geneid | 6492 |
---|---|
ensemblid | ENSG00000112246.10 |
hgncid | 10882 |
symbol | SIM1 |
name | SIM bHLH transcription factor 1 |
refseq_nuc | NM_005068.3 |
refseq_prot | NP_005059.2 |
ensembl_nuc | ENST00000369208.8 |
ensembl_prot | ENSP00000358210.4 |
mane_status | MANE Select |
chr | chr6 |
start | 100385009 |
end | 100464921 |
strand | - |
ver | v1.2 |
region | chr6:100385009-100464921 |
region5000 | chr6:100380009-100469921 |
regionname0 | SIM1_chr6_100385009_100464921 |
regionname5000 | SIM1_chr6_100380009_100469921 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 766 | 237 | 79 | 42 | 78 | 14 | 22 | 57 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002 | 0/0 | 766 | 79 | 0 | 12 | 55 | 4 | 8 | 43 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0003 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0004 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0005 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0006 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2301 | 231 | 78 | 42 | 77 | 13 | 19 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0002 | 0/0 | 2301 | 78 | 0 | 12 | 54 | 4 | 8 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0003 | 0/0 | 2301 | 4 | 0 | 0 | 0 | 1 | 3 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0004 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0005 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0006 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0007 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0008 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0009 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
c0010 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6122 | 53 | 0 | 6 | 36 | 4 | 7 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0002 | 0/0 | 6134 | 42 | 9 | 7 | 16 | 1 | 9 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0003 | 0/1 | 6132 | 36 | 8 | 7 | 14 | 4 | 2 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0004 | 0/0 | 6119 | 19 | 0 | 5 | 14 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0005 | 0/0 | 6122 | 18 | 1 | 1 | 13 | 1 | 2 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0006 | 0/0 | 6130 | 16 | 14 | 1 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0007 | 0/0 | 6124 | 13 | 0 | 4 | 9 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0008 | 0/0 | 6119 | 11 | 3 | 5 | 1 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0009 | 1/0 | 6128 | 9 | 4 | 3 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0010 | 0/0 | 6138 | 6 | 3 | 1 | 1 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0011 | 0/0 | 6136 | 5 | 3 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0012 | 0/0 | 6134 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0013 | 0/0 | 6124 | 4 | 0 | 0 | 2 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0014 | 0/0 | 6118 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0015 | 0/0 | 6122 | 3 | 3 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0016 | 0/0 | 6136 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0017 | 0/0 | 6122 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0018 | 0/0 | 6119 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0019 | 0/0 | 6132 | 2 | 0 | 1 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0020 | 0/0 | 6124 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0021 | 0/0 | 6136 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0022 | 0/0 | 6132 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0023 | 0/0 | 6136 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0024 | 0/0 | 6120 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0025 | 0/0 | 6124 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0026 | 0/0 | 6121 | 2 | 0 | 1 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0027 | 0/0 | 6121 | 2 | 1 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0028 | 0/0 | 6122 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0029 | 0/0 | 6140 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0030 | 0/0 | 6132 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0031 | 0/0 | 6119 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0032 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0033 | 0/0 | 6118 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0034 | 0/0 | 6134 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0035 | 0/0 | 6119 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0036 | 0/0 | 6136 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0037 | 0/0 | 6136 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0038 | 0/0 | 6134 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0039 | 0/0 | 6130 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0040 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0041 | 0/0 | 6122 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0042 | 0/0 | 6132 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0043 | 0/0 | 6130 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0044 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0045 | 0/0 | 6142 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0046 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0047 | 0/0 | 6134 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0048 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0049 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0050 | 0/0 | 6142 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0051 | 0/0 | 6136 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0052 | 0/0 | 6134 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0053 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0054 | 0/0 | 6136 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0055 | 0/0 | 6130 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0056 | 0/0 | 6130 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0057 | 0/0 | 6130 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0058 | 0/0 | 6130 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0059 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0060 | 0/0 | 6134 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0061 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0062 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0063 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0064 | 0/0 | 6118 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0065 | 0/0 | 6122 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0066 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0067 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0068 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0069 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0070 | 0/0 | 6116 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0071 | 0/0 | 6123 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0072 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0073 | 0/0 | 6117 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0074 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0075 | 0/0 | 6119 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0076 | 0/0 | 6134 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0077 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0078 | 0/0 | 6134 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
t0079 | 0/0 | 6132 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2301 | 231 | 78 | 42 | 77 | 13 | 19 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0003 | 0/0 | 2301 | 4 | 0 | 0 | 0 | 1 | 3 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0007 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0009 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002 | 0/0 | 2301 | 78 | 0 | 12 | 54 | 4 | 8 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0005 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0003c0006 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0004c0008 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0005c0010 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0006c0004 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0002 | 0/0 | 8434 | 42 | 9 | 7 | 16 | 1 | 9 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0003 | 0/1 | 8432 | 31 | 8 | 7 | 11 | 3 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0004 | 0/0 | 8419 | 17 | 0 | 5 | 12 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0005 | 0/0 | 8422 | 18 | 1 | 1 | 13 | 1 | 2 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0006 | 0/0 | 8430 | 15 | 14 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0008 | 0/0 | 8419 | 11 | 3 | 5 | 1 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0009 | 1/0 | 8428 | 9 | 4 | 3 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0010 | 0/0 | 8438 | 6 | 3 | 1 | 1 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0011 | 0/0 | 8436 | 5 | 3 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0012 | 0/0 | 8434 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0013 | 0/0 | 8424 | 4 | 0 | 0 | 2 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0015 | 0/0 | 8422 | 3 | 3 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0016 | 0/0 | 8436 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0018 | 0/0 | 8419 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0019 | 0/0 | 8432 | 2 | 0 | 1 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0020 | 0/0 | 8424 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0021 | 0/0 | 8436 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0022 | 0/0 | 8432 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0023 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0025 | 0/0 | 8424 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0026 | 0/0 | 8421 | 2 | 0 | 1 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0027 | 0/0 | 8421 | 2 | 1 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0028 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0029 | 0/0 | 8440 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0031 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0032 | 0/0 | 8438 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0034 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0035 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0036 | 0/0 | 8436 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0037 | 0/0 | 8436 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0038 | 0/0 | 8434 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0039 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0040 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0041 | 0/0 | 8422 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0042 | 0/0 | 8432 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0043 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0044 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0045 | 0/0 | 8442 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0046 | 0/0 | 8438 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0047 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0048 | 0/0 | 8438 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0049 | 0/0 | 8428 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0050 | 0/0 | 8442 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0051 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0052 | 0/0 | 8434 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0053 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0054 | 0/0 | 8436 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0055 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0056 | 0/0 | 8430 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0057 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0058 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0059 | 0/0 | 8428 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0060 | 0/0 | 8434 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0061 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0062 | 0/0 | 8428 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0063 | 0/0 | 8420 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0064 | 0/0 | 8418 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0068 | 0/0 | 8420 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0069 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0070 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0071 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0072 | 0/0 | 8429 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0073 | 0/0 | 8417 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0074 | 0/0 | 8413 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0075 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0076 | 0/0 | 8434 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0077 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0001t0078 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0003t0003 | 0/0 | 8432 | 2 | 0 | 0 | 0 | 1 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0003t0030 | 0/0 | 8432 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0003t0079 | 0/0 | 8432 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0007t0004 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0001c0009t0033 | 0/0 | 8418 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0001 | 0/0 | 8422 | 52 | 0 | 6 | 35 | 4 | 7 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0003 | 0/0 | 8432 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0006 | 0/0 | 8430 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0007 | 0/0 | 8424 | 13 | 0 | 4 | 9 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0014 | 0/0 | 8418 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0017 | 0/0 | 8422 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0024 | 0/0 | 8420 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0028 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0002t0066 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0002c0005t0065 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0003c0006t0004 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0004c0008t0023 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0005c0010t0067 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
a0006c0004t0003 | 0/0 | 8432 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | copy fasta | chr6 | 100380009 | 100469921 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0012g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0012g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0012g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0012g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0013g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0013g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0015g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0016g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0018g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0018g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0019g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0019g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0020g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0021g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0021g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0022g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0025g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0025g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0026g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0026g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0027g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0027g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0028g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0029g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0031g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0032g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0034g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0035g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0036g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0037g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0038g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0039g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0040g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0041g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0042g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0043g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0044g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0045g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0046g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0047g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0048g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0049g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0050g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0051g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0052g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0053g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0054g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0055g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0056g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0057g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0058g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0059g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0060g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0061g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0062g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0063g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0064g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0068g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0069g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0070g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0071g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0072g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0073g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0074g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0075g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0076g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0077g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0001t0078g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0003t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0003t0079g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0007t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0001c0009t0033g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0014g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0014g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0014g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0017g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0017g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0024g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0024g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0028g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0002t0066g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0002c0005t0065g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0003c0006t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0004c0008t0023g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0005c0010t0067g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
a0006c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0249 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00099 | hp2 | a0001 | c0001 | t0010 | g0279 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00140 | hp1 | a0001 | c0001 | t0037 | g0017 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0243 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00280 | hp1 | a0001 | c0001 | t0036 | g0305 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00280 | hp2 | a0001 | c0001 | t0013 | g0127 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00323 | hp2 | a0001 | c0001 | t0013 | g0142 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00423 | hp1 | a0001 | c0001 | t0026 | g0233 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00438 | hp1 | a0002 | c0002 | t0014 | g0269 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00558 | hp2 | a0002 | c0002 | t0024 | g0101 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0050 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00738 | hp1 | a0001 | c0001 | t0048 | g0107 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00738 | hp2 | a0002 | c0002 | t0007 | g0267 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01070 | hp1 | a0001 | c0001 | t0019 | g0018 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0209 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01074 | hp1 | a0002 | c0002 | t0017 | g0312 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01081 | hp1 | a0001 | c0001 | t0021 | g0266 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0284 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0070 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01167 | hp2 | a0001 | c0001 | t0021 | g0108 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0023 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01168 | hp2 | a0001 | c0001 | t0059 | g0178 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0081 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0072 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01175 | hp1 | a0001 | c0001 | t0027 | g0029 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01256 | hp1 | a0001 | c0001 | t0038 | g0015 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0099 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01346 | hp1 | a0001 | c0001 | t0016 | g0001 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0096 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01361 | hp1 | a0002 | c0002 | t0017 | g0313 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01433 | hp2 | a0001 | c0001 | t0076 | g0076 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01496 | hp2 | a0001 | c0001 | t0026 | g0202 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0079 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0317 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01516 | hp1 | a0001 | c0003 | t0003 | g0137 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0315 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0078 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0318 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0300 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01884 | hp2 | a0001 | c0001 | t0060 | g0153 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01891 | hp1 | a0001 | c0001 | t0015 | g0246 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01891 | hp2 | a0001 | c0001 | t0050 | g0155 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01934 | hp1 | a0002 | c0002 | t0007 | g0100 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01952 | hp2 | a0002 | c0002 | t0007 | g0268 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01993 | hp1 | a0001 | c0001 | t0029 | g0002 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02027 | hp1 | a0001 | c0001 | t0075 | g0179 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02027 | hp2 | a0001 | c0007 | t0004 | g0205 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02055 | hp1 | a0001 | c0001 | t0074 | g0051 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02056 | hp1 | a0002 | c0002 | t0007 | g0238 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02071 | hp2 | a0006 | c0004 | t0003 | g0093 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02083 | hp1 | a0001 | c0001 | t0018 | g0311 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02083 | hp2 | a0002 | c0002 | t0014 | g0272 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02129 | hp1 | a0001 | c0001 | t0012 | g0306 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02129 | hp2 | a0001 | c0001 | t0011 | g0125 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02145 | hp1 | a0001 | c0001 | t0069 | g0264 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02165 | hp2 | a0001 | c0001 | t0011 | g0290 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0297 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0283 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0160 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02280 | hp2 | a0001 | c0001 | t0053 | g0289 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0098 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02300 | hp2 | a0002 | c0002 | t0007 | g0121 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02451 | hp2 | a0001 | c0001 | t0025 | g0263 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02523 | hp2 | a0001 | c0001 | t0008 | g0102 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0163 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0077 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02602 | hp1 | a0002 | c0002 | t0006 | g0235 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02615 | hp1 | a0001 | c0001 | t0039 | g0012 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02615 | hp2 | a0001 | c0001 | t0071 | g0010 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02630 | hp2 | a0001 | c0001 | t0027 | g0089 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02647 | hp2 | a0001 | c0001 | t0051 | g0188 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02683 | hp1 | a0001 | c0001 | t0056 | g0025 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02717 | hp1 | a0001 | c0001 | t0077 | g0275 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02717 | hp2 | a0001 | c0001 | t0068 | g0294 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02723 | hp1 | a0001 | c0001 | t0041 | g0167 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02738 | hp2 | a0001 | c0003 | t0003 | g0024 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02809 | hp1 | a0001 | c0001 | t0043 | g0190 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02809 | hp2 | a0001 | c0001 | t0040 | g0011 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0286 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0159 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02965 | hp1 | a0001 | c0001 | t0057 | g0083 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0245 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03017 | hp1 | a0001 | c0001 | t0049 | g0073 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0219 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0287 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0285 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03098 | hp1 | a0001 | c0001 | t0055 | g0154 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0247 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03139 | hp1 | a0001 | c0001 | t0058 | g0084 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03139 | hp2 | a0001 | c0001 | t0032 | g0006 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03225 | hp1 | a0004 | c0008 | t0023 | g0223 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03225 | hp2 | a0001 | c0001 | t0042 | g0040 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03239 | hp2 | a0001 | c0001 | t0034 | g0007 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03490 | hp1 | a0001 | c0001 | t0078 | g0303 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03490 | hp2 | a0001 | c0003 | t0030 | g0003 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03491 | hp2 | a0001 | c0001 | t0035 | g0008 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03492 | hp1 | a0001 | c0003 | t0079 | g0304 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0299 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03516 | hp2 | a0001 | c0001 | t0025 | g0256 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03540 | hp2 | a0001 | c0001 | t0044 | g0168 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0172 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03831 | hp1 | a0001 | c0001 | t0009 | g0027 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0248 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04184 | hp2 | a0001 | c0001 | t0047 | g0208 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18522 | hp1 | a0001 | c0001 | t0022 | g0147 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18747 | hp2 | a0002 | c0002 | t0007 | g0176 | EAS | CHB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18943 | hp1 | a0001 | c0001 | t0045 | g0253 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18943 | hp2 | a0001 | c0001 | t0018 | g0307 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0309 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18946 | hp1 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18948 | hp2 | a0002 | c0002 | t0014 | g0270 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18953 | hp1 | a0001 | c0001 | t0064 | g0090 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18957 | hp1 | a0005 | c0010 | t0067 | g0021 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18957 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18966 | hp1 | a0002 | c0002 | t0007 | g0133 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18966 | hp2 | a0001 | c0001 | t0072 | g0181 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18967 | hp1 | a0002 | c0005 | t0065 | g0055 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18967 | hp2 | a0001 | c0001 | t0052 | g0296 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18973 | hp1 | a0002 | c0002 | t0007 | g0065 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18975 | hp2 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18978 | hp1 | a0002 | c0002 | t0028 | g0103 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18980 | hp1 | a0001 | c0001 | t0013 | g0126 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18982 | hp2 | a0002 | c0002 | t0007 | g0184 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18983 | hp2 | a0002 | c0002 | t0014 | g0057 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18989 | hp1 | a0001 | c0001 | t0046 | g0252 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18992 | hp1 | a0002 | c0002 | t0024 | g0273 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18994 | hp2 | a0001 | c0001 | t0013 | g0106 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18998 | hp1 | a0002 | c0002 | t0066 | g0062 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19007 | hp1 | a0001 | c0001 | t0012 | g0310 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0281 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19030 | hp2 | a0001 | c0009 | t0033 | g0005 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19062 | hp1 | a0001 | c0001 | t0073 | g0115 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19062 | hp2 | a0002 | c0002 | t0007 | g0183 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19063 | hp2 | a0001 | c0001 | t0028 | g0254 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19065 | hp2 | a0001 | c0001 | t0054 | g0197 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19066 | hp1 | a0002 | c0002 | t0007 | g0019 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19066 | hp2 | a0003 | c0006 | t0004 | g0130 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19068 | hp1 | a0001 | c0001 | t0012 | g0308 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19078 | hp2 | a0002 | c0002 | t0007 | g0237 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19082 | hp1 | a0002 | c0002 | t0007 | g0054 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19082 | hp2 | a0001 | c0001 | t0062 | g0109 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19240 | hp1 | a0001 | c0001 | t0061 | g0302 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20752 | hp1 | a0001 | c0001 | t0019 | g0016 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0143 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0032 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02109 | hp1 | a0001 | c0001 | t0023 | g0088 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02559 | hp1 | a0001 | c0001 | t0070 | g0177 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0216 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA21309 | hp1 | a0001 | c0001 | t0063 | g0075 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0009 | REF | REF | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0022 | REF | REF | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:100390489
|
C | T | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2173G>A | p.Glu725Lys | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2948/8428 | 2173/2301 | 725/766 | chr6 | 100390489 | ||
chr6:100420836
|
C | T | 1 | a0003 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1121G>A | p.Arg374Gln | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1896/8428 | 1121/2301 | 374/766 | chr6 | 100420836 | ||
chr6:100420845
|
G | A | 2 | a0002a0005 | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
missense_variant | MODERATE | c.1112C>T | p.Ala371Val | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1887/8428 | 1112/2301 | 371/766 | chr6 | 100420845 | ||
chr6:100420903
|
G | T | 2 | a0002a0005 | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
missense_variant | MODERATE | c.1054C>A | p.Pro352Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1829/8428 | 1054/2301 | 352/766 | chr6 | 100420903 | ||
chr6:100449650
|
T | C | 1 | a0005 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.398A>G | p.His133Arg | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/12 | 1173/8428 | 398/2301 | 133/766 | chr6 | 100449650 | ||
chr6:100453800
|
C | T | 1 | a0006 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.220G>A | p.Asp74Asn | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/12 | 995/8428 | 220/2301 | 74/766 | chr6 | 100453800 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:100390370
|
G | A | 1 | a0002c0005 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2292C>T | p.Asn764Asn | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3067/8428 | 2292/2301 | 764/766 | chr6 | 100390370 | ||
chr6:100390562
|
G | C | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2100C>G | p.Gly700Gly | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2875/8428 | 2100/2301 | 700/766 | chr6 | 100390562 | ||
chr6:100390703
|
G | A | 1 | a0001c0003 | 4 | HG01516.hp1 HG02738.hp2 HG03490.hp2 others(1): Show |
synonymous_variant | LOW | c.1959C>T | p.Thr653Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2734/8428 | 1959/2301 | 653/766 | chr6 | 100390703 | ||
chr6:100393821
|
G | T | 1 | a0001c0007 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1236C>A | p.Thr412Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/12 | 2011/8428 | 1236/2301 | 412/766 | chr6 | 100393821 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:100385194
|
A | G | 1 | a0002c0005t0065 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5167T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5167 | chr6 | 100385194 | |||||
chr6:100385200
|
A | G | 1 | a0001c0001t0051 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5161T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5161 | chr6 | 100385200 | |||||
chr6:100385266
|
C | T | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(13): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5095G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5095 | chr6 | 100385266 | |||||
chr6:100385267
|
G | A | 1 | a0001c0001t0052 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5094C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5094 | chr6 | 100385267 | |||||
chr6:100385392
|
C | T | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4969G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4969 | chr6 | 100385392 | |||||
chr6:100385393
|
G | A | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4968C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4968 | chr6 | 100385393 | |||||
chr6:100385411
|
G | A | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(35): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*4950C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4950 | chr6 | 100385411 | |||||
chr6:100385669
|
A | ATG | 8 | a0001c0001t0006a0001c0001t0039a0001c0001t0043others(5): Show | 22 | HG01346.hp2 HG01884.hp1 HG02258.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4690_*4691dupCA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTG | 9 | a0001c0001t0003a0001c0001t0019a0001c0001t0022others(6): Show | 43 | HG00544.hp1 HG00558.hp1 HG01070.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4688_*4691dupCACA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTGTG | 9 | a0001c0001t0002a0001c0001t0012a0001c0001t0034others(6): Show | 53 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4686_*4691dupCACA others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0011a0001c0001t0016a0001c0001t0021others(6): Show | 15 | HG00140.hp1 HG00280.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4684_*4691dupCACA others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0010a0001c0001t0032a0001c0001t0046others(1): Show | 9 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4682_*4691dupCACA others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0029 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4680_*4691dupCACA others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0045a0001c0001t0050 | 2 | HG01891.hp2 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4678_*4691dupCACA others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | |||||
chr6:100385669
|
A | G | 1 | a0001c0001t0049 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4692T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4692 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTG | A | 6 | a0001c0001t0013a0001c0001t0020a0001c0001t0025others(3): Show | 23 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4688_*4691delCACA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4688 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTGTG | A | 10 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(7): Show | 81 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4686_*4691delCACA others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4686 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0026a0001c0001t0027a0001c0001t0063others(2): Show | 8 | HG00423.hp1 HG00558.hp2 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4684_*4691delCACA others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4684 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(8): Show | 41 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4682_*4691delCACA others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4682 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0061a0001c0001t0070a0001c0001t0073others(1): Show | 4 | HG02559.hp1 HG02717.hp1 NA19062.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4680_*4691delCACA others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4680 | chr6 | 100385669 | |||||
chr6:100385669
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4676_*4691delCACA others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4676 | chr6 | 100385669 | |||||
chr6:100385885
|
C | T | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4476G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4476 | chr6 | 100385885 | |||||
chr6:100385903
|
C | T | 11 | a0001c0001t0001a0001c0001t0028a0002c0002t0001others(8): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4458G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4458 | chr6 | 100385903 | |||||
chr6:100386187
|
G | C | 5 | a0001c0001t0005a0001c0001t0013a0001c0001t0062others(2): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4174C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4174 | chr6 | 100386187 | |||||
chr6:100386226
|
T | C | 2 | a0001c0001t0025a0001c0001t0069 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4135A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4135 | chr6 | 100386226 | |||||
chr6:100386363
|
T | C | 1 | a0002c0002t0066 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3998A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3998 | chr6 | 100386363 | |||||
chr6:100386374
|
A | G | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3987T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3987 | chr6 | 100386374 | |||||
chr6:100386399
|
T | C | 16 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(13): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3962A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3962 | chr6 | 100386399 | |||||
chr6:100386409
|
G | T | 1 | a0001c0001t0034 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3952C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3952 | chr6 | 100386409 | |||||
chr6:100386521
|
A | G | 1 | a0001c0001t0061 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3840T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3840 | chr6 | 100386521 | |||||
chr6:100386555
|
A | G | 1 | a0001c0001t0022 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3806T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3806 | chr6 | 100386555 | |||||
chr6:100386556
|
T | C | 1 | a0001c0001t0053 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3805 | chr6 | 100386556 | |||||
chr6:100386627
|
C | T | 5 | a0001c0001t0016a0001c0001t0021a0001c0001t0029others(2): Show | 7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3734G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3734 | chr6 | 100386627 | |||||
chr6:100386798
|
C | T | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(13): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3563G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3563 | chr6 | 100386798 | |||||
chr6:100386882
|
A | G | 1 | a0001c0009t0033 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3479T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3479 | chr6 | 100386882 | |||||
chr6:100386904
|
C | T | 13 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(10): Show | 42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3457G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3457 | chr6 | 100386904 | |||||
chr6:100386996
|
A | G | 1 | a0001c0001t0047 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3365 | chr6 | 100386996 | |||||
chr6:100387067
|
A | T | 2 | a0001c0001t0045a0001c0001t0046 | 2 | NA18943.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3294T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3294 | chr6 | 100387067 | |||||
chr6:100387100
|
T | C | 2 | a0001c0001t0025a0001c0001t0069 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3261A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3261 | chr6 | 100387100 | |||||
chr6:100387345
|
T | C | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(29): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3016A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3016 | chr6 | 100387345 | |||||
chr6:100387359
|
T | C | 2 | a0001c0001t0025a0001c0001t0069 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3002A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3002 | chr6 | 100387359 | |||||
chr6:100387391
|
G | A | 1 | a0005c0010t0067 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2970C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2970 | chr6 | 100387391 | |||||
chr6:100387431
|
A | T | 10 | a0001c0001t0004a0001c0001t0018a0001c0001t0026others(7): Show | 28 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2930T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2930 | chr6 | 100387431 | |||||
chr6:100387453
|
A | G | 1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2908T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2908 | chr6 | 100387453 | |||||
chr6:100387479
|
T | C | 1 | a0001c0001t0054 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2882A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2882 | chr6 | 100387479 | |||||
chr6:100387717
|
G | A | 1 | a0001c0001t0070 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2644 | chr6 | 100387717 | |||||
chr6:100387782
|
T | C | 11 | a0001c0001t0001a0001c0001t0028a0002c0002t0001others(8): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2579A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2579 | chr6 | 100387782 | |||||
chr6:100387784
|
T | C | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(38): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2577A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2577 | chr6 | 100387784 | |||||
chr6:100387833
|
T | C | 1 | a0001c0001t0075 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2528A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2528 | chr6 | 100387833 | |||||
chr6:100387945
|
C | A | 1 | a0001c0001t0055 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2416 | chr6 | 100387945 | |||||
chr6:100388139
|
C | T | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(29): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2222 | chr6 | 100388139 | |||||
chr6:100388146
|
T | C | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(13): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2215A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2215 | chr6 | 100388146 | |||||
chr6:100388274
|
C | T | 1 | a0001c0001t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2087 | chr6 | 100388274 | |||||
chr6:100388315
|
A | T | 1 | a0001c0001t0071 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2046T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2046 | chr6 | 100388315 | |||||
chr6:100388356
|
G | GA | 16 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(13): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2004dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2004 | chr6 | 100388356 | |||||
chr6:100388400
|
G | A | 1 | a0001c0001t0056 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1961C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1961 | chr6 | 100388400 | |||||
chr6:100388584
|
C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1777 | chr6 | 100388584 | |||||
chr6:100388760
|
A | T | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(13): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1601T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1601 | chr6 | 100388760 | |||||
chr6:100388908
|
C | A | 16 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(13): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1453G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1453 | chr6 | 100388908 | |||||
chr6:100389229
|
T | G | 2 | a0001c0001t0057a0001c0001t0058 | 2 | HG02965.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1132 | chr6 | 100389229 | |||||
chr6:100389362
|
A | G | 1 | a0001c0001t0061 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 999 | chr6 | 100389362 | |||||
chr6:100389867
|
A | G | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG02809.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*494T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 494 | chr6 | 100389867 | |||||
chr6:100389891
|
G | A | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 470 | chr6 | 100389891 | |||||
chr6:100389986
|
G | A | 3 | a0001c0001t0023a0001c0001t0060a0004c0008t0023 | 3 | HG01884.hp2 HG02109.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 375 | chr6 | 100389986 | |||||
chr6:100390013
|
T | A | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(35): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*348A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 348 | chr6 | 100390013 | |||||
chr6:100390178
|
T | A | 2 | a0001c0001t0028a0002c0002t0028 | 2 | NA18978.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 183 | chr6 | 100390178 | |||||
chr6:100390248
|
T | A | 1 | a0001c0001t0076 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 113 | chr6 | 100390248 | |||||
chr6:100390274
|
C | A | 1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 87 | chr6 | 100390274 | |||||
chr6:100390310
|
C | T | 2 | a0001c0001t0020a0001c0001t0041 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 51 | chr6 | 100390310 | |||||
chr6:100463558
|
G | T | 2 | a0001c0001t0039a0001c0001t0040 | 2 | HG02615.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-90C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 90 | chr6 | 100463558 | |||||
chr6:100463595
|
A | G | 3 | a0001c0001t0019a0001c0001t0037a0001c0001t0038 | 4 | HG00140.hp1 HG01070.hp1 HG01256.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-127T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 127 | chr6 | 100463595 | |||||
chr6:100463642
|
G | A | 2 | a0001c0001t0078a0001c0003t0079 | 2 | HG03490.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-174C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 174 | chr6 | 100463642 | |||||
chr6:100463724
|
C | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0036others(1): Show | 9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-256G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 256 | chr6 | 100463724 | |||||
chr6:100464648
|
C | T | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG03239.hp2 HG03491.hp2 |
5_prime_UTR_variant | MODIFIER | c.-502G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1180 | chr6 | 100464648 | |||||
chr6:100464681
|
C | T | 2 | a0001c0001t0032a0001c0009t0033 | 2 | HG03139.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-535G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1213 | chr6 | 100464681 | |||||
chr6:100464749
|
C | G | 1 | a0001c0001t0031 | 1 | NA18975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-603G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1281 | chr6 | 100464749 | |||||
chr6:100464867
|
A | G | 3 | a0001c0001t0016a0001c0001t0029a0001c0003t0030 | 4 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-721T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1399 | chr6 | 100464867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:100391287
|
T | C | 104 | a0001c0001t0001g0141a0001c0001t0005g0032a0001c0001t0005g0045others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1571-196A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391287 | ||||||
chr6:100391322
|
T | C | 1 | a0001c0001t0056g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1571-231A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391322 | ||||||
chr6:100391418
|
T | C | 25 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0082others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1571-327A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391418 | ||||||
chr6:100391422
|
C | T | 1 | a0001c0001t0005g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1571-331G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391422 | ||||||
chr6:100391487
|
C | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0191a0001c0001t0003g0224others(1): Show | 4 | HG02071.hp2 HG02132.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-396G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391487 | ||||||
chr6:100391497
|
T | C | 1 | a0001c0001t0068g0294 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1571-406A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391497 | ||||||
chr6:100391554
|
C | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-463G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391554 | ||||||
chr6:100391863
|
A | G | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-772T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391863 | ||||||
chr6:100391910
|
C | A | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1571-819G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391910 | ||||||
chr6:100391913
|
C | G | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-822G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391913 | ||||||
chr6:100391990
|
T | C | 3 | a0001c0001t0002g0086a0001c0001t0003g0151a0001c0001t0003g0169 | 3 | HG02257.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1571-899A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391990 | ||||||
chr6:100392082
|
G | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-991C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392082 | ||||||
chr6:100392128
|
C | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-1037G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392128 | ||||||
chr6:100392130
|
C | T | 1 | a0001c0001t0004g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1571-1039G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392130 | ||||||
chr6:100392131
|
G | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-1040C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392131 | ||||||
chr6:100392152
|
C | T | 43 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1571-1061G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392152 | ||||||
chr6:100392183
|
T | A | 1 | a0002c0002t0007g0238 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1571-1092A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392183 | ||||||
chr6:100392200
|
T | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-1109A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392200 | ||||||
chr6:100392215
|
A | T | 104 | a0001c0001t0001g0141a0001c0001t0005g0032a0001c0001t0005g0045others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1571-1124T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392215 | ||||||
chr6:100392244
|
A | T | 2 | a0001c0001t0027g0089a0001c0001t0077g0275 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1571-1153T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392244 | ||||||
chr6:100392248
|
TG | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-1158delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392248 | ||||||
chr6:100392383
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1570+1104C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392383 | ||||||
chr6:100392504
|
G | A | 149 | a0001c0001t0001g0141a0001c0001t0004g0041a0001c0001t0004g0095others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1570+983C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392504 | ||||||
chr6:100392548
|
G | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1570+939C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392548 | ||||||
chr6:100392763
|
C | T | 1 | a0001c0001t0027g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1570+724G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392763 | ||||||
chr6:100392880
|
C | T | 104 | a0001c0001t0001g0141a0001c0001t0005g0032a0001c0001t0005g0045others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1570+607G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392880 | ||||||
chr6:100392972
|
G | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1570+515C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392972 | ||||||
chr6:100393091
|
T | G | 1 | a0001c0001t0074g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1570+396A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100393091 | ||||||
chr6:100393353
|
G | T | 167 | a0001c0001t0001g0141a0001c0001t0004g0041a0001c0001t0004g0095others(164): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1570+134C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100393353 | ||||||
chr6:100393996
|
G | T | 1 | a0001c0001t0004g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-107C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100393996 | ||||||
chr6:100394092
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-203T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394092 | ||||||
chr6:100394130
|
A | G | 5 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-241T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394130 | ||||||
chr6:100394220
|
TG | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-332delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394220 | ||||||
chr6:100394240
|
G | C | 1 | a0002c0002t0001g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1168-351C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394240 | ||||||
chr6:100394455
|
G | A | 152 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-566C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394455 | ||||||
chr6:100394575
|
T | A | 1 | a0002c0002t0001g0120 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1168-686A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394575 | ||||||
chr6:100394603
|
C | G | 26 | a0001c0001t0003g0033a0001c0001t0005g0032a0001c0001t0005g0045others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1168-714G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394603 | ||||||
chr6:100394613
|
C | G | 152 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-724G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394613 | ||||||
chr6:100394889
|
T | A | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1168-1000A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394889 | ||||||
chr6:100395019
|
C | T | 152 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-1130G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395019 | ||||||
chr6:100395212
|
T | A | 1 | a0001c0001t0010g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1168-1323A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395212 | ||||||
chr6:100395251
|
TATTCCAT others(4): Show |
T | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-1373_1168-136 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395251 | ||||||
chr6:100395308
|
C | T | 1 | a0001c0001t0012g0306 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1168-1419G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395308 | ||||||
chr6:100395433
|
C | T | 6 | a0001c0001t0002g0148a0001c0001t0002g0186a0001c0001t0006g0014others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-1544G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395433 | ||||||
chr6:100395605
|
G | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-1716C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395605 | ||||||
chr6:100395716
|
A | G | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-1827T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395716 | ||||||
chr6:100395964
|
T | C | 3 | a0002c0002t0014g0269a0002c0002t0014g0270a0002c0002t0014g0272 | 3 | HG00438.hp1 HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1168-2075A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395964 | ||||||
chr6:100395982
|
A | T | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-2093T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395982 | ||||||
chr6:100396038
|
A | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-2149T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396038 | ||||||
chr6:100396049
|
C | T | 1 | a0001c0001t0006g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1168-2160G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396049 | ||||||
chr6:100396082
|
T | C | 1 | a0001c0001t0010g0279 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1168-2193A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396082 | ||||||
chr6:100396125
|
C | T | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1168-2236G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396125 | ||||||
chr6:100396155
|
G | A | 1 | a0001c0001t0074g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1168-2266C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396155 | ||||||
chr6:100396219
|
T | C | 157 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1168-2330A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396219 | ||||||
chr6:100396229
|
T | C | 27 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-2340A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396229 | ||||||
chr6:100396392
|
T | C | 45 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(42): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1168-2503A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396392 | ||||||
chr6:100396545
|
G | T | 2 | a0001c0001t0012g0308a0001c0001t0012g0309 | 2 | NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1168-2656C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396545 | ||||||
chr6:100396599
|
A | C | 1 | a0002c0002t0007g0019 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1168-2710T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396599 | ||||||
chr6:100396632
|
A | T | 1 | a0002c0002t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1168-2743T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396632 | ||||||
chr6:100396799
|
G | T | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-2910C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396799 | ||||||
chr6:100396914
|
G | A | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-3025C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396914 | ||||||
chr6:100396950
|
T | C | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-3061A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396950 | ||||||
chr6:100397230
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1168-3341C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397230 | ||||||
chr6:100397478
|
A | G | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-3589T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397478 | ||||||
chr6:100397553
|
C | T | 78 | a0001c0001t0028g0254a0002c0002t0001g0030a0002c0002t0001g0035others(75): Show | 78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-3664G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397553 | ||||||
chr6:100397719
|
G | A | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-3830C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397719 | ||||||
chr6:100397759
|
C | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-3870G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397759 | ||||||
chr6:100397768
|
A | G | 78 | a0001c0001t0028g0254a0002c0002t0001g0030a0002c0002t0001g0035others(75): Show | 78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-3879T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397768 | ||||||
chr6:100397912
|
A | T | 1 | a0001c0001t0055g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1168-4023T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397912 | ||||||
chr6:100397963
|
A | G | 2 | a0001c0001t0020g0159a0001c0001t0020g0286 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4074T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397963 | ||||||
chr6:100397979
|
A | G | 2 | a0001c0001t0042g0040a0001c0001t0043g0190 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1168-4090T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397979 | ||||||
chr6:100398025
|
A | G | 42 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(39): Show | 42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1168-4136T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398025 | ||||||
chr6:100398280
|
G | A | 6 | a0001c0001t0006g0166a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-4391C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398280 | ||||||
chr6:100398325
|
T | C | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168-4436A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398325 | ||||||
chr6:100398450
|
T | A | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4561A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398450 | ||||||
chr6:100398489
|
T | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-4600A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398489 | ||||||
chr6:100398712
|
G | A | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4823C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398712 | ||||||
chr6:100398841
|
C | T | 5 | a0001c0001t0002g0066a0001c0001t0032g0006a0001c0001t0042g0040others(2): Show | 5 | HG01433.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-4952G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398841 | ||||||
chr6:100398842
|
G | A | 4 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167others(1): Show | 4 | HG01168.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-4953C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398842 | ||||||
chr6:100398894
|
C | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5005G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398894 | ||||||
chr6:100398933
|
T | TTG | 46 | a0001c0001t0002g0036a0001c0001t0002g0157a0001c0001t0003g0156others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1168-5046_1168-504 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | ||||||
chr6:100398933
|
T | TTGTGTG | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0061g0302 | 3 | HG02451.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1168-5050_1168-504 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | ||||||
chr6:100398933
|
TTG | T | 9 | a0001c0001t0002g0150a0001c0001t0002g0162a0001c0001t0002g0220others(6): Show | 9 | HG00735.hp1 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1168-5046_1168-504 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | ||||||
chr6:100398951
|
GTGTGTGT others(3): Show |
G | 5 | a0001c0001t0028g0254a0002c0002t0001g0085a0002c0002t0001g0274others(2): Show | 5 | HG01261.hp2 HG02071.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398951 | ||||||
chr6:100398953
|
GTGTGTGT others(1): Show |
G | 70 | a0002c0002t0001g0030a0002c0002t0001g0035a0002c0002t0001g0042others(67): Show | 70 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398953 | ||||||
chr6:100398955
|
GTGTGTA | G | 4 | a0001c0001t0006g0161a0001c0001t0006g0227a0002c0002t0001g0120others(1): Show | 4 | HG02976.hp2 HG06807.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398955 | ||||||
chr6:100398958
|
TGTATG | T | 25 | a0001c0001t0003g0033a0001c0001t0005g0032a0001c0001t0005g0045others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-5074_1168-507 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398958 | ||||||
chr6:100398961
|
A | G | 7 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(4): Show | 7 | HG01891.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1168-5072T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398961 | ||||||
chr6:100398963
|
G | A | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-5074C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398963 | ||||||
chr6:100398964
|
T | A | 28 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1168-5075A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398964 | ||||||
chr6:100398965
|
G | A | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5076C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398965 | ||||||
chr6:100398966
|
T | TG | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5078_1168-507 others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398966 | ||||||
chr6:100398966
|
TA | T | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-5078delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398966 | ||||||
chr6:100398967
|
A | T | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5078T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398967 | ||||||
chr6:100399305
|
A | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5416T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399305 | ||||||
chr6:100399334
|
A | C | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-5445T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399334 | ||||||
chr6:100399366
|
T | C | 1 | a0001c0001t0073g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1168-5477A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399366 | ||||||
chr6:100399423
|
G | C | 2 | a0001c0001t0003g0158a0001c0001t0009g0172 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1168-5534C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399423 | ||||||
chr6:100399744
|
C | A | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5855G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399744 | ||||||
chr6:100399752
|
A | G | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1168-5863T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399752 | ||||||
chr6:100399912
|
A | G | 1 | a0001c0001t0008g0026 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-6023T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399912 | ||||||
chr6:100399997
|
G | A | 4 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0284others(1): Show | 4 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-6108C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399997 | ||||||
chr6:100400194
|
G | A | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-6305C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400194 | ||||||
chr6:100400242
|
A | G | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0258 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1168-6353T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400242 | ||||||
chr6:100400258
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1168-6369A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400258 | ||||||
chr6:100400308
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1168-6419C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400308 | ||||||
chr6:100400443
|
C | A | 126 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1168-6554G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400443 | ||||||
chr6:100400980
|
GA | G | 82 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(79): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1168-7092delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400980 | ||||||
chr6:100400995
|
A | G | 43 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1168-7106T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400995 | ||||||
chr6:100401224
|
T | C | 131 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(128): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1168-7335A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401224 | ||||||
chr6:100401260
|
G | C | 1 | a0002c0002t0001g0218 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1168-7371C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401260 | ||||||
chr6:100401315
|
A | C | 4 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167others(1): Show | 4 | HG01168.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-7426T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401315 | ||||||
chr6:100401450
|
T | C | 165 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-7561A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401450 | ||||||
chr6:100401462
|
T | A | 29 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-7573A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401462 | ||||||
chr6:100401492
|
T | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-7603A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401492 | ||||||
chr6:100401790
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1168-7901G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401790 | ||||||
chr6:100401854
|
C | T | 165 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-7965G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401854 | ||||||
chr6:100401962
|
G | A | 5 | a0001c0001t0002g0170a0001c0001t0002g0173a0001c0001t0011g0149others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-8073C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401962 | ||||||
chr6:100402092
|
T | C | 1 | a0001c0001t0004g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1168-8203A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402092 | ||||||
chr6:100402165
|
A | G | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-8276T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402165 | ||||||
chr6:100402259
|
T | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-8370A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402259 | ||||||
chr6:100402265
|
G | T | 17 | a0002c0002t0001g0042a0002c0002t0001g0046a0002c0002t0001g0048others(14): Show | 17 | HG00621.hp2 HG02293.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.1168-8376C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402265 | ||||||
chr6:100402295
|
T | TA | 28 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(25): Show | 28 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1168-8407dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402295 | ||||||
chr6:100402420
|
T | A | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-8531A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402420 | ||||||
chr6:100402528
|
A | G | 29 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-8639T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402528 | ||||||
chr6:100402565
|
C | CTTTTCTC others(6): Show |
15 | a0001c0001t0028g0254a0002c0002t0001g0030a0002c0002t0001g0035others(12): Show | 15 | HG00738.hp2 HG01074.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
C | CTTTTCTC others(7): Show |
27 | a0002c0002t0001g0042a0002c0002t0001g0044a0002c0002t0001g0046others(24): Show | 27 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
C | CTTTTCTC others(8): Show |
20 | a0002c0002t0001g0048a0002c0002t0001g0059a0002c0002t0001g0060others(17): Show | 20 | HG00140.hp2 HG00423.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
C | CTTTTCTC others(9): Show |
10 | a0002c0002t0001g0063a0002c0002t0001g0194a0002c0002t0001g0257others(7): Show | 10 | HG00642.hp2 HG01106.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
C | CTTTTCTC others(10): Show |
1 | a0002c0002t0001g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1168-8677_1168-867 others(21): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
C | CTTTTCTC others(12): Show |
3 | a0002c0002t0001g0122a0002c0002t0001g0230a0002c0002t0066g0062 | 3 | HG01192.hp2 HG02135.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402565
|
CTCTTT | C | 27 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8681_1168-867 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | ||||||
chr6:100402567
|
C | CT | 22 | a0001c0001t0002g0066a0001c0001t0002g0251a0001c0001t0002g0261others(19): Show | 22 | HG00544.hp1 HG01169.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1168-8679dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402567
|
C | CTTT | 32 | a0001c0001t0004g0095a0001c0001t0004g0104a0001c0001t0004g0111others(29): Show | 32 | HG00733.hp1 HG01070.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1168-8681_1168-867 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402567
|
C | CTTTT | 11 | a0001c0001t0004g0041a0001c0001t0004g0185a0001c0001t0008g0072others(8): Show | 11 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-8682_1168-867 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402567
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0015g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1168-8688_1168-867 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402567
|
C | T | 78 | a0001c0001t0028g0254a0002c0002t0001g0030a0002c0002t0001g0035others(75): Show | 78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-8678G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402567
|
CT | C | 8 | a0001c0001t0002g0150a0001c0001t0003g0156a0001c0001t0009g0216others(5): Show | 8 | HG00735.hp1 HG01167.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168-8679delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | ||||||
chr6:100402569
|
T | C | 1 | a0001c0001t0025g0256 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1168-8680A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402569 | ||||||
chr6:100402570
|
T | C | 2 | a0001c0001t0025g0263a0001c0001t0069g0264 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1168-8681A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402570 | ||||||
chr6:100402571
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-8682A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402571 | ||||||
chr6:100402572
|
T | C | 1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-8683A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402572 | ||||||
chr6:100402573
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-8684A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402573 | ||||||
chr6:100402574
|
T | C | 1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-8685A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402574 | ||||||
chr6:100402575
|
T | C | 27 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8686A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402575 | ||||||
chr6:100402577
|
T | C | 27 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8688A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402577 | ||||||
chr6:100402622
|
G | GGCT | 107 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1168-8736_1168-873 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402622 | ||||||
chr6:100402673
|
G | A | 316 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1168-8784C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402673 | ||||||
chr6:100402678
|
C | T | 316 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1168-8789G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402678 | ||||||
chr6:100402785
|
C | T | 1 | a0002c0002t0001g0120 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1168-8896G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402785 | ||||||
chr6:100403100
|
T | C | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-9211A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403100 | ||||||
chr6:100403317
|
G | C | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-9428C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403317 | ||||||
chr6:100403568
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1168-9679T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403568 | ||||||
chr6:100403754
|
A | G | 1 | a0001c0001t0008g0026 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-9865T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403754 | ||||||
chr6:100403845
|
T | G | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-9956A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403845 | ||||||
chr6:100403942
|
A | G | 44 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10053T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403942 | ||||||
chr6:100404027
|
C | G | 1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-10138G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404027 | ||||||
chr6:100404098
|
C | T | 1 | a0001c0001t0037g0017 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1168-10209G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404098 | ||||||
chr6:100404140
|
C | T | 107 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1168-10251G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404140 | ||||||
chr6:100404158
|
A | G | 29 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-10269T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404158 | ||||||
chr6:100404229
|
C | T | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-10340G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404229 | ||||||
chr6:100404303
|
A | C | 27 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-10414T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404303 | ||||||
chr6:100404424
|
C | T | 1 | a0001c0001t0027g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1168-10535G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404424 | ||||||
chr6:100404491
|
G | T | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1168-10602C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404491 | ||||||
chr6:100404692
|
T | G | 1 | a0002c0002t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1168-10803A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404692 | ||||||
chr6:100404793
|
C | T | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1168-10904G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404793 | ||||||
chr6:100404877
|
T | C | 29 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-10988A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404877 | ||||||
chr6:100404886
|
G | A | 1 | a0001c0001t0008g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1168-10997C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404886 | ||||||
chr6:100405076
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-11187T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405076 | ||||||
chr6:100405116
|
T | C | 44 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11227A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405116 | ||||||
chr6:100405206
|
C | T | 154 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(151): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1168-11317G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405206 | ||||||
chr6:100405263
|
C | T | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-11374G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405263 | ||||||
chr6:100405344
|
C | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-11455G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405344 | ||||||
chr6:100405526
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1168-11637T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405526 | ||||||
chr6:100405551
|
C | T | 160 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1168-11662G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405551 | ||||||
chr6:100405729
|
C | A | 6 | a0001c0001t0002g0049a0001c0001t0002g0061a0001c0001t0002g0260others(3): Show | 6 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-11840G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405729 | ||||||
chr6:100405921
|
A | G | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1168-12032T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405921 | ||||||
chr6:100405972
|
A | G | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-12083T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405972 | ||||||
chr6:100405991
|
A | G | 1 | a0004c0008t0023g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-12102T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405991 | ||||||
chr6:100406034
|
G | T | 3 | a0001c0001t0002g0195a0001c0001t0012g0308a0001c0001t0012g0309 | 3 | NA18945.hp1 NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1168-12145C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406034 | ||||||
chr6:100406088
|
C | T | 34 | a0001c0001t0002g0261a0001c0001t0002g0276a0001c0001t0003g0009others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1168-12199G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406088 | ||||||
chr6:100406120
|
G | C | 154 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(151): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1168-12231C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406120 | ||||||
chr6:100406257
|
T | C | 165 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-12368A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406257 | ||||||
chr6:100406651
|
T | C | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-12762A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406651 | ||||||
chr6:100406689
|
T | C | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-12800A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406689 | ||||||
chr6:100406714
|
TTGTATAC others(5): Show |
T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-12837_1168-12 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406714 | ||||||
chr6:100406746
|
T | C | 48 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1168-12857A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406746 | ||||||
chr6:100406908
|
G | A | 6 | a0001c0001t0006g0166a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-13019C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406908 | ||||||
chr6:100406929
|
AC | A | 25 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-13041delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406929 | ||||||
chr6:100406931
|
A | G | 25 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-13042T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406931 | ||||||
chr6:100406972
|
C | T | 1 | a0001c0001t0005g0204 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1168-13083G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406972 | ||||||
chr6:100407059
|
T | C | 50 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1168-13170A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407059 | ||||||
chr6:100407119
|
T | C | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1168-13230A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407119 | ||||||
chr6:100407338
|
C | T | 83 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0028g0254others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1168-13449G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407338 | ||||||
chr6:100407513
|
T | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0236 | 2 | NA19078.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1167+13277A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407513 | ||||||
chr6:100407530
|
C | A | 1 | a0002c0002t0001g0060 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1167+13260G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407530 | ||||||
chr6:100407607
|
C | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+13183G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407607 | ||||||
chr6:100407670
|
C | T | 86 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0025g0256others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+13120G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407670 | ||||||
chr6:100407690
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+13100T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407690 | ||||||
chr6:100407742
|
C | T | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0258 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1167+13048G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407742 | ||||||
chr6:100407787
|
C | A | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+13003G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407787 | ||||||
chr6:100407793
|
T | A | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+12997A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407793 | ||||||
chr6:100408063
|
T | A | 3 | a0002c0002t0001g0200a0002c0002t0001g0278a0002c0002t0024g0101 | 3 | HG00558.hp2 NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1167+12727A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408063 | ||||||
chr6:100408206
|
T | C | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+12584A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408206 | ||||||
chr6:100408289
|
T | C | 1 | a0001c0001t0003g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1167+12501A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408289 | ||||||
chr6:100408566
|
T | C | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+12224A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408566 | ||||||
chr6:100408659
|
A | G | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+12131T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408659 | ||||||
chr6:100408870
|
T | C | 43 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+11920A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408870 | ||||||
chr6:100408916
|
G | T | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+11874C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408916 | ||||||
chr6:100408929
|
G | T | 1 | a0001c0001t0027g0029 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1167+11861C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408929 | ||||||
chr6:100408933
|
T | C | 6 | a0001c0001t0006g0166a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+11857A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408933 | ||||||
chr6:100409120
|
A | C | 1 | a0001c0001t0059g0178 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+11670T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409120 | ||||||
chr6:100409136
|
G | T | 1 | a0002c0002t0001g0046 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1167+11654C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409136 | ||||||
chr6:100409198
|
C | T | 2 | a0001c0001t0009g0023a0001c0001t0009g0081 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1167+11592G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409198 | ||||||
chr6:100409405
|
AT | A | 3 | a0001c0001t0003g0033a0001c0001t0005g0032a0001c0001t0005g0091 | 3 | HG01109.hp2 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1167+11384delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409405 | ||||||
chr6:100409428
|
A | AT | 46 | a0001c0001t0002g0135a0001c0001t0004g0041a0001c0001t0004g0095others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1167+11361dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409428 | ||||||
chr6:100409583
|
C | A | 6 | a0001c0001t0016g0001a0001c0001t0021g0108a0001c0001t0021g0266others(3): Show | 7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+11207G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409583 | ||||||
chr6:100409637
|
T | C | 2 | a0001c0001t0070g0177a0001c0001t0071g0010 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1167+11153A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409637 | ||||||
chr6:100409643
|
C | G | 11 | a0001c0001t0002g0043a0001c0001t0002g0064a0001c0001t0002g0138others(8): Show | 11 | HG00558.hp1 HG02132.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1167+11147G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409643 | ||||||
chr6:100409689
|
A | T | 86 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0025g0256others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+11101T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409689 | ||||||
chr6:100409769
|
T | C | 7 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+11021A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409769 | ||||||
chr6:100409890
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+10900T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409890 | ||||||
chr6:100409993
|
G | A | 131 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(128): Show | 131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1167+10797C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409993 | ||||||
chr6:100410351
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0162 | 2 | HG00735.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1167+10439T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410351 | ||||||
chr6:100410400
|
G | A | 1 | a0001c0001t0012g0310 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1167+10390C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410400 | ||||||
chr6:100410433
|
C | T | 1 | a0002c0002t0024g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1167+10357G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410433 | ||||||
chr6:100410462
|
A | C | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+10328T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410462 | ||||||
chr6:100410651
|
T | A | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1167+10139A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410651 | ||||||
chr6:100411060
|
A | T | 25 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+9730T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411060 | ||||||
chr6:100411164
|
G | T | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+9626C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411164 | ||||||
chr6:100411283
|
T | C | 138 | a0001c0001t0004g0041a0001c0001t0004g0095a0001c0001t0004g0104others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1167+9507A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411283 | ||||||
chr6:100411313
|
A | G | 86 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0025g0256others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+9477T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411313 | ||||||
chr6:100411452
|
T | C | 1 | a0002c0002t0024g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+9338A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411452 | ||||||
chr6:100411472
|
G | T | 83 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0028g0254others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+9318C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411472 | ||||||
chr6:100411510
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+9280C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411510 | ||||||
chr6:100411587
|
C | T | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+9203G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411587 | ||||||
chr6:100411598
|
T | G | 1 | a0002c0002t0014g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1167+9192A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411598 | ||||||
chr6:100411609
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0009g0172 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1167+9181T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411609 | ||||||
chr6:100411697
|
C | T | 137 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0111others(134): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1167+9093G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411697 | ||||||
chr6:100411727
|
A | T | 1 | a0002c0002t0007g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1167+9063T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411727 | ||||||
chr6:100411739
|
T | C | 1 | a0001c0001t0026g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1167+9051A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411739 | ||||||
chr6:100411832
|
C | T | 39 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0111others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1167+8958G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411832 | ||||||
chr6:100411867
|
G | A | 1 | a0001c0001t0060g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1167+8923C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411867 | ||||||
chr6:100411905
|
G | A | 39 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0111others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1167+8885C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411905 | ||||||
chr6:100411907
|
G | C | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+8883C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411907 | ||||||
chr6:100412035
|
C | T | 1 | a0001c0001t0040g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1167+8755G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412035 | ||||||
chr6:100412071
|
T | C | 167 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(164): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1167+8719A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412071 | ||||||
chr6:100412101
|
G | A | 3 | a0001c0001t0002g0157a0001c0001t0003g0156a0001c0001t0003g0171 | 3 | HG02055.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1167+8689C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412101 | ||||||
chr6:100412207
|
T | C | 2 | a0001c0001t0005g0144a0001c0001t0005g0145 | 2 | NA18982.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1167+8583A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412207 | ||||||
chr6:100412226
|
T | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0031 | 2 | HG03834.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1167+8564A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412226 | ||||||
chr6:100412461
|
C | A | 1 | a0002c0002t0001g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1167+8329G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412461 | ||||||
chr6:100412462
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1167+8328T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412462 | ||||||
chr6:100412534
|
CTAAGAAA others(34): Show |
C | 1 | a0002c0002t0001g0200 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1167+8215_1167+825 others(45): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412534 | ||||||
chr6:100412534
|
CTAAGAAA others(38): Show |
C | 1 | a0002c0002t0001g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1167+8211_1167+825 others(49): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412534 | ||||||
chr6:100412535
|
T | A | 81 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0028g0254others(78): Show | 81 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1167+8255A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412535 | ||||||
chr6:100412541
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+8249T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412541 | ||||||
chr6:100412542
|
GAAAGAAA others(6): Show |
G | 10 | a0001c0001t0005g0045a0001c0001t0005g0082a0001c0001t0005g0099others(7): Show | 10 | HG00544.hp2 HG01256.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8235_1167+824 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412542 | ||||||
chr6:100412546
|
GAAAGAAA others(2): Show |
G | 12 | a0001c0001t0005g0110a0001c0001t0005g0119a0001c0001t0005g0131others(9): Show | 12 | HG00621.hp1 HG00733.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167+8235_1167+824 others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412546 | ||||||
chr6:100412548
|
AAGAAAGA others(28): Show |
A | 1 | a0001c0001t0005g0248 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1167+8207_1167+824 others(39): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412548 | ||||||
chr6:100412550
|
GAAAGA | G | 7 | a0001c0001t0004g0196a0001c0001t0004g0198a0001c0001t0008g0087others(4): Show | 7 | HG01081.hp2 HG01168.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+8235_1167+823 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412550 | ||||||
chr6:100412551
|
AAAGAAAA others(1): Show |
A | 3 | a0001c0001t0006g0166a0001c0001t0006g0299a0001c0001t0006g0301 | 3 | HG03195.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412551 | ||||||
chr6:100412553
|
AGAAAAGA others(63): Show |
A | 1 | a0002c0002t0017g0312 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1167+8167_1167+823 others(74): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412553 | ||||||
chr6:100412554
|
GA | G | 118 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0104others(115): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1167+8235delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412554 | ||||||
chr6:100412555
|
A | AAAAG | 17 | a0001c0001t0002g0036a0001c0001t0002g0217a0001c0001t0003g0052others(14): Show | 17 | HG00140.hp1 HG00558.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAAGAAA others(1): Show |
5 | a0001c0001t0002g0295a0001c0001t0003g0058a0001c0001t0003g0224others(2): Show | 5 | HG01993.hp1 HG03491.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8227_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAAGAAA others(5): Show |
1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1167+8223_1167+823 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAG | 8 | a0001c0001t0004g0041a0001c0001t0004g0113a0001c0001t0004g0207others(5): Show | 8 | HG00438.hp2 HG02723.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAGAAAG | 4 | a0001c0001t0004g0114a0001c0001t0008g0026a0001c0001t0008g0077others(1): Show | 4 | HG01074.hp2 HG02572.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(11): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAGAAAG others(4): Show |
2 | a0001c0001t0008g0209a0001c0001t0026g0233 | 2 | HG00423.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
A | AAAGAAAG others(101): Show |
1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8234_1167+823 others(112): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
AAAAG | A | 57 | a0001c0001t0002g0028a0001c0001t0002g0061a0001c0001t0002g0066others(54): Show | 58 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
AAAAGAAA others(1): Show |
A | 22 | a0001c0001t0002g0071a0001c0001t0002g0148a0001c0001t0002g0157others(19): Show | 22 | HG01109.hp1 HG01433.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1167+8227_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0002g0043a0001c0001t0002g0064a0001c0001t0002g0138others(10): Show | 13 | HG00099.hp2 HG01256.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1167+8223_1167+823 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1167+8219_1167+823 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412555
|
AAAAGAAA others(21): Show |
A | 1 | a0001c0001t0047g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1167+8207_1167+823 others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | ||||||
chr6:100412559
|
G | A | 1 | a0001c0001t0006g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1167+8231C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412559 | ||||||
chr6:100412563
|
G | A | 4 | a0001c0001t0006g0166a0001c0001t0006g0299a0001c0001t0006g0301others(1): Show | 4 | HG02615.hp1 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8227C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412563 | ||||||
chr6:100412569
|
AAG | A | 5 | a0001c0001t0013g0106a0001c0001t0013g0127a0001c0001t0013g0142others(2): Show | 5 | HG00280.hp2 HG00323.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+8219_1167+822 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412569 | ||||||
chr6:100412575
|
GAAAGAAA others(55): Show |
G | 3 | a0001c0001t0028g0254a0002c0002t0001g0315a0002c0002t0001g0318 | 3 | HG01516.hp2 HG01517.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+821 others(66): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412575 | ||||||
chr6:100412579
|
GAAAGAAA others(51): Show |
G | 3 | a0002c0002t0001g0136a0002c0002t0001g0292a0002c0002t0001g0317 | 3 | HG01515.hp2 HG02071.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+821 others(62): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412579 | ||||||
chr6:100412581
|
AAG | A | 15 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0045others(12): Show | 15 | HG00544.hp2 HG01109.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1167+8207_1167+820 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412581 | ||||||
chr6:100412583
|
GAAAGAAA others(47): Show |
G | 4 | a0002c0002t0001g0192a0002c0002t0001g0319a0002c0002t0006g0235others(1): Show | 4 | HG02300.hp2 HG02602.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+820 others(58): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | ||||||
chr6:100412583
|
GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0001g0243 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1167+8151_1167+820 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | ||||||
chr6:100412583
|
GAAAGAAA others(53): Show |
G | 1 | a0002c0002t0024g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+8147_1167+820 others(64): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | ||||||
chr6:100412585
|
A | G | 2 | a0002c0002t0007g0133a0002c0005t0065g0055 | 2 | NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1167+8205T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412585 | ||||||
chr6:100412585
|
AAGAAAG | A | 5 | a0001c0001t0002g0288a0001c0003t0003g0024a0001c0003t0003g0137others(2): Show | 5 | HG01516.hp1 HG02738.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8199_1167+820 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412585 | ||||||
chr6:100412587
|
GAAAGAAA others(43): Show |
G | 2 | a0002c0002t0007g0267a0002c0002t0007g0268 | 2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+820 others(54): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | ||||||
chr6:100412587
|
GAAAGAAA others(45): Show |
G | 3 | a0002c0002t0001g0222a0002c0002t0001g0230a0002c0002t0007g0176 | 3 | HG02135.hp2 NA18747.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1167+8151_1167+820 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | ||||||
chr6:100412587
|
GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1167+8147_1167+820 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | ||||||
chr6:100412587
|
GAAAGAAA others(61): Show |
G | 1 | a0002c0002t0017g0313 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8135_1167+820 others(72): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | ||||||
chr6:100412589
|
A | G | 6 | a0001c0001t0008g0070a0001c0001t0008g0072a0002c0002t0001g0255others(3): Show | 6 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8201T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412589 | ||||||
chr6:100412590
|
A | G | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8200T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412590 | ||||||
chr6:100412591
|
GAAAGAAA others(39): Show |
G | 6 | a0002c0002t0001g0120a0002c0002t0001g0218a0002c0002t0001g0262others(3): Show | 6 | HG00642.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(50): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | ||||||
chr6:100412591
|
GAAAGAAA others(41): Show |
G | 1 | a0002c0002t0001g0255 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+819 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | ||||||
chr6:100412591
|
GAAAGAAA others(45): Show |
G | 2 | a0002c0002t0001g0232a0002c0002t0001g0257 | 2 | HG03239.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1167+8147_1167+819 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | ||||||
chr6:100412593
|
A | G | 9 | a0001c0001t0008g0070a0001c0001t0008g0072a0002c0002t0001g0030others(6): Show | 9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8197T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412593 | ||||||
chr6:100412595
|
G | GAA | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+8193_1167+819 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(23): Show |
G | 1 | a0002c0002t0007g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1167+8165_1167+819 others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(35): Show |
G | 5 | a0002c0002t0001g0030a0002c0002t0001g0047a0002c0002t0007g0019others(2): Show | 5 | HG04204.hp1 NA18966.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(46): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(37): Show |
G | 1 | a0002c0002t0007g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+819 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(41): Show |
G | 4 | a0001c0001t0070g0177a0002c0002t0001g0124a0002c0002t0001g0215others(1): Show | 4 | HG02559.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8147_1167+819 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(42): Show |
G | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+8146_1167+819 others(53): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(45): Show |
G | 1 | a0002c0002t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1167+8143_1167+819 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412595
|
GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1167+8139_1167+819 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | ||||||
chr6:100412596
|
AAAGAAAG others(17): Show |
A | 4 | a0001c0001t0013g0127a0001c0001t0013g0142a0001c0001t0062g0109others(1): Show | 4 | HG00280.hp2 HG00323.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8170_1167+819 others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412596 | ||||||
chr6:100412597
|
A | G | 8 | a0001c0001t0008g0070a0001c0001t0008g0072a0002c0002t0001g0035others(5): Show | 8 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8193T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412597 | ||||||
chr6:100412599
|
GAAAGAAA others(31): Show |
G | 2 | a0002c0002t0001g0277a0002c0002t0003g0039 | 2 | HG00741.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(42): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | ||||||
chr6:100412599
|
GAAAGAAA others(33): Show |
G | 4 | a0001c0001t0008g0072a0002c0002t0001g0035a0002c0002t0001g0274others(1): Show | 4 | HG01169.hp2 HG01261.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8151_1167+819 others(44): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | ||||||
chr6:100412599
|
GAAAGAAA others(36): Show |
G | 1 | a0002c0002t0024g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1167+8148_1167+819 others(47): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | ||||||
chr6:100412599
|
GAAAGAAA others(37): Show |
G | 1 | a0002c0002t0014g0270 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1167+8147_1167+819 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | ||||||
chr6:100412599
|
GAAAGAAA others(40): Show |
G | 1 | a0002c0002t0014g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1167+8144_1167+819 others(51): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | ||||||
chr6:100412601
|
A | G | 4 | a0001c0001t0008g0070a0002c0002t0001g0067a0002c0002t0001g0122others(1): Show | 4 | HG01167.hp1 HG01192.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8189T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412601 | ||||||
chr6:100412603
|
GAAAGAAA others(16): Show |
G | 1 | a0002c0002t0007g0184 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1167+8164_1167+818 others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | ||||||
chr6:100412603
|
GAAAGAAA others(27): Show |
G | 1 | a0002c0002t0001g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1167+8153_1167+818 others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | ||||||
chr6:100412603
|
GAAAGAAA others(29): Show |
G | 3 | a0002c0002t0001g0129a0002c0002t0001g0259a0002c0002t0066g0062 | 3 | HG01106.hp2 NA18998.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1167+8151_1167+818 others(40): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | ||||||
chr6:100412605
|
A | G | 5 | a0001c0001t0008g0070a0002c0002t0001g0053a0002c0002t0001g0067others(2): Show | 5 | HG01167.hp1 HG01192.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8185T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412605 | ||||||
chr6:100412607
|
GAAAGGAA others(23): Show |
G | 4 | a0002c0002t0001g0046a0002c0002t0001g0117a0002c0002t0001g0189others(1): Show | 4 | NA18950.hp2 NA18957.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+818 others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | ||||||
chr6:100412607
|
GAAAGGAA others(25): Show |
G | 1 | a0002c0002t0001g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+818 others(36): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | ||||||
chr6:100412607
|
GAAAGGAA others(37): Show |
G | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+8139_1167+818 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | ||||||
chr6:100412608
|
A | G | 20 | a0001c0001t0004g0111a0001c0001t0004g0128a0001c0001t0004g0185others(17): Show | 20 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1167+8182T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412608 | ||||||
chr6:100412609
|
A | G | 3 | a0002c0002t0001g0053a0002c0002t0001g0122a0002c0002t0014g0272 | 3 | HG01192.hp2 HG02083.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1167+8181T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412609 | ||||||
chr6:100412609
|
AAGGAAAG others(7): Show |
A | 1 | a0002c0002t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1167+8167_1167+818 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412609 | ||||||
chr6:100412610
|
AG | A | 8 | a0001c0001t0013g0106a0001c0001t0020g0159a0001c0001t0020g0286others(5): Show | 8 | HG02074.hp2 HG02886.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8179delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412610 | ||||||
chr6:100412610
|
AGGAAAGA others(6): Show |
A | 7 | a0001c0001t0022g0147a0002c0002t0001g0042a0002c0002t0001g0044others(4): Show | 7 | HG00621.hp2 HG02523.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+8167_1167+817 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412610 | ||||||
chr6:100412611
|
G | A | 22 | a0001c0001t0004g0111a0001c0001t0004g0128a0001c0001t0004g0185others(19): Show | 22 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1167+8179C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(8): Show |
G | 1 | a0002c0002t0001g0105 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1167+8164_1167+817 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(12): Show |
G | 3 | a0002c0002t0001g0059a0002c0002t0001g0063a0002c0002t0014g0057 | 3 | NA18965.hp1 NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1167+8160_1167+817 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(19): Show |
G | 2 | a0002c0002t0001g0069a0002c0002t0001g0080 | 2 | NA18989.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+817 others(30): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(20): Show |
G | 1 | a0002c0002t0007g0054 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1167+8152_1167+817 others(31): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(21): Show |
G | 2 | a0002c0002t0001g0053a0002c0002t0014g0272 | 2 | HG02083.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1167+8151_1167+817 others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(22): Show |
G | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167+8150_1167+817 others(33): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412611
|
GGAAAGAA others(29): Show |
G | 1 | a0002c0002t0001g0203 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1167+8143_1167+817 others(40): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | ||||||
chr6:100412614
|
A | G | 2 | a0001c0001t0008g0070a0002c0002t0001g0122 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8176T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412614 | ||||||
chr6:100412614
|
AAG | A | 3 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0068g0294 | 3 | HG01891.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1167+8174_1167+817 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412614 | ||||||
chr6:100412615
|
A | G | 1 | a0003c0006t0004g0130 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1167+8175T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412615 | ||||||
chr6:100412616
|
GAAAGAAG others(14): Show |
G | 1 | a0001c0001t0003g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1167+8153_1167+817 others(25): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | ||||||
chr6:100412616
|
GAAAGAAG others(16): Show |
G | 1 | a0002c0002t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+817 others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | ||||||
chr6:100412616
|
GAAAGAAG others(24): Show |
G | 2 | a0001c0001t0022g0160a0002c0002t0007g0237 | 2 | HG02280.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1167+8143_1167+817 others(35): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | ||||||
chr6:100412618
|
A | G | 3 | a0001c0001t0006g0227a0001c0001t0008g0070a0002c0002t0001g0122 | 3 | HG01167.hp1 HG01192.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1167+8172T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412618 | ||||||
chr6:100412619
|
A | G | 18 | a0001c0001t0004g0111a0001c0001t0004g0128a0001c0001t0004g0185others(15): Show | 18 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1167+8171T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412619 | ||||||
chr6:100412620
|
GAAGGAAA others(10): Show |
G | 2 | a0001c0001t0005g0110a0001c0001t0063g0075 | 2 | HG02165.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(21): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412620 | ||||||
chr6:100412622
|
A | G | 2 | a0001c0001t0008g0070a0002c0002t0001g0122 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8168T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412622 | ||||||
chr6:100412623
|
G | A | 50 | a0001c0001t0003g0214a0001c0001t0004g0111a0001c0001t0004g0128others(47): Show | 50 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1167+8167C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412623 | ||||||
chr6:100412623
|
G | GGAAA | 15 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0112others(12): Show | 15 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1167+8163_1167+816 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412623 | ||||||
chr6:100412624
|
GAAAGAAA others(6): Show |
G | 2 | a0001c0001t0003g0214a0001c0001t0005g0221 | 2 | HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412624 | ||||||
chr6:100412626
|
A | G | 3 | a0001c0001t0006g0227a0002c0002t0001g0122a0002c0002t0001g0210 | 3 | HG01192.hp2 HG02976.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1167+8164T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412626 | ||||||
chr6:100412628
|
GAAAGAAA others(2): Show |
G | 5 | a0001c0001t0005g0082a0001c0001t0005g0219a0001c0001t0005g0248others(2): Show | 5 | HG01168.hp2 HG02074.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412628 | ||||||
chr6:100412630
|
A | G | 6 | a0001c0001t0006g0227a0002c0002t0001g0060a0002c0002t0001g0092others(3): Show | 6 | HG02976.hp2 NA18971.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8160T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412630 | ||||||
chr6:100412632
|
GAAAGA | G | 4 | a0001c0001t0005g0099a0001c0001t0005g0139a0001c0001t0005g0204others(1): Show | 4 | HG01256.hp2 HG02129.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+815 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | ||||||
chr6:100412632
|
GAAAGAAA others(4): Show |
G | 1 | a0001c0001t0025g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+8147_1167+815 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | ||||||
chr6:100412632
|
GAAAGAAA others(8): Show |
G | 2 | a0001c0001t0025g0256a0001c0001t0069g0264 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+8143_1167+815 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | ||||||
chr6:100412634
|
A | G | 10 | a0001c0001t0006g0227a0002c0002t0001g0048a0002c0002t0001g0059others(7): Show | 10 | HG02976.hp2 NA18965.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8156T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412634 | ||||||
chr6:100412636
|
G | A | 1 | a0003c0006t0004g0130 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1167+8154C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | ||||||
chr6:100412636
|
GA | G | 18 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0091others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1167+8153delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | ||||||
chr6:100412636
|
GAAA | G | 6 | a0001c0001t0006g0227a0002c0002t0001g0042a0002c0002t0001g0059others(3): Show | 6 | HG02976.hp2 NA18965.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8151_1167+815 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | ||||||
chr6:100412637
|
A | AAAG | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+8152_1167+815 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | ||||||
chr6:100412637
|
A | G | 2 | a0001c0001t0015g0247a0003c0006t0004g0130 | 2 | HG03098.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1167+8153T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | ||||||
chr6:100412637
|
AAAAG | A | 3 | a0001c0001t0002g0162a0001c0001t0009g0216a0002c0002t0001g0118 | 3 | HG00621.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1167+8149_1167+815 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | ||||||
chr6:100412639
|
A | G | 24 | a0002c0002t0001g0030a0002c0002t0001g0047a0002c0002t0001g0048others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+8151T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412639 | ||||||
chr6:100412640
|
A | G | 9 | a0001c0001t0008g0026a0001c0001t0008g0077a0001c0001t0008g0209others(6): Show | 9 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8150T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412640 | ||||||
chr6:100412641
|
G | A | 5 | a0001c0001t0008g0026a0001c0001t0008g0077a0001c0001t0008g0209others(2): Show | 5 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8149C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412641 | ||||||
chr6:100412643
|
A | G | 59 | a0001c0001t0006g0227a0001c0001t0008g0072a0001c0001t0015g0247others(56): Show | 59 | HG00140.hp2 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1167+8147T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412643 | ||||||
chr6:100412644
|
A | G | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167+8146T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412644 | ||||||
chr6:100412647
|
A | G | 73 | a0001c0001t0005g0182a0001c0001t0008g0072a0001c0001t0015g0245others(70): Show | 73 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1167+8143T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412647 | ||||||
chr6:100412649
|
GAA | G | 6 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0131others(3): Show | 6 | NA18944.hp1 NA18948.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+8139_1167+814 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412649 | ||||||
chr6:100412649
|
GAAAGAAA others(27): Show |
G | 2 | a0001c0001t0008g0070a0002c0002t0001g0122 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8107_1167+814 others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412649 | ||||||
chr6:100412651
|
A | G | 87 | a0001c0001t0005g0091a0001c0001t0005g0182a0001c0001t0006g0161others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1167+8139T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412651 | ||||||
chr6:100412655
|
A | G | 100 | a0001c0001t0003g0151a0001c0001t0003g0171a0001c0001t0005g0032others(97): Show | 100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1167+8135T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | ||||||
chr6:100412655
|
AAG | A | 10 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0003g0068others(7): Show | 10 | HG00733.hp1 HG00733.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8133_1167+813 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | ||||||
chr6:100412655
|
AAGAGAGA others(7): Show |
A | 1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1167+8121_1167+813 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | ||||||
chr6:100412657
|
G | GAA | 4 | a0001c0001t0008g0026a0001c0001t0008g0077a0001c0001t0008g0209others(1): Show | 4 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8132_1167+813 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412657 | ||||||
chr6:100412659
|
G | A | 15 | a0001c0001t0003g0214a0001c0001t0005g0110a0001c0001t0005g0119others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1167+8131C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412659 | ||||||
chr6:100412661
|
G | A | 1 | a0001c0001t0005g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1167+8129C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412661 | ||||||
chr6:100412663
|
G | A | 1 | a0001c0001t0020g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1167+8127C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412663 | ||||||
chr6:100412665
|
G | A | 12 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0091others(9): Show | 12 | HG00544.hp2 HG01169.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1167+8125C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412665 | ||||||
chr6:100412667
|
G | A | 2 | a0001c0001t0013g0106a0002c0002t0001g0060 | 2 | NA18994.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1167+8123C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412667 | ||||||
chr6:100412669
|
G | A | 12 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0091others(9): Show | 12 | HG00544.hp2 HG01169.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1167+8121C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412669 | ||||||
chr6:100412671
|
G | A | 27 | a0001c0001t0003g0033a0001c0001t0003g0151a0001c0001t0005g0082others(24): Show | 27 | HG00544.hp2 HG00642.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1167+8119C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412671 | ||||||
chr6:100412671
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0003g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1167+8107_1167+811 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412671 | ||||||
chr6:100412673
|
G | A | 10 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0131others(7): Show | 10 | HG01169.hp2 HG02451.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8117C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412673 | ||||||
chr6:100412673
|
GAAAGAAA others(37): Show |
G | 2 | a0001c0001t0015g0245a0001c0001t0015g0246 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1167+8073_1167+811 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412673 | ||||||
chr6:100412675
|
A | G | 40 | a0001c0001t0004g0128a0001c0001t0020g0286a0001c0001t0028g0254others(37): Show | 40 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167+8115T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412675 | ||||||
chr6:100412677
|
G | A | 1 | a0001c0001t0013g0106 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1167+8113C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412677 | ||||||
chr6:100412679
|
A | G | 17 | a0001c0001t0013g0106a0001c0001t0028g0254a0001c0001t0071g0010others(14): Show | 17 | HG01074.hp1 HG01361.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1167+8111T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412679 | ||||||
chr6:100412681
|
G | A | 21 | a0001c0001t0003g0033a0001c0001t0003g0151a0001c0001t0005g0082others(18): Show | 21 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1167+8109C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412681 | ||||||
chr6:100412681
|
GAA | G | 12 | a0001c0001t0005g0032a0001c0001t0005g0045a0001c0001t0005g0131others(9): Show | 12 | HG00544.hp2 HG02451.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167+8107_1167+810 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412681 | ||||||
chr6:100412683
|
A | AAAAG | 30 | a0001c0001t0002g0061a0001c0001t0002g0193a0001c0001t0002g0195others(27): Show | 31 | HG00738.hp1 HG01167.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1167+8103_1167+810 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
A | AAAAGAAA others(1): Show |
9 | a0001c0001t0002g0157a0001c0001t0003g0009a0001c0001t0006g0297others(6): Show | 9 | HG01081.hp1 HG01256.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167+8099_1167+810 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
A | AAAAGAAA others(5): Show |
1 | a0001c0001t0039g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1167+8095_1167+810 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
A | AAG | 3 | a0001c0001t0005g0091a0001c0001t0008g0072a0002c0002t0001g0200 | 3 | HG01169.hp2 HG06807.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1167+8106_1167+810 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
A | G | 37 | a0001c0001t0002g0212a0001c0001t0003g0033a0001c0001t0003g0151others(34): Show | 37 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1167+8107T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAG | A | 32 | a0001c0001t0001g0141a0001c0001t0002g0043a0001c0001t0002g0066others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1167+8103_1167+810 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(1): Show |
A | 29 | a0001c0001t0002g0049a0001c0001t0002g0056a0001c0001t0002g0086others(26): Show | 29 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1167+8099_1167+810 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(5): Show |
A | 11 | a0001c0001t0002g0097a0001c0001t0002g0148a0001c0001t0003g0158others(8): Show | 11 | HG01261.hp1 HG02132.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1167+8095_1167+810 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(9): Show |
A | 6 | a0001c0001t0002g0260a0001c0001t0003g0094a0001c0001t0003g0134others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+8091_1167+810 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(13): Show |
A | 4 | a0001c0001t0003g0058a0001c0001t0003g0224a0001c0001t0019g0018others(1): Show | 4 | HG01070.hp1 HG02071.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8087_1167+810 others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(17): Show |
A | 1 | a0004c0008t0023g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+8083_1167+810 others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(37): Show |
A | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+8063_1167+810 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412683
|
AAAAGAAA others(41): Show |
A | 2 | a0001c0001t0015g0247a0001c0001t0068g0294 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1167+8059_1167+810 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | ||||||
chr6:100412685
|
A | G | 29 | a0001c0001t0002g0064a0001c0001t0004g0128a0001c0001t0020g0286others(26): Show | 29 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+8105T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412685 | ||||||
chr6:100412687
|
G | A | 24 | a0001c0001t0002g0064a0001c0001t0004g0128a0001c0001t0020g0286others(21): Show | 24 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+8103C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412687 | ||||||
chr6:100412689
|
A | G | 1 | a0002c0002t0017g0313 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8101T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412689 | ||||||
chr6:100412693
|
AAG | A | 9 | a0001c0001t0003g0175a0001c0001t0028g0254a0001c0001t0071g0010others(6): Show | 9 | HG00544.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8095_1167+809 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412693 | ||||||
chr6:100412695
|
G | A | 1 | a0002c0002t0017g0313 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8095C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412695 | ||||||
chr6:100412696
|
AAAGAAAG others(12): Show |
A | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1167+8075_1167+809 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412696 | ||||||
chr6:100412697
|
AAG | A | 4 | a0002c0002t0001g0136a0002c0002t0001g0194a0002c0002t0001g0222others(1): Show | 4 | HG02071.hp1 HG02602.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8091_1167+809 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412697 | ||||||
chr6:100412738
|
AGAAAG | A | 10 | a0001c0001t0004g0041a0001c0001t0004g0198a0001c0001t0004g0199others(7): Show | 10 | HG00438.hp2 HG00733.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+8047_1167+805 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412738 | ||||||
chr6:100412742
|
A | G | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+8048T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412742 | ||||||
chr6:100412742
|
AG | A | 8 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0196others(5): Show | 8 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+8047delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412742 | ||||||
chr6:100412746
|
AG | A | 4 | a0001c0001t0004g0112a0001c0001t0004g0185a0001c0001t0018g0311others(1): Show | 4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8043delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412746 | ||||||
chr6:100412751
|
G | A | 5 | a0001c0001t0004g0293a0001c0001t0008g0209a0001c0001t0027g0089others(2): Show | 5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8039C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412751 | ||||||
chr6:100412751
|
GAAAAAAG others(1): Show |
G | 19 | a0001c0001t0004g0041a0001c0001t0004g0113a0001c0001t0004g0114others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1167+8031_1167+803 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412751 | ||||||
chr6:100412754
|
A | G | 5 | a0001c0001t0004g0293a0001c0001t0008g0209a0001c0001t0027g0089others(2): Show | 5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8036T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412754 | ||||||
chr6:100412754
|
AAAAG | A | 4 | a0001c0001t0004g0112a0001c0001t0004g0185a0001c0001t0018g0311others(1): Show | 4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8032_1167+803 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412754 | ||||||
chr6:100412758
|
GA | G | 5 | a0001c0001t0004g0293a0001c0001t0008g0209a0001c0001t0027g0089others(2): Show | 5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8031delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412758 | ||||||
chr6:100412759
|
A | AAAG | 11 | a0001c0001t0004g0104a0001c0001t0004g0111a0001c0001t0004g0128others(8): Show | 11 | HG00099.hp1 HG01074.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1167+8030_1167+803 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412759 | ||||||
chr6:100412759
|
A | G | 4 | a0001c0001t0004g0112a0001c0001t0004g0185a0001c0001t0018g0311others(1): Show | 4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8031T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412759 | ||||||
chr6:100412788
|
C | T | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8002G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412788 | ||||||
chr6:100412807
|
C | T | 8 | a0001c0001t0002g0056a0001c0001t0002g0071a0001c0001t0002g0211others(5): Show | 8 | HG02129.hp1 NA18982.hp1 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+7983G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412807 | ||||||
chr6:100413274
|
T | C | 3 | a0001c0001t0020g0159a0001c0001t0020g0286a0001c0001t0041g0167 | 3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+7516A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413274 | ||||||
chr6:100413330
|
A | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+7460T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413330 | ||||||
chr6:100413450
|
C | T | 6 | a0001c0001t0016g0001a0001c0001t0021g0108a0001c0001t0021g0266others(3): Show | 7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+7340G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413450 | ||||||
chr6:100413550
|
G | A | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+7240C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413550 | ||||||
chr6:100413676
|
T | C | 1 | a0001c0001t0059g0178 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+7114A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413676 | ||||||
chr6:100413679
|
C | T | 1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1167+7111G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413679 | ||||||
chr6:100413726
|
G | A | 316 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1167+7064C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413726 | ||||||
chr6:100413841
|
G | A | 1 | a0002c0002t0007g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1167+6949C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413841 | ||||||
chr6:100413903
|
A | G | 1 | a0001c0001t0003g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1167+6887T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413903 | ||||||
chr6:100414072
|
G | A | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+6718C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414072 | ||||||
chr6:100414175
|
G | A | 31 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1167+6615C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414175 | ||||||
chr6:100414246
|
T | C | 6 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6544A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414246 | ||||||
chr6:100414272
|
C | T | 2 | a0001c0001t0003g0151a0001c0001t0003g0169 | 2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1167+6518G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414272 | ||||||
chr6:100414368
|
T | C | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+6422A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414368 | ||||||
chr6:100414401
|
C | A | 1 | a0001c0001t0004g0314 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1167+6389G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414401 | ||||||
chr6:100414415
|
C | T | 6 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6375G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414415 | ||||||
chr6:100414495
|
G | T | 6 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6295C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414495 | ||||||
chr6:100414551
|
T | C | 31 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1167+6239A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414551 | ||||||
chr6:100414614
|
A | G | 1 | a0002c0002t0001g0047 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1167+6176T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414614 | ||||||
chr6:100414662
|
G | T | 1 | a0002c0002t0024g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+6128C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414662 | ||||||
chr6:100414933
|
A | G | 7 | a0001c0001t0006g0161a0001c0001t0006g0227a0001c0001t0025g0256others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+5857T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414933 | ||||||
chr6:100415051
|
T | C | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5739A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415051 | ||||||
chr6:100415121
|
G | A | 1 | a0002c0002t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1167+5669C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415121 | ||||||
chr6:100415203
|
A | G | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5587T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415203 | ||||||
chr6:100415312
|
T | C | 7 | a0001c0001t0006g0161a0001c0001t0006g0227a0001c0001t0025g0256others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+5478A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415312 | ||||||
chr6:100415388
|
C | A | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5402G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415388 | ||||||
chr6:100415912
|
C | T | 1 | a0001c0001t0078g0303 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1167+4878G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415912 | ||||||
chr6:100416242
|
C | T | 83 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0028g0254others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+4548G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416242 | ||||||
chr6:100416260
|
C | A | 24 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+4530G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416260 | ||||||
chr6:100416298
|
T | C | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1167+4492A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416298 | ||||||
chr6:100416404
|
C | G | 4 | a0001c0001t0002g0066a0001c0001t0032g0006a0001c0001t0042g0040others(1): Show | 4 | HG01433.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+4386G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416404 | ||||||
chr6:100416604
|
C | T | 3 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264 | 3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+4186G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416604 | ||||||
chr6:100416948
|
T | A | 25 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+3842A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416948 | ||||||
chr6:100416953
|
T | C | 159 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0004g0041others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1167+3837A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416953 | ||||||
chr6:100416979
|
C | CA | 83 | a0001c0001t0002g0066a0001c0001t0008g0026a0001c0001t0008g0070others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1167+3810dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416979 | ||||||
chr6:100416979
|
C | CAA | 30 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1167+3809_1167+381 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416979 | ||||||
chr6:100416992
|
C | A | 5 | a0001c0001t0016g0001a0001c0001t0021g0108a0001c0001t0021g0266others(2): Show | 6 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+3798G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416992 | ||||||
chr6:100417062
|
T | G | 111 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1167+3728A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417062 | ||||||
chr6:100417084
|
A | G | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+3706T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417084 | ||||||
chr6:100417147
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+3643T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417147 | ||||||
chr6:100417209
|
C | T | 1 | a0001c0001t0010g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1167+3581G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417209 | ||||||
chr6:100417347
|
C | T | 1 | a0001c0001t0078g0303 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1167+3443G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417347 | ||||||
chr6:100417348
|
G | A | 4 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0061g0302others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+3442C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417348 | ||||||
chr6:100417395
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1167+3395A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417395 | ||||||
chr6:100417451
|
T | C | 1 | a0001c0001t0059g0178 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+3339A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417451 | ||||||
chr6:100417496
|
C | T | 5 | a0001c0001t0002g0170a0001c0001t0002g0173a0001c0001t0011g0149others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+3294G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417496 | ||||||
chr6:100417688
|
C | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+3102G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417688 | ||||||
chr6:100417822
|
T | C | 1 | a0001c0001t0019g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1167+2968A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417822 | ||||||
chr6:100417930
|
G | T | 83 | a0001c0001t0008g0070a0001c0001t0008g0072a0001c0001t0028g0254others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+2860C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417930 | ||||||
chr6:100418004
|
T | A | 1 | a0001c0001t0018g0307 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1167+2786A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418004 | ||||||
chr6:100418150
|
A | G | 275 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(272): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1167+2640T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418150 | ||||||
chr6:100418190
|
A | C | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1167+2600T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418190 | ||||||
chr6:100418198
|
A | T | 6 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0059g0178others(3): Show | 6 | HG01168.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+2592T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418198 | ||||||
chr6:100418321
|
C | T | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1167+2469G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418321 | ||||||
chr6:100418359
|
A | AAAAT | 110 | a0001c0001t0002g0097a0001c0001t0003g0033a0001c0001t0003g0094others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1167+2427_1167+243 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | ||||||
chr6:100418359
|
A | AAAATAAA others(1): Show |
7 | a0001c0001t0005g0045a0001c0001t0005g0132a0001c0001t0005g0271others(4): Show | 7 | HG03831.hp2 HG04184.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+2423_1167+243 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | ||||||
chr6:100418359
|
A | AAAATAAA others(5): Show |
8 | a0001c0001t0004g0114a0001c0001t0006g0227a0001c0001t0008g0050others(5): Show | 8 | HG00733.hp1 HG01168.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+2419_1167+243 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | ||||||
chr6:100418359
|
A | AAAATAAA others(9): Show |
40 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0112others(37): Show | 40 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167+2415_1167+243 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | ||||||
chr6:100418359
|
A | AAAATAAA others(13): Show |
8 | a0001c0001t0002g0086a0001c0001t0004g0111a0001c0001t0004g0293others(5): Show | 8 | HG01175.hp1 HG02083.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+2411_1167+243 others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | ||||||
chr6:100418506
|
G | A | 6 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+2284C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418506 | ||||||
chr6:100418740
|
A | G | 2 | a0001c0001t0020g0159a0001c0001t0041g0167 | 2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+2050T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418740 | ||||||
chr6:100418769
|
T | A | 4 | a0001c0001t0059g0178a0001c0001t0061g0302a0001c0001t0070g0177others(1): Show | 4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+2021A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418769 | ||||||
chr6:100418848
|
G | C | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+1942C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418848 | ||||||
chr6:100418888
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1167+1902G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418888 | ||||||
chr6:100418957
|
G | A | 6 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+1833C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418957 | ||||||
chr6:100419009
|
A | G | 3 | a0001c0001t0059g0178a0001c0001t0070g0177a0001c0001t0071g0010 | 3 | HG01168.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1167+1781T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419009 | ||||||
chr6:100419086
|
G | A | 128 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1167+1704C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419086 | ||||||
chr6:100419185
|
C | A | 1 | a0001c0001t0019g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1167+1605G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419185 | ||||||
chr6:100419329
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1167+1461A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419329 | ||||||
chr6:100419384
|
C | T | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+1406G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419384 | ||||||
chr6:100419662
|
G | T | 33 | a0002c0002t0001g0042a0002c0002t0001g0046a0002c0002t0001g0048others(30): Show | 33 | HG00621.hp2 HG02056.hp1 HG02293.hp1 others(30): Show |
intron_variant | MODIFIER | c.1167+1128C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419662 | ||||||
chr6:100419675
|
A | G | 1 | a0001c0007t0004g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1167+1115T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419675 | ||||||
chr6:100419753
|
A | T | 2 | a0001c0001t0023g0088a0001c0001t0060g0153 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1167+1037T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419753 | ||||||
chr6:100419787
|
A | G | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+1003T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419787 | ||||||
chr6:100419923
|
A | G | 48 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1167+867T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419923 | ||||||
chr6:100420039
|
G | T | 3 | a0002c0002t0001g0120a0002c0002t0001g0218a0002c0002t0006g0235 | 3 | HG02602.hp1 HG03704.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1167+751C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420039 | ||||||
chr6:100420072
|
T | A | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+718A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420072 | ||||||
chr6:100420133
|
T | C | 25 | a0001c0001t0003g0033a0001c0001t0003g0214a0001c0001t0005g0032others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+657A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420133 | ||||||
chr6:100420195
|
C | T | 6 | a0001c0001t0016g0001a0001c0001t0021g0108a0001c0001t0021g0266others(3): Show | 7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+595G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420195 | ||||||
chr6:100420359
|
G | A | 2 | a0001c0001t0022g0147a0001c0001t0022g0160 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+431C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420359 | ||||||
chr6:100420492
|
A | T | 1 | a0002c0002t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1167+298T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420492 | ||||||
chr6:100420499
|
G | A | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+291C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420499 | ||||||
chr6:100420584
|
A | G | 45 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(42): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1167+206T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420584 | ||||||
chr6:100420616
|
A | T | 164 | a0001c0001t0002g0086a0001c0001t0003g0033a0001c0001t0003g0214others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1167+174T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420616 | ||||||
chr6:100421463
|
C | G | 2 | a0002c0002t0003g0038a0002c0002t0003g0039 | 2 | NA18957.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.999-505G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421463 | ||||||
chr6:100421680
|
T | G | 1 | a0002c0002t0007g0065 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.999-722A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421680 | ||||||
chr6:100421722
|
T | G | 2 | a0001c0001t0057g0083a0001c0001t0058g0084 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.999-764A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421722 | ||||||
chr6:100421797
|
C | T | 8 | a0001c0001t0008g0026a0001c0001t0008g0050a0001c0001t0008g0077others(5): Show | 8 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.999-839G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421797 | ||||||
chr6:100421809
|
T | C | 1 | a0002c0002t0001g0317 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.999-851A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421809 | ||||||
chr6:100421818
|
A | G | 1 | a0002c0002t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.999-860T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421818 | ||||||
chr6:100421959
|
G | A | 2 | a0001c0001t0005g0045a0001c0001t0005g0132 | 2 | NA18944.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.999-1001C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421959 | ||||||
chr6:100421973
|
C | A | 45 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(42): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.999-1015G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421973 | ||||||
chr6:100422006
|
T | TC | 83 | a0001c0001t0003g0033a0001c0001t0005g0032a0001c0001t0005g0091others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.999-1049dupG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422006 | ||||||
chr6:100422214
|
T | C | 1 | a0001c0001t0013g0127 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.999-1256A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422214 | ||||||
chr6:100422329
|
G | A | 1 | a0001c0001t0073g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.999-1371C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422329 | ||||||
chr6:100422388
|
G | C | 1 | a0001c0001t0005g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.999-1430C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422388 | ||||||
chr6:100422390
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.999-1432C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422390 | ||||||
chr6:100422499
|
G | A | 1 | a0002c0002t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.999-1541C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422499 | ||||||
chr6:100422575
|
T | C | 1 | a0001c0001t0019g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.999-1617A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422575 | ||||||
chr6:100422661
|
A | C | 45 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(42): Show | 45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.999-1703T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422661 | ||||||
chr6:100422880
|
T | C | 2 | a0001c0001t0004g0128a0003c0006t0004g0130 | 2 | NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.999-1922A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422880 | ||||||
chr6:100422910
|
T | C | 22 | a0001c0001t0003g0214a0001c0001t0005g0045a0001c0001t0005g0082others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-1952A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422910 | ||||||
chr6:100422922
|
A | G | 1 | a0002c0002t0001g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.999-1964T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422922 | ||||||
chr6:100422954
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0239 | 2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.999-1996G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422954 | ||||||
chr6:100423048
|
C | A | 1 | a0001c0001t0002g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.999-2090G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423048 | ||||||
chr6:100423077
|
T | C | 6 | a0001c0001t0003g0214a0001c0001t0005g0110a0001c0001t0005g0119others(3): Show | 6 | HG00621.hp1 HG02165.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-2119A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423077 | ||||||
chr6:100423126
|
C | A | 2 | a0001c0001t0070g0177a0001c0009t0033g0005 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.999-2168G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423126 | ||||||
chr6:100423131
|
A | G | 1 | a0001c0001t0059g0178 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.999-2173T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423131 | ||||||
chr6:100423184
|
T | A | 4 | a0001c0001t0059g0178a0001c0001t0070g0177a0001c0001t0071g0010others(1): Show | 4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-2226A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423184 | ||||||
chr6:100423227
|
T | G | 1 | a0001c0001t0003g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.999-2269A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423227 | ||||||
chr6:100423286
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.999-2328G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423286 | ||||||
chr6:100423439
|
A | C | 1 | a0001c0001t0005g0119 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.999-2481T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423439 | ||||||
chr6:100423612
|
T | C | 164 | a0001c0001t0002g0086a0001c0001t0003g0033a0001c0001t0003g0214others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.999-2654A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423612 | ||||||
chr6:100423659
|
G | A | 22 | a0001c0001t0003g0214a0001c0001t0005g0045a0001c0001t0005g0082others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-2701C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423659 | ||||||
chr6:100423728
|
T | C | 1 | a0002c0002t0006g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.999-2770A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423728 | ||||||
chr6:100423853
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.999-2895G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423853 | ||||||
chr6:100424066
|
C | G | 2 | a0001c0001t0020g0159a0001c0001t0041g0167 | 2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-3108G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424066 | ||||||
chr6:100424078
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999-3120G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424078 | ||||||
chr6:100424092
|
A | T | 3 | a0001c0001t0006g0164a0001c0001t0057g0083a0001c0001t0058g0084 | 3 | HG02965.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.999-3134T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424092 | ||||||
chr6:100424180
|
T | A | 168 | a0001c0001t0002g0086a0001c0001t0003g0033a0001c0001t0003g0151others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.999-3222A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424180 | ||||||
chr6:100424232
|
A | G | 1 | a0002c0002t0007g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.999-3274T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424232 | ||||||
chr6:100424608
|
T | A | 1 | a0002c0002t0007g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.999-3650A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424608 | ||||||
chr6:100424679
|
G | A | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-3721C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424679 | ||||||
chr6:100424770
|
T | C | 3 | a0001c0001t0019g0016a0001c0001t0034g0007a0001c0001t0056g0025 | 3 | HG02683.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.999-3812A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424770 | ||||||
chr6:100424827
|
T | C | 44 | a0001c0001t0002g0086a0001c0001t0004g0041a0001c0001t0004g0104others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.999-3869A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424827 | ||||||
chr6:100424911
|
C | T | 119 | a0001c0001t0002g0086a0001c0001t0003g0033a0001c0001t0004g0041others(116): Show | 119 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.999-3953G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424911 | ||||||
chr6:100425381
|
T | C | 83 | a0001c0001t0003g0033a0001c0001t0005g0032a0001c0001t0005g0091others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.999-4423A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425381 | ||||||
chr6:100425404
|
T | C | 2 | a0001c0001t0006g0161a0001c0001t0006g0227 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.999-4446A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425404 | ||||||
chr6:100425425
|
A | C | 1 | a0001c0001t0005g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.999-4467T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425425 | ||||||
chr6:100425814
|
A | G | 4 | a0001c0001t0059g0178a0001c0001t0070g0177a0001c0001t0071g0010others(1): Show | 4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-4856T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425814 | ||||||
chr6:100425914
|
T | C | 1 | a0002c0005t0065g0055 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.999-4956A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425914 | ||||||
chr6:100426062
|
G | A | 26 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0111others(23): Show | 26 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.999-5104C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426062 | ||||||
chr6:100426219
|
A | G | 1 | a0001c0001t0074g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.999-5261T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426219 | ||||||
chr6:100426284
|
C | T | 6 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0027g0089others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-5326G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426284 | ||||||
chr6:100426441
|
C | T | 5 | a0001c0001t0002g0170a0001c0001t0002g0173a0001c0001t0011g0149others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-5483G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426441 | ||||||
chr6:100426474
|
G | A | 1 | a0001c0001t0037g0017 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.999-5516C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426474 | ||||||
chr6:100426658
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0009g0172 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.999-5700T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426658 | ||||||
chr6:100426709
|
TC | T | 5 | a0001c0001t0006g0226a0001c0001t0010g0280a0001c0001t0010g0281others(2): Show | 5 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-5752delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426709 | ||||||
chr6:100426713
|
G | C | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.999-5755C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426713 | ||||||
chr6:100426727
|
A | G | 4 | a0001c0001t0059g0178a0001c0001t0070g0177a0001c0001t0071g0010others(1): Show | 4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-5769T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426727 | ||||||
chr6:100426753
|
C | T | 4 | a0001c0001t0015g0245a0001c0001t0015g0246a0001c0001t0015g0247others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-5795G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426753 | ||||||
chr6:100426899
|
A | T | 4 | a0001c0001t0003g0228a0001c0001t0003g0298a0001c0001t0005g0045others(1): Show | 4 | HG02896.hp2 HG02970.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-5941T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426899 | ||||||
chr6:100427277
|
C | T | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0258 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.999-6319G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427277 | ||||||
chr6:100427640
|
T | C | 88 | a0001c0001t0003g0033a0001c0001t0004g0206a0001c0001t0005g0032others(85): Show | 88 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.999-6682A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427640 | ||||||
chr6:100427950
|
C | T | 1 | a0001c0001t0064g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-6992G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427950 | ||||||
chr6:100428050
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.999-7092A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428050 | ||||||
chr6:100428213
|
G | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-7255C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428213 | ||||||
chr6:100428380
|
A | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0239a0001c0001t0053g0289 | 3 | HG00642.hp1 HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.999-7422T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428380 | ||||||
chr6:100428436
|
A | C | 9 | a0001c0001t0002g0157a0001c0001t0003g0171a0001c0001t0003g0228others(6): Show | 9 | HG02055.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.999-7478T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428436 | ||||||
chr6:100428577
|
G | T | 10 | a0001c0001t0002g0043a0001c0001t0002g0174a0001c0001t0002g0261others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-7619C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428577 | ||||||
chr6:100428628
|
T | TAAGAATG others(318): Show |
2 | a0001c0001t0006g0226a0001c0001t0010g0163 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(327): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(328): Show |
4 | a0001c0001t0025g0256a0001c0001t0025g0263a0001c0001t0069g0264others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-7671_999-7670i others(337): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(329): Show |
2 | a0001c0001t0027g0089a0001c0001t0074g0051 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(338): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(330): Show |
1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(339): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(332): Show |
2 | a0001c0001t0006g0165a0001c0009t0033g0005 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(341): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(321): Show |
1 | a0001c0001t0002g0239 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(330): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(322): Show |
1 | a0001c0001t0002g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(331): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(324): Show |
1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(333): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(333): Show |
1 | a0001c0001t0063g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(342): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(339): Show |
1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(348): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(344): Show |
1 | a0001c0001t0006g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(353): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428628
|
T | TAAGAATG others(346): Show |
1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(355): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | ||||||
chr6:100428667
|
G | C | 4 | a0001c0001t0002g0231a0001c0001t0039g0012a0001c0001t0043g0190others(1): Show | 4 | HG00642.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-7709C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428667 | ||||||
chr6:100428668
|
C | G | 1 | a0001c0001t0039g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.999-7710G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428668 | ||||||
chr6:100428805
|
T | C | 1 | a0001c0001t0011g0285 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.999-7847A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428805 | ||||||
chr6:100428886
|
T | C | 1 | a0001c0001t0003g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.999-7928A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428886 | ||||||
chr6:100429018
|
G | A | 36 | a0001c0001t0002g0056a0001c0001t0002g0064a0001c0001t0002g0195others(33): Show | 36 | HG00558.hp1 HG00741.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.999-8060C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429018 | ||||||
chr6:100429068
|
A | T | 1 | a0002c0005t0065g0055 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.999-8110T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429068 | ||||||
chr6:100429076
|
T | G | 2 | a0001c0001t0010g0163a0001c0001t0040g0011 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-8118A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429076 | ||||||
chr6:100429084
|
C | T | 6 | a0001c0001t0012g0306a0001c0001t0012g0308a0001c0001t0012g0309others(3): Show | 6 | HG02083.hp1 HG02129.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-8126G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429084 | ||||||
chr6:100429116
|
C | T | 6 | a0001c0001t0012g0306a0001c0001t0012g0308a0001c0001t0012g0309others(3): Show | 6 | HG02083.hp1 HG02129.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-8158G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429116 | ||||||
chr6:100429174
|
A | G | 2 | a0001c0001t0004g0104a0001c0001t0005g0131 | 2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.999-8216T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429174 | ||||||
chr6:100429365
|
T | C | 97 | a0001c0001t0001g0141a0001c0001t0002g0036a0001c0001t0002g0043others(94): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.999-8407A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429365 | ||||||
chr6:100429368
|
CA | C | 289 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.999-8411delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429368 | ||||||
chr6:100429368
|
CAA | C | 8 | a0001c0001t0002g0135a0001c0001t0002g0276a0001c0001t0003g0009others(5): Show | 8 | HG00741.hp2 HG02109.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.999-8412_999-8411d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429368 | ||||||
chr6:100429584
|
G | A | 1 | a0001c0001t0003g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.999-8626C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429584 | ||||||
chr6:100429926
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.999-8968A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429926 | ||||||
chr6:100429952
|
T | C | 52 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(49): Show | 52 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.999-8994A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429952 | ||||||
chr6:100430022
|
A | G | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-9064T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430022 | ||||||
chr6:100430387
|
C | T | 1 | a0001c0001t0008g0026 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.999-9429G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430387 | ||||||
chr6:100430391
|
C | T | 137 | a0001c0001t0002g0028a0001c0001t0002g0049a0001c0001t0002g0056others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.999-9433G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430391 | ||||||
chr6:100430440
|
T | A | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-9482A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430440 | ||||||
chr6:100430466
|
C | G | 1 | a0001c0001t0063g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999-9508G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430466 | ||||||
chr6:100430582
|
G | T | 304 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.999-9624C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430582 | ||||||
chr6:100430716
|
A | G | 2 | a0001c0001t0057g0083a0001c0001t0058g0084 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.999-9758T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430716 | ||||||
chr6:100430762
|
T | C | 4 | a0002c0002t0014g0269a0002c0002t0014g0270a0002c0002t0014g0272others(1): Show | 4 | HG00438.hp1 HG02083.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-9804A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430762 | ||||||
chr6:100430775
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.999-9817T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430775 | ||||||
chr6:100430968
|
C | G | 3 | a0002c0002t0007g0019a0002c0002t0007g0065a0002c0002t0007g0237 | 3 | NA18973.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.999-10010G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430968 | ||||||
chr6:100430982
|
A | G | 132 | a0001c0001t0001g0141a0001c0001t0002g0036a0001c0001t0002g0043others(129): Show | 132 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.999-10024T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430982 | ||||||
chr6:100431093
|
T | G | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10135A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431093 | ||||||
chr6:100431140
|
C | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10182G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431140 | ||||||
chr6:100431183
|
T | C | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-10225A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431183 | ||||||
chr6:100431288
|
G | A | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999-10330C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431288 | ||||||
chr6:100431382
|
C | T | 1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999-10424G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431382 | ||||||
chr6:100431505
|
T | C | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10547A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431505 | ||||||
chr6:100431775
|
C | T | 172 | a0001c0001t0002g0028a0001c0001t0002g0049a0001c0001t0002g0056others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.999-10817G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431775 | ||||||
chr6:100431852
|
C | T | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.999-10894G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431852 | ||||||
chr6:100431977
|
C | T | 4 | a0001c0001t0006g0297a0001c0001t0006g0299a0001c0001t0006g0300others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11019G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431977 | ||||||
chr6:100432018
|
C | T | 1 | a0002c0002t0007g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.999-11060G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432018 | ||||||
chr6:100432151
|
A | G | 5 | a0001c0001t0002g0043a0001c0001t0002g0138a0001c0001t0005g0139others(2): Show | 5 | HG02132.hp1 HG02523.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-11193T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432151 | ||||||
chr6:100432256
|
G | C | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.999-11298C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432256 | ||||||
chr6:100432426
|
A | AGTG | 4 | a0001c0001t0018g0307a0001c0001t0018g0311a0002c0002t0017g0312others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11471_999-1146 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432426 | ||||||
chr6:100432429
|
GGTT | G | 4 | a0001c0001t0018g0307a0001c0001t0018g0311a0002c0002t0017g0312others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11474_999-1147 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432429 | ||||||
chr6:100432432
|
T | G | 7 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(4): Show | 7 | HG00280.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-11474A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432432 | ||||||
chr6:100432677
|
G | T | 1 | a0001c0001t0064g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-11719C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432677 | ||||||
chr6:100432820
|
A | G | 143 | a0001c0001t0001g0141a0001c0001t0002g0036a0001c0001t0002g0043others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.999-11862T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432820 | ||||||
chr6:100432956
|
G | A | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-11998C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432956 | ||||||
chr6:100433018
|
T | C | 1 | a0002c0002t0001g0232 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.999-12060A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433018 | ||||||
chr6:100433083
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.999-12125G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433083 | ||||||
chr6:100433202
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.999-12244G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433202 | ||||||
chr6:100433464
|
C | G | 4 | a0001c0001t0003g0078a0001c0001t0003g0079a0002c0002t0017g0312others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-12506G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433464 | ||||||
chr6:100433670
|
G | C | 1 | a0003c0006t0004g0130 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.999-12712C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433670 | ||||||
chr6:100433736
|
C | CCCACCCA others(4): Show |
1 | a0001c0001t0004g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.999-12779_999-1277 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433736 | ||||||
chr6:100433736
|
C | CCCACCCA others(6): Show |
1 | a0002c0002t0001g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.999-12779_999-1277 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433736 | ||||||
chr6:100433740
|
C | A | 2 | a0001c0001t0004g0095a0002c0002t0001g0030 | 2 | HG01993.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.999-12782G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CACACACA others(4): Show |
1 | a0001c0001t0003g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.999-12783_999-1278 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCA | 32 | a0001c0001t0002g0193a0001c0001t0002g0195a0001c0001t0003g0058others(29): Show | 32 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.999-12784_999-1278 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCACACA | 4 | a0001c0001t0002g0186a0001c0001t0006g0014a0001c0001t0006g0180others(1): Show | 4 | HG02559.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-12788_999-1278 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCACACAC others(1): Show |
3 | a0001c0001t0009g0146a0002c0002t0001g0044a0002c0002t0001g0105 | 3 | HG02523.hp1 NA18990.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.999-12790_999-1278 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCACACAC others(3): Show |
86 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.999-12792_999-1278 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCACACAC others(5): Show |
4 | a0001c0001t0005g0131a0001c0001t0027g0029a0001c0001t0071g0010others(1): Show | 4 | HG01175.hp1 HG02615.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-12794_999-1278 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433740
|
C | CCACCCAC others(3): Show |
1 | a0001c0001t0002g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999-12783_999-1278 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | ||||||
chr6:100433742
|
A | ACC | 8 | a0001c0001t0012g0306a0001c0001t0012g0308a0001c0001t0012g0309others(5): Show | 8 | HG00280.hp1 HG01074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.999-12785_999-1278 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433742 | ||||||
chr6:100433767
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.999-12809A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433767 | ||||||
chr6:100433986
|
C | T | 1 | a0001c0001t0064g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-13028G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433986 | ||||||
chr6:100434408
|
G | T | 1 | a0001c0001t0037g0017 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.998+12860C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434408 | ||||||
chr6:100434470
|
A | G | 1 | a0001c0001t0076g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.998+12798T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434470 | ||||||
chr6:100434520
|
C | G | 2 | a0001c0001t0002g0064a0001c0001t0003g0052 | 2 | HG00558.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.998+12748G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434520 | ||||||
chr6:100434529
|
G | A | 100 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(97): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+12739C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434529 | ||||||
chr6:100435126
|
T | C | 1 | a0002c0002t0001g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+12142A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435126 | ||||||
chr6:100435273
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.998+11995A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435273 | ||||||
chr6:100435458
|
C | A | 9 | a0001c0001t0002g0261a0001c0001t0021g0266a0002c0002t0001g0274others(6): Show | 9 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.998+11810G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435458 | ||||||
chr6:100435464
|
G | T | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+11804C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435464 | ||||||
chr6:100435492
|
C | T | 1 | a0001c0001t0004g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.998+11776G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435492 | ||||||
chr6:100435562
|
C | T | 4 | a0001c0001t0002g0186a0001c0001t0006g0014a0001c0001t0006g0180others(1): Show | 4 | HG02559.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+11706G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435562 | ||||||
chr6:100435609
|
A | C | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.998+11659T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435609 | ||||||
chr6:100435663
|
A | T | 2 | a0001c0001t0002g0162a0001c0001t0059g0178 | 2 | HG01168.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.998+11605T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435663 | ||||||
chr6:100435792
|
C | A | 1 | a0001c0001t0008g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.998+11476G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435792 | ||||||
chr6:100435912
|
G | A | 1 | a0001c0001t0005g0119 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.998+11356C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435912 | ||||||
chr6:100435975
|
A | C | 99 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(96): Show | 99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+11293T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435975 | ||||||
chr6:100435992
|
C | T | 1 | a0002c0002t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11276G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435992 | ||||||
chr6:100435993
|
A | C | 1 | a0002c0002t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11275T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435993 | ||||||
chr6:100435994
|
T | A | 1 | a0002c0002t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11274A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | ||||||
chr6:100435994
|
T | TCA | 98 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(95): Show | 98 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.998+11272_998+1127 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | ||||||
chr6:100435994
|
TCACA | T | 26 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(23): Show | 26 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+11270_998+1127 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | ||||||
chr6:100436033
|
G | C | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+11235C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436033 | ||||||
chr6:100436255
|
T | C | 5 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0036g0305others(2): Show | 5 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.998+11013A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436255 | ||||||
chr6:100436355
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.998+10913A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436355 | ||||||
chr6:100436701
|
G | A | 1 | a0001c0001t0034g0007 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.998+10567C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436701 | ||||||
chr6:100436742
|
A | AT | 7 | a0001c0001t0002g0036a0001c0001t0003g0123a0001c0001t0004g0293others(4): Show | 7 | HG01169.hp1 HG01255.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.998+10525dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | ||||||
chr6:100436742
|
A | ATT | 94 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0043others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.998+10524_998+1052 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | ||||||
chr6:100436742
|
AT | A | 8 | a0001c0001t0006g0287a0001c0001t0008g0282a0001c0001t0010g0280others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.998+10525delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | ||||||
chr6:100436972
|
G | A | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.998+10296C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436972 | ||||||
chr6:100437009
|
G | T | 115 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.998+10259C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437009 | ||||||
chr6:100437013
|
G | A | 1 | a0001c0001t0004g0293 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.998+10255C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437013 | ||||||
chr6:100437077
|
A | G | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.998+10191T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437077 | ||||||
chr6:100437126
|
G | A | 1 | a0001c0001t0003g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.998+10142C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437126 | ||||||
chr6:100437216
|
A | G | 1 | a0002c0002t0007g0019 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.998+10052T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437216 | ||||||
chr6:100437233
|
T | C | 1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998+10035A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437233 | ||||||
chr6:100437387
|
C | T | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+9881G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437387 | ||||||
chr6:100437429
|
C | T | 1 | a0001c0001t0061g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.998+9839G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437429 | ||||||
chr6:100437481
|
G | A | 2 | a0001c0001t0034g0007a0001c0001t0035g0008 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.998+9787C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437481 | ||||||
chr6:100437482
|
G | A | 1 | a0001c0001t0056g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.998+9786C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437482 | ||||||
chr6:100437579
|
GA | G | 13 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(10): Show | 13 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.998+9688delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437579 | ||||||
chr6:100437587
|
AAC | A | 101 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(98): Show | 101 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.998+9679_998+9680d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437587 | ||||||
chr6:100437618
|
G | T | 1 | a0002c0002t0006g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.998+9650C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437618 | ||||||
chr6:100437675
|
G | A | 1 | a0001c0001t0042g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.998+9593C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437675 | ||||||
chr6:100437829
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.998+9439C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437829 | ||||||
chr6:100437938
|
G | A | 1 | a0001c0001t0003g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.998+9330C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437938 | ||||||
chr6:100438042
|
C | T | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.998+9226G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438042 | ||||||
chr6:100438091
|
A | G | 26 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0043others(23): Show | 26 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+9177T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438091 | ||||||
chr6:100438217
|
C | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+9051G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438217 | ||||||
chr6:100438238
|
T | C | 305 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.998+9030A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438238 | ||||||
chr6:100438240
|
T | A | 305 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.998+9028A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438240 | ||||||
chr6:100438422
|
C | T | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.998+8846G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438422 | ||||||
chr6:100438530
|
A | C | 102 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(99): Show | 102 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.998+8738T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438530 | ||||||
chr6:100438532
|
T | C | 1 | a0001c0001t0005g0132 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.998+8736A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438532 | ||||||
chr6:100438579
|
A | G | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+8689T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438579 | ||||||
chr6:100438749
|
G | T | 102 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(99): Show | 102 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.998+8519C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438749 | ||||||
chr6:100438790
|
A | G | 2 | a0001c0001t0002g0288a0001c0001t0002g0295 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.998+8478T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438790 | ||||||
chr6:100438879
|
A | G | 1 | a0001c0001t0056g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.998+8389T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438879 | ||||||
chr6:100438987
|
G | T | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.998+8281C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438987 | ||||||
chr6:100439466
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.998+7802A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439466 | ||||||
chr6:100439491
|
A | C | 2 | a0001c0001t0026g0233a0002c0002t0007g0238 | 2 | HG00423.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.998+7777T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439491 | ||||||
chr6:100439649
|
C | T | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+7619G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439649 | ||||||
chr6:100439989
|
G | A | 12 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(9): Show | 12 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.998+7279C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439989 | ||||||
chr6:100440173
|
C | A | 7 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(4): Show | 7 | NA18944.hp2 NA18950.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.998+7095G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440173 | ||||||
chr6:100440182
|
A | C | 306 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.998+7086T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440182 | ||||||
chr6:100440532
|
G | C | 116 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.998+6736C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440532 | ||||||
chr6:100440597
|
C | T | 1 | a0002c0002t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.998+6671G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440597 | ||||||
chr6:100440749
|
C | T | 94 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.998+6519G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440749 | ||||||
chr6:100440775
|
A | C | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+6493T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440775 | ||||||
chr6:100441210
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.998+6058C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441210 | ||||||
chr6:100441624
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.998+5644G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441624 | ||||||
chr6:100441665
|
T | G | 14 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(11): Show | 14 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.998+5603A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441665 | ||||||
chr6:100441771
|
G | C | 1 | a0001c0001t0003g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.998+5497C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441771 | ||||||
chr6:100441790
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.998+5478C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441790 | ||||||
chr6:100441848
|
A | G | 2 | a0001c0003t0003g0024a0001c0003t0003g0137 | 2 | HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.998+5420T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441848 | ||||||
chr6:100441979
|
T | A | 99 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(96): Show | 99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+5289A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441979 | ||||||
chr6:100442067
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.998+5201T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442067 | ||||||
chr6:100442098
|
A | T | 1 | a0001c0001t0003g0228 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.998+5170T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442098 | ||||||
chr6:100442702
|
C | G | 1 | a0001c0001t0002g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.998+4566G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442702 | ||||||
chr6:100442737
|
T | A | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+4531A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442737 | ||||||
chr6:100442775
|
A | G | 1 | a0001c0001t0008g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.998+4493T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442775 | ||||||
chr6:100442778
|
T | A | 132 | a0001c0001t0002g0049a0001c0001t0002g0056a0001c0001t0002g0061others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.998+4490A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442778 | ||||||
chr6:100443081
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.998+4187T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443081 | ||||||
chr6:100443115
|
A | G | 171 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.998+4153T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443115 | ||||||
chr6:100443255
|
T | C | 3 | a0001c0001t0002g0086a0001c0001t0008g0087a0001c0001t0023g0088 | 3 | HG02109.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.998+4013A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443255 | ||||||
chr6:100443309
|
T | C | 22 | a0001c0001t0002g0193a0001c0001t0002g0195a0001c0001t0003g0201others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.998+3959A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443309 | ||||||
chr6:100443381
|
A | G | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+3887T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443381 | ||||||
chr6:100443824
|
A | G | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+3444T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443824 | ||||||
chr6:100443891
|
A | G | 2 | a0001c0001t0003g0033a0001c0001t0005g0032 | 2 | HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.998+3377T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443891 | ||||||
chr6:100443968
|
A | T | 1 | a0002c0002t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.998+3300T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443968 | ||||||
chr6:100444034
|
G | A | 1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998+3234C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444034 | ||||||
chr6:100444111
|
C | CATTTTCA | 100 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(97): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+3156_998+3157i others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444111 | ||||||
chr6:100444342
|
T | G | 1 | a0002c0002t0001g0319 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.998+2926A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444342 | ||||||
chr6:100444419
|
T | G | 2 | a0001c0001t0041g0167a0001c0001t0044g0168 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.998+2849A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444419 | ||||||
chr6:100444710
|
A | G | 1 | a0001c0001t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.998+2558T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444710 | ||||||
chr6:100444829
|
C | T | 1 | a0001c0001t0010g0279 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.998+2439G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444829 | ||||||
chr6:100444914
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.998+2354G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444914 | ||||||
chr6:100445387
|
G | T | 1 | a0002c0002t0001g0292 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.998+1881C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445387 | ||||||
chr6:100445644
|
G | C | 32 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(29): Show | 32 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.998+1624C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445644 | ||||||
chr6:100445715
|
C | G | 1 | a0001c0001t0040g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.998+1553G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445715 | ||||||
chr6:100445986
|
A | G | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.998+1282T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445986 | ||||||
chr6:100445986
|
A | T | 1 | a0002c0002t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+1282T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445986 | ||||||
chr6:100446040
|
AT | A | 51 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(48): Show | 51 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.998+1227delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446040 | ||||||
chr6:100446303
|
A | G | 100 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(97): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+965T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446303 | ||||||
chr6:100446638
|
G | T | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+630C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446638 | ||||||
chr6:100446641
|
C | T | 2 | a0001c0001t0006g0226a0001c0001t0006g0227 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.998+627G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446641 | ||||||
chr6:100446711
|
G | A | 99 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(96): Show | 99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+557C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446711 | ||||||
chr6:100446803
|
G | C | 1 | a0001c0001t0027g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.998+465C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446803 | ||||||
chr6:100446985
|
C | T | 3 | a0001c0001t0021g0266a0002c0002t0007g0267a0002c0002t0007g0268 | 3 | HG00738.hp2 HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.998+283G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446985 | ||||||
chr6:100447468
|
C | T | 304 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.851-53G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447468 | ||||||
chr6:100447586
|
G | T | 110 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.851-171C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447586 | ||||||
chr6:100447728
|
G | A | 4 | a0001c0001t0002g0157a0001c0001t0022g0147a0001c0001t0022g0160others(1): Show | 4 | HG02280.hp1 HG02647.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-313C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447728 | ||||||
chr6:100447749
|
C | G | 95 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(92): Show | 95 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.851-334G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447749 | ||||||
chr6:100447776
|
C | T | 2 | a0001c0001t0002g0260a0002c0002t0001g0259 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.851-361G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447776 | ||||||
chr6:100448042
|
G | T | 3 | a0001c0001t0002g0174a0001c0001t0003g0175a0002c0002t0007g0176 | 3 | HG00544.hp1 NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.850+104C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100448042 | ||||||
chr6:100448305
|
C | T | 1 | a0002c0002t0006g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.744-53G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448305 | ||||||
chr6:100448320
|
C | A | 16 | a0001c0001t0002g0056a0001c0001t0002g0071a0001c0001t0003g0058others(13): Show | 16 | NA18946.hp2 NA18950.hp2 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.744-68G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448320 | ||||||
chr6:100448367
|
A | G | 96 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(93): Show | 96 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.743+112T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448367 | ||||||
chr6:100448367
|
A | T | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.743+112T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448367 | ||||||
chr6:100448413
|
T | G | 97 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.743+66A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448413 | ||||||
chr6:100448693
|
T | G | 112 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.544-15A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448693 | ||||||
chr6:100448738
|
G | A | 22 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(19): Show | 22 | HG00544.hp1 HG00735.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-60C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448738 | ||||||
chr6:100448969
|
A | G | 1 | a0002c0002t0006g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.544-291T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448969 | ||||||
chr6:100449134
|
C | G | 1 | a0001c0001t0018g0307 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.543+229G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449134 | ||||||
chr6:100449137
|
G | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+226C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449137 | ||||||
chr6:100449303
|
C | G | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+60G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449303 | ||||||
chr6:100449508
|
C | T | 1 | a0001c0001t0019g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.458-60G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/11 | chr6 | 100449508 | ||||||
chr6:100449519
|
C | T | 1 | a0001c0001t0068g0294 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-71G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/11 | chr6 | 100449519 | ||||||
chr6:100449907
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0003g0158 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.349-208G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 4/11 | chr6 | 100449907 | ||||||
chr6:100450243
|
G | A | 1 | a0001c0001t0008g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.348+24C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 4/11 | chr6 | 100450243 | ||||||
chr6:100450410
|
T | C | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.259-54A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450410 | ||||||
chr6:100450544
|
C | G | 1 | a0001c0001t0004g0293 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.259-188G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450544 | ||||||
chr6:100450665
|
G | GTCTCTCT others(1): Show |
8 | a0001c0001t0009g0013a0001c0001t0016g0001a0001c0001t0053g0289others(5): Show | 9 | HG00438.hp1 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-317_259-310dup others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | ||||||
chr6:100450665
|
G | GTCTCTCT others(3): Show |
1 | a0002c0002t0001g0318 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.259-319_259-310dup others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | ||||||
chr6:100450665
|
G | GTCTCTCT others(5): Show |
2 | a0001c0001t0029g0002a0002c0002t0001g0243 | 2 | HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.259-321_259-310dup others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | ||||||
chr6:100450665
|
GTC | G | 6 | a0001c0001t0003g0034a0001c0001t0071g0010a0002c0002t0001g0120others(3): Show | 6 | HG01496.hp1 HG02071.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-311_259-310del others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | ||||||
chr6:100450665
|
GTCTC | G | 10 | a0001c0001t0002g0043a0001c0001t0002g0138a0001c0001t0003g0031others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-313_259-310del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | ||||||
chr6:100450692
|
TCTCTCAC others(3): Show |
T | 13 | a0001c0001t0002g0193a0001c0001t0003g0201a0001c0001t0004g0185others(10): Show | 13 | HG00423.hp2 HG00735.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-346_259-337del others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450692 | ||||||
chr6:100450694
|
T | TCACA | 6 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0308others(3): Show | 6 | HG01361.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-339_259-338ins others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | ||||||
chr6:100450694
|
TCTCA | T | 64 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0086others(61): Show | 64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.259-342_259-339del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | ||||||
chr6:100450694
|
TCTCACA | T | 9 | a0001c0001t0002g0097a0001c0001t0003g0123a0001c0001t0003g0134others(6): Show | 9 | HG01106.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-344_259-339del others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | ||||||
chr6:100450694
|
TCTCACAC others(3): Show |
T | 8 | a0001c0001t0002g0195a0001c0001t0004g0207a0001c0001t0004g0291others(5): Show | 8 | HG02165.hp2 HG02602.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-348_259-339del others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | ||||||
chr6:100450694
|
TCTCACAC others(5): Show |
T | 1 | a0001c0001t0006g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-350_259-339del others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | ||||||
chr6:100450696
|
T | A | 15 | a0001c0001t0003g0034a0001c0001t0003g0078a0001c0001t0003g0079others(12): Show | 15 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-340A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCAC others(1): Show |
6 | a0001c0001t0002g0236a0001c0001t0002g0240a0001c0001t0003g0191others(3): Show | 6 | HG01256.hp1 HG02132.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCAC others(3): Show |
5 | a0001c0001t0002g0276a0001c0001t0003g0009a0001c0001t0019g0016others(2): Show | 5 | HG01070.hp1 HG02109.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCAC others(5): Show |
2 | a0001c0001t0003g0265a0001c0001t0010g0279 | 2 | HG00099.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCAC others(7): Show |
1 | a0001c0001t0008g0209 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(3): Show |
9 | a0001c0001t0003g0052a0001c0001t0003g0258a0001c0001t0006g0161others(6): Show | 9 | HG00140.hp1 HG00558.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(5): Show |
4 | a0001c0001t0043g0190a0001c0001t0072g0181a0001c0001t0075g0179others(1): Show | 4 | HG02027.hp1 HG02809.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(7): Show |
2 | a0001c0001t0002g0064a0001c0001t0002g0211 | 2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(9): Show |
2 | a0001c0001t0003g0228a0002c0002t0007g0184 | 2 | HG02896.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(3): Show |
6 | a0001c0001t0004g0293a0001c0001t0004g0314a0001c0001t0005g0271others(3): Show | 6 | HG02602.hp1 NA18947.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(5): Show |
16 | a0001c0001t0002g0229a0001c0001t0002g0234a0001c0001t0002g0239others(13): Show | 16 | HG00423.hp1 HG00544.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(7): Show |
5 | a0001c0001t0002g0231a0001c0001t0002g0260a0001c0001t0003g0244others(2): Show | 5 | HG00323.hp1 HG00642.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(9): Show |
3 | a0001c0001t0005g0221a0002c0002t0001g0215a0002c0002t0007g0065 | 3 | HG00621.hp1 NA18973.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(5): Show |
11 | a0001c0001t0002g0220a0001c0001t0005g0219a0001c0001t0008g0249others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(7): Show |
5 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0217others(2): Show | 5 | HG03704.hp1 NA18946.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(9): Show |
19 | a0001c0001t0002g0056a0001c0001t0002g0071a0001c0001t0003g0058others(16): Show | 19 | HG01891.hp1 HG02723.hp2 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(11): Show |
3 | a0001c0001t0010g0281a0002c0002t0001g0048a0002c0002t0001g0230 | 3 | HG02135.hp2 NA18978.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(17): Show |
1 | a0001c0001t0002g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(7): Show |
1 | a0002c0002t0024g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(9): Show |
4 | a0001c0001t0002g0288a0001c0001t0002g0295a0002c0002t0001g0069others(1): Show | 4 | HG03491.hp1 HG03492.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(11): Show |
7 | a0001c0001t0006g0226a0001c0001t0010g0284a0001c0001t0011g0283others(4): Show | 7 | HG00741.hp2 HG01109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(13): Show |
1 | a0001c0001t0006g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(15): Show |
1 | a0001c0001t0003g0214 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
T | TCTCTCTC others(11): Show |
1 | a0002c0002t0001g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
TCA | T | 5 | a0001c0001t0001g0141a0001c0001t0032g0006a0001c0001t0039g0012others(2): Show | 5 | HG02615.hp1 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-342_259-341del others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
TCACA | T | 3 | a0001c0001t0061g0302a0002c0002t0007g0121a0002c0002t0024g0101 | 3 | HG00558.hp2 HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259-344_259-341del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450696
|
TCACACAC others(1): Show |
T | 30 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(27): Show | 30 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.259-348_259-341del others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | ||||||
chr6:100450698
|
A | T | 9 | a0001c0001t0002g0186a0001c0001t0003g0242a0001c0001t0006g0014others(6): Show | 10 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-342T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450698 | ||||||
chr6:100450700
|
A | T | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-344T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450700 | ||||||
chr6:100450706
|
A | T | 29 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(26): Show | 29 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.259-350T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450706 | ||||||
chr6:100450803
|
A | T | 1 | a0001c0001t0011g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.259-447T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450803 | ||||||
chr6:100450908
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.259-552G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450908 | ||||||
chr6:100450909
|
G | A | 4 | a0001c0001t0002g0157a0001c0001t0022g0147a0001c0001t0022g0160others(1): Show | 4 | HG02280.hp1 HG02647.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-553C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450909 | ||||||
chr6:100450999
|
C | G | 2 | a0001c0001t0002g0288a0001c0001t0002g0295 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.259-643G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450999 | ||||||
chr6:100451210
|
C | T | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-854G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451210 | ||||||
chr6:100451225
|
C | T | 1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-869G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451225 | ||||||
chr6:100451315
|
G | T | 3 | a0001c0001t0002g0217a0001c0001t0002g0234a0001c0001t0002g0240 | 3 | HG03704.hp1 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.259-959C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451315 | ||||||
chr6:100451584
|
A | G | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.259-1228T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451584 | ||||||
chr6:100451983
|
G | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-1627C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451983 | ||||||
chr6:100452000
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.259-1644G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452000 | ||||||
chr6:100452083
|
G | T | 1 | a0001c0001t0034g0007 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.258+1679C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452083 | ||||||
chr6:100452209
|
CCTT | C | 6 | a0001c0001t0003g0298a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1550_258+1552d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452209 | ||||||
chr6:100452289
|
A | C | 2 | a0001c0001t0010g0163a0001c0001t0055g0154 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258+1473T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452289 | ||||||
chr6:100452299
|
T | C | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+1463A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452299 | ||||||
chr6:100452360
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.258+1402C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452360 | ||||||
chr6:100452380
|
G | A | 2 | a0002c0002t0001g0122a0002c0002t0007g0121 | 2 | HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.258+1382C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452380 | ||||||
chr6:100452386
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0003g0171a0001c0001t0009g0172 | 3 | HG02055.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.258+1376G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452386 | ||||||
chr6:100452418
|
C | T | 3 | a0001c0001t0021g0266a0002c0002t0007g0267a0002c0002t0007g0268 | 3 | HG00738.hp2 HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.258+1344G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452418 | ||||||
chr6:100452630
|
C | T | 5 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0036g0305others(2): Show | 5 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1132G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452630 | ||||||
chr6:100452632
|
G | A | 317 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.258+1130C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452632 | ||||||
chr6:100452738
|
G | A | 1 | a0001c0001t0003g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.258+1024C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452738 | ||||||
chr6:100452865
|
G | A | 2 | a0001c0001t0006g0226a0001c0001t0006g0227 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.258+897C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452865 | ||||||
chr6:100453286
|
G | A | 2 | a0001c0001t0070g0177a0001c0001t0071g0010 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.258+476C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453286 | ||||||
chr6:100453492
|
C | T | 2 | a0001c0001t0008g0070a0001c0001t0008g0072 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.258+270G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453492 | ||||||
chr6:100453518
|
A | G | 1 | a0002c0002t0001g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258+244T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453518 | ||||||
chr6:100453644
|
T | TG | 110 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.258+117dupC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453644 | ||||||
chr6:100453666
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.258+96A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453666 | ||||||
chr6:100453913
|
C | A | 2 | a0001c0001t0070g0177a0001c0001t0071g0010 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-69G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453913 | ||||||
chr6:100453961
|
G | A | 51 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(48): Show | 51 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.176-117C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453961 | ||||||
chr6:100453978
|
G | T | 2 | a0001c0001t0002g0260a0002c0002t0001g0259 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.176-134C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453978 | ||||||
chr6:100454166
|
A | T | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.176-322T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454166 | ||||||
chr6:100454225
|
G | A | 2 | a0001c0001t0002g0231a0001c0001t0002g0239 | 2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.176-381C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454225 | ||||||
chr6:100454319
|
C | A | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.176-475G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454319 | ||||||
chr6:100454323
|
C | T | 1 | a0002c0002t0001g0092 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.176-479G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454323 | ||||||
chr6:100454384
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.176-540G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454384 | ||||||
chr6:100454518
|
C | A | 1 | a0001c0001t0026g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-674G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454518 | ||||||
chr6:100454555
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.176-711G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454555 | ||||||
chr6:100454595
|
G | T | 1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.176-751C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454595 | ||||||
chr6:100454657
|
C | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-813G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454657 | ||||||
chr6:100454715
|
C | T | 2 | a0001c0001t0070g0177a0001c0001t0071g0010 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-871G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454715 | ||||||
chr6:100454932
|
C | T | 1 | a0001c0001t0009g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.176-1088G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454932 | ||||||
chr6:100455105
|
T | A | 1 | a0001c0001t0018g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.176-1261A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455105 | ||||||
chr6:100455110
|
A | G | 2 | a0001c0001t0057g0083a0001c0001t0058g0084 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.176-1266T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455110 | ||||||
chr6:100455302
|
C | T | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-1458G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455302 | ||||||
chr6:100455370
|
T | C | 1 | a0001c0001t0011g0285 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.176-1526A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455370 | ||||||
chr6:100455405
|
G | A | 2 | a0001c0001t0070g0177a0001c0001t0071g0010 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-1561C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455405 | ||||||
chr6:100455688
|
G | C | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.176-1844C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455688 | ||||||
chr6:100455689
|
G | A | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.176-1845C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455689 | ||||||
chr6:100455934
|
C | A | 1 | a0001c0001t0003g0123 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.176-2090G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455934 | ||||||
chr6:100455947
|
C | T | 1 | a0001c0001t0044g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.176-2103G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455947 | ||||||
chr6:100456157
|
C | T | 1 | a0001c0001t0074g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-2313G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456157 | ||||||
chr6:100456229
|
G | C | 94 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.176-2385C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456229 | ||||||
chr6:100456312
|
A | G | 303 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.176-2468T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456312 | ||||||
chr6:100456567
|
A | G | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.176-2723T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456567 | ||||||
chr6:100456988
|
G | T | 1 | a0001c0001t0064g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.176-3144C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456988 | ||||||
chr6:100457090
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.176-3246A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457090 | ||||||
chr6:100457265
|
A | G | 2 | a0001c0001t0005g0182a0001c0001t0072g0181 | 2 | HG00544.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.176-3421T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457265 | ||||||
chr6:100457350
|
C | G | 44 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.176-3506G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457350 | ||||||
chr6:100457419
|
G | T | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-3575C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457419 | ||||||
chr6:100457435
|
G | A | 1 | a0001c0001t0009g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.176-3591C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457435 | ||||||
chr6:100457780
|
G | C | 1 | a0001c0001t0074g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-3936C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457780 | ||||||
chr6:100457795
|
G | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-3951C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457795 | ||||||
chr6:100457822
|
G | A | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-3978C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457822 | ||||||
chr6:100457886
|
T | C | 1 | a0001c0001t0039g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.176-4042A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457886 | ||||||
chr6:100458005
|
TTTCTCTC others(6): Show |
T | 2 | a0001c0001t0003g0079a0001c0001t0044g0168 | 2 | HG01515.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-4174_176-4162d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | ||||||
chr6:100458005
|
TTTCTCTC others(8): Show |
T | 3 | a0001c0001t0003g0158a0001c0001t0006g0300a0005c0010t0067g0021 | 3 | HG01884.hp1 HG03471.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.176-4176_176-4162d others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | ||||||
chr6:100458005
|
TTTCTCTC others(16): Show |
T | 1 | a0001c0001t0006g0164 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.176-4184_176-4162d others(25): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | ||||||
chr6:100458005
|
TTTCTCTC others(18): Show |
T | 1 | a0001c0001t0005g0045 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.176-4186_176-4162d others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | ||||||
chr6:100458006
|
T | C | 1 | a0002c0002t0001g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-4162A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
T | TTCTCTCT others(3): Show |
1 | a0001c0001t0053g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.176-4172_176-4163d others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
T | TTCTCTCT others(5): Show |
1 | a0004c0008t0023g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.176-4163_176-4162i others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
T | TTCTCTCT others(13): Show |
1 | a0002c0002t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.176-4163_176-4162i others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTC | T | 7 | a0001c0001t0002g0229a0001c0001t0010g0280a0001c0001t0010g0281others(4): Show | 7 | HG02135.hp2 HG02723.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-4164_176-4163d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTC | T | 8 | a0001c0001t0002g0231a0001c0001t0008g0282a0001c0001t0010g0284others(5): Show | 8 | HG00642.hp1 HG01109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-4166_176-4163d others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTC | T | 11 | a0001c0001t0002g0234a0001c0001t0002g0236a0001c0001t0002g0239others(8): Show | 11 | HG00642.hp2 HG02056.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-4168_176-4163d others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(1): Show |
T | 22 | a0001c0001t0002g0071a0001c0001t0002g0240a0001c0001t0003g0074others(19): Show | 22 | HG00140.hp2 HG00423.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.176-4170_176-4163d others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(3): Show |
T | 19 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0003g0258others(16): Show | 19 | HG00280.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-4172_176-4163d others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(5): Show |
T | 27 | a0001c0001t0002g0217a0001c0001t0002g0260a0001c0001t0002g0261others(24): Show | 27 | HG00323.hp1 HG01070.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.176-4174_176-4163d others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(7): Show |
T | 39 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0195others(36): Show | 39 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.176-4176_176-4163d others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(9): Show |
T | 19 | a0001c0001t0002g0056a0001c0001t0002g0061a0001c0001t0002g0173others(16): Show | 19 | HG00558.hp1 HG01192.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-4178_176-4163d others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(11): Show |
T | 20 | a0001c0001t0002g0049a0001c0001t0002g0148a0001c0001t0002g0150others(17): Show | 20 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.176-4180_176-4163d others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(13): Show |
T | 9 | a0001c0001t0002g0162a0001c0001t0002g0170a0001c0001t0002g0186others(6): Show | 9 | HG00544.hp1 HG01168.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-4182_176-4163d others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(15): Show |
T | 1 | a0001c0001t0006g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-4184_176-4163d others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(17): Show |
T | 2 | a0001c0001t0010g0163a0001c0001t0039g0012 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.176-4186_176-4163d others(26): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(19): Show |
T | 1 | a0001c0001t0002g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.176-4188_176-4163d others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(21): Show |
T | 4 | a0001c0001t0005g0082a0001c0001t0040g0011a0001c0001t0055g0154others(1): Show | 4 | HG02074.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-4190_176-4163d others(30): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(23): Show |
T | 2 | a0001c0001t0002g0135a0001c0001t0003g0134 | 2 | HG01106.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.176-4192_176-4163d others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(25): Show |
T | 11 | a0001c0001t0004g0128a0001c0001t0005g0131a0001c0001t0005g0132others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-4194_176-4163d others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(27): Show |
T | 49 | a0001c0001t0001g0141a0001c0001t0002g0036a0001c0001t0002g0097others(46): Show | 49 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.176-4196_176-4163d others(36): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458006
|
TTCTCTCT others(29): Show |
T | 24 | a0001c0001t0002g0028a0001c0001t0002g0043a0001c0001t0002g0086others(21): Show | 24 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.176-4198_176-4163d others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | ||||||
chr6:100458007
|
T | TCTCTCTC others(3): Show |
1 | a0001c0001t0003g0224 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.176-4164_176-4163i others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458007 | ||||||
chr6:100458007
|
TCTCTCTC others(6): Show |
T | 1 | a0002c0002t0001g0067 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-4176_176-4164d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458007 | ||||||
chr6:100458009
|
T | TCTCTCTC others(1): Show |
3 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0003g0214 | 3 | NA18950.hp1 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.176-4166_176-4165i others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458009 | ||||||
chr6:100458011
|
TCTCTCTC others(4): Show |
T | 1 | a0001c0007t0004g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.176-4178_176-4168d others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458011 | ||||||
chr6:100458011
|
TCTCTCTC others(6): Show |
T | 1 | a0002c0002t0001g0203 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.176-4180_176-4168d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458011 | ||||||
chr6:100458012
|
C | T | 1 | a0001c0001t0032g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.176-4168G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458012 | ||||||
chr6:100458015
|
T | TCC | 4 | a0001c0001t0002g0225a0001c0001t0006g0226a0001c0001t0006g0227others(1): Show | 4 | HG02135.hp1 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-4172_176-4171i others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458015 | ||||||
chr6:100458016
|
C | T | 1 | a0001c0009t0033g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-4172G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | ||||||
chr6:100458016
|
CTCTCTCT | C | 4 | a0001c0001t0026g0233a0002c0002t0001g0187a0002c0002t0001g0232others(1): Show | 4 | HG00423.hp1 HG01516.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-4179_176-4173d others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | ||||||
chr6:100458016
|
CTCTCTCT others(4): Show |
C | 1 | a0001c0001t0008g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.176-4183_176-4173d others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | ||||||
chr6:100458017
|
T | C | 2 | a0001c0001t0003g0228a0001c0001t0008g0209 | 2 | HG01070.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.176-4173A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458017 | ||||||
chr6:100458018
|
C | T | 1 | a0001c0001t0004g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-4174G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458018 | ||||||
chr6:100458019
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0010g0280a0001c0001t0010g0281others(2): Show | 5 | HG02135.hp2 HG02723.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-4175A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458019 | ||||||
chr6:100458020
|
C | T | 1 | a0001c0001t0004g0206 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.176-4176G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458020 | ||||||
chr6:100458021
|
T | C | 5 | a0001c0001t0002g0231a0001c0001t0008g0282a0001c0001t0010g0284others(2): Show | 5 | HG00642.hp1 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-4177A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458021 | ||||||
chr6:100458022
|
C | T | 1 | a0001c0001t0005g0204 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.176-4178G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458022 | ||||||
chr6:100458023
|
T | C | 8 | a0001c0001t0002g0234a0001c0001t0002g0236a0001c0001t0002g0239others(5): Show | 8 | HG00642.hp2 HG02056.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-4179A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458023 | ||||||
chr6:100458024
|
C | T | 3 | a0001c0001t0003g0201a0001c0001t0004g0291a0001c0001t0026g0202 | 3 | HG01496.hp2 NA18971.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.176-4180G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458024 | ||||||
chr6:100458025
|
T | C | 15 | a0001c0001t0002g0240a0001c0001t0003g0191a0001c0001t0003g0242others(12): Show | 15 | HG00140.hp2 HG00423.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.176-4181A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458025 | ||||||
chr6:100458026
|
C | T | 9 | a0001c0001t0002g0195a0001c0001t0004g0185a0001c0001t0004g0196others(6): Show | 9 | HG00735.hp2 HG01081.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-4182G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458026 | ||||||
chr6:100458027
|
T | C | 12 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0003g0258others(9): Show | 12 | HG01175.hp2 HG02809.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-4183A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458027 | ||||||
chr6:100458028
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.176-4184G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458028 | ||||||
chr6:100458029
|
T | C | 18 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0288others(15): Show | 18 | HG00323.hp1 HG01070.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-4185A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458029 | ||||||
chr6:100458030
|
C | T | 2 | a0001c0001t0052g0296a0002c0002t0001g0192 | 2 | HG03831.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.176-4186G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458030 | ||||||
chr6:100458031
|
T | C | 20 | a0001c0001t0002g0276a0001c0001t0003g0009a0001c0001t0004g0293others(17): Show | 20 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.176-4187A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458031 | ||||||
chr6:100458033
|
T | C | 1 | a0002c0002t0001g0278 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.176-4189A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458033 | ||||||
chr6:100458071
|
T | C | 1 | a0001c0001t0010g0279 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.176-4227A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458071 | ||||||
chr6:100458122
|
C | T | 1 | a0001c0001t0075g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.176-4278G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458122 | ||||||
chr6:100458170
|
G | T | 89 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(86): Show | 89 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.176-4326C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458170 | ||||||
chr6:100458319
|
G | T | 1 | a0001c0001t0005g0082 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.176-4475C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458319 | ||||||
chr6:100458328
|
C | A | 6 | a0001c0001t0003g0298a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-4484G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458328 | ||||||
chr6:100458445
|
C | G | 2 | a0001c0001t0009g0023a0001c0001t0009g0081 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.176-4601G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458445 | ||||||
chr6:100458628
|
G | A | 21 | a0001c0001t0002g0193a0001c0001t0002g0195a0001c0001t0003g0201others(18): Show | 21 | HG00735.hp2 HG01081.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.175+4666C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458628 | ||||||
chr6:100458700
|
C | A | 8 | a0001c0001t0006g0287a0001c0001t0008g0282a0001c0001t0010g0280others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+4594G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458700 | ||||||
chr6:100458731
|
T | A | 1 | a0001c0001t0010g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175+4563A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458731 | ||||||
chr6:100458773
|
A | T | 6 | a0001c0001t0003g0298a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+4521T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458773 | ||||||
chr6:100458786
|
C | A | 33 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(30): Show | 33 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+4508G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458786 | ||||||
chr6:100458789
|
C | A | 1 | a0001c0001t0070g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175+4505G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458789 | ||||||
chr6:100459301
|
G | A | 1 | a0001c0003t0003g0137 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.175+3993C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459301 | ||||||
chr6:100459333
|
G | A | 11 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0012g0306others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+3961C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459333 | ||||||
chr6:100459688
|
A | G | 3 | a0001c0001t0016g0001a0001c0001t0029g0002a0001c0003t0030g0003 | 4 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+3606T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459688 | ||||||
chr6:100459911
|
C | T | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | NA18950.hp1 NA18971.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+3383G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459911 | ||||||
chr6:100460254
|
A | T | 1 | a0001c0001t0003g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.175+3040T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460254 | ||||||
chr6:100460258
|
G | A | 2 | a0001c0001t0006g0164a0001c0001t0006g0165 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175+3036C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460258 | ||||||
chr6:100460304
|
T | C | 31 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(28): Show | 31 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.175+2990A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460304 | ||||||
chr6:100460760
|
C | T | 1 | a0001c0001t0008g0209 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.175+2534G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460760 | ||||||
chr6:100460862
|
G | C | 33 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(30): Show | 33 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+2432C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460862 | ||||||
chr6:100460921
|
C | A | 1 | a0002c0002t0001g0044 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.175+2373G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460921 | ||||||
chr6:100460996
|
C | T | 32 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(29): Show | 32 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.175+2298G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460996 | ||||||
chr6:100461259
|
T | C | 1 | a0001c0001t0068g0294 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+2035A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461259 | ||||||
chr6:100461382
|
T | A | 2 | a0001c0001t0002g0288a0001c0001t0002g0295 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.175+1912A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461382 | ||||||
chr6:100461422
|
G | T | 1 | a0002c0002t0001g0080 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.175+1872C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461422 | ||||||
chr6:100461507
|
C | A | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+1787G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461507 | ||||||
chr6:100461522
|
C | T | 122 | a0001c0001t0002g0186a0001c0001t0002g0211a0001c0001t0002g0212others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.175+1772G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461522 | ||||||
chr6:100461637
|
C | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0138a0001c0001t0005g0139others(2): Show | 5 | HG02132.hp1 HG02523.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1657G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461637 | ||||||
chr6:100461777
|
C | T | 279 | a0001c0001t0001g0141a0001c0001t0002g0028a0001c0001t0002g0036others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.175+1517G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461777 | ||||||
chr6:100461783
|
A | C | 2 | a0001c0001t0032g0006a0001c0009t0033g0005 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.175+1511T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461783 | ||||||
chr6:100461827
|
T | TTC | 9 | a0001c0001t0002g0162a0001c0001t0002g0170a0001c0001t0003g0171others(6): Show | 9 | HG01168.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+1465_175+1466d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461827 | ||||||
chr6:100461840
|
TC | T | 4 | a0001c0001t0002g0162a0001c0001t0006g0164a0001c0001t0006g0165others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+1453delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461840 | ||||||
chr6:100461841
|
C | CTT | 6 | a0001c0001t0006g0166a0001c0001t0009g0013a0001c0001t0041g0167others(3): Show | 6 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+1451_175+1452d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
C | CTTT | 11 | a0001c0001t0002g0157a0001c0001t0002g0174a0001c0001t0003g0156others(8): Show | 11 | HG00544.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+1450_175+1452d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
C | CTTTT | 7 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0173others(4): Show | 7 | HG00735.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+1449_175+1452d others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
C | T | 1 | a0001c0001t0055g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175+1453G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
CT | C | 92 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0043others(89): Show | 92 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.175+1452delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
CTT | C | 161 | a0001c0001t0002g0086a0001c0001t0002g0097a0001c0001t0002g0135others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.175+1451_175+1452d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461841
|
CTTT | C | 11 | a0001c0001t0001g0141a0001c0001t0002g0295a0001c0001t0004g0293others(8): Show | 11 | HG00323.hp2 HG01070.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+1450_175+1452d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | ||||||
chr6:100461846
|
T | C | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.175+1448A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461846 | ||||||
chr6:100462293
|
C | T | 1 | a0001c0001t0022g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.175+1001G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462293 | ||||||
chr6:100462610
|
G | A | 9 | a0001c0001t0012g0306a0001c0001t0012g0308a0001c0001t0012g0309others(6): Show | 9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+684C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462610 | ||||||
chr6:100462898
|
C | CA | 7 | a0001c0001t0005g0144a0001c0001t0005g0145a0001c0001t0008g0143others(4): Show | 8 | HG01255.hp2 HG01346.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+395dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | ||||||
chr6:100462898
|
C | CAA | 11 | a0001c0001t0009g0013a0001c0001t0012g0306a0001c0001t0012g0308others(8): Show | 11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+394_175+395dup others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | ||||||
chr6:100462898
|
C | CAAA | 26 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(23): Show | 26 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.175+393_175+395dup others(3): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | ||||||
chr6:100462898
|
C | CAAAA | 6 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0175others(3): Show | 6 | HG00544.hp1 HG01168.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+392_175+395dup others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | ||||||
chr6:100462922
|
G | A | 191 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0157others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.175+372C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462922 | ||||||
chr6:100463080
|
G | A | 1 | a0001c0001t0031g0004 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.175+214C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463080 | ||||||
chr6:100463093
|
G | C | 6 | a0001c0001t0003g0298a0001c0001t0006g0297a0001c0001t0006g0299others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+201C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463093 | ||||||
chr6:100463196
|
ATATGT | A | 145 | a0001c0001t0002g0186a0001c0001t0002g0193a0001c0001t0002g0195others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.175+93_175+97delAC others(3): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463196 | ||||||
chr6:100463973
|
G | T | 1 | a0001c0001t0006g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-467-38C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100463973 | ||||||
chr6:100464019
|
C | A | 9 | a0001c0001t0012g0306a0001c0001t0012g0308a0001c0001t0012g0309others(6): Show | 9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-467-84G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464019 | ||||||
chr6:100464196
|
C | T | 1 | a0001c0001t0009g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-467-261G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464196 | ||||||
chr6:100464201
|
G | A | 1 | a0001c0001t0004g0314 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-467-266C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464201 | ||||||
chr6:100464241
|
G | A | 4 | a0002c0002t0001g0315a0002c0002t0001g0316a0002c0002t0001g0317others(1): Show | 4 | HG00642.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-467-306C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464241 | ||||||
chr6:100464260
|
G | A | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-467-325C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464260 | ||||||
chr6:100464261
|
C | T | 2 | a0001c0001t0039g0012a0001c0001t0040g0011 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-467-326G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464261 | ||||||
chr6:100464326
|
G | T | 1 | a0001c0001t0071g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-468+288C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464326 | ||||||
chr6:100464497
|
G | C | 1 | a0002c0002t0001g0319 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-468+117C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464497 | ||||||
chr6:100464500
|
C | T | 1 | a0001c0001t0003g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-468+114G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464500 |