geneid | 23531 |
---|---|
ensemblid | ENSG00000108960.9 |
hgncid | 7153 |
symbol | MMD |
name | monocyte to macrophage differentiation associated |
refseq_nuc | NM_012329.3 |
refseq_prot | NP_036461.2 |
ensembl_nuc | ENST00000262065.8 |
ensembl_prot | ENSP00000262065.3 |
mane_status | MANE Select |
chr | chr17 |
start | 55392622 |
end | 55421835 |
strand | - |
ver | v1.2 |
region | chr17:55392622-55421835 |
region5000 | chr17:55387622-55426835 |
regionname0 | MMD_chr17_55392622_55421835 |
regionname5000 | MMD_chr17_55387622_55426835 |
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 | 238 | 408 | 94 | 70 | 178 | 16 | 48 | MMD_chr17_55387622_55426835 | MMD | 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 | 717 | 393 | 81 | 69 | 178 | 16 | 47 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
c0002 | 0/0 | 717 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
c0003 | 0/0 | 717 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
c0004 | 0/0 | 717 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | 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 | 1853 | 143 | 39 | 16 | 73 | 1 | 13 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0002 | 0/1 | 1852 | 63 | 3 | 27 | 19 | 4 | 9 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0003 | 0/0 | 1852 | 62 | 4 | 13 | 25 | 8 | 12 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0004 | 0/0 | 1851 | 53 | 0 | 2 | 42 | 0 | 9 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0005 | 0/0 | 1852 | 12 | 0 | 7 | 0 | 3 | 2 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0006 | 0/0 | 1853 | 11 | 0 | 0 | 10 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0007 | 0/0 | 1852 | 11 | 11 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0008 | 0/0 | 1853 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0009 | 0/0 | 1852 | 10 | 9 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0010 | 0/0 | 1851 | 7 | 6 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0011 | 0/0 | 1852 | 7 | 0 | 0 | 7 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0012 | 0/0 | 1851 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0013 | 0/0 | 1852 | 3 | 2 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0014 | 0/0 | 1853 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0015 | 0/0 | 1853 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0016 | 0/0 | 1853 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0017 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0018 | 0/0 | 1852 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0019 | 0/0 | 1852 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0020 | 0/0 | 1852 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0021 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0022 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0023 | 0/0 | 1851 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
t0024 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | 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 | 32 | 0 | 6 | 24 | 1 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0002 | 0/0 | 16 | 0 | 0 | 7 | 4 | 5 | MMD_chr17_55387622_55426835 | MMD |
g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0004 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD |
g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0012 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0015 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0024 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MMD_chr17_55387622_55426835 | MMD |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0051 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
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 | 393 | 81 | 69 | 178 | 16 | 47 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0004 | a0001 | c0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | 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 | 142 | 39 | 16 | 73 | 1 | 12 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/1 | 63 | 3 | 27 | 19 | 4 | 9 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 62 | 4 | 13 | 25 | 8 | 12 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 53 | 0 | 2 | 42 | 0 | 9 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 12 | 0 | 7 | 0 | 3 | 2 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0003t0009 | a0001 | c0003 | t0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD | copy fasta |
a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD | 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 | 32 | 0 | 6 | 24 | 1 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0014 | a0001 | c0001 | t0002 | g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0217 | a0001 | c0001 | t0002 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0226 | a0001 | c0001 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0227 | a0001 | c0001 | t0002 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0228 | a0001 | c0001 | t0002 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0239 | a0001 | c0001 | t0002 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0240 | a0001 | c0001 | t0002 | g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0241 | a0001 | c0001 | t0002 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0242 | a0001 | c0001 | t0002 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0002g0243 | a0001 | c0001 | t0002 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0002 | a0001 | c0001 | t0003 | g0002 | 0/0 | 16 | 0 | 0 | 7 | 4 | 5 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0042 | a0001 | c0001 | t0003 | g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0043 | a0001 | c0001 | t0003 | g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0044 | a0001 | c0001 | t0003 | g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0045 | a0001 | c0001 | t0003 | g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0047 | a0001 | c0001 | t0003 | g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0048 | a0001 | c0001 | t0003 | g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0108 | a0001 | c0001 | t0003 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0109 | a0001 | c0001 | t0003 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0112 | a0001 | c0001 | t0003 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0160 | a0001 | c0001 | t0003 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0165 | a0001 | c0001 | t0003 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0169 | a0001 | c0001 | t0003 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0170 | a0001 | c0001 | t0003 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0171 | a0001 | c0001 | t0003 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0172 | a0001 | c0001 | t0003 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0173 | a0001 | c0001 | t0003 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0174 | a0001 | c0001 | t0003 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0175 | a0001 | c0001 | t0003 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0176 | a0001 | c0001 | t0003 | g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0177 | a0001 | c0001 | t0003 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0178 | a0001 | c0001 | t0003 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0180 | a0001 | c0001 | t0003 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0181 | a0001 | c0001 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0182 | a0001 | c0001 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0183 | a0001 | c0001 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0184 | a0001 | c0001 | t0003 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0185 | a0001 | c0001 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0186 | a0001 | c0001 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0187 | a0001 | c0001 | t0003 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0188 | a0001 | c0001 | t0003 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0189 | a0001 | c0001 | t0003 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0190 | a0001 | c0001 | t0003 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0191 | a0001 | c0001 | t0003 | g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0192 | a0001 | c0001 | t0003 | g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0193 | a0001 | c0001 | t0003 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0197 | a0001 | c0001 | t0003 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0198 | a0001 | c0001 | t0003 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0214 | a0001 | c0001 | t0003 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0246 | a0001 | c0001 | t0003 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0003g0247 | a0001 | c0001 | t0003 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0003 | a0001 | c0001 | t0004 | g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0007 | a0001 | c0001 | t0004 | g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0010 | a0001 | c0001 | t0004 | g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0016 | a0001 | c0001 | t0004 | g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0023 | a0001 | c0001 | t0004 | g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0028 | a0001 | c0001 | t0004 | g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0031 | a0001 | c0001 | t0004 | g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0050 | a0001 | c0001 | t0004 | g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0065 | a0001 | c0001 | t0004 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0066 | a0001 | c0001 | t0004 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0067 | a0001 | c0001 | t0004 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0068 | a0001 | c0001 | t0004 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0069 | a0001 | c0001 | t0004 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0070 | a0001 | c0001 | t0004 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0071 | a0001 | c0001 | t0004 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0072 | a0001 | c0001 | t0004 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0073 | a0001 | c0001 | t0004 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0074 | a0001 | c0001 | t0004 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0075 | a0001 | c0001 | t0004 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0076 | a0001 | c0001 | t0004 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0077 | a0001 | c0001 | t0004 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0078 | a0001 | c0001 | t0004 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0079 | a0001 | c0001 | t0004 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0080 | a0001 | c0001 | t0004 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0081 | a0001 | c0001 | t0004 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0082 | a0001 | c0001 | t0004 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0004g0218 | a0001 | c0001 | t0004 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0022 | a0001 | c0001 | t0005 | g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0089 | a0001 | c0001 | t0005 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0230 | a0001 | c0001 | t0005 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0231 | a0001 | c0001 | t0005 | g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0232 | a0001 | c0001 | t0005 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0233 | a0001 | c0001 | t0005 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0234 | a0001 | c0001 | t0005 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0236 | a0001 | c0001 | t0005 | g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0237 | a0001 | c0001 | t0005 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0005g0245 | a0001 | c0001 | t0005 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0017 | a0001 | c0001 | t0006 | g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0111 | a0001 | c0001 | t0006 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0115 | a0001 | c0001 | t0006 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0116 | a0001 | c0001 | t0006 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0117 | a0001 | c0001 | t0006 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0123 | a0001 | c0001 | t0006 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0138 | a0001 | c0001 | t0006 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0139 | a0001 | c0001 | t0006 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0006g0151 | a0001 | c0001 | t0006 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0020 | a0001 | c0001 | t0007 | g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0025 | a0001 | c0001 | t0007 | g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0107 | a0001 | c0001 | t0007 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0161 | a0001 | c0001 | t0007 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0162 | a0001 | c0001 | t0007 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0203 | a0001 | c0001 | t0007 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0210 | a0001 | c0001 | t0007 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0007g0213 | a0001 | c0001 | t0007 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0009g0029 | a0001 | c0001 | t0009 | g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0009g0030 | a0001 | c0001 | t0009 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0009g0064 | a0001 | c0001 | t0009 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0009g0148 | a0001 | c0001 | t0009 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0009g0209 | a0001 | c0001 | t0009 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0046 | a0001 | c0001 | t0010 | g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0167 | a0001 | c0001 | t0010 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0168 | a0001 | c0001 | t0010 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0196 | a0001 | c0001 | t0010 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0215 | a0001 | c0001 | t0010 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0010g0216 | a0001 | c0001 | t0010 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0011g0021 | a0001 | c0001 | t0011 | g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0011g0054 | a0001 | c0001 | t0011 | g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0011g0223 | a0001 | c0001 | t0011 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0011g0238 | a0001 | c0001 | t0011 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0012g0095 | a0001 | c0001 | t0012 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0012g0200 | a0001 | c0001 | t0012 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0012g0201 | a0001 | c0001 | t0012 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0013g0026 | a0001 | c0001 | t0013 | g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0013g0091 | a0001 | c0001 | t0013 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0014g0098 | a0001 | c0001 | t0014 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0014g0110 | a0001 | c0001 | t0014 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0015g0141 | a0001 | c0001 | t0015 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0016g0142 | a0001 | c0001 | t0016 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0017g0121 | a0001 | c0001 | t0017 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0018g0179 | a0001 | c0001 | t0018 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0019g0163 | a0001 | c0001 | t0019 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0020g0211 | a0001 | c0001 | t0020 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0021g0157 | a0001 | c0001 | t0021 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0022g0166 | a0001 | c0001 | t0022 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0023g0229 | a0001 | c0001 | t0023 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0001t0024g0087 | a0001 | c0001 | t0024 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0013 | a0001 | c0002 | t0008 | g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0035 | a0001 | c0002 | t0008 | g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0099 | a0001 | c0002 | t0008 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0100 | a0001 | c0002 | t0008 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0101 | a0001 | c0002 | t0008 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0102 | a0001 | c0002 | t0008 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0002t0008g0103 | a0001 | c0002 | t0008 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0003t0009g0063 | a0001 | c0003 | t0009 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0003t0009g0084 | a0001 | c0003 | t0009 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0003t0009g0085 | a0001 | c0003 | t0009 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD_chr17_55387622_55426835 | MMD |
a0001c0004t0001g0134 | a0001 | c0004 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD_chr17_55387622_55426835 | MMD |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0247 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0236 | EUR | GBR | MMD_chr17_55387622_55426835 | MMD |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0169 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0233 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | MMD_chr17_55387622_55426835 | MMD |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | MMD_chr17_55387622_55426835 | MMD |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01081 | hp1 | a0001 | c0001 | t0013 | g0026 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01109 | hp1 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0029 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MMD_chr17_55387622_55426835 | MMD |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0234 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0185 | EUR | IBS | MMD_chr17_55387622_55426835 | MMD |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0196 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02055 | hp2 | a0001 | c0002 | t0008 | g0103 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0238 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02135 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0216 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | CDX | MMD_chr17_55387622_55426835 | MMD |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0099 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02258 | hp1 | a0001 | c0001 | t0023 | g0229 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | MMD_chr17_55387622_55426835 | MMD |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0201 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MMD_chr17_55387622_55426835 | MMD |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0046 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02622 | hp2 | a0001 | c0001 | t0021 | g0157 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02717 | hp1 | a0001 | c0002 | t0008 | g0100 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02723 | hp1 | a0001 | c0002 | t0008 | g0101 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0098 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0209 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0148 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02896 | hp1 | a0001 | c0003 | t0009 | g0084 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02897 | hp1 | a0001 | c0003 | t0009 | g0085 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0035 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03195 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0046 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | MMD_chr17_55387622_55426835 | MMD |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MMD_chr17_55387622_55426835 | MMD |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03579 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03710 | hp2 | a0001 | c0001 | t0018 | g0179 | SAS | PJL | MMD_chr17_55387622_55426835 | MMD |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0077 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0134 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | MMD_chr17_55387622_55426835 | MMD |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0139 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | STU | MMD_chr17_55387622_55426835 | MMD |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA18522 | hp2 | a0001 | c0002 | t0008 | g0035 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | MMD_chr17_55387622_55426835 | MMD |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18943 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18956 | hp2 | a0001 | c0001 | t0011 | g0223 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18981 | hp1 | a0001 | c0001 | t0017 | g0121 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18985 | hp1 | a0001 | c0001 | t0024 | g0087 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19030 | hp1 | a0001 | c0001 | t0014 | g0110 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
NA19030 | hp2 | a0001 | c0001 | t0020 | g0211 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19070 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19080 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19089 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | YRI | MMD_chr17_55387622_55426835 | MMD |
NA20129 | hp1 | a0001 | c0001 | t0022 | g0166 | AFR | ASW | MMD_chr17_55387622_55426835 | MMD |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ASW | MMD_chr17_55387622_55426835 | MMD |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0022 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | MMD_chr17_55387622_55426835 | MMD |
NA20905 | hp1 | a0001 | c0001 | t0016 | g0142 | SAS | GIH | MMD_chr17_55387622_55426835 | MMD |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | MMD_chr17_55387622_55426835 | MMD |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG01123 | hp2 | a0001 | c0001 | t0015 | g0141 | AMR | CLM | MMD_chr17_55387622_55426835 | MMD |
HG02109 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02109 | hp2 | a0001 | c0001 | t0010 | g0215 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02486 | hp1 | a0001 | c0003 | t0009 | g0063 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02559 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | MMD_chr17_55387622_55426835 | MMD |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0168 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | MSL | MMD_chr17_55387622_55426835 | MMD |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | MMD_chr17_55387622_55426835 | MMD |
HG06807 | hp2 | a0001 | c0001 | t0012 | g0095 | AFR | USA | MMD_chr17_55387622_55426835 | MMD |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MMD_chr17_55387622_55426835 | MMD |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0167 | AFR | USA | MMD_chr17_55387622_55426835 | MMD |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | USA | MMD_chr17_55387622_55426835 | MMD |
NA21309 | hp1 | a0001 | c0002 | t0008 | g0102 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | LWK | MMD_chr17_55387622_55426835 | MMD |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0051 | REF | REF | MMD_chr17_55387622_55426835 | MMD |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | MMD_chr17_55387622_55426835 | MMD |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:55394523
|
A | G | 1 | a0001c0002 | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
synonymous_variant | LOW | c.528T>C | p.Asp176Asp | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 668/2569 | 528/717 | 176/238 | chr17 | 55394523 | ||
chr17:55411322
|
T | A | 1 | a0001c0004 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.204A>T | p.Gly68Gly | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/7 | 344/2569 | 204/717 | 68/238 | chr17 | 55411322 | ||
chr17:55411403
|
C | T | 1 | a0001c0003 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/7 | 263/2569 | 123/717 | 41/238 | chr17 | 55411403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:55392643
|
A | G | 1 | a0001c0001t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1691T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1691 | chr17 | 55392643 | |||||
chr17:55392739
|
T | G | 1 | a0001c0001t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1595 | chr17 | 55392739 | |||||
chr17:55392933
|
G | T | 1 | a0001c0001t0014 | 2 | HG02818.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1401C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1401 | chr17 | 55392933 | |||||
chr17:55392964
|
G | C | 4 | a0001c0001t0007a0001c0001t0012a0001c0001t0019others(1): Show | 16 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1370C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1370 | chr17 | 55392964 | |||||
chr17:55393037
|
G | A | 1 | a0001c0001t0011 | 7 | HG02132.hp1 HG02135.hp2 NA18943.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1297C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1297 | chr17 | 55393037 | |||||
chr17:55393054
|
A | G | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1280T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1280 | chr17 | 55393054 | |||||
chr17:55393101
|
C | T | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(6): Show | 139 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1233G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1233 | chr17 | 55393101 | |||||
chr17:55393202
|
G | T | 1 | a0001c0001t0018 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1132 | chr17 | 55393202 | |||||
chr17:55393251
|
GA | G | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(8): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1082delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1082 | chr17 | 55393251 | |||||
chr17:55393251
|
GAA | G | 4 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(1): Show | 64 | HG00735.hp2 HG01123.hp1 HG01891.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1081_*1082delTT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1081 | chr17 | 55393251 | |||||
chr17:55393266
|
A | C | 1 | a0001c0001t0006 | 11 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1068T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 1068 | chr17 | 55393266 | |||||
chr17:55393658
|
G | A | 1 | a0001c0002t0008 | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*676C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 676 | chr17 | 55393658 | |||||
chr17:55393744
|
T | G | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(3): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 590 | chr17 | 55393744 | |||||
chr17:55393815
|
A | T | 1 | a0001c0001t0017 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 519 | chr17 | 55393815 | |||||
chr17:55393830
|
T | A | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(2): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 504 | chr17 | 55393830 | |||||
chr17:55393897
|
T | C | 1 | a0001c0001t0013 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 437 | chr17 | 55393897 | |||||
chr17:55394146
|
C | T | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG01123.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 188 | chr17 | 55394146 | |||||
chr17:55394214
|
C | G | 1 | a0001c0001t0015 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 7/7 | 120 | chr17 | 55394214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:55394595
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517-61T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394595 | ||||||
chr17:55394858
|
G | A | 1 | a0001c0001t0001g0009 | 6 | NA18747.hp1 NA18960.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-324C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394858 | ||||||
chr17:55394898
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0041 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-364G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55394898 | ||||||
chr17:55395539
|
G | T | 1 | a0001c0001t0005g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.517-1005C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395539 | ||||||
chr17:55395575
|
T | C | 1 | a0001c0001t0006g0116 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-1041A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395575 | ||||||
chr17:55395637
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.517-1103A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395637 | ||||||
chr17:55395648
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.517-1114G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395648 | ||||||
chr17:55395728
|
A | G | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.517-1194T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395728 | ||||||
chr17:55395797
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517-1263A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55395797 | ||||||
chr17:55396076
|
C | T | 1 | a0001c0001t0003g0043 | 2 | HG01074.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.517-1542G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396076 | ||||||
chr17:55396207
|
A | G | 1 | a0001c0001t0018g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.517-1673T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396207 | ||||||
chr17:55396347
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.517-1813G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396347 | ||||||
chr17:55396535
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.517-2001A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396535 | ||||||
chr17:55396556
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-2022A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396556 | ||||||
chr17:55396601
|
T | G | 5 | a0001c0001t0001g0122a0001c0001t0002g0052a0001c0001t0002g0217others(2): Show | 6 | HG01261.hp1 HG01496.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-2067A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396601 | ||||||
chr17:55396604
|
G | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(70): Show | 111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.517-2070C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396604 | ||||||
chr17:55396607
|
G | T | 42 | a0001c0001t0001g0199a0001c0001t0003g0002a0001c0001t0003g0042others(39): Show | 63 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-2073C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396607 | ||||||
chr17:55396622
|
CT | C | 6 | a0001c0001t0003g0173a0001c0001t0003g0175a0001c0001t0003g0178others(3): Show | 6 | HG01934.hp1 HG01993.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-2089delA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396622 | ||||||
chr17:55396639
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517-2105A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396639 | ||||||
chr17:55396675
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.517-2141C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396675 | ||||||
chr17:55396677
|
A | G | 3 | a0001c0003t0009g0063a0001c0003t0009g0084a0001c0003t0009g0085 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.517-2143T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396677 | ||||||
chr17:55396761
|
C | T | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.517-2227G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396761 | ||||||
chr17:55396775
|
C | T | 2 | a0001c0001t0003g0183a0001c0001t0018g0179 | 2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.517-2241G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396775 | ||||||
chr17:55396830
|
T | C | 1 | a0001c0001t0007g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.517-2296A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396830 | ||||||
chr17:55396906
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.517-2372G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55396906 | ||||||
chr17:55397159
|
G | GTTTA | 3 | a0001c0001t0010g0046a0001c0001t0010g0196a0001c0001t0010g0215 | 4 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2629_517-2626d others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397159 | ||||||
chr17:55397165
|
T | G | 2 | a0001c0001t0013g0026a0001c0001t0013g0091 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517-2631A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397165 | ||||||
chr17:55397387
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.517-2853G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397387 | ||||||
chr17:55397391
|
C | T | 1 | a0001c0001t0005g0022 | 3 | HG01175.hp1 HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.517-2857G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397391 | ||||||
chr17:55397478
|
C | T | 198 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(195): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.517-2944G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397478 | ||||||
chr17:55397557
|
T | G | 1 | a0001c0001t0002g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517-3023A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397557 | ||||||
chr17:55397617
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0137 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.517-3083G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397617 | ||||||
chr17:55397665
|
C | T | 1 | a0001c0001t0012g0095 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-3131G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397665 | ||||||
chr17:55397680
|
A | G | 11 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-3146T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397680 | ||||||
chr17:55397687
|
T | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.517-3153A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397687 | ||||||
chr17:55397703
|
A | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.517-3169T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397703 | ||||||
chr17:55397788
|
C | T | 1 | a0001c0001t0002g0056 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517-3254G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397788 | ||||||
chr17:55397849
|
CA | C | 5 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0203others(2): Show | 8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-3316delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397849 | ||||||
chr17:55397863
|
C | T | 4 | a0001c0001t0002g0014a0001c0001t0002g0228a0001c0001t0002g0243others(1): Show | 7 | HG00558.hp2 NA18953.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-3329G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397863 | ||||||
chr17:55397934
|
T | TTC | 5 | a0001c0001t0004g0016a0001c0001t0004g0070a0001c0001t0004g0073others(2): Show | 7 | HG00735.hp2 HG02015.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-3402_517-3401d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397934 | ||||||
chr17:55397954
|
A | G | 4 | a0001c0001t0009g0029a0001c0001t0009g0030a0001c0001t0009g0064others(1): Show | 6 | HG01243.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-3420T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397954 | ||||||
chr17:55397974
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0227 | 2 | HG00639.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.517-3440C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55397974 | ||||||
chr17:55398111
|
C | CA | 83 | a0001c0001t0001g0061a0001c0001t0001g0126a0001c0001t0002g0004others(80): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.516+3357dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | ||||||
chr17:55398111
|
C | CAA | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0086others(20): Show | 26 | HG01433.hp2 HG02258.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.516+3356_516+3357d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | ||||||
chr17:55398111
|
CAAAA | C | 76 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(73): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.516+3354_516+3357d others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398111 | ||||||
chr17:55398126
|
A | AG | 2 | a0001c0001t0002g0011a0001c0001t0002g0088 | 5 | HG00140.hp1 HG01070.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+3342_516+3343i others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398126 | ||||||
chr17:55398126
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.516+3343T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398126 | ||||||
chr17:55398254
|
G | A | 1 | a0001c0001t0006g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.516+3215C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398254 | ||||||
chr17:55398331
|
A | C | 1 | a0001c0001t0006g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+3138T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398331 | ||||||
chr17:55398377
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516+3092A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398377 | ||||||
chr17:55398473
|
C | G | 3 | a0001c0001t0004g0007a0001c0001t0004g0065a0001c0001t0004g0072 | 8 | NA18953.hp2 NA18961.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+2996G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398473 | ||||||
chr17:55398566
|
G | T | 3 | a0001c0003t0009g0063a0001c0003t0009g0084a0001c0003t0009g0085 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.516+2903C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398566 | ||||||
chr17:55398568
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.516+2901A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398568 | ||||||
chr17:55398592
|
T | C | 1 | a0001c0001t0022g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.516+2877A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398592 | ||||||
chr17:55398649
|
A | C | 1 | a0001c0001t0005g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.516+2820T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398649 | ||||||
chr17:55398876
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.516+2593G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398876 | ||||||
chr17:55398969
|
G | A | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+2500C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55398969 | ||||||
chr17:55399038
|
A | G | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+2431T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399038 | ||||||
chr17:55399246
|
CA | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(94): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.516+2222delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399246 | ||||||
chr17:55399251
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+2218T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399251 | ||||||
chr17:55399316
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.516+2153G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399316 | ||||||
chr17:55399562
|
G | A | 7 | a0001c0002t0008g0013a0001c0002t0008g0035a0001c0002t0008g0099others(4): Show | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+1907C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399562 | ||||||
chr17:55399564
|
C | A | 45 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0003g0002others(42): Show | 66 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.516+1905G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399564 | ||||||
chr17:55399613
|
A | G | 1 | a0001c0002t0008g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.516+1856T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399613 | ||||||
chr17:55399677
|
A | G | 198 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(195): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.516+1792T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399677 | ||||||
chr17:55399794
|
G | A | 1 | a0001c0001t0002g0033 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.516+1675C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399794 | ||||||
chr17:55399961
|
C | T | 15 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(12): Show | 19 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+1508G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55399961 | ||||||
chr17:55400060
|
T | C | 5 | a0001c0001t0010g0046a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1409A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400060 | ||||||
chr17:55400129
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(65): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.516+1340C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400129 | ||||||
chr17:55400155
|
T | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0049a0001c0001t0001g0202others(6): Show | 12 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+1314A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400155 | ||||||
chr17:55400225
|
T | C | 60 | a0001c0001t0001g0039a0001c0001t0001g0049a0001c0001t0001g0202others(57): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.516+1244A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400225 | ||||||
chr17:55400399
|
A | C | 5 | a0001c0001t0007g0161a0001c0001t0007g0210a0001c0001t0012g0095others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+1070T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400399 | ||||||
chr17:55400401
|
T | C | 51 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(48): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.516+1068A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400401 | ||||||
chr17:55400481
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.516+988C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400481 | ||||||
chr17:55400556
|
G | GA | 188 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(185): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.516+912dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400556 | ||||||
chr17:55400662
|
T | C | 1 | a0001c0001t0004g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.516+807A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400662 | ||||||
chr17:55400757
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(65): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.516+712C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55400757 | ||||||
chr17:55401051
|
G | A | 15 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(12): Show | 19 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+418C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401051 | ||||||
chr17:55401174
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG03139.hp1 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+295A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401174 | ||||||
chr17:55401314
|
A | G | 198 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(195): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.516+155T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401314 | ||||||
chr17:55401375
|
A | G | 11 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+94T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 6/6 | chr17 | 55401375 | ||||||
chr17:55401618
|
T | C | 1 | a0001c0001t0002g0053 | 2 | HG00733.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.447-80A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401618 | ||||||
chr17:55401705
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(76): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.447-167G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401705 | ||||||
chr17:55401737
|
C | T | 5 | a0001c0001t0010g0046a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.447-199G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401737 | ||||||
chr17:55401739
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.447-201G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401739 | ||||||
chr17:55401879
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.447-341G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401879 | ||||||
chr17:55401978
|
AGAATGGC others(8): Show |
A | 138 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.447-455_447-441del others(15): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55401978 | ||||||
chr17:55402087
|
C | CA | 28 | a0001c0001t0001g0158a0001c0001t0002g0033a0001c0001t0002g0057others(25): Show | 37 | HG00323.hp1 HG00558.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.447-550dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402087 | ||||||
chr17:55402087
|
CA | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0027others(84): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.447-550delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402087 | ||||||
chr17:55402104
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-566T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402104 | ||||||
chr17:55402105
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-567C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402105 | ||||||
chr17:55402134
|
G | C | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.447-596C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402134 | ||||||
chr17:55402136
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.447-598G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402136 | ||||||
chr17:55402186
|
C | T | 50 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(47): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.447-648G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402186 | ||||||
chr17:55402260
|
T | C | 10 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(7): Show | 13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.447-722A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402260 | ||||||
chr17:55402678
|
C | T | 5 | a0001c0001t0010g0046a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.446+1089G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402678 | ||||||
chr17:55402812
|
T | C | 1 | a0001c0001t0003g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.446+955A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402812 | ||||||
chr17:55402965
|
C | T | 10 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(7): Show | 13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.446+802G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55402965 | ||||||
chr17:55403056
|
A | T | 1 | a0001c0001t0005g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.446+711T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403056 | ||||||
chr17:55403159
|
A | T | 1 | a0001c0001t0004g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.446+608T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403159 | ||||||
chr17:55403231
|
A | G | 11 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.446+536T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403231 | ||||||
chr17:55403453
|
G | A | 1 | a0001c0001t0010g0167 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.446+314C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403453 | ||||||
chr17:55403655
|
T | C | 5 | a0001c0001t0007g0161a0001c0001t0007g0210a0001c0001t0012g0095others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+112A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403655 | ||||||
chr17:55403698
|
G | A | 4 | a0001c0001t0009g0029a0001c0001t0009g0030a0001c0001t0009g0064others(1): Show | 6 | HG01243.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+69C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 5/6 | chr17 | 55403698 | ||||||
chr17:55403902
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.345-34C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55403902 | ||||||
chr17:55404291
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0126a0001c0001t0001g0154others(1): Show | 5 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-423C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404291 | ||||||
chr17:55404319
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.345-451G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404319 | ||||||
chr17:55404330
|
G | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-462C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404330 | ||||||
chr17:55404415
|
G | A | 5 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0203others(2): Show | 8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-547C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404415 | ||||||
chr17:55404443
|
C | T | 34 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0010others(31): Show | 62 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.345-575G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404443 | ||||||
chr17:55404565
|
C | T | 1 | a0001c0001t0003g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-697G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404565 | ||||||
chr17:55404588
|
G | C | 3 | a0001c0001t0007g0107a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02970.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.345-720C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404588 | ||||||
chr17:55404836
|
C | A | 1 | a0001c0001t0003g0188 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.345-968G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404836 | ||||||
chr17:55404889
|
C | T | 1 | a0001c0001t0006g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.345-1021G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55404889 | ||||||
chr17:55405070
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.345-1202A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405070 | ||||||
chr17:55405197
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0105a0001c0001t0001g0106 | 4 | NA18997.hp2 NA19072.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1329T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405197 | ||||||
chr17:55405379
|
GA | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 169 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.345-1512delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405379 | ||||||
chr17:55405379
|
GAA | G | 50 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(47): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.345-1513_345-1512d others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405379 | ||||||
chr17:55405653
|
G | T | 5 | a0001c0001t0010g0046a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1785C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405653 | ||||||
chr17:55405666
|
C | T | 5 | a0001c0001t0010g0046a0001c0001t0010g0167a0001c0001t0010g0168others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1798G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405666 | ||||||
chr17:55405678
|
C | G | 1 | a0001c0001t0003g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.345-1810G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405678 | ||||||
chr17:55405687
|
GTTC | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.345-1822_345-1820d others(5): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405687 | ||||||
chr17:55405751
|
T | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-1883A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405751 | ||||||
chr17:55405936
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.344+1810T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55405936 | ||||||
chr17:55406022
|
A | G | 1 | a0001c0001t0004g0067 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.344+1724T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406022 | ||||||
chr17:55406103
|
TTCAAAAA others(18): Show |
T | 16 | a0001c0001t0003g0109a0001c0001t0007g0020a0001c0001t0007g0025others(13): Show | 20 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.344+1618_344+1642d others(27): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406103 | ||||||
chr17:55406149
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.344+1597G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406149 | ||||||
chr17:55406263
|
C | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0034others(11): Show | 23 | HG00544.hp2 HG00597.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.344+1483G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406263 | ||||||
chr17:55406313
|
G | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.344+1433C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406313 | ||||||
chr17:55406408
|
C | G | 40 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0158others(37): Show | 70 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.344+1338G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406408 | ||||||
chr17:55406535
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.344+1211A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406535 | ||||||
chr17:55406551
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.344+1195A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406551 | ||||||
chr17:55406610
|
G | A | 10 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(7): Show | 13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+1136C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406610 | ||||||
chr17:55406620
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.344+1126T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406620 | ||||||
chr17:55406629
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1117G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406629 | ||||||
chr17:55406695
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1051C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406695 | ||||||
chr17:55406701
|
A | G | 1 | a0001c0001t0007g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.344+1045T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406701 | ||||||
chr17:55406710
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.344+1036G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406710 | ||||||
chr17:55406743
|
C | A | 1 | a0001c0001t0006g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.344+1003G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406743 | ||||||
chr17:55406842
|
C | T | 7 | a0001c0002t0008g0013a0001c0002t0008g0035a0001c0002t0008g0099others(4): Show | 11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+904G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406842 | ||||||
chr17:55406858
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344+888G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55406858 | ||||||
chr17:55407142
|
A | G | 1 | a0001c0001t0003g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.344+604T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407142 | ||||||
chr17:55407149
|
T | C | 1 | a0001c0001t0022g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344+597A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407149 | ||||||
chr17:55407158
|
G | A | 10 | a0001c0001t0007g0020a0001c0001t0007g0025a0001c0001t0007g0161others(7): Show | 13 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+588C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407158 | ||||||
chr17:55407229
|
T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+517A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407229 | ||||||
chr17:55407237
|
G | A | 1 | a0001c0001t0006g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.344+509C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407237 | ||||||
chr17:55407298
|
C | CTAAA | 3 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0093 | 3 | HG02258.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.344+447_344+448ins others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407298 | ||||||
chr17:55407299
|
A | AAAAT | 13 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0113others(10): Show | 22 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+443_344+446dup others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
A | AAAATAAA others(1): Show |
3 | a0001c0001t0014g0098a0001c0001t0018g0179a0001c0002t0008g0102 | 3 | HG02818.hp1 HG03710.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.344+439_344+446dup others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
A | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 8 | HG02258.hp2 HG02451.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+447T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
AAAAT | A | 57 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0049others(54): Show | 94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.344+443_344+446del others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
AAAATAAA others(1): Show |
A | 11 | a0001c0001t0003g0109a0001c0001t0007g0107a0001c0001t0007g0162others(8): Show | 11 | HG02486.hp1 HG02886.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+439_344+446del others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.344+435_344+446del others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407299
|
AAAATAAA others(9): Show |
A | 39 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0010others(36): Show | 69 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.344+431_344+446del others(16): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407299 | ||||||
chr17:55407327
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0158others(3): Show | 8 | HG01891.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+419A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407327 | ||||||
chr17:55407355
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.344+391G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407355 | ||||||
chr17:55407391
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.344+355A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407391 | ||||||
chr17:55407489
|
C | T | 1 | a0001c0001t0022g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344+257G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407489 | ||||||
chr17:55407490
|
A | T | 4 | a0001c0001t0007g0107a0001c0001t0007g0161a0001c0001t0007g0162others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+256T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407490 | ||||||
chr17:55407613
|
A | G | 1 | a0001c0001t0007g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.344+133T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 4/6 | chr17 | 55407613 | ||||||
chr17:55407825
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
splice_region_variant&intron_variant | LOW | c.270-5G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55407825 | ||||||
chr17:55407944
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-124A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55407944 | ||||||
chr17:55408050
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-230T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408050 | ||||||
chr17:55408056
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.270-236A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408056 | ||||||
chr17:55408065
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.270-245C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408065 | ||||||
chr17:55408197
|
C | T | 1 | a0001c0001t0003g0044 | 2 | HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.270-377G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408197 | ||||||
chr17:55408198
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0003g0198 | 2 | NA18981.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.270-378C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408198 | ||||||
chr17:55408275
|
C | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270-455G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408275 | ||||||
chr17:55408382
|
CA | C | 4 | a0001c0001t0007g0210a0001c0001t0012g0095a0001c0001t0012g0200others(1): Show | 4 | HG02451.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-563delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408382 | ||||||
chr17:55408388
|
C | CA | 4 | a0001c0001t0007g0107a0001c0001t0007g0161a0001c0001t0007g0162others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-569dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408388 | ||||||
chr17:55408458
|
G | GA | 6 | a0001c0001t0001g0212a0001c0001t0007g0020a0001c0001t0007g0025others(3): Show | 9 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.270-639dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408458 | ||||||
chr17:55408654
|
C | T | 3 | a0001c0003t0009g0063a0001c0003t0009g0084a0001c0003t0009g0085 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.270-834G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408654 | ||||||
chr17:55408655
|
G | A | 2 | a0001c0001t0006g0116a0001c0001t0006g0117 | 2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.270-835C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408655 | ||||||
chr17:55408874
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.270-1054C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408874 | ||||||
chr17:55408955
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.270-1135G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55408955 | ||||||
chr17:55409119
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.270-1299T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409119 | ||||||
chr17:55409225
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270-1405G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409225 | ||||||
chr17:55409400
|
C | T | 2 | a0001c0001t0006g0116a0001c0001t0006g0117 | 2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.270-1580G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409400 | ||||||
chr17:55409443
|
A | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-1623T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409443 | ||||||
chr17:55409453
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.270-1633G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409453 | ||||||
chr17:55409563
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.269+1694C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409563 | ||||||
chr17:55409715
|
G | T | 1 | a0001c0001t0006g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.269+1542C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409715 | ||||||
chr17:55409722
|
G | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.269+1535C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409722 | ||||||
chr17:55409786
|
G | C | 1 | a0001c0001t0007g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.269+1471C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409786 | ||||||
chr17:55409954
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.269+1303G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409954 | ||||||
chr17:55409957
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.269+1300T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55409957 | ||||||
chr17:55410075
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.269+1182T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410075 | ||||||
chr17:55410303
|
A | C | 92 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0060others(89): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.269+954T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410303 | ||||||
chr17:55410348
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 116 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.269+909C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410348 | ||||||
chr17:55410471
|
A | G | 1 | a0001c0001t0002g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.269+786T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410471 | ||||||
chr17:55410567
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.269+690A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410567 | ||||||
chr17:55410675
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 116 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.269+582G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410675 | ||||||
chr17:55410707
|
C | T | 8 | a0001c0001t0014g0098a0001c0002t0008g0013a0001c0002t0008g0035others(5): Show | 12 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.269+550G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410707 | ||||||
chr17:55410766
|
A | G | 1 | a0001c0001t0022g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.269+491T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410766 | ||||||
chr17:55410985
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.269+272C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55410985 | ||||||
chr17:55411044
|
G | T | 1 | a0001c0001t0001g0113 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.269+213C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 3/6 | chr17 | 55411044 | ||||||
chr17:55411640
|
G | C | 32 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0010others(29): Show | 58 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-223C>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411640 | ||||||
chr17:55411681
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0034others(11): Show | 23 | HG00544.hp2 HG00597.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.109-264A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411681 | ||||||
chr17:55411694
|
G | GT | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-278_109-277ins others(1): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411694 | ||||||
chr17:55411695
|
G | T | 35 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(32): Show | 61 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.109-278C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411695 | ||||||
chr17:55411695
|
GT | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 135 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.109-279delA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411695 | ||||||
chr17:55411724
|
A | G | 5 | a0001c0001t0001g0212a0001c0001t0007g0020a0001c0001t0007g0025others(2): Show | 8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-307T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411724 | ||||||
chr17:55411729
|
G | A | 4 | a0001c0001t0007g0107a0001c0001t0007g0161a0001c0001t0007g0162others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-312C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411729 | ||||||
chr17:55411826
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109-409G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55411826 | ||||||
chr17:55412212
|
T | A | 1 | a0001c0001t0003g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.109-795A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412212 | ||||||
chr17:55412238
|
G | A | 92 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0060others(89): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.109-821C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412238 | ||||||
chr17:55412863
|
A | AT | 6 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+1287dupA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412863 | ||||||
chr17:55412932
|
T | A | 26 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0010others(23): Show | 50 | HG00735.hp2 HG01123.hp1 HG02015.hp1 others(47): Show |
intron_variant | MODIFIER | c.108+1219A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412932 | ||||||
chr17:55412999
|
C | T | 1 | a0001c0001t0012g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+1152G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55412999 | ||||||
chr17:55413000
|
G | A | 1 | a0001c0001t0003g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108+1151C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413000 | ||||||
chr17:55413006
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1145T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413006 | ||||||
chr17:55413026
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1125G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413026 | ||||||
chr17:55413033
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1118T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413033 | ||||||
chr17:55413040
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1111T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413040 | ||||||
chr17:55413053
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1098G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413053 | ||||||
chr17:55413058
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1093G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413058 | ||||||
chr17:55413060
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1091G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413060 | ||||||
chr17:55413061
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1090G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413061 | ||||||
chr17:55413064
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1087A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413064 | ||||||
chr17:55413065
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1086A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413065 | ||||||
chr17:55413066
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1085T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413066 | ||||||
chr17:55413069
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1082A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413069 | ||||||
chr17:55413070
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1081T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413070 | ||||||
chr17:55413071
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+1080T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413071 | ||||||
chr17:55413161
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+990T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413161 | ||||||
chr17:55413167
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+984C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413167 | ||||||
chr17:55413195
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+956A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413195 | ||||||
chr17:55413205
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+946T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413205 | ||||||
chr17:55413209
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+942A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413209 | ||||||
chr17:55413211
|
A | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+940T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413211 | ||||||
chr17:55413219
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+932T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413219 | ||||||
chr17:55413246
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+905T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413246 | ||||||
chr17:55413248
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+903A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413248 | ||||||
chr17:55413259
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+892G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413259 | ||||||
chr17:55413273
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+878G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413273 | ||||||
chr17:55413280
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+871A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413280 | ||||||
chr17:55413281
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+870G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413281 | ||||||
chr17:55413285
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+866A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413285 | ||||||
chr17:55413286
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+865A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413286 | ||||||
chr17:55413288
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+863A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413288 | ||||||
chr17:55413289
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+862G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413289 | ||||||
chr17:55413290
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+861T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413290 | ||||||
chr17:55413292
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+859T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413292 | ||||||
chr17:55413293
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+858G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413293 | ||||||
chr17:55413294
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+857A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413294 | ||||||
chr17:55413295
|
G | T | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+856C>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413295 | ||||||
chr17:55413299
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+852G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413299 | ||||||
chr17:55413300
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+851G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413300 | ||||||
chr17:55413301
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+850G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413301 | ||||||
chr17:55413310
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+841A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413310 | ||||||
chr17:55413312
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+839A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413312 | ||||||
chr17:55413318
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+833A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413318 | ||||||
chr17:55413319
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+832G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413319 | ||||||
chr17:55413322
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.108+829A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413322 | ||||||
chr17:55413323
|
G | A | 1 | a0001c0001t0004g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.108+828C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413323 | ||||||
chr17:55413464
|
T | C | 35 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(32): Show | 61 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.108+687A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413464 | ||||||
chr17:55413674
|
TCTC | T | 4 | a0001c0001t0007g0107a0001c0001t0007g0161a0001c0001t0007g0162others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+474_108+476del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413674 | ||||||
chr17:55413704
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+447T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413704 | ||||||
chr17:55413880
|
A | G | 3 | a0001c0001t0002g0024a0001c0001t0002g0220a0001c0001t0002g0221 | 5 | HG01516.hp1 HG01934.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+271T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55413880 | ||||||
chr17:55414060
|
C | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+91G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414060 | ||||||
chr17:55414094
|
C | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.108+57G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414094 | ||||||
chr17:55414097
|
C | T | 32 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0010others(29): Show | 58 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+54G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414097 | ||||||
chr17:55414142
|
T | A | 1 | a0001c0001t0003g0190 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.108+9A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 2/6 | chr17 | 55414142 | ||||||
chr17:55414448
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.27-216A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414448 | ||||||
chr17:55414554
|
A | G | 2 | a0001c0001t0013g0026a0001c0001t0013g0091 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-322T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414554 | ||||||
chr17:55414555
|
T | TACACAC | 3 | a0001c0003t0009g0063a0001c0003t0009g0084a0001c0003t0009g0085 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.27-324_27-323insGT others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414555 | ||||||
chr17:55414555
|
TTC | T | 2 | a0001c0001t0013g0026a0001c0001t0013g0091 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-325_27-324delGA | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414555 | ||||||
chr17:55414556
|
T | A | 3 | a0001c0003t0009g0063a0001c0003t0009g0084a0001c0003t0009g0085 | 3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.27-324A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCA | 34 | a0001c0001t0001g0040a0001c0001t0001g0140a0001c0001t0001g0143others(31): Show | 55 | HG00735.hp2 HG01123.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.27-326_27-325dupTG | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACA | 16 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(13): Show | 23 | HG00597.hp2 HG02004.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.27-328_27-325dupTG others(2): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACACA | 12 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0049others(9): Show | 21 | HG00544.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-330_27-325dupTG others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACACAC others(1): Show |
6 | a0001c0001t0001g0034a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 7 | HG01167.hp1 HG02965.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-332_27-325dupTG others(6): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACACAC others(3): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.27-334_27-325dupTG others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACACAC others(5): Show |
3 | a0001c0001t0001g0096a0001c0001t0010g0046a0001c0001t0010g0215 | 4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-336_27-325dupTG others(10): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0010g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27-338_27-325dupTG others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCA | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0036others(52): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.27-326_27-325delTG | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCACA | T | 80 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0094others(77): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.27-328_27-325delTG others(2): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCACACA | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0244others(1): Show | 4 | HG01256.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-330_27-325delTG others(4): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27-334_27-325delTG others(8): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCACACAC others(7): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.27-338_27-325delTG others(12): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414556
|
TCACACAC others(9): Show |
T | 4 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0158others(1): Show | 6 | HG01891.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-340_27-325delTG others(14): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414556 | ||||||
chr17:55414602
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.27-370A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414602 | ||||||
chr17:55414610
|
G | GA | 10 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(7): Show | 11 | HG00408.hp1 HG00597.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-379dupT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414610 | ||||||
chr17:55414610
|
GA | G | 16 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0060others(13): Show | 17 | HG02258.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-379delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414610 | ||||||
chr17:55414620
|
A | C | 1 | a0001c0001t0007g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.27-388T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414620 | ||||||
chr17:55414643
|
T | C | 4 | a0001c0001t0001g0199a0001c0001t0003g0047a0001c0001t0003g0172others(1): Show | 5 | HG02132.hp2 NA18981.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-411A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414643 | ||||||
chr17:55414721
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 7 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-489A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55414721 | ||||||
chr17:55415073
|
C | T | 1 | a0001c0001t0009g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-841G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415073 | ||||||
chr17:55415274
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-1042G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415274 | ||||||
chr17:55415276
|
TA | T | 34 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0001t0002g0219others(31): Show | 60 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-1045delT | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415276 | ||||||
chr17:55415377
|
A | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-1145T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415377 | ||||||
chr17:55415754
|
TG | T | 8 | a0001c0001t0014g0098a0001c0002t0008g0013a0001c0002t0008g0035others(5): Show | 12 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-1523delC | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415754 | ||||||
chr17:55415837
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27-1605T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55415837 | ||||||
chr17:55416089
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.27-1857G>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416089 | ||||||
chr17:55416151
|
T | C | 1 | a0001c0001t0007g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.27-1919A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416151 | ||||||
chr17:55416352
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.27-2120G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416352 | ||||||
chr17:55416371
|
G | A | 1 | a0001c0001t0011g0238 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.27-2139C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416371 | ||||||
chr17:55416384
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.27-2152A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416384 | ||||||
chr17:55416463
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2231A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416463 | ||||||
chr17:55416579
|
T | C | 7 | a0001c0001t0002g0015a0001c0001t0002g0056a0001c0001t0002g0057others(4): Show | 12 | HG01070.hp2 HG01192.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.27-2347A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416579 | ||||||
chr17:55416609
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.27-2377T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416609 | ||||||
chr17:55416647
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0158others(2): Show | 7 | HG01891.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-2415A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416647 | ||||||
chr17:55416650
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2418T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416650 | ||||||
chr17:55416653
|
C | T | 1 | a0001c0003t0009g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27-2421G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416653 | ||||||
chr17:55416710
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0096 | 3 | HG02280.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.27-2478G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416710 | ||||||
chr17:55416790
|
A | T | 1 | a0001c0001t0003g0172 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.27-2558T>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416790 | ||||||
chr17:55416923
|
T | G | 1 | a0001c0001t0022g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27-2691A>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416923 | ||||||
chr17:55416944
|
C | T | 4 | a0001c0001t0007g0210a0001c0001t0012g0095a0001c0001t0012g0200others(1): Show | 4 | HG02451.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2712G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55416944 | ||||||
chr17:55417045
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG03139.hp1 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-2813T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417045 | ||||||
chr17:55417201
|
C | T | 1 | a0001c0001t0002g0032 | 2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.27-2969G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417201 | ||||||
chr17:55417353
|
C | T | 85 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0002g0004others(82): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.27-3121G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417353 | ||||||
chr17:55417401
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.27-3169G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417401 | ||||||
chr17:55417440
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27-3208G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417440 | ||||||
chr17:55417446
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.27-3214A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417446 | ||||||
chr17:55417633
|
A | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.27-3401T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417633 | ||||||
chr17:55417706
|
G | A | 1 | a0001c0001t0002g0024 | 3 | HG02055.hp1 HG03490.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.27-3474C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417706 | ||||||
chr17:55417725
|
G | A | 3 | a0001c0001t0007g0161a0001c0001t0007g0162a0001c0001t0019g0163 | 3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.27-3493C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417725 | ||||||
chr17:55417959
|
A | C | 1 | a0001c0001t0003g0169 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.26+3711T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417959 | ||||||
chr17:55417962
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.26+3708C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55417962 | ||||||
chr17:55418562
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.26+3108A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418562 | ||||||
chr17:55418612
|
C | T | 2 | a0001c0001t0013g0026a0001c0001t0013g0091 | 3 | HG01081.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.26+3058G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418612 | ||||||
chr17:55418949
|
T | C | 1 | a0001c0001t0002g0243 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26+2721A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55418949 | ||||||
chr17:55419326
|
T | A | 1 | a0001c0001t0003g0048 | 2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.26+2344A>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419326 | ||||||
chr17:55419358
|
A | G | 2 | a0001c0001t0010g0167a0001c0001t0010g0168 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26+2312T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419358 | ||||||
chr17:55419393
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+2277T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419393 | ||||||
chr17:55419604
|
GTAC | G | 87 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0060others(84): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.26+2063_26+2065del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419604 | ||||||
chr17:55419843
|
C | T | 36 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0086others(33): Show | 63 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.26+1827G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419843 | ||||||
chr17:55419885
|
C | T | 85 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0086others(82): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.26+1785G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419885 | ||||||
chr17:55419980
|
TAAA | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0062 | 3 | HG02280.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.26+1687_26+1689del others(3): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55419980 | ||||||
chr17:55420243
|
A | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0165 | 3 | NA18957.hp1 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.26+1427T>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420243 | ||||||
chr17:55420404
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.26+1266T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420404 | ||||||
chr17:55420548
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.26+1122T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420548 | ||||||
chr17:55420555
|
T | TG | 20 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(17): Show | 25 | HG01081.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.26+1114dupC | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420555 | ||||||
chr17:55420846
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+824A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55420846 | ||||||
chr17:55421307
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02258.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.26+363C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421307 | ||||||
chr17:55421437
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.26+233C>T | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421437 | ||||||
chr17:55421485
|
C | T | 51 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(48): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.26+185G>A | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421485 | ||||||
chr17:55421501
|
C | G | 1 | a0001c0001t0013g0026 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26+169G>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421501 | ||||||
chr17:55421541
|
TCCCTGGC others(10): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26+112_26+128delCC others(15): Show |
MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421541 | ||||||
chr17:55421622
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+48T>C | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421622 | ||||||
chr17:55421629
|
T | C | 47 | a0001c0001t0001g0058a0001c0001t0001g0244a0001c0001t0002g0004others(44): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.26+41A>G | MMD | ENSG00000108960.9 | transcript | ENST00000262065.8 | protein_coding | 1/6 | chr17 | 55421629 |