | 3 | 2 | AGA_chr4_177425774_177447437 | AGA |
| g0010 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0011 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0012 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0014 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0015 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0016 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0019 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0020 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0021 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0022 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | AGA_chr4_177425774_177447437 | AGA |
| g0023 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0024 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0025 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0026 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0027 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0031 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | AGA_chr4_177425774_177447437 | AGA |
| g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0034 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0058 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0059 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0063 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0064 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0065 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0066 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/1 | 404 | 65 | 72 | 204 | 16 | 46 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0002c0002 | a0002 | c0002 | 1/0 | 25 | 22 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0005c0006 | a0005 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0006c0008 | a0006 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0007c0007 | a0007 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 194 | 48 | 28 | 89 | 8 | 21 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/1 | 178 | 13 | 42 | 90 | 8 | 24 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0005t0002 | a0001 | c0005 | t0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 1/0 | 17 | 16 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0004c0004t0002 | a0004 | c0004 | t0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0005c0006t0001 | a0005 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0006c0008t0002 | a0006 | c0008 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| a0007c0007t0002 | a0007 | c0007 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 36 | 0 | 5 | 26 | 3 | 2 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 12 | 5 | 3 | 0 | 2 | 2 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 9 | 2 | 4 | 2 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 41 | 0 | 9 | 22 | 1 | 9 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 29 | 0 | 0 | 28 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 14 | 1 | 6 | 3 | 0 | 4 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/1 | 8 | 0 | 1 | 1 | 3 | 2 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0135 | a0001 | c0001 | t0002 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0137 | a0001 | c0001 | t0002 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0140 | a0001 | c0001 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0141 | a0001 | c0001 | t0002 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0154 | a0001 | c0001 | t0002 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0155 | a0001 | c0001 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0003g0014 | a0001 | c0001 | t0003 | g0014 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0003g0105 | a0001 | c0001 | t0003 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0004g0021 | a0001 | c0001 | t0004 | g0021 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0004g0049 | a0001 | c0001 | t0004 | g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0004g0062 | a0001 | c0001 | t0004 | g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0004g0067 | a0001 | c0001 | t0004 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0004g0075 | a0001 | c0001 | t0004 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0005g0033 | a0001 | c0001 | t0005 | g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0006g0052 | a0001 | c0001 | t0006 | g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0007g0109 | a0001 | c0001 | t0007 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0008g0108 | a0001 | c0001 | t0008 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0001t0009g0126 | a0001 | c0001 | t0009 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0005t0002g0059 | a0001 | c0005 | t0002 | g0059 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0001c0009t0001g0151 | a0001 | c0009 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0018 | a0002 | c0002 | t0001 | g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0040 | a0002 | c0002 | t0001 | g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0088 | a0002 | c0002 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0093 | a0002 | c0002 | t0001 | g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0094 | a0002 | c0002 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0095 | a0002 | c0002 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0096 | a0002 | c0002 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0097 | a0002 | c0002 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0098 | a0002 | c0002 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0099 | a0002 | c0002 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0104 | a0002 | c0002 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0001g0147 | a0002 | c0002 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0002g0024 | a0002 | c0002 | t0002 | g0024 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0002g0041 | a0002 | c0002 | t0002 | g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0002c0002t0002g0042 | a0002 | c0002 | t0002 | g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0003c0003t0001g0053 | a0003 | c0003 | t0001 | g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0003c0003t0001g0118 | a0003 | c0003 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0003c0003t0001g0128 | a0003 | c0003 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0004c0004t0002g0034 | a0004 | c0004 | t0002 | g0034 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0005c0006t0001g0124 | a0005 | c0006 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0006c0008t0002g0139 | a0006 | c0008 | t0002 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| a0007c0007t0002g0138 | a0007 | c0007 | t0002 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGA_chr4_177425774_177447437 | AGA |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | AGA_chr4_177425774_177447437 | AGA |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | GBR | AGA_chr4_177425774_177447437 | AGA |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | AGA_chr4_177425774_177447437 | AGA |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AGA_chr4_177425774_177447437 | AGA |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | AGA_chr4_177425774_177447437 | AGA |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | AGA_chr4_177425774_177447437 | AGA |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | AGA_chr4_177425774_177447437 | AGA |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | AGA_chr4_177425774_177447437 | AGA |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AGA_chr4_177425774_177447437 | AGA |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00733 | hp1 | a0004 | c0004 | t0002 | g0034 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01081 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01099 | hp1 | a0004 | c0004 | t0002 | g0034 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01167 | hp1 | a0004 | c0004 | t0002 | g0034 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01192 | hp1 | a0001 | c0005 | t0002 | g0059 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | AGA_chr4_177425774_177447437 | AGA |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | IBS | AGA_chr4_177425774_177447437 | AGA |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | AGA_chr4_177425774_177447437 | AGA |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | AGA_chr4_177425774_177447437 | AGA |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | AGA_chr4_177425774_177447437 | AGA |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02055 | hp2 | a0001 | c0009 | t0001 | g0151 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | CDX | AGA_chr4_177425774_177447437 | AGA |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | AGA_chr4_177425774_177447437 | AGA |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CDX | AGA_chr4_177425774_177447437 | AGA |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | AGA_chr4_177425774_177447437 | AGA |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | AGA_chr4_177425774_177447437 | AGA |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AGA_chr4_177425774_177447437 | AGA |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0124 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0118 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0053 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0053 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | AGA_chr4_177425774_177447437 | AGA |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | AGA_chr4_177425774_177447437 | AGA |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AGA_chr4_177425774_177447437 | AGA |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | AGA_chr4_177425774_177447437 | AGA |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AGA_chr4_177425774_177447437 | AGA |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | AGA_chr4_177425774_177447437 | AGA |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0128 | AFR | YRI | AGA_chr4_177425774_177447437 | AGA |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | AGA_chr4_177425774_177447437 | AGA |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | AGA_chr4_177425774_177447437 | AGA |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | AGA_chr4_177425774_177447437 | AGA |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | AGA_chr4_177425774_177447437 | AGA |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA19240 | hp1 | a0006 | c0008 | t0002 | g0139 | AFR | YRI | AGA_chr4_177425774_177447437 | AGA |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | YRI | AGA_chr4_177425774_177447437 | AGA |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | AGA_chr4_177425774_177447437 | AGA |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | ASW | AGA_chr4_177425774_177447437 | AGA |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | AGA_chr4_177425774_177447437 | AGA |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AGA_chr4_177425774_177447437 | AGA |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | AGA_chr4_177425774_177447437 | AGA |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AGA_chr4_177425774_177447437 | AGA |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | AGA_chr4_177425774_177447437 | AGA |
| HG02109 | hp1 | a0007 | c0007 | t0002 | g0138 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG02559 | hp2 | a0001 | c0005 | t0002 | g0059 | AFR | ACB | AGA_chr4_177425774_177447437 | AGA |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | AGA_chr4_177425774_177447437 | AGA |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | AGA_chr4_177425774_177447437 | AGA |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | USA | AGA_chr4_177425774_177447437 | AGA |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGA_chr4_177425774_177447437 | AGA |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | AGA_chr4_177425774_177447437 | AGA |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | AGA_chr4_177425774_177447437 | AGA |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | AGA_chr4_177425774_177447437 | AGA |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0009 | REF | REF | AGA_chr4_177425774_177447437 | AGA |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0093 | REF | REF | AGA_chr4_177425774_177447437 | AGA |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:177431763
|
A | G | 1 | a0007 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.986T>C | p.Met329Thr | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 1048/2037 | 986/1041 | 329/346 | chr4 | 177431763 | ||
| chr4:177431784
|
G | A | 2 | a0006a0007 | 2 | HG02109.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.965C>T | p.Thr322Ile | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 1027/2037 | 965/1041 | 322/346 | chr4 | 177431784 | ||
| chr4:177433252
|
A | G | 1 | a0003 | 4 | HG03195.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.902T>C | p.Phe301Ser | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/9 | 964/2037 | 902/1041 | 301/346 | chr4 | 177433252 | ||
| chr4:177434396
|
C | T | 1 | a0005 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.792G>A | p.Met264Ile | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/9 | 854/2037 | 792/1041 | 264/346 | chr4 | 177434396 | ||
| chr4:177438806
|
G | C | 6 | a0001a0003a0004others(3): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
missense_variant | MODERATE | c.446C>G | p.Thr149Ser | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/9 | 508/2037 | 446/1041 | 149/346 | chr4 | 177438806 | ||
| chr4:177442342
|
C | A | 1 | a0004 | 3 | HG00733.hp1 HG01099.hp1 HG01167.hp1 |
missense_variant | MODERATE | c.34G>T | p.Val12Leu | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/9 | 96/2037 | 34/1041 | 12/346 | chr4 | 177442342 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:177431726
|
T | C | 1 | a0001c0005 | 2 | HG01192.hp1 HG02559.hp2 |
synonymous_variant | LOW | c.1023A>G | p.Glu341Glu | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 1085/2037 | 1023/1041 | 341/346 | chr4 | 177431726 | ||
| chr4:177439667
|
T | A | 1 | a0001c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.303A>T | p.Ala101Ala | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/9 | 365/2037 | 303/1041 | 101/346 | chr4 | 177439667 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:177430826
|
T | G | 1 | a0001c0001t0004 | 11 | HG00438.hp1 HG02015.hp2 HG02155.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*882A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 882 | chr4 | 177430826 | |||||
| chr4:177430857
|
C | T | 1 | a0001c0001t0009 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 851 | chr4 | 177430857 | |||||
| chr4:177430990
|
C | T | 1 | a0001c0001t0006 | 2 | HG02965.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*718G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 718 | chr4 | 177430990 | |||||
| chr4:177431251
|
T | C | 1 | a0001c0001t0003 | 13 | HG03491.hp1 NA18946.hp1 NA18949.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*457A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 457 | chr4 | 177431251 | |||||
| chr4:177431488
|
C | G | 1 | a0001c0001t0005 | 3 | HG01255.hp2 NA18943.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*220G>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 220 | chr4 | 177431488 | |||||
| chr4:177431525
|
T | G | 6 | a0001c0001t0002a0001c0005t0002a0002c0002t0002others(3): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*183A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 183 | chr4 | 177431525 | |||||
| chr4:177431538
|
A | G | 1 | a0001c0001t0008 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 170 | chr4 | 177431538 | |||||
| chr4:177431700
|
A | G | 1 | a0001c0001t0007 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 9/9 | 8 | chr4 | 177431700 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:177431813
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.941-5C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177431813 | ||||||
| chr4:177431875
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.941-67A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177431875 | ||||||
| chr4:177431892
|
G | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0017others(89): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.941-84C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177431892 | ||||||
| chr4:177431994
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.941-186C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177431994 | ||||||
| chr4:177432018
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.941-210A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432018 | ||||||
| chr4:177432035
|
T | G | 1 | a0001c0001t0002g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.941-227A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432035 | ||||||
| chr4:177432036
|
TTTGTTG | T | 3 | a0003c0003t0001g0053a0003c0003t0001g0118a0003c0003t0001g0128 | 4 | HG03195.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-234_941-229del others(6): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432036 | ||||||
| chr4:177432061
|
C | T | 3 | a0003c0003t0001g0053a0003c0003t0001g0118a0003c0003t0001g0128 | 4 | HG03195.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-253G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432061 | ||||||
| chr4:177432097
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.941-289G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432097 | ||||||
| chr4:177432319
|
A | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0017others(30): Show | 95 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.941-511T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432319 | ||||||
| chr4:177432477
|
TAATTTTT others(31): Show |
T | 1 | a0001c0001t0002g0156 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.940+699_941-670del others(38): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432477 | ||||||
| chr4:177432515
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.940+699C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432515 | ||||||
| chr4:177432675
|
T | C | 1 | a0001c0001t0005g0033 | 3 | HG01255.hp2 NA18943.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.940+539A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432675 | ||||||
| chr4:177432754
|
T | C | 1 | a0001c0009t0001g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.940+460A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 8/8 | chr4 | 177432754 | ||||||
| chr4:177433400
|
A | G | 1 | a0002c0002t0002g0041 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.807-53T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433400 | ||||||
| chr4:177433512
|
C | T | 1 | a0001c0009t0001g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.807-165G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433512 | ||||||
| chr4:177433513
|
C | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0017others(95): Show | 295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.807-166G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433513 | ||||||
| chr4:177433526
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 382 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.807-179T>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433526 | ||||||
| chr4:177433651
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.807-304G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433651 | ||||||
| chr4:177433710
|
A | G | 2 | a0001c0001t0002g0136a0001c0001t0003g0013 | 7 | NA18946.hp1 NA18949.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.807-363T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433710 | ||||||
| chr4:177433732
|
G | A | 56 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(53): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.807-385C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433732 | ||||||
| chr4:177433936
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0113 | 4 | HG02280.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+446A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177433936 | ||||||
| chr4:177434110
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.806+272G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177434110 | ||||||
| chr4:177434150
|
T | C | 3 | a0001c0001t0002g0064a0001c0001t0002g0114a0001c0001t0002g0159 | 4 | HG00735.hp1 HG01175.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+232A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177434150 | ||||||
| chr4:177434180
|
G | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0017others(33): Show | 103 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.806+202C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177434180 | ||||||
| chr4:177434256
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.806+126C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 7/8 | chr4 | 177434256 | ||||||
| chr4:177434514
|
C | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.699-25G>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434514 | ||||||
| chr4:177434629
|
C | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0150 | 4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-140G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434629 | ||||||
| chr4:177434701
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.699-212C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434701 | ||||||
| chr4:177434712
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.699-223T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434712 | ||||||
| chr4:177434726
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.699-237G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434726 | ||||||
| chr4:177434788
|
G | A | 1 | a0002c0002t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.699-299C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434788 | ||||||
| chr4:177434904
|
A | AT | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 238 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.699-416dupA | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177434904 | ||||||
| chr4:177435076
|
ATT | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(54): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.699-589_699-588del others(2): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435076 | ||||||
| chr4:177435159
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.699-670G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435159 | ||||||
| chr4:177435195
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 8 | HG01243.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.699-706C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435195 | ||||||
| chr4:177435307
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(25): Show | 94 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.699-818A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435307 | ||||||
| chr4:177435476
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(7): Show | 22 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.698+800A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435476 | ||||||
| chr4:177435506
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0116others(4): Show | 15 | HG00140.hp1 HG01978.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.698+770A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435506 | ||||||
| chr4:177435573
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+703A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435573 | ||||||
| chr4:177435590
|
T | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0157others(10): Show | 24 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.698+686A>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435590 | ||||||
| chr4:177435612
|
C | A | 1 | a0001c0001t0002g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.698+664G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435612 | ||||||
| chr4:177435679
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.698+597G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435679 | ||||||
| chr4:177435693
|
C | A | 1 | a0001c0001t0001g0038 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.698+583G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435693 | ||||||
| chr4:177435747
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.698+529T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435747 | ||||||
| chr4:177435776
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(41): Show | 167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.698+500T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435776 | ||||||
| chr4:177435784
|
G | GCGTGCAC others(31): Show |
1 | a0001c0001t0002g0156 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.698+454_698+491dup others(38): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435784 | ||||||
| chr4:177435851
|
GCA | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0125a0001c0001t0002g0130others(14): Show | 32 | HG00738.hp2 HG01081.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.698+423_698+424del others(2): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435851 | ||||||
| chr4:177435851
|
GCACA | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.698+421_698+424del others(4): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435851 | ||||||
| chr4:177435855
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.698+421T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435855 | ||||||
| chr4:177435856
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0146a0001c0001t0004g0021others(1): Show | 10 | HG00438.hp1 HG00597.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.698+420G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435856 | ||||||
| chr4:177435857
|
A | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(69): Show | 238 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.698+419T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435857 | ||||||
| chr4:177435873
|
A | C | 1 | a0002c0002t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.698+403T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435873 | ||||||
| chr4:177435943
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0006g0052 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.698+317_698+332del others(16): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435943 | ||||||
| chr4:177435990
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.698+286C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177435990 | ||||||
| chr4:177436076
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0155 | 2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.698+200G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177436076 | ||||||
| chr4:177436101
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.698+175T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177436101 | ||||||
| chr4:177436212
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(8): Show | 23 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.698+64G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 6/8 | chr4 | 177436212 | ||||||
| chr4:177436358
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | splice_region_variant&intron_variant | LOW | c.623-7C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436358 | ||||||
| chr4:177436412
|
A | ATAATTG | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(24): Show | 68 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.623-67_623-62dupCA others(4): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436412 | ||||||
| chr4:177436524
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0116others(6): Show | 17 | HG00140.hp1 HG01978.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.623-173C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436524 | ||||||
| chr4:177436613
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.623-262G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436613 | ||||||
| chr4:177436635
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(8): Show | 23 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.623-284C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436635 | ||||||
| chr4:177436659
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0125others(2): Show | 10 | HG01081.hp2 HG02451.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.623-308C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436659 | ||||||
| chr4:177436660
|
C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0125others(2): Show | 10 | HG01081.hp2 HG02451.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.623-309G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436660 | ||||||
| chr4:177436782
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(8): Show | 23 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.623-431T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436782 | ||||||
| chr4:177436797
|
CATT | C | 2 | a0001c0001t0001g0025a0001c0001t0002g0047 | 6 | HG02055.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-449_623-447del others(3): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177436797 | ||||||
| chr4:177437107
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.622+298A>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177437107 | ||||||
| chr4:177437152
|
TG | T | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+252delC | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177437152 | ||||||
| chr4:177437385
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.622+20G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 5/8 | chr4 | 177437385 | ||||||
| chr4:177437712
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(8): Show | 23 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.508-193G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177437712 | ||||||
| chr4:177437869
|
A | C | 1 | a0001c0001t0008g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.508-350T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177437869 | ||||||
| chr4:177437915
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0002g0056 | 3 | HG01256.hp1 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.508-396G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177437915 | ||||||
| chr4:177437918
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.508-399T>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177437918 | ||||||
| chr4:177437974
|
A | C | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-455T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177437974 | ||||||
| chr4:177438075
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.508-556T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438075 | ||||||
| chr4:177438120
|
G | A | 1 | a0002c0002t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508-601C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438120 | ||||||
| chr4:177438390
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0002g0037 | 4 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+355G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438390 | ||||||
| chr4:177438492
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.507+253G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438492 | ||||||
| chr4:177438513
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0101 | 3 | HG02630.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.507+232C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438513 | ||||||
| chr4:177438525
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(23): Show | 67 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.507+220A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438525 | ||||||
| chr4:177438564
|
C | T | 1 | a0005c0006t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.507+181G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438564 | ||||||
| chr4:177438565
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(67): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.507+180T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 4/8 | chr4 | 177438565 | ||||||
| chr4:177438932
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.395-75T>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177438932 | ||||||
| chr4:177438991
|
C | T | 13 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0157others(10): Show | 24 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.395-134G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177438991 | ||||||
| chr4:177439012
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-155G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439012 | ||||||
| chr4:177439042
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.395-185A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439042 | ||||||
| chr4:177439070
|
T | C | 1 | a0001c0001t0002g0145 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.395-213A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439070 | ||||||
| chr4:177439111
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0002g0084 | 5 | HG00735.hp2 HG02074.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-254C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439111 | ||||||
| chr4:177439157
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.395-300A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439157 | ||||||
| chr4:177439291
|
G | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0116others(6): Show | 17 | HG00140.hp1 HG01978.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+285C>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439291 | ||||||
| chr4:177439322
|
C | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.394+254G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439322 | ||||||
| chr4:177439396
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(28): Show | 97 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.394+180G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439396 | ||||||
| chr4:177439441
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.394+135A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439441 | ||||||
| chr4:177439523
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.394+53A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 3/8 | chr4 | 177439523 | ||||||
| chr4:177439741
|
G | C | 1 | a0001c0001t0002g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.282-53C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439741 | ||||||
| chr4:177439759
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.282-71A>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439759 | ||||||
| chr4:177439845
|
C | G | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-157G>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439845 | ||||||
| chr4:177439863
|
GA | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.282-176delT | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439863 | ||||||
| chr4:177439897
|
C | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0020others(36): Show | 111 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.282-209G>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439897 | ||||||
| chr4:177439945
|
T | C | 1 | a0001c0001t0001g0061 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.282-257A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177439945 | ||||||
| chr4:177440008
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(64): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.281+265A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440008 | ||||||
| chr4:177440013
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.281+260C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440013 | ||||||
| chr4:177440165
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.281+108C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440165 | ||||||
| chr4:177440219
|
C | T | 1 | a0001c0001t0002g0010 | 8 | NA18939.hp2 NA18947.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.281+54G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440219 | ||||||
| chr4:177440242
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.281+31T>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440242 | ||||||
| chr4:177440260
|
A | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(23): Show | 67 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.281+13T>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 2/8 | chr4 | 177440260 | ||||||
| chr4:177440467
|
T | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(84): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.128-41A>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440467 | ||||||
| chr4:177440651
|
G | GTT | 10 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0157others(7): Show | 20 | HG01175.hp1 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.128-227_128-226dup others(2): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440651 | ||||||
| chr4:177440651
|
GT | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 12 | HG01243.hp2 HG01981.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-226delA | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440651 | ||||||
| chr4:177440654
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.128-228A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440654 | ||||||
| chr4:177440693
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(8): Show | 23 | HG00140.hp1 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-267C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440693 | ||||||
| chr4:177440833
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0020others(39): Show | 118 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.128-407A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440833 | ||||||
| chr4:177440902
|
C | T | 1 | a0002c0002t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128-476G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440902 | ||||||
| chr4:177440968
|
C | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(29): Show | 98 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.128-542G>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440968 | ||||||
| chr4:177440998
|
G | A | 1 | a0001c0001t0004g0062 | 2 | NA18979.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.128-572C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177440998 | ||||||
| chr4:177441156
|
A | ACACTTCA others(5): Show |
82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.128-731_128-730ins others(12): Show |
AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441156 | ||||||
| chr4:177441413
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+836A>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441413 | ||||||
| chr4:177441419
|
T | C | 1 | a0001c0001t0001g0046 | 2 | NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.127+830A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441419 | ||||||
| chr4:177441429
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127+820A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441429 | ||||||
| chr4:177441469
|
G | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 19 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.127+780C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441469 | ||||||
| chr4:177441512
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.127+737C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441512 | ||||||
| chr4:177441541
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.127+708C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441541 | ||||||
| chr4:177441561
|
C | G | 2 | a0001c0001t0001g0025a0001c0001t0002g0047 | 6 | HG02055.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+688G>C | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441561 | ||||||
| chr4:177441857
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 19 | HG00280.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.127+392A>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441857 | ||||||
| chr4:177441914
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+335C>G | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441914 | ||||||
| chr4:177441920
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0004g0067 | 7 | HG00609.hp2 HG02015.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+329G>A | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441920 | ||||||
| chr4:177441974
|
T | A | 1 | a0002c0002t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+275A>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177441974 | ||||||
| chr4:177442046
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0005g0033 | 4 | HG01255.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+203C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177442046 | ||||||
| chr4:177442224
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.127+25C>T | AGA | ENSG00000038002.9 | transcript | ENST00000264595.7 | protein_coding | 1/8 | chr4 | 177442224 |