geneid | 10492 |
---|---|
ensemblid | ENSG00000135316.20 |
hgncid | 16918 |
symbol | SYNCRIP |
name | synaptotagmin binding cytoplasmic RNA interacting protein |
refseq_nuc | NM_006372.5 |
refseq_prot | NP_006363.4 |
ensembl_nuc | ENST00000369622.8 |
ensembl_prot | ENSP00000358635.3 |
mane_status | MANE Select |
chr | chr6 |
start | 85613976 |
end | 85642886 |
strand | - |
ver | v1.2 |
region | chr6:85613976-85642886 |
region5000 | chr6:85608976-85647886 |
regionname0 | SYNCRIP_chr6_85613976_85642886 |
regionname5000 | SYNCRIP_chr6_85608976_85647886 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 623 | 361 | 84 | 48 | 179 | 14 | 34 | 141 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0002 | 0/0 | 623 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0003 | 0/0 | 623 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1872 | 359 | 84 | 48 | 177 | 14 | 34 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
c0002 | 0/0 | 1872 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
c0003 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
c0004 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
c0005 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 883 | 361 | 84 | 50 | 178 | 14 | 33 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
t0002 | 0/0 | 883 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
t0003 | 0/0 | 883 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
t0004 | 0/0 | 883 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0002 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0003 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0006 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0014 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0015 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1872 | 359 | 84 | 48 | 177 | 14 | 34 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0003 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0004 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0002c0002 | 0/0 | 1872 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0003c0005 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2754 | 356 | 84 | 48 | 175 | 14 | 33 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0001t0002 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0001t0003 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0001t0004 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0003t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0001c0004t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0002c0002t0001 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
a0003c0005t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | copy fasta | chr6 | 85608976 | 85647886 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0002 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0003 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0014 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
a0003c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18957 | hp1 | a0003 | c0005 | t0001 | g0242 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18977 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | GIH | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0280 | REF | REF | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85614856
|
G | A | 1 | a0002 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.1772C>T | p.Ala591Val | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 11/11 | 1874/2754 | 1772/1872 | 591/623 | chr6 | 85614856 | ||
chr6:85641393
|
T | G | 1 | a0003 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.47A>C | p.Asp16Ala | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/11 | 149/2754 | 47/1872 | 16/623 | chr6 | 85641393 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85615152
|
T | C | 1 | a0001c0003 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1476A>G | p.Gln492Gln | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 11/11 | 1578/2754 | 1476/1872 | 492/623 | chr6 | 85615152 | ||
chr6:85637279
|
G | A | 1 | a0001c0004 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.453C>T | p.Ser151Ser | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 5/11 | 555/2754 | 453/1872 | 151/623 | chr6 | 85637279 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85642807
|
G | A | 1 | a0001c0001t0002 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1368 | chr6 | 85642807 | |||||
chr6:85642817
|
G | A | 1 | a0001c0001t0003 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1378 | chr6 | 85642817 | |||||
chr6:85642860
|
T | G | 1 | a0001c0001t0004 | 1 | HG02080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1421 | chr6 | 85642860 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85615548
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1281-201A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615548 | ||||||
chr6:85615633
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1281-286A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615633 | ||||||
chr6:85615855
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0184a0001c0001t0001g0194 | 3 | NA18980.hp1 NA18995.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1281-508A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615855 | ||||||
chr6:85615914
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(176): Show | 216 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1281-567G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615914 | ||||||
chr6:85615947
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1281-600T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615947 | ||||||
chr6:85616084
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1281-737T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616084 | ||||||
chr6:85616190
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1281-843G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616190 | ||||||
chr6:85616295
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01258.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1281-948C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616295 | ||||||
chr6:85616387
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-1040C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616387 | ||||||
chr6:85616567
|
ACCCACCT others(17): Show |
A | 2 | a0001c0001t0001g0165a0001c0001t0001g0181 | 2 | HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1281-1244_1281-122 others(28): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616567 | ||||||
chr6:85616693
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1281-1346G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616693 | ||||||
chr6:85616750
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0206 | 2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1281-1403A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616750 | ||||||
chr6:85616782
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281-1435G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616782 | ||||||
chr6:85616898
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281-1551C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616898 | ||||||
chr6:85616924
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1281-1577A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616924 | ||||||
chr6:85616945
|
C | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1598G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616945 | ||||||
chr6:85617013
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1666T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617013 | ||||||
chr6:85617152
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1280+1666C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617152 | ||||||
chr6:85617160
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1280+1658C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617160 | ||||||
chr6:85617174
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280+1644C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617174 | ||||||
chr6:85617197
|
T | TA | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0053others(6): Show | 11 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280+1620dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617197 | ||||||
chr6:85617197
|
TA | T | 16 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 16 | HG01070.hp2 HG01517.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280+1620delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617197 | ||||||
chr6:85617229
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1280+1589T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617229 | ||||||
chr6:85617283
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1280+1535T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617283 | ||||||
chr6:85617327
|
CCTCT | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0235 | 3 | HG00423.hp1 HG02074.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1280+1487_1280+149 others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617327 | ||||||
chr6:85617453
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0152a0001c0001t0001g0192others(1): Show | 7 | HG01175.hp1 HG01261.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280+1365G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617453 | ||||||
chr6:85617488
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1280+1330C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617488 | ||||||
chr6:85617647
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1280+1171C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617647 | ||||||
chr6:85617751
|
G | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0001g0241others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280+1067C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617751 | ||||||
chr6:85617778
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0031others(1): Show | 10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1280+1040C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617778 | ||||||
chr6:85617975
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1280+843T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617975 | ||||||
chr6:85618019
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280+799A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618019 | ||||||
chr6:85618142
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(142): Show | 174 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1280+676G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618142 | ||||||
chr6:85618149
|
A | AG | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+668dupC | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618149 | ||||||
chr6:85618230
|
T | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+588A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618230 | ||||||
chr6:85618256
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1280+562T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618256 | ||||||
chr6:85618425
|
C | CAGCT | 8 | a0001c0001t0001g0121a0001c0001t0001g0241a0001c0001t0001g0244others(5): Show | 8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1280+389_1280+392d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618425 | ||||||
chr6:85618635
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1280+183A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618635 | ||||||
chr6:85618713
|
A | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(142): Show | 174 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1280+105T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618713 | ||||||
chr6:85619049
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1159-110G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619049 | ||||||
chr6:85619075
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1159-136A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619075 | ||||||
chr6:85619174
|
CA | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1158+93delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619174 | ||||||
chr6:85619187
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18991.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1158+81T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619187 | ||||||
chr6:85619421
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA18959.hp2 | splice_region_variant&intron_variant | LOW | c.1009-4C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619421 | ||||||
chr6:85619535
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1009-118A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619535 | ||||||
chr6:85619535
|
T | TA | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(78): Show | 90 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1009-119dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619535 | ||||||
chr6:85619715
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0173 | 2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1009-298G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619715 | ||||||
chr6:85619797
|
G | GTA | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1009-382_1009-381d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619797 | ||||||
chr6:85619824
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-407G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619824 | ||||||
chr6:85619842
|
A | C | 1 | a0001c0001t0001g0255 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1009-425T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619842 | ||||||
chr6:85619886
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1009-469G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619886 | ||||||
chr6:85620111
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-694A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620111 | ||||||
chr6:85620141
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1009-724C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620141 | ||||||
chr6:85620204
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1009-787G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620204 | ||||||
chr6:85620359
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1009-942A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620359 | ||||||
chr6:85620397
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1009-980A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620397 | ||||||
chr6:85620415
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1009-998C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620415 | ||||||
chr6:85620880
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1009-1463T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620880 | ||||||
chr6:85621322
|
A | G | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1160T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621322 | ||||||
chr6:85621347
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1008+1135G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621347 | ||||||
chr6:85621409
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0181 | 2 | HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1008+1073G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621409 | ||||||
chr6:85621601
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008+881C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621601 | ||||||
chr6:85621607
|
T | TA | 8 | a0001c0001t0001g0027a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 9 | HG00280.hp1 HG00544.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+874dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | ||||||
chr6:85621607
|
TA | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 132 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1008+874delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | ||||||
chr6:85621607
|
TAA | T | 14 | a0001c0001t0001g0058a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01168.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+873_1008+874d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | ||||||
chr6:85621609
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1008+873T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621609 | ||||||
chr6:85621640
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0033 | 3 | HG02280.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1008+842T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621640 | ||||||
chr6:85621731
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1008+751C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621731 | ||||||
chr6:85621800
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1008+682C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621800 | ||||||
chr6:85621819
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1008+663A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621819 | ||||||
chr6:85621913
|
T | TGTAGGCG others(41): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1008+521_1008+568d others(50): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621913 | ||||||
chr6:85621918
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1008+564C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621918 | ||||||
chr6:85621935
|
T | C | 1 | a0001c0001t0001g0280 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1008+547A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621935 | ||||||
chr6:85622016
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1008+466G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622016 | ||||||
chr6:85622031
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1008+451G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622031 | ||||||
chr6:85622064
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1008+418A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622064 | ||||||
chr6:85622155
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1008+327G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622155 | ||||||
chr6:85622169
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(58): Show | 81 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1008+313G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622169 | ||||||
chr6:85622181
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008+301C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622181 | ||||||
chr6:85622231
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(18): Show | 29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1008+251G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622231 | ||||||
chr6:85622256
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1008+226A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622256 | ||||||
chr6:85622274
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1008+208G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622274 | ||||||
chr6:85622416
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+66G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622416 | ||||||
chr6:85622725
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0155 | 4 | HG02451.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-38T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85622725 | ||||||
chr6:85622875
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.803-188A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85622875 | ||||||
chr6:85623044
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 6 | HG02559.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-357T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623044 | ||||||
chr6:85623258
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0031others(1): Show | 10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-571C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623258 | ||||||
chr6:85623311
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.803-624G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623311 | ||||||
chr6:85623374
|
G | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+603C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623374 | ||||||
chr6:85623532
|
C | G | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.802+445G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623532 | ||||||
chr6:85623561
|
C | CCCAAAAA others(6): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0094 | 2 | HG00408.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.802+415_802+416ins others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623561 | ||||||
chr6:85623562
|
C | CAAAAAA | 15 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(12): Show | 23 | HG00423.hp1 HG01070.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.802+409_802+414dup others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.802+401_802+414dup others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.802+397_802+414dup others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+396_802+414dup others(19): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAA | 4 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0125others(1): Show | 4 | HG03098.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(3): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAA | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0126 | 3 | HG02145.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.802+414_802+415ins others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA | 7 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0259others(4): Show | 8 | HG01168.hp2 HG01169.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(7): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(4): Show |
15 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0054others(12): Show | 17 | HG01168.hp1 HG01358.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(11): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(5): Show |
19 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0041others(16): Show | 22 | HG00735.hp2 HG01109.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(6): Show |
12 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(9): Show | 12 | HG02165.hp2 HG02523.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(7): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 17 | HG00423.hp2 HG02135.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(8): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0063others(7): Show | 10 | HG01255.hp1 HG01975.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(15): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(9): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0093 | 2 | HG01928.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.802+414_802+415ins others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(10): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0074 | 2 | HG03471.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.802+414_802+415ins others(17): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(11): Show |
1 | a0001c0001t0001g0070 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.802+414_802+415ins others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
C | CCAAAAAA others(13): Show |
1 | a0001c0001t0001g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.802+414_802+415ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
CA | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.802+414delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623562
|
CAAA | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0241a0001c0001t0001g0244others(5): Show | 8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+412_802+414del others(3): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | ||||||
chr6:85623563
|
A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(47): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.802+414T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623563 | ||||||
chr6:85623566
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.802+411T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623566 | ||||||
chr6:85623567
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.802+410T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623567 | ||||||
chr6:85623571
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.802+405_802+406ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | ||||||
chr6:85623571
|
A | AAAAAAAA others(13): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02630.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.802+405_802+406ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | ||||||
chr6:85623571
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.802+405_802+406ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | ||||||
chr6:85623571
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.802+406T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | ||||||
chr6:85623573
|
A | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0086others(1): Show | 6 | NA18956.hp2 NA18969.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+404T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623573 | ||||||
chr6:85623579
|
A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0251a0001c0001t0001g0257a0001c0001t0001g0274others(1): Show | 4 | HG02071.hp2 NA19058.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623579
|
A | AAAAAAAC others(14): Show |
1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623579
|
A | AAAAAAAC others(13): Show |
42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(39): Show | 61 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.802+397_802+398ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623579
|
A | AAAAAAAC others(13): Show |
1 | a0001c0001t0001g0258 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.802+397_802+398ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623579
|
A | AAAAAAAC others(14): Show |
1 | a0001c0001t0001g0291 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623579
|
A | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0259a0001c0001t0001g0262others(4): Show | 8 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+398T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | ||||||
chr6:85623583
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.802+393_802+394ins others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623583 | ||||||
chr6:85623595
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.802+382C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623595 | ||||||
chr6:85623888
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.802+89A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623888 | ||||||
chr6:85624115
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0130 | 2 | HG02523.hp1 NA18979.hp2 |
splice_region_variant&intron_variant | LOW | c.667-3C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624115 | ||||||
chr6:85624138
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.667-26A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624138 | ||||||
chr6:85624186
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.667-74T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624186 | ||||||
chr6:85624303
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.667-191A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624303 | ||||||
chr6:85624342
|
C | G | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-230G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624342 | ||||||
chr6:85624372
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-260C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624372 | ||||||
chr6:85624654
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.667-542C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624654 | ||||||
chr6:85624669
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.667-557A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624669 | ||||||
chr6:85624681
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.667-569T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624681 | ||||||
chr6:85624708
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.667-596T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624708 | ||||||
chr6:85624716
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.667-604A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624716 | ||||||
chr6:85624718
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667-606C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624718 | ||||||
chr6:85624956
|
A | G | 9 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0001g0241others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-844T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624956 | ||||||
chr6:85625130
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.667-1018G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625130 | ||||||
chr6:85625212
|
T | A | 1 | a0001c0001t0001g0255 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.667-1100A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625212 | ||||||
chr6:85625243
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-1131G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625243 | ||||||
chr6:85625246
|
C | G | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.667-1134G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625246 | ||||||
chr6:85625358
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0235 | 3 | HG00423.hp1 HG02074.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.667-1246A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625358 | ||||||
chr6:85625363
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.667-1251T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625363 | ||||||
chr6:85625379
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.667-1267C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625379 | ||||||
chr6:85625380
|
G | GT | 10 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0074others(7): Show | 11 | HG02055.hp1 HG02109.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1269dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625380 | ||||||
chr6:85625432
|
A | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.667-1320T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625432 | ||||||
chr6:85625466
|
C | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0113 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.667-1354G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625466 | ||||||
chr6:85625513
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.667-1401C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625513 | ||||||
chr6:85625576
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.667-1464G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625576 | ||||||
chr6:85625584
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-1472G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625584 | ||||||
chr6:85625632
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.667-1520G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625632 | ||||||
chr6:85625747
|
C | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | NA18944.hp1 NA19009.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1635G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625747 | ||||||
chr6:85626080
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 11 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-1968A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626080 | ||||||
chr6:85626315
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.667-2203T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626315 | ||||||
chr6:85626340
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 6 | HG02559.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-2228A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626340 | ||||||
chr6:85626385
|
GA | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667-2274delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626385 | ||||||
chr6:85626491
|
T | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0291 | 3 | HG00609.hp2 NA18981.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.667-2379A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626491 | ||||||
chr6:85626582
|
T | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.667-2470A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626582 | ||||||
chr6:85626619
|
G | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(143): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.667-2507C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626619 | ||||||
chr6:85626686
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.667-2574T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626686 | ||||||
chr6:85626949
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-2837G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626949 | ||||||
chr6:85626972
|
T | C | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.667-2860A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626972 | ||||||
chr6:85627037
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.667-2925C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627037 | ||||||
chr6:85627083
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.667-2971G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627083 | ||||||
chr6:85627092
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.667-2980C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627092 | ||||||
chr6:85627270
|
C | CA | 18 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01928.hp2 HG02135.hp1 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.667-3159dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627270 | ||||||
chr6:85627271
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.667-3159T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627271 | ||||||
chr6:85627393
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-3281T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627393 | ||||||
chr6:85627465
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.667-3353G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627465 | ||||||
chr6:85627607
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0206 | 2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.667-3495T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627607 | ||||||
chr6:85627619
|
T | TAATTTAA others(3): Show |
1 | a0001c0001t0001g0197 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.667-3517_667-3508d others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627619 | ||||||
chr6:85627705
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-3593G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627705 | ||||||
chr6:85627729
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.667-3617A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627729 | ||||||
chr6:85628089
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-3977A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628089 | ||||||
chr6:85628271
|
G | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0068 | 2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.667-4159C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628271 | ||||||
chr6:85628276
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.667-4164C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628276 | ||||||
chr6:85628330
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0273 | 2 | NA18985.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.667-4218T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628330 | ||||||
chr6:85628340
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG02132.hp1 NA18940.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-4228A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628340 | ||||||
chr6:85628561
|
G | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-4449C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628561 | ||||||
chr6:85628562
|
A | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-4450T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628562 | ||||||
chr6:85628679
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.667-4567C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628679 | ||||||
chr6:85628868
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-4756G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628868 | ||||||
chr6:85629009
|
CT | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-4898delA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629009 | ||||||
chr6:85629052
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.667-4940T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629052 | ||||||
chr6:85629066
|
A | C | 1 | a0001c0001t0001g0255 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.667-4954T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629066 | ||||||
chr6:85629088
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-4976A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629088 | ||||||
chr6:85629176
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667-5064T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629176 | ||||||
chr6:85629378
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.667-5266A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629378 | ||||||
chr6:85629516
|
C | CA | 68 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0025others(65): Show | 72 | HG00423.hp1 HG00609.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.667-5405dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | ||||||
chr6:85629516
|
C | CAA | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(37): Show | 55 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.667-5406_667-5405d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | ||||||
chr6:85629516
|
C | CAAA | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0250others(20): Show | 32 | HG00609.hp2 HG02071.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.667-5407_667-5405d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | ||||||
chr6:85629552
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.667-5440C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629552 | ||||||
chr6:85629587
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(18): Show | 29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-5475C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629587 | ||||||
chr6:85629683
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.667-5571C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629683 | ||||||
chr6:85629846
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0299 | 2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.667-5734A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629846 | ||||||
chr6:85629853
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667-5741C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629853 | ||||||
chr6:85629917
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-5805C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629917 | ||||||
chr6:85629961
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.667-5849A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629961 | ||||||
chr6:85629979
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667-5867G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629979 | ||||||
chr6:85629981
|
C | CA | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 90 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.667-5870dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629981 | ||||||
chr6:85630084
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667-5972C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630084 | ||||||
chr6:85630205
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.667-6093G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630205 | ||||||
chr6:85630255
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.667-6143C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630255 | ||||||
chr6:85630310
|
G | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0241a0001c0001t0001g0244others(5): Show | 8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-6198C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630310 | ||||||
chr6:85630363
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.667-6251T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630363 | ||||||
chr6:85630388
|
C | T | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.667-6276G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630388 | ||||||
chr6:85630519
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0054a0001c0001t0001g0055others(21): Show | 26 | HG00735.hp2 HG01168.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-6407G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630519 | ||||||
chr6:85630678
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+6289A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630678 | ||||||
chr6:85630690
|
A | AT | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.666+6276dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630690 | ||||||
chr6:85630978
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.666+5989G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630978 | ||||||
chr6:85631025
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.666+5942G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631025 | ||||||
chr6:85631119
|
A | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.666+5848T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631119 | ||||||
chr6:85631130
|
G | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.666+5837C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631130 | ||||||
chr6:85631310
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.666+5657C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631310 | ||||||
chr6:85631339
|
C | CA | 7 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(4): Show | 7 | HG00544.hp2 HG01496.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+5627dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAA | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(44): Show | 67 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.666+5625_666+5627d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAA | 6 | a0001c0001t0001g0060a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00597.hp1 HG03017.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+5624_666+5627d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA | 8 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 9 | HG01433.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.666+5621_666+5627d others(9): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.666+5617_666+5627d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(5): Show |
28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022others(25): Show | 33 | HG00423.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+5616_666+5627d others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(6): Show |
27 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0056others(24): Show | 30 | HG00408.hp2 HG00735.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.666+5615_666+5627d others(15): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001g0067a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG01358.hp2 HG03017.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+5614_666+5627d others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0107others(1): Show | 4 | HG01109.hp1 HG03942.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+5613_666+5627d others(17): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0122 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.666+5612_666+5627d others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG01891.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.666+5627_666+5628i others(19): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0109 | 2 | HG02895.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.666+5627_666+5628i others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.666+5627_666+5628i others(27): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(47): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631339
|
C | CAAAAAAA others(44): Show |
1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(53): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | ||||||
chr6:85631721
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.666+5246G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631721 | ||||||
chr6:85631754
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.666+5213G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631754 | ||||||
chr6:85631849
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+5118G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631849 | ||||||
chr6:85631891
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+5076G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631891 | ||||||
chr6:85631893
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0241 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+5074A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631893 | ||||||
chr6:85632041
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.666+4926C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632041 | ||||||
chr6:85632198
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.666+4769T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632198 | ||||||
chr6:85632260
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.666+4707A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632260 | ||||||
chr6:85632463
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.666+4504A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632463 | ||||||
chr6:85632641
|
T | TA | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+4325dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632641 | ||||||
chr6:85632765
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.666+4202C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632765 | ||||||
chr6:85632936
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+4031C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632936 | ||||||
chr6:85632961
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.666+4006C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632961 | ||||||
chr6:85632981
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.666+3986C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632981 | ||||||
chr6:85633088
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.666+3868_666+3878d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633088 | ||||||
chr6:85633180
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3787G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633180 | ||||||
chr6:85633188
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3779T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633188 | ||||||
chr6:85633257
|
AAAAC | A | 73 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 81 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.666+3706_666+3709d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633257 | ||||||
chr6:85633261
|
C | CAAAT | 6 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0254others(3): Show | 6 | HG01175.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+3702_666+3705d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | ||||||
chr6:85633261
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.666+3706G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | ||||||
chr6:85633261
|
CAAAT | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0020others(45): Show | 57 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.666+3702_666+3705d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | ||||||
chr6:85633269
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+3698A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633269 | ||||||
chr6:85633294
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.666+3673A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633294 | ||||||
chr6:85633355
|
G | C | 1 | a0001c0001t0001g0024 | 2 | NA18948.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.666+3612C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633355 | ||||||
chr6:85633373
|
C | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0120 | 3 | HG02818.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.666+3594G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633373 | ||||||
chr6:85633528
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0031others(1): Show | 10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+3439A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633528 | ||||||
chr6:85633575
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | NA18948.hp2 NA18961.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+3392T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633575 | ||||||
chr6:85633688
|
T | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0141others(11): Show | 15 | HG00735.hp1 HG01106.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.666+3279A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633688 | ||||||
chr6:85633731
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.666+3236G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633731 | ||||||
chr6:85633763
|
C | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3204G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633763 | ||||||
chr6:85633793
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.666+3174G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633793 | ||||||
chr6:85633950
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.666+3017C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633950 | ||||||
chr6:85633996
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.666+2971C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633996 | ||||||
chr6:85634161
|
T | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0205a0001c0001t0001g0295 | 3 | HG00597.hp2 HG02027.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.666+2806A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634161 | ||||||
chr6:85634237
|
C | CTCGA | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02647.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2726_666+2729d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634237 | ||||||
chr6:85634239
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2728G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634239 | ||||||
chr6:85634240
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2727C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634240 | ||||||
chr6:85634317
|
C | CTATAAAT others(4): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.666+2639_666+2649d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634317 | ||||||
chr6:85634386
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.666+2581C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634386 | ||||||
chr6:85634512
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.666+2455C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634512 | ||||||
chr6:85634522
|
C | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2445G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634522 | ||||||
chr6:85634532
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00280.hp2 HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.666+2435T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634532 | ||||||
chr6:85634542
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.666+2425G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634542 | ||||||
chr6:85634578
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.666+2389C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634578 | ||||||
chr6:85634581
|
G | GT | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(56): Show | 79 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.666+2385dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634581 | ||||||
chr6:85634633
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+2334C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634633 | ||||||
chr6:85634907
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+2060A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634907 | ||||||
chr6:85634949
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.666+2018A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634949 | ||||||
chr6:85634990
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.666+1977G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634990 | ||||||
chr6:85635168
|
A | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG01433.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.666+1799T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635168 | ||||||
chr6:85635321
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.666+1646A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635321 | ||||||
chr6:85635353
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.666+1614A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635353 | ||||||
chr6:85635553
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.666+1414A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635553 | ||||||
chr6:85635702
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.666+1265C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635702 | ||||||
chr6:85635774
|
C | CA | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 135 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.666+1192dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | ||||||
chr6:85635774
|
C | CAA | 39 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0031others(36): Show | 43 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.666+1191_666+1192d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | ||||||
chr6:85635774
|
C | CAAA | 8 | a0001c0001t0001g0059a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG01884.hp2 HG03098.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+1190_666+1192d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | ||||||
chr6:85635774
|
CA | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0140a0001c0001t0001g0141others(5): Show | 11 | HG01257.hp1 HG01975.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+1192delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | ||||||
chr6:85635774
|
CAAA | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(18): Show | 29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.666+1190_666+1192d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | ||||||
chr6:85636071
|
A | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01258.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.666+896T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636071 | ||||||
chr6:85636119
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG03492.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.666+848T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636119 | ||||||
chr6:85636177
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.666+790C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636177 | ||||||
chr6:85636216
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.666+751C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636216 | ||||||
chr6:85636220
|
G | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.666+747C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636220 | ||||||
chr6:85636287
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+680T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636287 | ||||||
chr6:85636326
|
A | G | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.666+641T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636326 | ||||||
chr6:85636424
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0241 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+543C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636424 | ||||||
chr6:85636784
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.666+183T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636784 | ||||||
chr6:85636841
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+126T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636841 | ||||||
chr6:85636891
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0206 | 2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.666+76A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636891 | ||||||
chr6:85637471
|
TAA | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-117_376-116del others(2): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637471 | ||||||
chr6:85637527
|
T | C | 40 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 44 | HG00408.hp2 HG00423.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.376-171A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637527 | ||||||
chr6:85637830
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376-474C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637830 | ||||||
chr6:85637887
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-531G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637887 | ||||||
chr6:85637972
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-616C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637972 | ||||||
chr6:85638286
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376-930A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638286 | ||||||
chr6:85638341
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.376-985T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638341 | ||||||
chr6:85638380
|
C | CA | 15 | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0041others(12): Show | 16 | HG01168.hp1 HG01975.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-1025dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAA | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(28): Show | 36 | HG00423.hp2 HG00735.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.376-1026_376-1025d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAA | 17 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0089others(14): Show | 17 | HG00408.hp2 HG01255.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.376-1027_376-1025d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAA | 21 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0048others(18): Show | 24 | HG01109.hp1 HG02109.hp1 HG02165.hp1 others(21): Show |
intron_variant | MODIFIER | c.376-1028_376-1025d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAA | 11 | a0001c0001t0001g0056a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 11 | HG01891.hp2 HG02132.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.376-1029_376-1025d others(7): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAAA | 13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0118others(10): Show | 15 | HG00280.hp1 HG00544.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1030_376-1025d others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAAAA | 8 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 8 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-1031_376-1025d others(9): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0029others(5): Show | 15 | HG00099.hp1 HG01433.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1032_376-1025d others(10): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0286others(7): Show | 12 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-1033_376-1025d others(11): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.376-1034_376-1025d others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
CA | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.376-1025delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
CAAAAAA | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0053others(17): Show | 29 | HG02027.hp2 HG02083.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.376-1030_376-1025d others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638380
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0121a0001c0001t0001g0241 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.376-1035_376-1025d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | ||||||
chr6:85638463
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.376-1107T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638463 | ||||||
chr6:85638585
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.376-1229A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638585 | ||||||
chr6:85638620
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376-1264T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638620 | ||||||
chr6:85638820
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(18): Show | 29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.375+1401C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638820 | ||||||
chr6:85638848
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0132others(1): Show | 7 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+1373G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638848 | ||||||
chr6:85638992
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.375+1229C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638992 | ||||||
chr6:85639002
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.375+1219C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639002 | ||||||
chr6:85639025
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(22): Show | 33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.375+1196A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639025 | ||||||
chr6:85639080
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+1141G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639080 | ||||||
chr6:85639150
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0241 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.375+1071C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639150 | ||||||
chr6:85639385
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.375+836A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639385 | ||||||
chr6:85639415
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.375+806A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639415 | ||||||
chr6:85639453
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG03492.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.375+768G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639453 | ||||||
chr6:85639584
|
C | T | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+637G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639584 | ||||||
chr6:85639636
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.375+585T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639636 | ||||||
chr6:85639672
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18991.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.375+549C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639672 | ||||||
chr6:85639688
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.375+533A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639688 | ||||||
chr6:85639714
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.375+507T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639714 | ||||||
chr6:85639726
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.375+495G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639726 | ||||||
chr6:85639852
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(58): Show | 81 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.375+369A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639852 | ||||||
chr6:85639952
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.375+269T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639952 | ||||||
chr6:85639969
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.375+252A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639969 | ||||||
chr6:85640027
|
G | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0208a0001c0001t0001g0209others(6): Show | 12 | HG02074.hp2 HG02683.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.375+194C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640027 | ||||||
chr6:85640097
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.375+124A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640097 | ||||||
chr6:85640135
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.375+86T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640135 | ||||||
chr6:85640676
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 217 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.149-112G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640676 | ||||||
chr6:85640687
|
G | GA | 33 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(30): Show | 41 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.149-124dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640687 | ||||||
chr6:85640698
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.149-134T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640698 | ||||||
chr6:85640779
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-215A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640779 | ||||||
chr6:85640838
|
TAC | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-276_149-275del others(2): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640838 | ||||||
chr6:85641007
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.148+285T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85641007 | ||||||
chr6:85641046
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.148+246A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85641046 | ||||||
chr6:85641496
|
G | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-45C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85641496 | ||||||
chr6:85641865
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-12-414C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85641865 | ||||||
chr6:85642004
|
G | C | 1 | a0001c0001t0003g0301 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-12-553C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642004 | ||||||
chr6:85642083
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12-632G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642083 | ||||||
chr6:85642223
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+574C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642223 | ||||||
chr6:85642298
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(54): Show | 77 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-13+499C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642298 | ||||||
chr6:85642339
|
C | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0034others(6): Show | 11 | HG00609.hp1 HG02040.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+458G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642339 | ||||||
chr6:85642449
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-13+348C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642449 | ||||||
chr6:85642458
|
C | T | 1 | a0001c0001t0001g0009 | 3 | NA18951.hp1 NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-13+339G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642458 | ||||||
chr6:85642468
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0033 | 5 | HG02280.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+329G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642468 | ||||||
chr6:85642651
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+146A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642651 | ||||||
chr6:85642711
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-13+86G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642711 | ||||||
chr6:85642718
|
T | C | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-13+79A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642718 | ||||||
chr6:85642761
|
G | C | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-13+36C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642761 |