geneid | 23787 |
---|---|
ensemblid | ENSG00000137409.21 |
hgncid | 17586 |
symbol | MTCH1 |
name | mitochondrial carrier 1 |
refseq_nuc | NM_001271641.2 |
refseq_prot | NP_001258570.1 |
ensembl_nuc | ENST00000373627.10 |
ensembl_prot | ENSP00000362730.5 |
mane_status | MANE Select |
chr | chr6 |
start | 36968141 |
end | 36986196 |
strand | - |
ver | v1.2 |
region | chr6:36968141-36986196 |
region5000 | chr6:36963141-36991196 |
regionname0 | MTCH1_chr6_36968141_36986196 |
regionname5000 | MTCH1_chr6_36963141_36991196 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 389 | 394 | 94 | 71 | 175 | 13 | 39 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0002 | 0/0 | 91 | 16 | 1 | 0 | 13 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0003 | 0/0 | 389 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0004 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0005 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1170 | 329 | 77 | 68 | 140 | 10 | 32 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0002 | 0/0 | 1170 | 30 | 14 | 3 | 5 | 3 | 5 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0003 | 0/0 | 1170 | 29 | 0 | 0 | 27 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0004 | 0/0 | 1169 | 14 | 1 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0005 | 0/0 | 1170 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0006 | 0/0 | 1170 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0007 | 0/0 | 1170 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0008 | 0/0 | 1169 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0009 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
c0011 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | 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 | 786 | 370 | 72 | 61 | 187 | 9 | 40 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0002 | 0/0 | 786 | 25 | 21 | 4 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0003 | 0/0 | 786 | 8 | 2 | 2 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0004 | 0/1 | 786 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0005 | 0/0 | 786 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0006 | 0/0 | 786 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0007 | 0/0 | 786 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0008 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
t0009 | 0/0 | 786 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | 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 | 31 | 1 | 1 | 28 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0002 | 1/0 | 20 | 0 | 5 | 7 | 0 | 7 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0003 | 0/0 | 16 | 3 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0004 | 0/0 | 15 | 1 | 11 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0005 | 0/0 | 14 | 0 | 1 | 11 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0006 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0007 | 0/0 | 9 | 0 | 3 | 2 | 0 | 4 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0009 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0011 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0012 | 0/1 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0015 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0016 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0018 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0019 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0020 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0023 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0024 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0028 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0029 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0031 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0032 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0035 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0037 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0038 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0039 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/1 | 329 | 77 | 68 | 140 | 10 | 32 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 30 | 14 | 3 | 5 | 3 | 5 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 29 | 0 | 0 | 27 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0009 | a0001 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0002c0004 | a0002 | c0004 | 0/0 | 14 | 1 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0002c0008 | a0002 | c0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0003c0007 | a0003 | c0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0004c0010 | a0004 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0005c0011 | a0005 | c0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | 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 | 1/0 | 301 | 63 | 59 | 139 | 8 | 31 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 17 | 13 | 4 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/1 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 18 | 8 | 1 | 5 | 0 | 4 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 8 | 2 | 2 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 29 | 0 | 0 | 27 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0005t0002 | a0001 | c0005 | t0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 14 | 1 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0002c0008t0001 | a0002 | c0008 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0004c0010t0002 | a0004 | c0010 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
a0005c0011t0001 | a0005 | c0011 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 31 | 1 | 1 | 28 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 1/0 | 20 | 0 | 5 | 7 | 0 | 7 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 16 | 3 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 15 | 1 | 11 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 14 | 0 | 1 | 11 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 9 | 0 | 3 | 2 | 0 | 4 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0061 | a0001 | c0001 | t0002 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0004g0012 | a0001 | c0001 | t0004 | g0012 | 0/1 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0005g0116 | a0001 | c0001 | t0005 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0006g0120 | a0001 | c0001 | t0006 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0007g0060 | a0001 | c0001 | t0007 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0008g0095 | a0001 | c0001 | t0008 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0001t0009g0184 | a0001 | c0001 | t0009 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0018 | a0001 | c0002 | t0001 | g0018 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0042 | a0001 | c0002 | t0001 | g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0099 | a0001 | c0002 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0100 | a0001 | c0002 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0126 | a0001 | c0002 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0131 | a0001 | c0002 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0132 | a0001 | c0002 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0133 | a0001 | c0002 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0140 | a0001 | c0002 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0161 | a0001 | c0002 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0163 | a0001 | c0002 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0001g0174 | a0001 | c0002 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0002g0038 | a0001 | c0002 | t0002 | g0038 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0002g0159 | a0001 | c0002 | t0002 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0003g0016 | a0001 | c0002 | t0003 | g0016 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0003g0080 | a0001 | c0002 | t0003 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0003g0084 | a0001 | c0002 | t0003 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0002t0003g0093 | a0001 | c0002 | t0003 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0006 | a0001 | c0003 | t0001 | g0006 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0021 | a0001 | c0003 | t0001 | g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0022 | a0001 | c0003 | t0001 | g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0036 | a0001 | c0003 | t0001 | g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0109 | a0001 | c0003 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0115 | a0001 | c0003 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0121 | a0001 | c0003 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0123 | a0001 | c0003 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0124 | a0001 | c0003 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0130 | a0001 | c0003 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0003t0001g0155 | a0001 | c0003 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0005t0002g0041 | a0001 | c0005 | t0002 | g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0005t0002g0056 | a0001 | c0005 | t0002 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0006t0001g0040 | a0001 | c0006 | t0001 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0001c0009t0001g0055 | a0001 | c0009 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0004t0001g0008 | a0002 | c0004 | t0001 | g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0004t0001g0039 | a0002 | c0004 | t0001 | g0039 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0004t0001g0180 | a0002 | c0004 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0004t0001g0182 | a0002 | c0004 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0008t0001g0181 | a0002 | c0008 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0002c0008t0001g0183 | a0002 | c0008 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0003c0007t0001g0177 | a0003 | c0007 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0003c0007t0001g0178 | a0003 | c0007 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0004c0010t0002g0176 | a0004 | c0010 | t0002 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 |
a0005c0011t0001g0179 | a0005 | c0011 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | GBR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | FIN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00597 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00597 | hp2 | a0001 | c0009 | t0001 | g0055 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00609 | hp1 | a0001 | c0006 | t0001 | g0040 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0060 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01168 | hp2 | a0001 | c0001 | t0009 | g0184 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0080 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01517 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02258 | hp2 | a0001 | c0005 | t0002 | g0041 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02280 | hp1 | a0004 | c0010 | t0002 | g0176 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02572 | hp1 | a0001 | c0005 | t0002 | g0056 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02723 | hp2 | a0001 | c0005 | t0002 | g0041 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0084 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0120 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0109 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04115 | hp1 | a0002 | c0008 | t0001 | g0181 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0132 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18747 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18939 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18941 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18946 | hp2 | a0002 | c0004 | t0001 | g0182 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18947 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18963 | hp1 | a0001 | c0006 | t0001 | g0040 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0039 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18979 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0039 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18997 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19054 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19066 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19076 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19088 | hp1 | a0002 | c0004 | t0001 | g0039 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ASW | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20805 | hp1 | a0003 | c0007 | t0001 | g0177 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20905 | hp1 | a0005 | c0011 | t0001 | g0179 | SAS | GIH | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20905 | hp2 | a0002 | c0008 | t0001 | g0183 | SAS | GIH | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01123 | hp1 | a0003 | c0007 | t0001 | g0178 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0180 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0093 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0012 | REF | REF | MTCH1_chr6_36963141_36991196 | MTCH1 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | MTCH1_chr6_36963141_36991196 | MTCH1 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36986004
|
G | A | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.170C>T | p.Ala57Val | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 193/1955 | 170/1170 | 57/389 | chr6 | 36986004 | ||
chr6:36986127
|
G | A | 1 | a0003 | 2 | HG01123.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.47C>T | p.Ala16Val | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 70/1955 | 47/1170 | 16/389 | chr6 | 36986127 | ||
chr6:36986128
|
C | A | 1 | a0005 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.46G>T | p.Ala16Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 69/1955 | 46/1170 | 16/389 | chr6 | 36986128 | ||
chr6:36986143
|
AG | A | 1 | a0002 | 16 | HG00597.hp1 HG04115.hp1 NA18747.hp2 others(13): Show |
frameshift_variant | HIGH | c.30delC | p.Trp11fs | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 53/1955 | 30/1170 | 10/389 | chr6 | 36986143 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968921
|
T | C | 1 | a0001c0002 | 30 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(27): Show |
synonymous_variant | LOW | c.1152A>G | p.Ser384Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 1175/1955 | 1152/1170 | 384/389 | chr6 | 36968921 | ||
chr6:36970656
|
G | A | 3 | a0001c0003a0001c0009a0002c0008 | 32 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(29): Show |
synonymous_variant | LOW | c.945C>T | p.Phe315Phe | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 9/12 | 968/1955 | 945/1170 | 315/389 | chr6 | 36970656 | ||
chr6:36986087
|
G | T | 1 | a0001c0005 | 3 | HG02258.hp2 HG02572.hp1 HG02723.hp2 |
synonymous_variant | LOW | c.87C>A | p.Arg29Arg | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 110/1955 | 87/1170 | 29/389 | chr6 | 36986087 | ||
chr6:36986162
|
C | T | 2 | a0001c0006a0001c0009 | 3 | HG00597.hp2 HG00609.hp1 NA18963.hp1 |
synonymous_variant | LOW | c.12G>A | p.Ser4Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 35/1955 | 12/1170 | 4/389 | chr6 | 36986162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968435
|
C | T | 1 | a0001c0001t0007 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 468 | chr6 | 36968435 | |||||
chr6:36968676
|
C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 227 | chr6 | 36968676 | |||||
chr6:36968707
|
C | T | 1 | a0001c0002t0003 | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*196G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 196 | chr6 | 36968707 | |||||
chr6:36968740
|
A | C | 1 | a0001c0001t0006 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 163 | chr6 | 36968740 | |||||
chr6:36968803
|
C | T | 1 | a0001c0001t0005 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 100 | chr6 | 36968803 | |||||
chr6:36968830
|
T | C | 5 | a0001c0001t0002a0001c0001t0008a0001c0002t0002others(2): Show | 26 | HG00733.hp2 HG00741.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*73A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 73 | chr6 | 36968830 | |||||
chr6:36968864
|
G | A | 1 | a0001c0001t0004 | 6 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 39 | chr6 | 36968864 | |||||
chr6:36986189
|
G | C | 1 | a0001c0001t0009 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 16 | chr6 | 36986189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968995
|
A | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(44): Show | 93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1099-21T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36968995 | ||||||
chr6:36969089
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0089 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1099-115C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969089 | ||||||
chr6:36969181
|
T | C | 1 | a0002c0004t0001g0182 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1099-207A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969181 | ||||||
chr6:36969282
|
G | A | 5 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-308C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969282 | ||||||
chr6:36969310
|
T | G | 4 | a0001c0002t0003g0016a0001c0002t0003g0080a0001c0002t0003g0084others(1): Show | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-336A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969310 | ||||||
chr6:36969320
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1099-346A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969320 | ||||||
chr6:36969352
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1099-378A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969352 | ||||||
chr6:36969480
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1099-506G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969480 | ||||||
chr6:36969505
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0102 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1099-531G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969505 | ||||||
chr6:36969506
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-532C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969506 | ||||||
chr6:36969585
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1098+454T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969585 | ||||||
chr6:36969658
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1098+381G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969658 | ||||||
chr6:36969864
|
C | T | 4 | a0001c0002t0003g0016a0001c0002t0003g0080a0001c0002t0003g0084others(1): Show | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+175G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969864 | ||||||
chr6:36969871
|
T | C | 1 | a0001c0001t0001g0014 | 6 | HG00639.hp1 HG01070.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+168A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969871 | ||||||
chr6:36969899
|
T | C | 2 | a0001c0001t0002g0065a0001c0001t0002g0089 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1098+140A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969899 | ||||||
chr6:36969906
|
C | G | 4 | a0001c0002t0003g0016a0001c0002t0003g0080a0001c0002t0003g0084others(1): Show | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+133G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969906 | ||||||
chr6:36969993
|
T | C | 2 | a0001c0002t0002g0038a0001c0002t0002g0159 | 4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+46A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969993 | ||||||
chr6:36970021
|
C | T | 1 | a0001c0001t0001g0030 | 3 | HG02809.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1098+18G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36970021 | ||||||
chr6:36970022
|
G | A | 13 | a0001c0002t0001g0018a0001c0002t0001g0042a0001c0002t0001g0063others(10): Show | 18 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+17C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36970022 | ||||||
chr6:36970168
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1023-54C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970168 | ||||||
chr6:36970248
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1023-134C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970248 | ||||||
chr6:36970272
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1022+134T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970272 | ||||||
chr6:36970375
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0027 | 8 | NA18957.hp1 NA18983.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+31A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970375 | ||||||
chr6:36970731
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.907-37G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970731 | ||||||
chr6:36970853
|
G | C | 1 | a0001c0003t0001g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.907-159C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970853 | ||||||
chr6:36970975
|
C | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0157 | 3 | HG02258.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.907-281G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970975 | ||||||
chr6:36970991
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.907-297G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970991 | ||||||
chr6:36971102
|
C | T | 1 | a0003c0007t0001g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.907-408G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971102 | ||||||
chr6:36971123
|
T | G | 9 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.907-429A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971123 | ||||||
chr6:36971192
|
C | G | 4 | a0001c0002t0003g0016a0001c0002t0003g0080a0001c0002t0003g0084others(1): Show | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-498G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971192 | ||||||
chr6:36971275
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-581C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971275 | ||||||
chr6:36971430
|
C | T | 2 | a0001c0001t0002g0061a0001c0002t0001g0174 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.907-736G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971430 | ||||||
chr6:36971437
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(47): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.907-743G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971437 | ||||||
chr6:36971466
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.907-772T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971466 | ||||||
chr6:36971503
|
C | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(23): Show | 55 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.907-809G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971503 | ||||||
chr6:36971506
|
G | A | 2 | a0001c0002t0003g0080a0001c0002t0003g0084 | 2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.907-812C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971506 | ||||||
chr6:36971587
|
C | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(31): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.907-893G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971587 | ||||||
chr6:36971587
|
C | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(47): Show | 91 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.907-893G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971587 | ||||||
chr6:36971606
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.907-912G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971606 | ||||||
chr6:36971752
|
C | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(44): Show | 88 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.906+900G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971752 | ||||||
chr6:36971947
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.906+705A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971947 | ||||||
chr6:36972041
|
G | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0030others(11): Show | 27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.906+611C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972041 | ||||||
chr6:36972361
|
C | T | 1 | a0001c0001t0004g0012 | 6 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+291G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972361 | ||||||
chr6:36972425
|
C | CT | 52 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(49): Show | 93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.906+226_906+227ins others(1): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972425 | ||||||
chr6:36972430
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0062 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906+222T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972430 | ||||||
chr6:36972483
|
C | T | 1 | a0001c0002t0003g0016 | 5 | HG01433.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+169G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972483 | ||||||
chr6:36972484
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.906+168C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972484 | ||||||
chr6:36972497
|
G | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(42): Show | 82 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.906+155C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972497 | ||||||
chr6:36972567
|
G | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(49): Show | 93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.906+85C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972567 | ||||||
chr6:36972619
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906+33G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972619 | ||||||
chr6:36972959
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-163G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972959 | ||||||
chr6:36972973
|
C | G | 1 | a0001c0009t0001g0055 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.762-177G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972973 | ||||||
chr6:36972995
|
T | A | 2 | a0001c0002t0002g0038a0001c0002t0002g0159 | 4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.762-199A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972995 | ||||||
chr6:36973001
|
G | C | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.762-205C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973001 | ||||||
chr6:36973009
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.762-213C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973009 | ||||||
chr6:36973029
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(90): Show | 162 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(159): Show |
intron_variant | MODIFIER | c.762-233A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973029 | ||||||
chr6:36973302
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.762-506G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973302 | ||||||
chr6:36973319
|
A | C | 1 | a0001c0001t0002g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.762-523T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973319 | ||||||
chr6:36973335
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.762-539C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973335 | ||||||
chr6:36973360
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.762-564T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973360 | ||||||
chr6:36973486
|
T | A | 5 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.762-690A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973486 | ||||||
chr6:36973486
|
T | TA | 12 | a0001c0002t0001g0018a0001c0002t0001g0042a0001c0002t0001g0063others(9): Show | 17 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.762-691dupT | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973486 | ||||||
chr6:36973660
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.762-864A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973660 | ||||||
chr6:36973791
|
G | T | 1 | a0001c0001t0001g0026 | 3 | HG02735.hp1 HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.762-995C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973791 | ||||||
chr6:36973836
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-1040C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973836 | ||||||
chr6:36973847
|
C | T | 1 | a0001c0001t0001g0052 | 2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.762-1051G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973847 | ||||||
chr6:36974040
|
C | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(24): Show | 56 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.762-1244G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974040 | ||||||
chr6:36974086
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.762-1290G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974086 | ||||||
chr6:36974156
|
A | G | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.762-1360T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974156 | ||||||
chr6:36974168
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.762-1372G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974168 | ||||||
chr6:36974275
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0134 | 3 | HG02486.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.761+1383T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974275 | ||||||
chr6:36974325
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.761+1333G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974325 | ||||||
chr6:36974342
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0102 | 3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.761+1316T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974342 | ||||||
chr6:36974456
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1202A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974456 | ||||||
chr6:36974489
|
T | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(38): Show | 74 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.761+1169A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974489 | ||||||
chr6:36974498
|
C | G | 41 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(38): Show | 74 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.761+1160G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974498 | ||||||
chr6:36974534
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0166 | 3 | NA18946.hp1 NA18989.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.761+1124G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974534 | ||||||
chr6:36974641
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1017C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974641 | ||||||
chr6:36974688
|
A | G | 2 | a0001c0005t0002g0041a0001c0005t0002g0056 | 3 | HG02258.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.761+970T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974688 | ||||||
chr6:36974696
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.761+962A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974696 | ||||||
chr6:36974705
|
A | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+953T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974705 | ||||||
chr6:36974706
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.761+952A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974706 | ||||||
chr6:36974707
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0170a0001c0001t0001g0172others(3): Show | 9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+951T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974707 | ||||||
chr6:36974887
|
T | TGTATGTC others(10): Show |
1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.761+770_761+771ins others(17): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974887 | ||||||
chr6:36974888
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.761+770T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974888 | ||||||
chr6:36974970
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+688G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974970 | ||||||
chr6:36975101
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0151 | 10 | NA18964.hp2 NA18981.hp1 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.761+557A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975101 | ||||||
chr6:36975152
|
A | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+506T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975152 | ||||||
chr6:36975157
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.761+501G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975157 | ||||||
chr6:36975203
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+455A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975203 | ||||||
chr6:36975240
|
A | G | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0030others(11): Show | 27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.761+418T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975240 | ||||||
chr6:36975348
|
C | G | 1 | a0001c0001t0002g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.761+310G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975348 | ||||||
chr6:36975563
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.761+95C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975563 | ||||||
chr6:36975737
|
G | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-20C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975737 | ||||||
chr6:36975746
|
G | A | 1 | a0001c0001t0001g0049 | 2 | HG01192.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.702-29C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975746 | ||||||
chr6:36975755
|
G | A | 4 | a0001c0002t0003g0016a0001c0002t0003g0080a0001c0002t0003g0084others(1): Show | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.702-38C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975755 | ||||||
chr6:36975778
|
T | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0030others(11): Show | 27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.702-61A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975778 | ||||||
chr6:36975797
|
A | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-80T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975797 | ||||||
chr6:36975799
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0002t0003g0016others(3): Show | 15 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.702-82G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975799 | ||||||
chr6:36975829
|
A | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-112T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975829 | ||||||
chr6:36975915
|
T | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-198A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975915 | ||||||
chr6:36976011
|
A | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-294T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976011 | ||||||
chr6:36976035
|
G | A | 5 | a0001c0002t0001g0042a0001c0002t0001g0063a0001c0002t0001g0100others(2): Show | 6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-318C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976035 | ||||||
chr6:36976052
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.702-335G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976052 | ||||||
chr6:36976135
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-418C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976135 | ||||||
chr6:36976147
|
G | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(45): Show | 85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-430C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976147 | ||||||
chr6:36976180
|
AC | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0170a0001c0001t0001g0172others(3): Show | 9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-464delG | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976180 | ||||||
chr6:36976365
|
C | A | 1 | a0001c0001t0008g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-648G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976365 | ||||||
chr6:36976462
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0102 | 3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.701+737A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976462 | ||||||
chr6:36976703
|
T | C | 32 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0051others(29): Show | 52 | HG01069.hp2 HG01257.hp1 HG01258.hp2 others(49): Show |
intron_variant | MODIFIER | c.701+496A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976703 | ||||||
chr6:36976719
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.701+480T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976719 | ||||||
chr6:36976778
|
C | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(24): Show | 56 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.701+421G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976778 | ||||||
chr6:36976825
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+374G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976825 | ||||||
chr6:36976852
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.701+347G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976852 | ||||||
chr6:36977115
|
G | A | 2 | a0001c0002t0003g0080a0001c0002t0003g0084 | 2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.701+84C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36977115 | ||||||
chr6:36977126
|
T | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0083others(18): Show | 29 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.701+73A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36977126 | ||||||
chr6:36977257
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18979.hp2 | splice_region_variant&intron_variant | LOW | c.650-7T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977257 | ||||||
chr6:36977286
|
G | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(21): Show | 47 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.650-36C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977286 | ||||||
chr6:36977360
|
C | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-110G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977360 | ||||||
chr6:36977402
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG00438.hp2 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-152G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977402 | ||||||
chr6:36977506
|
C | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(21): Show | 47 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.649+128G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977506 | ||||||
chr6:36977583
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.649+51G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977583 | ||||||
chr6:36977617
|
G | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.649+17C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977617 | ||||||
chr6:36977622
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.649+12C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977622 | ||||||
chr6:36977761
|
T | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0134a0001c0002t0003g0016others(3): Show | 11 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-70A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977761 | ||||||
chr6:36977804
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.592-113A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977804 | ||||||
chr6:36977872
|
C | T | 1 | a0001c0002t0001g0042 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.592-181G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977872 | ||||||
chr6:36977970
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+108T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977970 | ||||||
chr6:36977978
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+100T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977978 | ||||||
chr6:36978005
|
C | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+73G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36978005 | ||||||
chr6:36978162
|
C | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.514-7G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978162 | ||||||
chr6:36978162
|
CAG | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0164 | 7 | HG00735.hp1 HG01358.hp2 HG01433.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.514-9_514-8delCT | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978162 | ||||||
chr6:36978169
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.514-14C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978169 | ||||||
chr6:36978213
|
G | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-58C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978213 | ||||||
chr6:36978310
|
G | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-155C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978310 | ||||||
chr6:36978665
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.407-54A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978665 | ||||||
chr6:36978682
|
C | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 16 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-71G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978682 | ||||||
chr6:36978694
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.407-83G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978694 | ||||||
chr6:36978735
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-124C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978735 | ||||||
chr6:36978829
|
G | A | 1 | a0002c0004t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.407-218C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978829 | ||||||
chr6:36978872
|
C | T | 5 | a0001c0002t0001g0042a0001c0002t0001g0063a0001c0002t0001g0100others(2): Show | 6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-261G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978872 | ||||||
chr6:36978873
|
TCC | T | 5 | a0001c0002t0001g0042a0001c0002t0001g0063a0001c0002t0001g0100others(2): Show | 6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-264_407-263del others(2): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978873 | ||||||
chr6:36978875
|
C | CT | 15 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0047others(12): Show | 21 | HG02257.hp1 HG02523.hp2 HG02723.hp1 others(18): Show |
intron_variant | MODIFIER | c.407-265dupA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
C | CTTT | 6 | a0001c0001t0001g0024a0001c0001t0001g0170a0001c0001t0001g0172others(3): Show | 9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-267_407-265dup others(3): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
C | CTTTT | 10 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 15 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-268_407-265dup others(4): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
CT | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(40): Show | 87 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.407-265delA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
CTT | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0066a0001c0001t0001g0086others(4): Show | 10 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.407-266_407-265del others(2): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.407-274_407-265del others(10): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36978875
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407-276_407-265del others(12): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | ||||||
chr6:36979041
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-430C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979041 | ||||||
chr6:36979128
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0027 | 8 | NA18957.hp1 NA18983.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-517G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979128 | ||||||
chr6:36979170
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.407-559T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979170 | ||||||
chr6:36979172
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(18): Show | 42 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.407-561G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979172 | ||||||
chr6:36979192
|
A | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.407-581T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979192 | ||||||
chr6:36979194
|
A | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.407-583T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979194 | ||||||
chr6:36979355
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407-744C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979355 | ||||||
chr6:36979482
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.407-871G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979482 | ||||||
chr6:36979502
|
G | A | 1 | a0001c0002t0001g0042 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.407-891C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979502 | ||||||
chr6:36979530
|
T | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.407-919A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979530 | ||||||
chr6:36979610
|
T | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.407-999A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979610 | ||||||
chr6:36979741
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.407-1130C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979741 | ||||||
chr6:36979923
|
C | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0102 | 3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.407-1312G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979923 | ||||||
chr6:36979973
|
T | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0030others(11): Show | 27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-1362A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979973 | ||||||
chr6:36980259
|
A | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(18): Show | 42 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.406+1329T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980259 | ||||||
chr6:36980306
|
T | C | 4 | a0001c0003t0001g0022a0001c0003t0001g0036a0001c0003t0001g0124others(1): Show | 9 | HG02015.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1282A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980306 | ||||||
chr6:36980348
|
A | T | 6 | a0001c0001t0001g0066a0001c0001t0002g0058a0001c0001t0002g0062others(3): Show | 8 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+1240T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980348 | ||||||
chr6:36980386
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.406+1202C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980386 | ||||||
chr6:36980439
|
T | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0134a0001c0002t0003g0016others(3): Show | 11 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.406+1149A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980439 | ||||||
chr6:36980470
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(20): Show | 46 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.406+1118G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980470 | ||||||
chr6:36980532
|
G | C | 12 | a0001c0002t0001g0018a0001c0002t0001g0042a0001c0002t0001g0063others(9): Show | 17 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.406+1056C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980532 | ||||||
chr6:36980583
|
C | T | 4 | a0001c0002t0001g0042a0001c0002t0001g0063a0001c0002t0001g0100others(1): Show | 5 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+1005G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980583 | ||||||
chr6:36980588
|
A | G | 1 | a0001c0002t0001g0140 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.406+1000T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980588 | ||||||
chr6:36980752
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0075others(23): Show | 35 | HG00741.hp2 HG01069.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.406+836T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980752 | ||||||
chr6:36981029
|
A | G | 80 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(77): Show | 145 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(142): Show |
intron_variant | MODIFIER | c.406+559T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981029 | ||||||
chr6:36981060
|
C | G | 1 | a0001c0005t0002g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.406+528G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981060 | ||||||
chr6:36981318
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+270A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981318 | ||||||
chr6:36981341
|
G | T | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.406+247C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981341 | ||||||
chr6:36981419
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.406+169G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981419 | ||||||
chr6:36981502
|
A | G | 5 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+86T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981502 | ||||||
chr6:36981508
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.406+80G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981508 | ||||||
chr6:36981536
|
TG | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0099a0001c0002t0001g0100others(3): Show | 10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+51delC | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981536 | ||||||
chr6:36981751
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(117): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.322-79G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981751 | ||||||
chr6:36981760
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-88G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981760 | ||||||
chr6:36981764
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.322-92T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981764 | ||||||
chr6:36981822
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.322-150G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981822 | ||||||
chr6:36981859
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0102a0001c0001t0001g0127others(5): Show | 15 | HG00733.hp2 HG01243.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-187G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981859 | ||||||
chr6:36982032
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-360G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982032 | ||||||
chr6:36982033
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-361A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982033 | ||||||
chr6:36982034
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-362G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982034 | ||||||
chr6:36982036
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-364A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982036 | ||||||
chr6:36982037
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-365G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982037 | ||||||
chr6:36982038
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-366A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982038 | ||||||
chr6:36982039
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-367G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982039 | ||||||
chr6:36982040
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-368G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982040 | ||||||
chr6:36982042
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-370C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982042 | ||||||
chr6:36982044
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-372A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982044 | ||||||
chr6:36982045
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-373C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982045 | ||||||
chr6:36982052
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-380A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982052 | ||||||
chr6:36982053
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-381A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982053 | ||||||
chr6:36982054
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-382G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982054 | ||||||
chr6:36982056
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-384A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982056 | ||||||
chr6:36982057
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-385A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982057 | ||||||
chr6:36982059
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-387G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982059 | ||||||
chr6:36982063
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-391G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982063 | ||||||
chr6:36982064
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-392A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982064 | ||||||
chr6:36982065
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-393G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982065 | ||||||
chr6:36982068
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-396A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982068 | ||||||
chr6:36982070
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-398G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982070 | ||||||
chr6:36982072
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-400T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982072 | ||||||
chr6:36982073
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-401T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982073 | ||||||
chr6:36982074
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-402T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982074 | ||||||
chr6:36982076
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-404C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982076 | ||||||
chr6:36982078
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-406C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982078 | ||||||
chr6:36982079
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-407C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982079 | ||||||
chr6:36982084
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-412T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982084 | ||||||
chr6:36982085
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-413T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982085 | ||||||
chr6:36982088
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-416T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982088 | ||||||
chr6:36982089
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-417T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982089 | ||||||
chr6:36982093
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-421G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982093 | ||||||
chr6:36982104
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-432T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982104 | ||||||
chr6:36982106
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-434G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982106 | ||||||
chr6:36982107
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-435G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982107 | ||||||
chr6:36982109
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-437G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982109 | ||||||
chr6:36982111
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-439C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982111 | ||||||
chr6:36982114
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-442T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982114 | ||||||
chr6:36982116
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-444C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982116 | ||||||
chr6:36982117
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-445A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982117 | ||||||
chr6:36982118
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-446G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982118 | ||||||
chr6:36982120
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-448C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982120 | ||||||
chr6:36982122
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-450G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982122 | ||||||
chr6:36982125
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-453A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982125 | ||||||
chr6:36982126
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-454T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982126 | ||||||
chr6:36982128
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-456C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982128 | ||||||
chr6:36982129
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-457A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982129 | ||||||
chr6:36982130
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-458G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982130 | ||||||
chr6:36982131
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.322-459T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982131 | ||||||
chr6:36982132
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-460A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982132 | ||||||
chr6:36982133
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-461G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982133 | ||||||
chr6:36982139
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-467G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982139 | ||||||
chr6:36982231
|
CT | C | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(33): Show | 85 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.322-560delA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982231 | ||||||
chr6:36982285
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.322-613T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982285 | ||||||
chr6:36982384
|
A | AT | 6 | a0001c0001t0001g0083a0001c0002t0001g0018a0001c0002t0001g0099others(3): Show | 10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-713dupA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982384 | ||||||
chr6:36982384
|
A | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 17 | HG00733.hp2 HG01243.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.322-712T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982384 | ||||||
chr6:36982387
|
T | TA | 3 | a0001c0002t0001g0100a0001c0002t0001g0131a0001c0002t0001g0132 | 3 | HG02970.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-716_322-715ins others(1): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982387 | ||||||
chr6:36982388
|
T | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(34): Show | 80 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.322-716A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982388 | ||||||
chr6:36982391
|
T | A | 1 | a0001c0002t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.322-719A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982391 | ||||||
chr6:36982439
|
C | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 11 | HG01255.hp2 HG01261.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.322-767G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982439 | ||||||
chr6:36982548
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.322-876G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982548 | ||||||
chr6:36982636
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(9): Show | 43 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.322-964C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982636 | ||||||
chr6:36982709
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322-1037G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982709 | ||||||
chr6:36982710
|
G | A | 2 | a0001c0001t0001g0175a0001c0002t0001g0174 | 2 | HG02922.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.322-1038C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982710 | ||||||
chr6:36982733
|
T | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0002g0009others(1): Show | 10 | HG00733.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-1061A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982733 | ||||||
chr6:36982838
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(11): Show | 31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.322-1166A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982838 | ||||||
chr6:36982843
|
C | T | 1 | a0001c0001t0001g0044 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.322-1171G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982843 | ||||||
chr6:36983003
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0170a0005c0011t0001g0179 | 6 | HG01069.hp2 HG01496.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-1331C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983003 | ||||||
chr6:36983010
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.322-1338C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983010 | ||||||
chr6:36983113
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.322-1441A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983113 | ||||||
chr6:36983157
|
T | C | 1 | a0001c0001t0001g0037 | 3 | HG03130.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.322-1485A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983157 | ||||||
chr6:36983208
|
A | G | 1 | a0002c0004t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.322-1536T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983208 | ||||||
chr6:36983229
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.322-1557G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983229 | ||||||
chr6:36983285
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(11): Show | 31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.322-1613C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983285 | ||||||
chr6:36983356
|
T | C | 1 | a0001c0003t0001g0130 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.322-1684A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983356 | ||||||
chr6:36983389
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322-1717A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983389 | ||||||
chr6:36983434
|
T | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(12): Show | 32 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.322-1762A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983434 | ||||||
chr6:36983578
|
G | A | 1 | a0001c0001t0008g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.322-1906C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983578 | ||||||
chr6:36983610
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0002g0065 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322-1938T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983610 | ||||||
chr6:36983696
|
C | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0099a0001c0002t0001g0100others(3): Show | 10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-2024G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983696 | ||||||
chr6:36983720
|
T | C | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-2048A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983720 | ||||||
chr6:36983749
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.322-2077C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983749 | ||||||
chr6:36983931
|
A | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(11): Show | 31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1922T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983931 | ||||||
chr6:36984056
|
A | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(11): Show | 31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1797T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984056 | ||||||
chr6:36984060
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.321+1793T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984060 | ||||||
chr6:36984089
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0025others(11): Show | 34 | HG00673.hp1 HG00738.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.321+1764G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984089 | ||||||
chr6:36984133
|
T | G | 1 | a0001c0002t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.321+1720A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984133 | ||||||
chr6:36984177
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.321+1676G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984177 | ||||||
chr6:36984206
|
G | GTCCCACC others(3): Show |
105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.321+1646_321+1647i others(12): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984206 | ||||||
chr6:36984216
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(11): Show | 31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1637G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984216 | ||||||
chr6:36984450
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0019others(36): Show | 106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.321+1403C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984450 | ||||||
chr6:36984518
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+1335C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984518 | ||||||
chr6:36984566
|
A | G | 1 | a0001c0001t0004g0012 | 6 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+1287T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984566 | ||||||
chr6:36984592
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0154a0001c0001t0001g0156others(1): Show | 8 | HG00673.hp2 HG02004.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.321+1261A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984592 | ||||||
chr6:36984643
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1210G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984643 | ||||||
chr6:36984693
|
C | T | 3 | a0001c0001t0001g0064a0001c0002t0001g0042a0001c0002t0001g0063 | 4 | HG02615.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1160G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984693 | ||||||
chr6:36984754
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.321+1099G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984754 | ||||||
chr6:36985026
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+827A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985026 | ||||||
chr6:36985255
|
C | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 6 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+598G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985255 | ||||||
chr6:36985260
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 5 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+593C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985260 | ||||||
chr6:36985363
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.321+490A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985363 | ||||||
chr6:36985454
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+399G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985454 | ||||||
chr6:36985491
|
A | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0059a0001c0001t0002g0058others(4): Show | 14 | HG00099.hp1 HG00738.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+362T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985491 | ||||||
chr6:36985566
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+287G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985566 | ||||||
chr6:36985615
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0024others(12): Show | 32 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.321+238C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985615 | ||||||
chr6:36985651
|
T | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 6 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+202A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985651 | ||||||
chr6:36985685
|
C | A | 2 | a0001c0001t0001g0175a0001c0002t0001g0174 | 2 | HG02922.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.321+168G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985685 | ||||||
chr6:36985807
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0057 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+46G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985807 |