geneid | 22944 |
---|---|
ensemblid | ENSG00000151657.12 |
hgncid | 6327 |
symbol | KIN |
name | Kin17 DNA and RNA binding protein |
refseq_nuc | NM_012311.4 |
refseq_prot | NP_036443.1 |
ensembl_nuc | ENST00000379562.9 |
ensembl_prot | ENSP00000368881.3 |
mane_status | MANE Select |
chr | chr10 |
start | 7750962 |
end | 7787993 |
strand | - |
ver | v1.2 |
region | chr10:7750962-7787993 |
region5000 | chr10:7745962-7792993 |
regionname0 | KIN_chr10_7750962_7787993 |
regionname5000 | KIN_chr10_7745962_7792993 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 393 | 422 | 81 | 68 | 218 | 16 | 37 | 178 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0002 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0003 | 0/0 | 393 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0004 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1182 | 406 | 66 | 67 | 218 | 16 | 37 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
c0002 | 0/0 | 1182 | 16 | 15 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
c0003 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
c0004 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
c0005 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4963 | 64 | 4 | 10 | 41 | 3 | 6 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0002 | 0/0 | 4963 | 56 | 7 | 21 | 22 | 2 | 4 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0003 | 0/0 | 4962 | 33 | 1 | 5 | 26 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0004 | 0/0 | 4963 | 27 | 0 | 2 | 22 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0005 | 0/0 | 4959 | 27 | 2 | 4 | 20 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0006 | 0/0 | 4963 | 19 | 0 | 2 | 17 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0007 | 0/0 | 4959 | 13 | 0 | 0 | 12 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0008 | 0/0 | 4962 | 10 | 0 | 4 | 0 | 0 | 6 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0009 | 0/0 | 4963 | 10 | 10 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0010 | 0/0 | 4963 | 8 | 5 | 1 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0011 | 0/0 | 4962 | 7 | 0 | 5 | 0 | 1 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0012 | 0/0 | 4962 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0013 | 0/0 | 4959 | 6 | 0 | 2 | 0 | 2 | 2 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0014 | 0/0 | 4963 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0015 | 0/0 | 4963 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0016 | 0/0 | 5183 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0017 | 0/0 | 4963 | 5 | 5 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0018 | 0/0 | 4963 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0019 | 0/0 | 4963 | 4 | 0 | 1 | 2 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0020 | 0/0 | 4963 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0021 | 0/0 | 4963 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0022 | 0/0 | 4962 | 3 | 0 | 1 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0023 | 0/0 | 4963 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0024 | 0/0 | 4959 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0025 | 0/0 | 4963 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0026 | 0/0 | 4963 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0027 | 0/0 | 4963 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0028 | 0/0 | 4963 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0029 | 0/0 | 4962 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0030 | 0/0 | 4963 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0031 | 0/0 | 4963 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0032 | 0/0 | 4963 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0033 | 0/0 | 4963 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0034 | 0/0 | 4963 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0035 | 0/0 | 5179 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0036 | 1/0 | 5179 | 2 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0037 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0038 | 0/0 | 4959 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0039 | 0/0 | 4959 | 2 | 1 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0040 | 0/0 | 4959 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0041 | 0/0 | 5177 | 2 | 0 | 0 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0042 | 0/0 | 4962 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0043 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0044 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0045 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0046 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0047 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0048 | 0/0 | 4963 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0049 | 0/0 | 5181 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0050 | 0/0 | 5181 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0051 | 0/1 | 5182 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0052 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0053 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0054 | 0/0 | 4962 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0055 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0056 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0057 | 0/0 | 5182 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0058 | 0/0 | 5183 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0059 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0060 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0061 | 0/0 | 4962 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0062 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0063 | 0/0 | 4962 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0064 | 0/0 | 4962 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0065 | 0/0 | 4962 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0066 | 0/0 | 4962 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0067 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0068 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0069 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0070 | 0/0 | 4963 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0071 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0072 | 0/0 | 5318 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0073 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0074 | 0/0 | 4963 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0075 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0076 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0077 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0078 | 0/0 | 4963 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0079 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0080 | 0/0 | 4963 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0081 | 0/0 | 5183 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0082 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0083 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0084 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0085 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0086 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0087 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0088 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0089 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0090 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0091 | 0/0 | 5178 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0092 | 0/0 | 5179 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0093 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0094 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0095 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0096 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0097 | 0/0 | 5177 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0098 | 0/0 | 5177 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0099 | 0/0 | 5178 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0100 | 0/0 | 5178 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0101 | 0/0 | 5179 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0102 | 0/0 | 5179 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
t0103 | 0/0 | 5179 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 3 | 7 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0002 | 0/0 | 9 | 2 | 5 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0007 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0043 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1182 | 406 | 66 | 67 | 218 | 16 | 37 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002 | 0/0 | 1182 | 16 | 15 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0002c0003 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0003c0004 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0004c0005 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6144 | 64 | 4 | 10 | 41 | 3 | 6 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0002 | 0/0 | 6144 | 56 | 7 | 21 | 22 | 2 | 4 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0003 | 0/0 | 6143 | 33 | 1 | 5 | 26 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0004 | 0/0 | 6144 | 27 | 0 | 2 | 22 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0005 | 0/0 | 6140 | 27 | 2 | 4 | 20 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0006 | 0/0 | 6144 | 19 | 0 | 2 | 17 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0007 | 0/0 | 6140 | 13 | 0 | 0 | 12 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0008 | 0/0 | 6143 | 9 | 0 | 4 | 0 | 0 | 5 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0010 | 0/0 | 6144 | 8 | 5 | 1 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0011 | 0/0 | 6143 | 7 | 0 | 5 | 0 | 1 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0012 | 0/0 | 6143 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0013 | 0/0 | 6140 | 6 | 0 | 2 | 0 | 2 | 2 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0014 | 0/0 | 6144 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0015 | 0/0 | 6144 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0016 | 0/0 | 6364 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0017 | 0/0 | 6144 | 5 | 5 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0018 | 0/0 | 6144 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0019 | 0/0 | 6144 | 4 | 0 | 1 | 2 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0020 | 0/0 | 6144 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0021 | 0/0 | 6144 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0022 | 0/0 | 6143 | 3 | 0 | 1 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0023 | 0/0 | 6144 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0024 | 0/0 | 6140 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0025 | 0/0 | 6144 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0026 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0027 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0029 | 0/0 | 6143 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0030 | 0/0 | 6144 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0031 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0032 | 0/0 | 6144 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0033 | 0/0 | 6144 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0034 | 0/0 | 6144 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0035 | 0/0 | 6360 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0036 | 1/0 | 6360 | 2 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0037 | 0/0 | 6140 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0038 | 0/0 | 6140 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0039 | 0/0 | 6140 | 2 | 1 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0040 | 0/0 | 6140 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0041 | 0/0 | 6358 | 2 | 0 | 0 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0042 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0043 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0044 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0045 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0046 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0048 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0049 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0050 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0051 | 0/1 | 6363 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0053 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0054 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0055 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0056 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0057 | 0/0 | 6363 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0058 | 0/0 | 6364 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0059 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0060 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0061 | 0/0 | 6143 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0062 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0063 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0064 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0065 | 0/0 | 6143 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0066 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0067 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0073 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0074 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0075 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0076 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0077 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0078 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0079 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0080 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0081 | 0/0 | 6364 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0082 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0083 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0084 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0085 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0086 | 0/0 | 6140 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0087 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0088 | 0/0 | 6361 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0089 | 0/0 | 6140 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0090 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0091 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0092 | 0/0 | 6360 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0093 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0094 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0095 | 0/0 | 6348 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0096 | 0/0 | 6348 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0097 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0098 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0099 | 0/0 | 6359 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0100 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0101 | 0/0 | 6360 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0102 | 0/0 | 6360 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0001t0103 | 0/0 | 6360 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0009 | 0/0 | 6144 | 10 | 10 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0052 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0068 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0069 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0070 | 0/0 | 6144 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0071 | 0/0 | 6500 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0001c0002t0072 | 0/0 | 6499 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0002c0003t0028 | 0/0 | 6144 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0003c0004t0008 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
a0004c0005t0047 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | copy fasta | chr10 | 7745962 | 7792993 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 0 | 3 | 7 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0002 | 0/0 | 9 | 2 | 5 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0008g0007 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0008g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0008g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0011g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0011g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0011g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0012g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0012g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0012g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0012g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0014g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0015g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0015g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0016g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0016g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0016g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0016g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0016g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0017g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0017g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0017g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0018g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0018g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0019g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0019g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0019g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0019g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0020g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0021g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0021g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0021g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0022g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0022g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0023g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0024g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0024g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0025g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0026g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0026g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0027g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0027g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0029g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0030g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0030g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0031g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0031g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0032g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0032g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0033g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0033g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0034g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0035g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0035g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0036g0043 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0037g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0037g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0038g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0039g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0039g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0040g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0040g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0041g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0041g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0042g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0043g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0044g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0045g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0046g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0048g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0049g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0050g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0051g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0053g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0054g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0055g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0056g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0057g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0058g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0059g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0060g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0061g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0062g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0063g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0064g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0065g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0066g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0067g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0073g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0074g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0075g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0076g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0077g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0078g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0079g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0080g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0081g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0082g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0083g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0084g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0085g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0086g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0087g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0088g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0089g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0090g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0091g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0092g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0093g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0094g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0095g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0096g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0097g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0098g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0099g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0100g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0101g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0102g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0001t0103g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0052g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0068g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0069g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0070g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0071g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0001c0002t0072g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0002c0003t0028g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0002c0003t0028g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0003c0004t0008g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
a0004c0005t0047g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0013 | g0048 | EUR | GBR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00099 | hp2 | a0001 | c0001 | t0049 | g0322 | EUR | GBR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00280 | hp1 | a0001 | c0001 | t0032 | g0060 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0282 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00323 | hp2 | a0001 | c0001 | t0066 | g0078 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00408 | hp1 | a0001 | c0001 | t0012 | g0223 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00438 | hp1 | a0002 | c0003 | t0028 | g0206 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00438 | hp2 | a0001 | c0001 | t0025 | g0030 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00558 | hp2 | a0001 | c0001 | t0045 | g0169 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00609 | hp2 | a0001 | c0001 | t0007 | g0167 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0142 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00642 | hp2 | a0001 | c0001 | t0011 | g0283 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00673 | hp2 | a0001 | c0001 | t0022 | g0038 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00733 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01069 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01070 | hp1 | a0001 | c0001 | t0038 | g0044 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01070 | hp2 | a0001 | c0001 | t0061 | g0285 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01071 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01071 | hp2 | a0001 | c0001 | t0038 | g0044 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01081 | hp1 | a0001 | c0001 | t0091 | g0109 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0291 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01175 | hp1 | a0001 | c0001 | t0019 | g0256 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01243 | hp1 | a0001 | c0002 | t0070 | g0140 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01243 | hp2 | a0001 | c0001 | t0089 | g0090 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0289 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01257 | hp2 | a0001 | c0001 | t0013 | g0156 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0320 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01433 | hp2 | a0001 | c0001 | t0086 | g0329 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0157 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01515 | hp1 | a0001 | c0001 | t0034 | g0024 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01516 | hp2 | a0001 | c0001 | t0048 | g0220 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01517 | hp2 | a0001 | c0001 | t0034 | g0024 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01884 | hp1 | a0001 | c0001 | t0081 | g0118 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01884 | hp2 | a0001 | c0001 | t0082 | g0284 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01891 | hp1 | a0001 | c0001 | t0027 | g0129 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01891 | hp2 | a0001 | c0001 | t0062 | g0288 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01981 | hp2 | a0001 | c0001 | t0100 | g0105 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01993 | hp1 | a0001 | c0001 | t0022 | g0280 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01993 | hp2 | a0001 | c0001 | t0065 | g0296 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02015 | hp1 | a0001 | c0001 | t0032 | g0059 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02015 | hp2 | a0001 | c0001 | t0093 | g0112 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02027 | hp1 | a0001 | c0001 | t0083 | g0168 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02055 | hp1 | a0001 | c0001 | t0026 | g0217 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02055 | hp2 | a0001 | c0002 | t0009 | g0093 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02056 | hp1 | a0001 | c0001 | t0092 | g0119 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02056 | hp2 | a0001 | c0001 | t0012 | g0308 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02080 | hp1 | a0001 | c0001 | t0064 | g0187 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02129 | hp2 | a0001 | c0001 | t0012 | g0295 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02132 | hp1 | a0001 | c0001 | t0007 | g0150 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02132 | hp2 | a0001 | c0001 | t0021 | g0134 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02135 | hp2 | a0002 | c0003 | t0028 | g0207 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | CDX | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CDX | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0326 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02257 | hp2 | a0001 | c0002 | t0009 | g0097 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02258 | hp1 | a0001 | c0001 | t0085 | g0163 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02280 | hp1 | a0001 | c0001 | t0096 | g0107 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02280 | hp2 | a0001 | c0001 | t0018 | g0017 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02300 | hp1 | a0001 | c0001 | t0025 | g0030 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02523 | hp1 | a0001 | c0001 | t0022 | g0038 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02602 | hp2 | a0001 | c0001 | t0040 | g0226 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02615 | hp1 | a0001 | c0001 | t0036 | g0043 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02615 | hp2 | a0001 | c0001 | t0031 | g0204 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02622 | hp1 | a0001 | c0002 | t0009 | g0095 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02622 | hp2 | a0001 | c0001 | t0094 | g0099 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02630 | hp1 | a0001 | c0002 | t0009 | g0094 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02630 | hp2 | a0001 | c0001 | t0101 | g0111 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02647 | hp1 | a0001 | c0001 | t0080 | g0081 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0312 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02698 | hp2 | a0001 | c0001 | t0041 | g0219 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0218 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02717 | hp2 | a0001 | c0002 | t0068 | g0098 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02723 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02723 | hp2 | a0001 | c0001 | t0095 | g0124 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0106 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02735 | hp2 | a0001 | c0001 | t0097 | g0162 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02738 | hp1 | a0001 | c0001 | t0098 | g0115 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02809 | hp1 | a0001 | c0001 | t0087 | g0328 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02809 | hp2 | a0001 | c0001 | t0037 | g0123 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0138 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0143 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02896 | hp1 | a0001 | c0002 | t0069 | g0089 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02970 | hp1 | a0001 | c0002 | t0072 | g0141 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02970 | hp2 | a0001 | c0002 | t0052 | g0096 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02976 | hp1 | a0001 | c0001 | t0023 | g0054 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02976 | hp2 | a0001 | c0001 | t0024 | g0045 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03017 | hp1 | a0003 | c0004 | t0008 | g0313 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03017 | hp2 | a0001 | c0001 | t0050 | g0281 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0277 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03041 | hp2 | a0001 | c0002 | t0009 | g0092 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0019 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03130 | hp1 | a0001 | c0001 | t0060 | g0086 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03130 | hp2 | a0001 | c0001 | t0018 | g0017 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03139 | hp1 | a0001 | c0001 | t0024 | g0327 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03139 | hp2 | a0001 | c0001 | t0039 | g0110 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03209 | hp1 | a0001 | c0001 | t0037 | g0088 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03225 | hp1 | a0004 | c0005 | t0047 | g0144 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03225 | hp2 | a0001 | c0001 | t0020 | g0014 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03453 | hp2 | a0001 | c0001 | t0067 | g0216 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0276 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0290 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03491 | hp2 | a0001 | c0001 | t0040 | g0114 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03492 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03516 | hp2 | a0001 | c0001 | t0027 | g0130 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03669 | hp1 | a0001 | c0001 | t0078 | g0061 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03669 | hp2 | a0001 | c0001 | t0063 | g0292 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03688 | hp1 | a0001 | c0001 | t0039 | g0051 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03688 | hp2 | a0001 | c0001 | t0011 | g0279 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03704 | hp2 | a0001 | c0001 | t0013 | g0160 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03710 | hp2 | a0001 | c0001 | t0103 | g0108 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03831 | hp1 | a0001 | c0001 | t0058 | g0257 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03834 | hp2 | a0001 | c0001 | t0013 | g0164 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03927 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03927 | hp2 | a0001 | c0001 | t0019 | g0260 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0148 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0017 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18522 | hp2 | a0001 | c0002 | t0009 | g0025 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18906 | hp1 | a0001 | c0001 | t0077 | g0077 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18906 | hp2 | a0001 | c0002 | t0071 | g0047 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18939 | hp2 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18940 | hp1 | a0001 | c0001 | t0033 | g0213 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18941 | hp1 | a0001 | c0001 | t0044 | g0126 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18941 | hp2 | a0001 | c0001 | t0012 | g0040 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18945 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18946 | hp1 | a0001 | c0001 | t0043 | g0182 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18949 | hp2 | a0001 | c0001 | t0021 | g0128 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18950 | hp1 | a0001 | c0001 | t0016 | g0242 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18951 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18953 | hp1 | a0001 | c0001 | t0056 | g0229 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18954 | hp2 | a0001 | c0001 | t0079 | g0063 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18960 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18964 | hp1 | a0001 | c0001 | t0084 | g0152 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18964 | hp2 | a0001 | c0001 | t0029 | g0039 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18966 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18967 | hp1 | a0001 | c0001 | t0016 | g0255 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18967 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18968 | hp1 | a0001 | c0001 | t0033 | g0211 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18972 | hp1 | a0001 | c0001 | t0016 | g0232 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18979 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18980 | hp1 | a0001 | c0001 | t0016 | g0241 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18984 | hp1 | a0001 | c0001 | t0015 | g0203 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18987 | hp1 | a0001 | c0001 | t0019 | g0251 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18988 | hp1 | a0001 | c0001 | t0057 | g0240 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18988 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18989 | hp2 | a0001 | c0001 | t0016 | g0231 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18990 | hp1 | a0001 | c0001 | t0054 | g0286 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0040 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18994 | hp1 | a0001 | c0001 | t0090 | g0153 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19001 | hp1 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19003 | hp1 | a0001 | c0001 | t0076 | g0071 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19005 | hp1 | a0001 | c0001 | t0099 | g0165 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19007 | hp1 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0275 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19030 | hp2 | a0001 | c0001 | t0031 | g0202 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19043 | hp1 | a0001 | c0002 | t0009 | g0025 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19043 | hp2 | a0001 | c0001 | t0059 | g0191 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19055 | hp1 | a0001 | c0001 | t0102 | g0159 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19057 | hp1 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19059 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19059 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19060 | hp1 | a0001 | c0001 | t0042 | g0175 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19062 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19062 | hp2 | a0001 | c0001 | t0041 | g0158 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19065 | hp1 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19075 | hp2 | a0001 | c0001 | t0012 | g0311 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19076 | hp2 | a0001 | c0001 | t0019 | g0237 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19077 | hp1 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19079 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19080 | hp1 | a0001 | c0001 | t0046 | g0176 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19080 | hp2 | a0001 | c0001 | t0055 | g0247 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19082 | hp2 | a0001 | c0001 | t0021 | g0133 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19085 | hp1 | a0001 | c0001 | t0029 | g0039 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19087 | hp1 | a0001 | c0001 | t0030 | g0245 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19087 | hp2 | a0001 | c0001 | t0073 | g0302 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19090 | hp1 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19240 | hp1 | a0001 | c0001 | t0017 | g0274 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA19240 | hp2 | a0001 | c0001 | t0020 | g0014 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | ASW | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20752 | hp1 | a0001 | c0001 | t0074 | g0069 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20752 | hp2 | a0001 | c0001 | t0013 | g0166 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20805 | hp1 | a0001 | c0001 | t0030 | g0192 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | GIH | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0155 | SAS | GIH | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01123 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02109 | hp1 | a0001 | c0001 | t0075 | g0053 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02109 | hp2 | a0001 | c0001 | t0020 | g0014 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02486 | hp1 | a0001 | c0001 | t0035 | g0325 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02486 | hp2 | a0001 | c0001 | t0026 | g0139 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02559 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0091 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0045 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG06807 | hp1 | a0001 | c0001 | t0023 | g0019 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18955 | hp1 | a0001 | c0001 | t0053 | g0190 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20300 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
NA21309 | hp2 | a0001 | c0001 | t0088 | g0122 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0051 | g0323 | REF | REF | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0036 | g0043 | REF | REF | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:7759942
|
G | A | 1 | a0002 | 2 | HG00438.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.1067C>T | p.Thr356Ile | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/13 | 1127/6360 | 1067/1182 | 356/393 | chr10 | 7759942 | ||
chr10:7763783
|
A | C | 1 | a0003 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.858T>G | p.Ile286Met | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/13 | 918/6360 | 858/1182 | 286/393 | chr10 | 7763783 | ||
chr10:7775762
|
T | A | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.596A>T | p.Asp199Val | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/13 | 656/6360 | 596/1182 | 199/393 | chr10 | 7775762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:7778871
|
C | T | 1 | a0001c0002 | 16 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
synonymous_variant | LOW | c.525G>A | p.Glu175Glu | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/13 | 585/6360 | 525/1182 | 175/393 | chr10 | 7778871 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:7751072
|
A | C | 20 | a0001c0001t0003a0001c0001t0011a0001c0001t0014others(17): Show | 72 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5008T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 5008 | chr10 | 7751072 | |||||
chr10:7751086
|
T | A | 1 | a0001c0001t0056 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4994A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4994 | chr10 | 7751086 | |||||
chr10:7751159
|
C | T | 1 | a0001c0001t0076 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4921G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4921 | chr10 | 7751159 | |||||
chr10:7751426
|
T | C | 2 | a0001c0001t0021a0001c0001t0054 | 4 | HG02132.hp2 NA18949.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4654A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4654 | chr10 | 7751426 | |||||
chr10:7751472
|
G | A | 1 | a0001c0001t0075 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4608C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4608 | chr10 | 7751472 | |||||
chr10:7751807
|
C | T | 44 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(41): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*4273G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4273 | chr10 | 7751807 | |||||
chr10:7751825
|
T | TC | 89 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(86): Show | 404 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*4254_*4255insG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4254 | chr10 | 7751825 | |||||
chr10:7751827
|
T | C | 3 | a0001c0001t0023a0001c0001t0038a0001c0001t0087 | 6 | HG01070.hp1 HG01071.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4253A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4253 | chr10 | 7751827 | |||||
chr10:7751851
|
T | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 394 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(391): Show |
3_prime_UTR_variant | MODIFIER | c.*4229A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4229 | chr10 | 7751851 | |||||
chr10:7751854
|
TAAAAGTA others(214): Show |
T | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 395 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*4005_*4225del | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4005 | chr10 | 7751854 | |||||
chr10:7751867
|
G | GTACTAAA others(127): Show |
1 | a0001c0002t0072 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4212_*4213insGAGA others(130): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4212 | chr10 | 7751867 | |||||
chr10:7751892
|
G | A | 2 | a0001c0001t0096a0001c0001t0098 | 2 | HG02280.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4188C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4188 | chr10 | 7751892 | |||||
chr10:7751895
|
C | T | 1 | a0001c0001t0095 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4185G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4185 | chr10 | 7751895 | |||||
chr10:7751897
|
C | T | 8 | a0001c0001t0041a0001c0001t0050a0001c0001t0081others(5): Show | 9 | HG01884.hp1 HG02280.hp1 HG02698.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4183G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4183 | chr10 | 7751897 | |||||
chr10:7751898
|
G | GGTGGCTC others(128): Show |
1 | a0001c0002t0071 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4181_*4182insTACG others(131): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4181 | chr10 | 7751898 | |||||
chr10:7751903
|
C | T | 2 | a0001c0001t0095a0001c0001t0096 | 2 | HG02280.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4177G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4177 | chr10 | 7751903 | |||||
chr10:7751904
|
G | C | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4176C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4176 | chr10 | 7751904 | |||||
chr10:7751928
|
G | T | 1 | a0001c0001t0035 | 2 | HG02257.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4152C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4152 | chr10 | 7751928 | |||||
chr10:7751953
|
T | G | 1 | a0001c0001t0098 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4127A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4127 | chr10 | 7751953 | |||||
chr10:7751964
|
A | G | 4 | a0001c0001t0049a0001c0001t0095a0001c0001t0096others(1): Show | 4 | HG00099.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4116T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4116 | chr10 | 7751964 | |||||
chr10:7752021
|
G | A | 4 | a0001c0001t0081a0001c0001t0088a0001c0002t0071others(1): Show | 4 | HG01884.hp1 HG02970.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4059C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4059 | chr10 | 7752021 | |||||
chr10:7752028
|
C | T | 1 | a0001c0001t0058 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4052G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4052 | chr10 | 7752028 | |||||
chr10:7752041
|
CA | C | 7 | a0001c0001t0051a0001c0001t0057a0001c0001t0058others(4): Show | 7 | HG01884.hp1 HG01981.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4038delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4038 | chr10 | 7752041 | |||||
chr10:7752041
|
CAA | C | 6 | a0001c0001t0041a0001c0001t0049a0001c0001t0050others(3): Show | 7 | HG00099.hp2 HG01081.hp1 HG02698.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4037_*4038delTT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4037 | chr10 | 7752041 | |||||
chr10:7752041
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0095a0001c0001t0096 | 2 | HG02280.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4026_*4038delTTTT others(9): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4026 | chr10 | 7752041 | |||||
chr10:7752178
|
C | T | 28 | a0001c0001t0010a0001c0001t0011a0001c0001t0017others(25): Show | 66 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3902G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3902 | chr10 | 7752178 | |||||
chr10:7752331
|
A | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*3749T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3749 | chr10 | 7752331 | |||||
chr10:7752336
|
A | G | 1 | a0002c0003t0028 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3744T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3744 | chr10 | 7752336 | |||||
chr10:7752391
|
T | G | 1 | a0001c0001t0079 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3689A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3689 | chr10 | 7752391 | |||||
chr10:7752435
|
G | A | 1 | a0001c0001t0064 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3645C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3645 | chr10 | 7752435 | |||||
chr10:7752472
|
G | A | 1 | a0001c0001t0058 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3608 | chr10 | 7752472 | |||||
chr10:7752572
|
G | A | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(6): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3508C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3508 | chr10 | 7752572 | |||||
chr10:7752685
|
T | G | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(27): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3395A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3395 | chr10 | 7752685 | |||||
chr10:7752843
|
G | C | 2 | a0001c0001t0037a0001c0001t0088 | 3 | HG02809.hp2 HG03209.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3237C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3237 | chr10 | 7752843 | |||||
chr10:7752902
|
G | A | 1 | a0001c0001t0067 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3178C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3178 | chr10 | 7752902 | |||||
chr10:7752965
|
A | C | 3 | a0001c0001t0010a0001c0001t0048a0004c0005t0047 | 10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3115T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3115 | chr10 | 7752965 | |||||
chr10:7753046
|
A | C | 1 | a0001c0001t0018 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3034T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3034 | chr10 | 7753046 | |||||
chr10:7753122
|
G | A | 1 | a0001c0001t0034 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2958C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2958 | chr10 | 7753122 | |||||
chr10:7753202
|
A | G | 1 | a0001c0001t0060 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2878T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2878 | chr10 | 7753202 | |||||
chr10:7753351
|
G | C | 1 | a0001c0002t0052 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2729 | chr10 | 7753351 | |||||
chr10:7753460
|
C | A | 1 | a0001c0001t0059 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2620G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2620 | chr10 | 7753460 | |||||
chr10:7753476
|
C | G | 1 | a0001c0001t0055 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2604 | chr10 | 7753476 | |||||
chr10:7753479
|
G | C | 2 | a0001c0001t0038a0001c0001t0089 | 3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2601C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2601 | chr10 | 7753479 | |||||
chr10:7753498
|
T | A | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(6): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2582A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2582 | chr10 | 7753498 | |||||
chr10:7753742
|
A | G | 1 | a0001c0001t0093 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2338T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2338 | chr10 | 7753742 | |||||
chr10:7753860
|
C | T | 1 | a0001c0001t0043 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2220 | chr10 | 7753860 | |||||
chr10:7753933
|
C | T | 2 | a0001c0001t0080a0001c0001t0081 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2147G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2147 | chr10 | 7753933 | |||||
chr10:7753948
|
A | G | 61 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(58): Show | 256 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*2132T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2132 | chr10 | 7753948 | |||||
chr10:7753962
|
C | T | 5 | a0001c0001t0007a0001c0001t0013a0001c0001t0083others(2): Show | 22 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2118G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2118 | chr10 | 7753962 | |||||
chr10:7753970
|
T | A | 1 | a0001c0001t0048 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2110 | chr10 | 7753970 | |||||
chr10:7754065
|
C | T | 1 | a0001c0001t0091 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2015 | chr10 | 7754065 | |||||
chr10:7754166
|
C | A | 2 | a0001c0001t0080a0001c0001t0081 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1914G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1914 | chr10 | 7754166 | |||||
chr10:7754191
|
C | A | 1 | a0001c0001t0090 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1889G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1889 | chr10 | 7754191 | |||||
chr10:7754360
|
C | T | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(6): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1720G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1720 | chr10 | 7754360 | |||||
chr10:7754502
|
G | A | 1 | a0002c0003t0028 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1578 | chr10 | 7754502 | |||||
chr10:7754558
|
G | A | 17 | a0001c0001t0005a0001c0001t0039a0001c0001t0040others(14): Show | 46 | HG00738.hp2 HG01081.hp1 HG01257.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1522C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1522 | chr10 | 7754558 | |||||
chr10:7754590
|
A | G | 1 | a0001c0002t0069 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1490T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1490 | chr10 | 7754590 | |||||
chr10:7754629
|
G | C | 27 | a0001c0001t0002a0001c0001t0010a0001c0001t0017others(24): Show | 112 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1451C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1451 | chr10 | 7754629 | |||||
chr10:7754633
|
GA | G | 17 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(14): Show | 71 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1446delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1446 | chr10 | 7754633 | |||||
chr10:7754718
|
T | C | 50 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(47): Show | 192 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1362A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1362 | chr10 | 7754718 | |||||
chr10:7754799
|
G | A | 1 | a0001c0001t0081 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1281 | chr10 | 7754799 | |||||
chr10:7754928
|
A | G | 5 | a0001c0001t0011a0001c0001t0022a0001c0001t0029others(2): Show | 14 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1152T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1152 | chr10 | 7754928 | |||||
chr10:7755023
|
G | A | 3 | a0001c0001t0017a0001c0001t0080a0001c0001t0081 | 7 | HG01884.hp1 HG02647.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1057C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1057 | chr10 | 7755023 | |||||
chr10:7755128
|
G | T | 1 | a0001c0001t0018 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*952C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 952 | chr10 | 7755128 | |||||
chr10:7755159
|
C | T | 1 | a0002c0003t0028 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*921G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 921 | chr10 | 7755159 | |||||
chr10:7755262
|
A | G | 1 | a0001c0001t0027 | 2 | HG01891.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 818 | chr10 | 7755262 | |||||
chr10:7755278
|
C | T | 4 | a0001c0001t0010a0001c0001t0048a0001c0001t0053others(1): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*802G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 802 | chr10 | 7755278 | |||||
chr10:7755402
|
C | A | 1 | a0001c0001t0082 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*678G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 678 | chr10 | 7755402 | |||||
chr10:7755467
|
A | G | 9 | a0001c0001t0010a0001c0001t0021a0001c0001t0026others(6): Show | 19 | HG00099.hp2 HG00642.hp1 HG01516.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*613T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 613 | chr10 | 7755467 | |||||
chr10:7755561
|
C | T | 1 | a0001c0001t0018 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 519 | chr10 | 7755561 | |||||
chr10:7755910
|
T | C | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(6): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*170A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 170 | chr10 | 7755910 | |||||
chr10:7755940
|
C | CAACT | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*136_*139dupAGTT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 139 | chr10 | 7755940 | |||||
chr10:7756070
|
A | T | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(6): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 10 | chr10 | 7756070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:7756187
|
C | T | 52 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(49): Show | 69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1120-45G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756187 | ||||||
chr10:7756387
|
A | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(255): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1120-245T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756387 | ||||||
chr10:7756637
|
C | T | 1 | a0001c0001t0004g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1120-495G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756637 | ||||||
chr10:7756682
|
T | C | 3 | a0001c0001t0049g0322a0001c0001t0050g0281a0001c0001t0051g0323 | 3 | HG00099.hp2 HG03017.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1120-540A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756682 | ||||||
chr10:7756686
|
G | A | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-544C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756686 | ||||||
chr10:7756772
|
C | CA | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(255): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1120-631_1120-630i others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756772 | ||||||
chr10:7756785
|
T | C | 61 | a0001c0001t0004g0008a0001c0001t0004g0029a0001c0001t0004g0031others(58): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1120-643A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756785 | ||||||
chr10:7756807
|
T | C | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120-665A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756807 | ||||||
chr10:7756825
|
T | C | 1 | a0001c0001t0094g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1120-683A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756825 | ||||||
chr10:7757007
|
A | G | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1120-865T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757007 | ||||||
chr10:7757222
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1120-1080C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757222 | ||||||
chr10:7757265
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(64): Show | 85 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1120-1123C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757265 | ||||||
chr10:7757521
|
A | T | 4 | a0001c0001t0005g0027a0001c0001t0005g0101a0001c0001t0005g0121others(1): Show | 5 | HG03453.hp2 NA18981.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-1379T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757521 | ||||||
chr10:7757526
|
T | A | 106 | a0001c0001t0001g0244a0001c0001t0001g0268a0001c0001t0002g0020others(103): Show | 145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1120-1384A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757526 | ||||||
chr10:7757531
|
T | A | 93 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(90): Show | 131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1120-1389A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757531 | ||||||
chr10:7757536
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(116): Show | 157 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1120-1394T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757536 | ||||||
chr10:7757632
|
C | A | 16 | a0001c0001t0003g0011a0001c0001t0003g0041a0001c0001t0003g0042others(13): Show | 21 | HG02074.hp1 HG02129.hp1 NA18944.hp2 others(18): Show |
intron_variant | MODIFIER | c.1120-1490G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757632 | ||||||
chr10:7757717
|
A | G | 91 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(88): Show | 127 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1120-1575T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757717 | ||||||
chr10:7757855
|
C | G | 52 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(49): Show | 69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1120-1713G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757855 | ||||||
chr10:7757908
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(255): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1120-1766A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757908 | ||||||
chr10:7757941
|
C | T | 1 | a0001c0001t0077g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120-1799G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757941 | ||||||
chr10:7757975
|
G | A | 1 | a0001c0001t0002g0020 | 2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1120-1833C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757975 | ||||||
chr10:7758010
|
A | AT | 72 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(69): Show | 92 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1120-1869dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758010 | ||||||
chr10:7758010
|
ATTT | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(62): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1120-1871_1120-186 others(7): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758010 | ||||||
chr10:7758078
|
C | CT | 65 | a0001c0001t0001g0264a0001c0001t0002g0002a0001c0001t0002g0012others(62): Show | 83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1119+1811dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | ||||||
chr10:7758078
|
CT | C | 39 | a0001c0001t0001g0084a0001c0001t0004g0008a0001c0001t0004g0029others(36): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1119+1811delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | ||||||
chr10:7758078
|
CTT | C | 10 | a0001c0001t0004g0171a0001c0001t0006g0177a0001c0001t0010g0015others(7): Show | 12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1119+1810_1119+181 others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | ||||||
chr10:7758197
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(64): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1119+1693G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758197 | ||||||
chr10:7758226
|
C | T | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+1664G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758226 | ||||||
chr10:7758258
|
T | C | 1 | a0001c0001t0026g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1119+1632A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758258 | ||||||
chr10:7758280
|
G | A | 5 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1610C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758280 | ||||||
chr10:7758353
|
A | C | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1119+1537T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758353 | ||||||
chr10:7758391
|
G | A | 5 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1499C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758391 | ||||||
chr10:7758435
|
G | A | 1 | a0001c0001t0026g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1119+1455C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758435 | ||||||
chr10:7758550
|
T | C | 4 | a0001c0001t0010g0142a0001c0001t0010g0148a0001c0001t0010g0149others(1): Show | 4 | HG00642.hp1 HG01516.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+1340A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758550 | ||||||
chr10:7758571
|
C | G | 1 | a0001c0001t0003g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1119+1319G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758571 | ||||||
chr10:7758612
|
A | G | 3 | a0001c0001t0002g0056a0001c0001t0032g0059a0001c0001t0076g0071 | 3 | HG02015.hp1 NA18946.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1119+1278T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758612 | ||||||
chr10:7758675
|
CA | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(183): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1119+1214delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758675 | ||||||
chr10:7758675
|
CAA | C | 51 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(48): Show | 68 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1119+1213_1119+121 others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758675 | ||||||
chr10:7758743
|
T | C | 5 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1147A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758743 | ||||||
chr10:7758815
|
T | TC | 5 | a0001c0001t0001g0235a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG00423.hp1 HG02027.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+1074dupG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758815 | ||||||
chr10:7758845
|
G | A | 142 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(139): Show | 182 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1119+1045C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758845 | ||||||
chr10:7758918
|
T | C | 54 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(51): Show | 73 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.1119+972A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758918 | ||||||
chr10:7759241
|
A | G | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+649T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759241 | ||||||
chr10:7759425
|
A | C | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119+465T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759425 | ||||||
chr10:7759544
|
C | A | 2 | a0001c0001t0038g0044a0001c0001t0089g0090 | 3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1119+346G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759544 | ||||||
chr10:7759608
|
T | C | 4 | a0001c0001t0003g0188a0001c0001t0003g0224a0001c0001t0003g0309others(1): Show | 4 | NA18961.hp1 NA18982.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+282A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759608 | ||||||
chr10:7759615
|
T | C | 6 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(3): Show | 6 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+275A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759615 | ||||||
chr10:7759709
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1119+181T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759709 | ||||||
chr10:7759997
|
T | C | 39 | a0001c0001t0004g0008a0001c0001t0004g0029a0001c0001t0004g0031others(36): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1019-7A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7759997 | ||||||
chr10:7760155
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1019-165C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760155 | ||||||
chr10:7760194
|
C | A | 1 | a0001c0001t0003g0307 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1019-204G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760194 | ||||||
chr10:7760285
|
C | A | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-295G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760285 | ||||||
chr10:7760380
|
CAT | C | 15 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(12): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1019-392_1019-391d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760380 | ||||||
chr10:7760521
|
A | G | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1019-531T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760521 | ||||||
chr10:7760547
|
T | C | 1 | a0001c0002t0009g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1019-557A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760547 | ||||||
chr10:7760590
|
C | A | 2 | a0001c0001t0003g0299a0001c0001t0003g0301 | 2 | NA18987.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1019-600G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760590 | ||||||
chr10:7760649
|
T | A | 59 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(56): Show | 77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1019-659A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760649 | ||||||
chr10:7760660
|
A | G | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-670T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760660 | ||||||
chr10:7760668
|
TTATTA | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(62): Show | 86 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1019-683_1019-679d others(7): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760668 | ||||||
chr10:7760750
|
G | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(56): Show | 77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1019-760C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760750 | ||||||
chr10:7760812
|
T | C | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1019-822A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760812 | ||||||
chr10:7760822
|
G | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(120): Show | 163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1019-832C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760822 | ||||||
chr10:7760846
|
G | A | 4 | a0001c0001t0004g0032a0001c0001t0004g0052a0001c0001t0004g0170others(1): Show | 5 | NA18747.hp2 NA18977.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-856C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760846 | ||||||
chr10:7760973
|
C | T | 1 | a0001c0001t0062g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1019-983G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760973 | ||||||
chr10:7761058
|
G | A | 14 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(11): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1019-1068C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761058 | ||||||
chr10:7761136
|
A | G | 4 | a0001c0001t0005g0087a0001c0001t0039g0110a0001c0001t0091g0109others(1): Show | 4 | HG01081.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-1146T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761136 | ||||||
chr10:7761142
|
T | C | 3 | a0001c0001t0017g0275a0001c0001t0017g0276a0001c0001t0017g0277 | 3 | HG03041.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1019-1152A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761142 | ||||||
chr10:7761184
|
A | G | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1019-1194T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761184 | ||||||
chr10:7761200
|
A | C | 1 | a0001c0001t0011g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1019-1210T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761200 | ||||||
chr10:7761256
|
C | G | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1018+1201G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761256 | ||||||
chr10:7761318
|
G | C | 40 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(37): Show | 59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1018+1139C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761318 | ||||||
chr10:7761493
|
C | G | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1018+964G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761493 | ||||||
chr10:7761656
|
T | C | 7 | a0001c0001t0007g0016a0001c0001t0007g0151a0001c0001t0007g0154others(4): Show | 9 | HG00609.hp2 NA18964.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018+801A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761656 | ||||||
chr10:7761754
|
C | A | 1 | a0001c0001t0081g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1018+703G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761754 | ||||||
chr10:7761757
|
T | C | 59 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(56): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1018+700A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761757 | ||||||
chr10:7761880
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0023g0019a0001c0001t0023g0054 | 4 | HG02976.hp1 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+577A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761880 | ||||||
chr10:7761883
|
T | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0273 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1018+574A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761883 | ||||||
chr10:7762132
|
C | G | 1 | a0001c0001t0002g0034 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1018+325G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762132 | ||||||
chr10:7762179
|
A | G | 8 | a0001c0001t0010g0015a0001c0001t0010g0142a0001c0001t0010g0143others(5): Show | 10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018+278T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762179 | ||||||
chr10:7762305
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1018+152G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762305 | ||||||
chr10:7762345
|
C | T | 318 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(315): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.1018+112G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762345 | ||||||
chr10:7762347
|
G | A | 8 | a0001c0001t0010g0015a0001c0001t0010g0142a0001c0001t0010g0143others(5): Show | 10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018+110C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762347 | ||||||
chr10:7762563
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0196others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.919-7A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762563 | ||||||
chr10:7762624
|
CAAATG | C | 6 | a0001c0001t0002g0062a0001c0001t0002g0075a0001c0001t0002g0076others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-73_919-69delCA others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762624 | ||||||
chr10:7762732
|
A | C | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.919-176T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762732 | ||||||
chr10:7762741
|
C | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-185G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762741 | ||||||
chr10:7763085
|
G | A | 1 | a0001c0002t0009g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.919-529C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763085 | ||||||
chr10:7763088
|
T | G | 3 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0052g0096 | 3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.919-532A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763088 | ||||||
chr10:7763119
|
G | A | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.919-563C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763119 | ||||||
chr10:7763345
|
C | G | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.918+378G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763345 | ||||||
chr10:7763518
|
C | T | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.918+205G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763518 | ||||||
chr10:7763613
|
A | C | 1 | a0001c0001t0079g0063 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.918+110T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763613 | ||||||
chr10:7763662
|
T | G | 1 | a0001c0001t0002g0021 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.918+61A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763662 | ||||||
chr10:7763838
|
G | A | 8 | a0001c0001t0010g0015a0001c0001t0010g0142a0001c0001t0010g0143others(5): Show | 10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-47C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763838 | ||||||
chr10:7763865
|
C | G | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-74G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763865 | ||||||
chr10:7763905
|
C | T | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-114G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763905 | ||||||
chr10:7763964
|
A | T | 5 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-173T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763964 | ||||||
chr10:7764011
|
G | GA | 8 | a0001c0001t0004g0029a0001c0001t0004g0032a0001c0001t0004g0052others(5): Show | 10 | HG00597.hp1 NA18747.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-221dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764011 | ||||||
chr10:7764237
|
G | A | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.850-446C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764237 | ||||||
chr10:7764239
|
A | G | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.850-448T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764239 | ||||||
chr10:7764435
|
G | A | 5 | a0001c0001t0001g0234a0001c0001t0001g0246a0001c0001t0001g0254others(2): Show | 5 | HG00673.hp1 NA18940.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-644C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764435 | ||||||
chr10:7764607
|
T | C | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.850-816A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764607 | ||||||
chr10:7764632
|
G | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0248a0001c0001t0001g0253others(4): Show | 8 | NA18747.hp1 NA18953.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764632 | ||||||
chr10:7764752
|
C | T | 15 | a0001c0001t0010g0015a0001c0001t0010g0142a0001c0001t0010g0143others(12): Show | 19 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850-961G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764752 | ||||||
chr10:7764886
|
G | A | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-1095C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764886 | ||||||
chr10:7764989
|
G | A | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+1064C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764989 | ||||||
chr10:7765114
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.849+939C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765114 | ||||||
chr10:7765159
|
C | CA | 69 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(66): Show | 91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.849+893dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765159 | ||||||
chr10:7765159
|
CA | C | 25 | a0001c0001t0001g0230a0001c0001t0001g0265a0001c0001t0003g0301others(22): Show | 28 | HG00323.hp1 HG01069.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.849+893delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765159 | ||||||
chr10:7765368
|
G | A | 40 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(37): Show | 59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.849+685C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765368 | ||||||
chr10:7765375
|
G | A | 1 | a0001c0001t0031g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+678C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765375 | ||||||
chr10:7765405
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(121): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.849+648C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765405 | ||||||
chr10:7765439
|
T | TA | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.849+613dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765439 | ||||||
chr10:7765650
|
A | G | 5 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+403T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765650 | ||||||
chr10:7765696
|
C | T | 318 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(315): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.849+357G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765696 | ||||||
chr10:7765901
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(60): Show | 84 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.849+152G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765901 | ||||||
chr10:7766123
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(121): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.799-20A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766123 | ||||||
chr10:7766726
|
T | C | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-623A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766726 | ||||||
chr10:7766727
|
C | T | 1 | a0001c0001t0005g0324 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.799-624G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766727 | ||||||
chr10:7766799
|
G | A | 4 | a0001c0001t0020g0014a0001c0001t0020g0091a0001c0001t0031g0202others(1): Show | 6 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-696C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766799 | ||||||
chr10:7766810
|
T | C | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.799-707A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766810 | ||||||
chr10:7766849
|
G | A | 1 | a0001c0001t0023g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.799-746C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766849 | ||||||
chr10:7766954
|
C | T | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-851G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766954 | ||||||
chr10:7767001
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(121): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.799-898G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767001 | ||||||
chr10:7767022
|
C | CA | 28 | a0001c0001t0006g0178a0001c0001t0006g0181a0001c0001t0007g0016others(25): Show | 32 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.799-920dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767022 | ||||||
chr10:7767032
|
A | C | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.799-929T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767032 | ||||||
chr10:7767035
|
AAAACCTC others(14): Show |
A | 1 | a0001c0001t0001g0265 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.799-953_799-933del others(21): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767035 | ||||||
chr10:7767036
|
AAACCTCA others(13): Show |
A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(51): Show | 75 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.799-953_799-934del others(20): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767036 | ||||||
chr10:7767037
|
AACCTCAT others(12): Show |
A | 9 | a0001c0001t0001g0189a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 9 | HG02027.hp2 HG02738.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-953_799-935del others(19): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767037 | ||||||
chr10:7767105
|
A | G | 1 | a0001c0001t0037g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-1002T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767105 | ||||||
chr10:7767112
|
G | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.799-1009C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767112 | ||||||
chr10:7767248
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.799-1145C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767248 | ||||||
chr10:7767335
|
G | A | 1 | a0001c0001t0003g0300 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.799-1232C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767335 | ||||||
chr10:7767405
|
G | A | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-1302C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767405 | ||||||
chr10:7767585
|
G | A | 1 | a0001c0001t0007g0154 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.799-1482C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767585 | ||||||
chr10:7767699
|
A | T | 1 | a0001c0001t0003g0287 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.798+1517T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767699 | ||||||
chr10:7767736
|
G | A | 11 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(8): Show | 14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+1480C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767736 | ||||||
chr10:7767769
|
G | C | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+1447C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767769 | ||||||
chr10:7767786
|
G | A | 8 | a0001c0001t0004g0029a0001c0001t0004g0032a0001c0001t0004g0052others(5): Show | 10 | HG00597.hp1 NA18747.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.798+1430C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767786 | ||||||
chr10:7767842
|
G | C | 3 | a0001c0001t0020g0014a0001c0001t0020g0091a0001c0002t0068g0098 | 5 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+1374C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767842 | ||||||
chr10:7767865
|
C | CA | 28 | a0001c0001t0002g0270a0001c0001t0003g0301a0001c0001t0007g0151others(25): Show | 34 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.798+1350dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767865 | ||||||
chr10:7767865
|
CA | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(107): Show | 150 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.798+1350delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767865 | ||||||
chr10:7767997
|
C | T | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.798+1219G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767997 | ||||||
chr10:7768054
|
A | G | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.798+1162T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768054 | ||||||
chr10:7768108
|
C | T | 88 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(85): Show | 113 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.798+1108G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768108 | ||||||
chr10:7768163
|
T | C | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.798+1053A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768163 | ||||||
chr10:7768281
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(117): Show | 160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.798+935T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768281 | ||||||
chr10:7768431
|
G | C | 2 | a0001c0001t0020g0014a0001c0001t0020g0091 | 4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+785C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768431 | ||||||
chr10:7768469
|
C | G | 3 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0052g0096 | 3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.798+747G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768469 | ||||||
chr10:7768541
|
C | CA | 56 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(53): Show | 74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.798+674dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768541 | ||||||
chr10:7768575
|
G | A | 6 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(3): Show | 6 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.798+641C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768575 | ||||||
chr10:7768576
|
C | T | 15 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(12): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.798+640G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768576 | ||||||
chr10:7768600
|
A | G | 9 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(6): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+616T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768600 | ||||||
chr10:7768643
|
G | C | 1 | a0001c0001t0001g0261 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.798+573C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768643 | ||||||
chr10:7768845
|
C | T | 1 | a0001c0001t0077g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798+371G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768845 | ||||||
chr10:7768912
|
G | T | 3 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0052g0096 | 3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.798+304C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768912 | ||||||
chr10:7769185
|
A | C | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.798+31T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7769185 | ||||||
chr10:7769365
|
T | C | 1 | a0001c0001t0021g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.669-20A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769365 | ||||||
chr10:7769415
|
T | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-70A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769415 | ||||||
chr10:7769444
|
G | C | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.669-99C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769444 | ||||||
chr10:7769582
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-237C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769582 | ||||||
chr10:7769692
|
GT | G | 9 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(6): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-348delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769692 | ||||||
chr10:7769700
|
C | CTA | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-357_669-356dup others(2): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769700 | ||||||
chr10:7769786
|
T | C | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-441A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769786 | ||||||
chr10:7769815
|
T | C | 2 | a0001c0002t0070g0140a0001c0002t0071g0047 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669-470A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769815 | ||||||
chr10:7769827
|
C | T | 3 | a0001c0001t0013g0048a0001c0001t0013g0156a0001c0001t0013g0157 | 3 | HG00099.hp1 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.669-482G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769827 | ||||||
chr10:7769851
|
T | C | 16 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(13): Show | 20 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.669-506A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769851 | ||||||
chr10:7769886
|
G | A | 11 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(8): Show | 14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.669-541C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769886 | ||||||
chr10:7769940
|
C | G | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.669-595G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769940 | ||||||
chr10:7769969
|
C | T | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.669-624G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769969 | ||||||
chr10:7769992
|
G | A | 14 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(11): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-647C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769992 | ||||||
chr10:7770017
|
G | A | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.669-672C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770017 | ||||||
chr10:7770040
|
C | T | 52 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(49): Show | 69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.669-695G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770040 | ||||||
chr10:7770045
|
C | T | 2 | a0001c0001t0005g0026a0001c0001t0005g0117 | 3 | NA18986.hp2 NA19011.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.669-700G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770045 | ||||||
chr10:7770128
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0154 | 2 | NA19001.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.669-783C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770128 | ||||||
chr10:7770238
|
T | C | 3 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0052g0096 | 3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.669-893A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770238 | ||||||
chr10:7770379
|
G | C | 2 | a0001c0001t0020g0014a0001c0001t0020g0091 | 4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-1034C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770379 | ||||||
chr10:7770483
|
C | T | 1 | a0001c0001t0024g0327 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.669-1138G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770483 | ||||||
chr10:7770577
|
TAGGG | T | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669-1236_669-1233d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770577 | ||||||
chr10:7770578
|
A | G | 40 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(37): Show | 59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.669-1233T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770578 | ||||||
chr10:7770923
|
T | C | 9 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(6): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-1578A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770923 | ||||||
chr10:7770950
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(117): Show | 160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.669-1605A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770950 | ||||||
chr10:7770974
|
C | G | 6 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(3): Show | 6 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-1629G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770974 | ||||||
chr10:7771014
|
C | T | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.669-1669G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771014 | ||||||
chr10:7771016
|
C | T | 17 | a0001c0001t0018g0017a0001c0001t0018g0218a0001c0001t0026g0139others(14): Show | 22 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.669-1671G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771016 | ||||||
chr10:7771145
|
T | TA | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(210): Show | 278 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.669-1801dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771145 | ||||||
chr10:7771161
|
A | G | 56 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(53): Show | 75 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.669-1816T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771161 | ||||||
chr10:7771190
|
G | A | 89 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0012others(86): Show | 114 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.669-1845C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771190 | ||||||
chr10:7771192
|
T | C | 1 | a0001c0001t0010g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.669-1847A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771192 | ||||||
chr10:7771421
|
A | C | 1 | a0001c0001t0017g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.669-2076T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771421 | ||||||
chr10:7771535
|
G | C | 3 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0052g0096 | 3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.669-2190C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771535 | ||||||
chr10:7771643
|
G | A | 9 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(6): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-2298C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771643 | ||||||
chr10:7771665
|
G | A | 7 | a0001c0001t0005g0004a0001c0001t0005g0027a0001c0001t0005g0101others(4): Show | 13 | NA18949.hp1 NA18956.hp1 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.669-2320C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771665 | ||||||
chr10:7771666
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0019g0237 | 2 | NA19072.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.669-2321C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771666 | ||||||
chr10:7771801
|
A | C | 4 | a0001c0001t0010g0015a0001c0001t0010g0143a0001c0001t0010g0145others(1): Show | 6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-2456T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771801 | ||||||
chr10:7771860
|
G | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.669-2515C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771860 | ||||||
chr10:7771874
|
A | G | 1 | a0001c0001t0004g0318 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.669-2529T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771874 | ||||||
chr10:7771895
|
CA | C | 92 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0002g0002others(89): Show | 117 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.669-2551delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771895 | ||||||
chr10:7771908
|
A | G | 1 | a0001c0001t0003g0304 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.669-2563T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771908 | ||||||
chr10:7772048
|
T | C | 1 | a0001c0001t0059g0191 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.669-2703A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772048 | ||||||
chr10:7772138
|
G | A | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.668+2693C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772138 | ||||||
chr10:7772206
|
G | C | 1 | a0001c0001t0003g0041 | 2 | NA18944.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.668+2625C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772206 | ||||||
chr10:7772227
|
C | T | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.668+2604G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772227 | ||||||
chr10:7772307
|
G | A | 9 | a0001c0001t0001g0238a0001c0001t0010g0015a0001c0001t0010g0142others(6): Show | 11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.668+2524C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772307 | ||||||
chr10:7772363
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.668+2468A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772363 | ||||||
chr10:7772366
|
A | G | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.668+2465T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772366 | ||||||
chr10:7772421
|
C | T | 2 | a0001c0001t0095g0124a0001c0001t0096g0107 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.668+2410G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772421 | ||||||
chr10:7772620
|
T | A | 15 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(12): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.668+2211A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772620 | ||||||
chr10:7772763
|
AAATT | A | 4 | a0001c0001t0010g0015a0001c0001t0010g0143a0001c0001t0010g0145others(1): Show | 6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.668+2064_668+2067d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772763 | ||||||
chr10:7772782
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.668+2049T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772782 | ||||||
chr10:7772995
|
T | C | 1 | a0001c0001t0097g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.668+1836A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772995 | ||||||
chr10:7773028
|
C | T | 1 | a0001c0001t0018g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.668+1803G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773028 | ||||||
chr10:7773140
|
G | A | 11 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(8): Show | 14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.668+1691C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773140 | ||||||
chr10:7773218
|
G | T | 89 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0012others(86): Show | 114 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.668+1613C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773218 | ||||||
chr10:7773331
|
C | T | 1 | a0001c0001t0007g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.668+1500G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773331 | ||||||
chr10:7773343
|
A | G | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.668+1488T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773343 | ||||||
chr10:7773466
|
G | A | 3 | a0001c0001t0020g0014a0001c0001t0020g0091a0001c0002t0068g0098 | 5 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+1365C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773466 | ||||||
chr10:7773482
|
T | G | 1 | a0001c0001t0079g0063 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.668+1349A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773482 | ||||||
chr10:7773761
|
G | C | 1 | a0001c0001t0026g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.668+1070C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773761 | ||||||
chr10:7773767
|
T | C | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.668+1064A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773767 | ||||||
chr10:7773809
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(63): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.668+1022A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773809 | ||||||
chr10:7773829
|
T | G | 1 | a0001c0002t0009g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.668+1002A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773829 | ||||||
chr10:7773988
|
C | T | 1 | a0001c0001t0100g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.668+843G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773988 | ||||||
chr10:7774019
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.668+812G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774019 | ||||||
chr10:7774112
|
A | G | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.668+719T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774112 | ||||||
chr10:7774182
|
T | C | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.668+649A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774182 | ||||||
chr10:7774183
|
T | C | 1 | a0001c0001t0003g0316 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.668+648A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774183 | ||||||
chr10:7774271
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0189a0001c0001t0001g0199others(1): Show | 5 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+560C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774271 | ||||||
chr10:7774338
|
G | T | 318 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(315): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.668+493C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774338 | ||||||
chr10:7774397
|
T | C | 46 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(43): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.668+434A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774397 | ||||||
chr10:7774399
|
T | C | 4 | a0001c0001t0010g0015a0001c0001t0010g0143a0001c0001t0010g0145others(1): Show | 6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.668+432A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774399 | ||||||
chr10:7774501
|
T | A | 1 | a0001c0001t0005g0101 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.668+330A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774501 | ||||||
chr10:7774557
|
G | A | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.668+274C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774557 | ||||||
chr10:7774578
|
G | C | 6 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(3): Show | 6 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.668+253C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774578 | ||||||
chr10:7774634
|
C | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.668+197G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774634 | ||||||
chr10:7774699
|
G | A | 52 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(49): Show | 69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.668+132C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774699 | ||||||
chr10:7774812
|
C | T | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.668+19G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774812 | ||||||
chr10:7774813
|
G | A | 3 | a0001c0001t0049g0322a0001c0001t0050g0281a0001c0001t0051g0323 | 3 | HG00099.hp2 HG03017.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.668+18C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774813 | ||||||
chr10:7775028
|
G | A | 1 | a0001c0001t0026g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608-137C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775028 | ||||||
chr10:7775052
|
G | A | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.608-161C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775052 | ||||||
chr10:7775066
|
G | A | 1 | a0001c0001t0061g0285 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.608-175C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775066 | ||||||
chr10:7775085
|
T | C | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.608-194A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775085 | ||||||
chr10:7775101
|
C | T | 1 | a0001c0001t0003g0297 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.608-210G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775101 | ||||||
chr10:7775372
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(255): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.607+379A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775372 | ||||||
chr10:7775594
|
A | G | 1 | a0001c0001t0003g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.607+157T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775594 | ||||||
chr10:7775906
|
C | T | 6 | a0001c0001t0005g0026a0001c0001t0005g0100a0001c0001t0005g0102others(3): Show | 7 | NA18942.hp1 NA18947.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-107G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7775906 | ||||||
chr10:7775955
|
G | A | 22 | a0001c0001t0003g0011a0001c0001t0003g0041a0001c0001t0003g0042others(19): Show | 28 | HG00408.hp1 HG02056.hp2 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.559-156C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7775955 | ||||||
chr10:7776025
|
G | A | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-226C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776025 | ||||||
chr10:7776087
|
G | A | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-288C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776087 | ||||||
chr10:7776093
|
G | A | 1 | a0001c0002t0070g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.559-294C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776093 | ||||||
chr10:7776127
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.559-328C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776127 | ||||||
chr10:7776177
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(122): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.559-378G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776177 | ||||||
chr10:7776229
|
CA | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(129): Show | 178 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.559-431delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776229 | ||||||
chr10:7776248
|
T | C | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-449A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776248 | ||||||
chr10:7776293
|
C | G | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-494G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776293 | ||||||
chr10:7776300
|
C | T | 13 | a0001c0001t0004g0008a0001c0001t0004g0029a0001c0001t0004g0032others(10): Show | 18 | HG00597.hp1 NA18747.hp2 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.559-501G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776300 | ||||||
chr10:7776357
|
G | A | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.559-558C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776357 | ||||||
chr10:7776440
|
G | T | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.559-641C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776440 | ||||||
chr10:7776498
|
T | G | 1 | a0001c0001t0004g0179 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.559-699A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776498 | ||||||
chr10:7776546
|
C | T | 58 | a0001c0001t0005g0004a0001c0001t0005g0026a0001c0001t0005g0027others(55): Show | 68 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.559-747G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776546 | ||||||
chr10:7776560
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.559-761C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776560 | ||||||
chr10:7776588
|
C | T | 1 | a0001c0001t0094g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.559-789G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776588 | ||||||
chr10:7776589
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(119): Show | 163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.559-790C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776589 | ||||||
chr10:7776603
|
C | T | 1 | a0001c0001t0026g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.559-804G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776603 | ||||||
chr10:7776604
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.559-805C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776604 | ||||||
chr10:7776663
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.559-864C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776663 | ||||||
chr10:7776677
|
G | A | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559-878C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776677 | ||||||
chr10:7776688
|
G | A | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-889C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776688 | ||||||
chr10:7776716
|
G | A | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-917C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776716 | ||||||
chr10:7776732
|
C | CA | 66 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(63): Show | 86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.559-934dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776732 | ||||||
chr10:7776747
|
AG | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(131): Show | 177 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.559-949delC | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776747 | ||||||
chr10:7776748
|
G | A | 66 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(63): Show | 90 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.559-949C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776748 | ||||||
chr10:7776815
|
C | T | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.559-1016G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776815 | ||||||
chr10:7776895
|
TA | T | 6 | a0001c0001t0002g0065a0001c0001t0002g0215a0001c0001t0004g0184others(3): Show | 6 | HG02809.hp2 HG03209.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-1097delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776895 | ||||||
chr10:7777053
|
C | CA | 47 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(44): Show | 63 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.559-1255dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777053
|
C | CAA | 7 | a0001c0001t0002g0022a0001c0001t0002g0066a0001c0001t0002g0070others(4): Show | 8 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.559-1256_559-1255d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777053
|
CA | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(125): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.559-1255delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777053
|
CAA | C | 23 | a0001c0001t0001g0193a0001c0001t0001g0265a0001c0001t0004g0146others(20): Show | 25 | HG00438.hp1 HG00642.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.559-1256_559-1255d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777053
|
CAAA | C | 6 | a0001c0001t0017g0274a0001c0001t0017g0275a0001c0001t0017g0276others(3): Show | 8 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.559-1257_559-1255d others(5): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777053
|
CAAAAAAA others(6): Show |
C | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.559-1267_559-1255d others(15): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | ||||||
chr10:7777246
|
C | CT | 60 | a0001c0001t0001g0236a0001c0001t0002g0002a0001c0001t0002g0012others(57): Show | 77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.559-1448dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777246 | ||||||
chr10:7777246
|
CT | C | 57 | a0001c0001t0001g0174a0001c0001t0001g0265a0001c0001t0004g0008others(54): Show | 79 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.559-1448delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777246 | ||||||
chr10:7777318
|
T | C | 14 | a0001c0001t0026g0139a0001c0001t0026g0217a0001c0002t0009g0013others(11): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.559-1519A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777318 | ||||||
chr10:7777323
|
A | T | 5 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(2): Show | 5 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+1515T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777323 | ||||||
chr10:7777329
|
G | C | 57 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0041others(54): Show | 76 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.558+1509C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777329 | ||||||
chr10:7777353
|
C | G | 1 | a0001c0001t0081g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.558+1485G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777353 | ||||||
chr10:7777420
|
G | A | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.558+1418C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777420 | ||||||
chr10:7777446
|
G | A | 1 | a0001c0001t0005g0028 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.558+1392C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777446 | ||||||
chr10:7777452
|
T | C | 1 | a0001c0001t0018g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.558+1386A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777452 | ||||||
chr10:7777624
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.558+1214C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777624 | ||||||
chr10:7777640
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.558+1198C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777640 | ||||||
chr10:7777691
|
A | C | 2 | a0001c0001t0002g0070a0001c0001t0074g0069 | 2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.558+1147T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777691 | ||||||
chr10:7777788
|
A | G | 4 | a0001c0001t0017g0274a0001c0001t0017g0275a0001c0001t0017g0276others(1): Show | 4 | HG03041.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1050T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777788 | ||||||
chr10:7777807
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0066g0078 | 2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.558+1031C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777807 | ||||||
chr10:7777831
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(53): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.558+1007C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777831 | ||||||
chr10:7777871
|
C | T | 2 | a0001c0001t0049g0322a0001c0001t0051g0323 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.558+967G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777871 | ||||||
chr10:7777895
|
TC | T | 68 | a0001c0001t0001g0174a0001c0001t0001g0235a0001c0001t0004g0008others(65): Show | 92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.558+942delG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777895 | ||||||
chr10:7777902
|
C | CA | 4 | a0001c0001t0002g0068a0001c0001t0002g0073a0001c0001t0018g0017others(1): Show | 6 | HG01175.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+935_558+936ins others(1): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777902 | ||||||
chr10:7777903
|
C | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.558+935G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777903 | ||||||
chr10:7777903
|
C | CA | 8 | a0001c0001t0001g0234a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 8 | HG00673.hp1 NA18940.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+934_558+935ins others(1): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777903 | ||||||
chr10:7777904
|
C | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(277): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.558+934G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777904 | ||||||
chr10:7777995
|
C | T | 10 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(7): Show | 12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+843G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777995 | ||||||
chr10:7778012
|
A | G | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.558+826T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778012 | ||||||
chr10:7778178
|
A | G | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+660T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778178 | ||||||
chr10:7778266
|
G | A | 2 | a0001c0001t0080g0081a0001c0001t0081g0118 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.558+572C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778266 | ||||||
chr10:7778407
|
G | C | 10 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(7): Show | 12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+431C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778407 | ||||||
chr10:7778449
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(255): Show | 342 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.558+389C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778449 | ||||||
chr10:7778462
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.558+376A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778462 | ||||||
chr10:7778478
|
C | T | 12 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+360G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778478 | ||||||
chr10:7778479
|
G | C | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.558+359C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778479 | ||||||
chr10:7778696
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.558+142C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778696 | ||||||
chr10:7778741
|
A | AAACAAC | 171 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(168): Show | 231 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.558+91_558+96dupGT others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778741 | ||||||
chr10:7778759
|
A | C | 12 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(9): Show | 14 | HG00438.hp1 HG00642.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+79T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778759 | ||||||
chr10:7779044
|
A | T | 5 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(2): Show | 5 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-25T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779044 | ||||||
chr10:7779118
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(196): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.377-99T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779118 | ||||||
chr10:7779118
|
A | T | 58 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(55): Show | 81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.377-99T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779118 | ||||||
chr10:7779162
|
C | T | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.377-143G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779162 | ||||||
chr10:7779220
|
C | T | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.377-201G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779220 | ||||||
chr10:7779225
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(120): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.377-206A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779225 | ||||||
chr10:7779230
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(214): Show | 282 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.377-211T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779230 | ||||||
chr10:7779366
|
C | T | 1 | a0001c0001t0041g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.377-347G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779366 | ||||||
chr10:7779393
|
G | A | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377-374C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779393 | ||||||
chr10:7779534
|
G | A | 1 | a0001c0001t0077g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.377-515C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779534 | ||||||
chr10:7779632
|
T | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(170): Show | 236 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.376+424A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779632 | ||||||
chr10:7779656
|
A | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(53): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.376+400T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779656 | ||||||
chr10:7779675
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(62): Show | 87 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.376+381C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779675 | ||||||
chr10:7779756
|
G | A | 9 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(6): Show | 12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.376+300C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779756 | ||||||
chr10:7779761
|
T | C | 1 | a0001c0001t0075g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.376+295A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779761 | ||||||
chr10:7779783
|
G | C | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.376+273C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779783 | ||||||
chr10:7779806
|
C | T | 4 | a0001c0001t0020g0014a0001c0001t0020g0091a0001c0001t0031g0202others(1): Show | 6 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+250G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779806 | ||||||
chr10:7779831
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(189): Show | 259 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+225G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779831 | ||||||
chr10:7779847
|
T | C | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376+209A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779847 | ||||||
chr10:7780052
|
T | G | 10 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0094others(7): Show | 13 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.376+4A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7780052 | ||||||
chr10:7780319
|
A | C | 2 | a0001c0001t0026g0139a0001c0001t0026g0217 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.210-12T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780319 | ||||||
chr10:7780383
|
T | C | 1 | a0001c0001t0059g0191 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210-76A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780383 | ||||||
chr10:7780424
|
C | T | 1 | a0001c0001t0100g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.210-117G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780424 | ||||||
chr10:7780430
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0030g0192 | 2 | NA18946.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.210-123G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780430 | ||||||
chr10:7780455
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(253): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.210-148A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780455 | ||||||
chr10:7780482
|
C | T | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.210-175G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780482 | ||||||
chr10:7780571
|
G | A | 8 | a0001c0001t0010g0145a0001c0001t0017g0138a0001c0001t0017g0274others(5): Show | 10 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.210-264C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780571 | ||||||
chr10:7780579
|
C | T | 9 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(6): Show | 12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.210-272G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780579 | ||||||
chr10:7780711
|
T | C | 1 | a0001c0001t0004g0032 | 2 | NA19083.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.210-404A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780711 | ||||||
chr10:7780746
|
G | C | 1 | a0001c0002t0052g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.210-439C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780746 | ||||||
chr10:7780803
|
C | T | 2 | a0001c0001t0031g0202a0001c0001t0031g0204 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210-496G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780803 | ||||||
chr10:7781015
|
G | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(235): Show | 320 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.210-708C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781015 | ||||||
chr10:7781016
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(62): Show | 87 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.210-709C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781016 | ||||||
chr10:7781022
|
C | T | 16 | a0001c0001t0003g0293a0001c0001t0011g0010a0001c0001t0011g0279others(13): Show | 23 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.210-715G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781022 | ||||||
chr10:7781112
|
G | A | 1 | a0001c0001t0013g0166 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210-805C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781112 | ||||||
chr10:7781319
|
G | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.210-1012C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781319 | ||||||
chr10:7781534
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210-1227G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781534 | ||||||
chr10:7781587
|
T | TAC | 11 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(8): Show | 13 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.210-1282_210-1281d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACAC | 6 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(3): Show | 6 | HG00099.hp2 HG00558.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-1284_210-1281d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(1): Show |
201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0037others(198): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.210-1288_210-1281d others(10): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(3): Show |
23 | a0001c0001t0001g0035a0001c0001t0001g0199a0001c0001t0002g0012others(20): Show | 29 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.210-1290_210-1281d others(12): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(5): Show |
2 | a0001c0001t0034g0024a0001c0002t0071g0047 | 3 | HG01515.hp1 HG01517.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.210-1292_210-1281d others(14): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0002g0070others(1): Show | 4 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-1294_210-1281d others(16): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(25): Show |
1 | a0002c0003t0028g0206 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(34): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TACACACA others(27): Show |
1 | a0002c0003t0028g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.210-1281_210-1280i others(36): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TCTACACA others(13): Show |
1 | a0001c0001t0017g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(22): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TCTACACA others(15): Show |
1 | a0001c0001t0017g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(24): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TCTACACA others(21): Show |
2 | a0001c0001t0017g0275a0001c0001t0017g0276 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.210-1281_210-1280i others(30): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781587
|
T | TCTACACA others(23): Show |
3 | a0001c0001t0017g0277a0001c0001t0018g0017a0001c0001t0018g0218 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-1281_210-1280i others(32): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | ||||||
chr10:7781645
|
C | G | 1 | a0001c0001t0017g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.210-1338G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781645 | ||||||
chr10:7781687
|
C | T | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.210-1380G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781687 | ||||||
chr10:7781688
|
G | A | 7 | a0001c0001t0017g0138a0001c0001t0017g0274a0001c0001t0017g0275others(4): Show | 9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-1381C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781688 | ||||||
chr10:7781750
|
C | CA | 85 | a0001c0001t0001g0174a0001c0001t0002g0023a0001c0001t0002g0055others(82): Show | 111 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.209+1330dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | ||||||
chr10:7781750
|
C | CAA | 46 | a0001c0001t0002g0303a0001c0001t0003g0011a0001c0001t0003g0018others(43): Show | 59 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.209+1329_209+1330d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | ||||||
chr10:7781750
|
C | CAAA | 57 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(54): Show | 72 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.209+1328_209+1330d others(5): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | ||||||
chr10:7781750
|
C | CAAAA | 23 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0201others(20): Show | 33 | HG00544.hp2 HG00597.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.209+1327_209+1330d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | ||||||
chr10:7781875
|
G | A | 2 | a0001c0001t0020g0014a0001c0001t0020g0091 | 4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1206C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781875 | ||||||
chr10:7781920
|
T | C | 1 | a0001c0001t0037g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.209+1161A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781920 | ||||||
chr10:7781971
|
T | C | 1 | a0001c0001t0008g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209+1110A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781971 | ||||||
chr10:7782044
|
G | A | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.209+1037C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782044 | ||||||
chr10:7782080
|
A | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(247): Show | 334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.209+1001T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782080 | ||||||
chr10:7782096
|
T | G | 1 | a0001c0001t0024g0327 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209+985A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782096 | ||||||
chr10:7782101
|
T | A | 17 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(14): Show | 21 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.209+980A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782101 | ||||||
chr10:7782212
|
T | C | 1 | a0001c0001t0017g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209+869A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782212 | ||||||
chr10:7782250
|
G | T | 1 | a0001c0001t0062g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.209+831C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782250 | ||||||
chr10:7782252
|
A | G | 125 | a0001c0001t0001g0174a0001c0001t0002g0002a0001c0001t0002g0012others(122): Show | 168 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.209+829T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782252 | ||||||
chr10:7782400
|
C | T | 4 | a0001c0001t0017g0274a0001c0001t0017g0275a0001c0001t0017g0276others(1): Show | 4 | HG03041.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+681G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782400 | ||||||
chr10:7782401
|
A | AT | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(128): Show | 172 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.209+679dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782401 | ||||||
chr10:7782401
|
A | T | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.209+680T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782401 | ||||||
chr10:7782492
|
C | G | 10 | a0001c0001t0002g0055a0001c0001t0002g0075a0001c0001t0002g0076others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.209+589G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782492 | ||||||
chr10:7782522
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.209+559G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782522 | ||||||
chr10:7782529
|
G | A | 10 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(7): Show | 12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.209+552C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782529 | ||||||
chr10:7782666
|
G | C | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.209+415C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782666 | ||||||
chr10:7782864
|
T | A | 1 | a0003c0004t0008g0313 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.209+217A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782864 | ||||||
chr10:7782909
|
G | T | 54 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(51): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.209+172C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782909 | ||||||
chr10:7782939
|
AAAG | A | 5 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0027g0129others(2): Show | 5 | HG01891.hp1 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+139_209+141del others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782939 | ||||||
chr10:7783231
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.115-56T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783231 | ||||||
chr10:7783237
|
A | C | 1 | a0001c0001t0075g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.115-62T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783237 | ||||||
chr10:7783308
|
A | G | 1 | a0001c0001t0003g0287 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.115-133T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783308 | ||||||
chr10:7783334
|
A | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(244): Show | 331 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.115-159T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783334 | ||||||
chr10:7783352
|
T | G | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.115-177A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783352 | ||||||
chr10:7783567
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(254): Show | 341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.115-392A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783567 | ||||||
chr10:7783586
|
C | T | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-411G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783586 | ||||||
chr10:7783601
|
A | G | 2 | a0001c0001t0016g0231a0001c0001t0016g0232 | 2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.115-426T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783601 | ||||||
chr10:7783753
|
T | C | 2 | a0001c0001t0003g0314a0001c0001t0003g0315 | 2 | NA18982.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.115-578A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783753 | ||||||
chr10:7783827
|
C | T | 1 | a0001c0001t0007g0150 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.115-652G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783827 | ||||||
chr10:7784169
|
G | C | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.115-994C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784169 | ||||||
chr10:7784242
|
A | G | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-1067T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784242 | ||||||
chr10:7784277
|
C | T | 1 | a0001c0001t0017g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.115-1102G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784277 | ||||||
chr10:7784286
|
T | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(322): Show | 421 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(418): Show |
intron_variant | MODIFIER | c.115-1111A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784286 | ||||||
chr10:7784341
|
G | C | 1 | a0001c0001t0034g0024 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.115-1166C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784341 | ||||||
chr10:7784351
|
G | A | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.115-1176C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784351 | ||||||
chr10:7784414
|
T | G | 44 | a0001c0001t0002g0303a0001c0001t0003g0011a0001c0001t0003g0018others(41): Show | 56 | HG00408.hp1 HG00741.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.115-1239A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784414 | ||||||
chr10:7784450
|
G | A | 38 | a0001c0001t0001g0174a0001c0001t0004g0008a0001c0001t0004g0029others(35): Show | 57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.115-1275C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784450 | ||||||
chr10:7784498
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.115-1323C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784498 | ||||||
chr10:7784551
|
G | A | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-1376C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784551 | ||||||
chr10:7784580
|
T | C | 2 | a0002c0003t0028g0206a0002c0003t0028g0207 | 2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.115-1405A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784580 | ||||||
chr10:7784643
|
G | T | 1 | a0001c0001t0003g0278 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.115-1468C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784643 | ||||||
chr10:7784814
|
C | T | 1 | a0001c0001t0004g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115-1639G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784814 | ||||||
chr10:7784969
|
G | A | 10 | a0001c0001t0004g0146a0001c0001t0004g0147a0001c0001t0010g0015others(7): Show | 12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-1794C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784969 | ||||||
chr10:7785016
|
G | A | 5 | a0001c0001t0021g0128a0001c0001t0021g0133a0001c0001t0021g0134others(2): Show | 5 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-1841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785016 | ||||||
chr10:7785070
|
G | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(253): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.115-1895C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785070 | ||||||
chr10:7785171
|
G | A | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-1996C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785171 | ||||||
chr10:7785202
|
T | C | 9 | a0001c0002t0009g0013a0001c0002t0009g0025a0001c0002t0009g0092others(6): Show | 12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-2027A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785202 | ||||||
chr10:7785233
|
C | T | 1 | a0001c0001t0067g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-2058G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785233 | ||||||
chr10:7785251
|
C | CA | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(84): Show | 114 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.115-2077dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785251 | ||||||
chr10:7785251
|
C | CAA | 44 | a0001c0001t0001g0174a0001c0001t0001g0205a0001c0001t0001g0267others(41): Show | 63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.115-2078_115-2077d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785251 | ||||||
chr10:7785510
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(197): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.114+2310G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785510 | ||||||
chr10:7785583
|
G | A | 4 | a0001c0002t0009g0025a0001c0002t0068g0098a0002c0003t0028g0206others(1): Show | 5 | HG00438.hp1 HG02135.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+2237C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785583 | ||||||
chr10:7785795
|
C | T | 23 | a0001c0001t0017g0138a0001c0001t0018g0218a0001c0001t0020g0091others(20): Show | 26 | HG00099.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+2025G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785795 | ||||||
chr10:7785813
|
G | T | 53 | a0001c0001t0002g0303a0001c0001t0003g0011a0001c0001t0003g0018others(50): Show | 70 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.114+2007C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | ||||||
chr10:7785813
|
GA | G | 8 | a0001c0001t0002g0215a0001c0001t0017g0274a0001c0001t0017g0275others(5): Show | 8 | HG02647.hp1 HG02896.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+2006delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | ||||||
chr10:7785813
|
GAA | G | 52 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(49): Show | 69 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.114+2005_114+2006d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | ||||||
chr10:7785872
|
T | C | 5 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0027g0129others(2): Show | 5 | HG01891.hp1 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1948A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785872 | ||||||
chr10:7785891
|
G | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.114+1929C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785891 | ||||||
chr10:7785979
|
G | A | 2 | a0001c0001t0067g0216a0001c0001t0080g0081 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.114+1841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785979 | ||||||
chr10:7785996
|
T | C | 1 | a0001c0001t0026g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.114+1824A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785996 | ||||||
chr10:7786066
|
T | C | 2 | a0001c0001t0002g0079a0001c0001t0066g0078 | 2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.114+1754A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786066 | ||||||
chr10:7786152
|
A | G | 4 | a0001c0001t0021g0133a0001c0001t0021g0134a0001c0001t0049g0322others(1): Show | 4 | HG00099.hp2 HG02132.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1668T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786152 | ||||||
chr10:7786154
|
G | A | 4 | a0001c0001t0021g0133a0001c0001t0021g0134a0001c0001t0049g0322others(1): Show | 4 | HG00099.hp2 HG02132.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1666C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786154 | ||||||
chr10:7786169
|
C | G | 2 | a0001c0001t0005g0087a0001c0001t0037g0088 | 2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.114+1651G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786169 | ||||||
chr10:7786245
|
T | C | 1 | a0001c0001t0018g0017 | 3 | HG02280.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+1575A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786245 | ||||||
chr10:7786257
|
T | C | 2 | a0001c0001t0018g0017a0001c0001t0018g0218 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1563A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786257 | ||||||
chr10:7786268
|
T | G | 2 | a0001c0001t0021g0133a0001c0001t0021g0134 | 2 | HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1552A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786268 | ||||||
chr10:7786270
|
C | T | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+1550G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786270 | ||||||
chr10:7786279
|
G | T | 4 | a0001c0001t0018g0017a0001c0001t0018g0218a0001c0001t0021g0133others(1): Show | 6 | HG02132.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1541C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786279 | ||||||
chr10:7786281
|
G | A | 4 | a0001c0001t0018g0017a0001c0001t0018g0218a0001c0001t0021g0133others(1): Show | 6 | HG02132.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1539C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786281 | ||||||
chr10:7786553
|
G | T | 1 | a0001c0001t0004g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.114+1267C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786553 | ||||||
chr10:7786710
|
G | A | 1 | a0001c0001t0041g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114+1110C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786710 | ||||||
chr10:7786767
|
T | C | 1 | a0001c0001t0005g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.114+1053A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786767 | ||||||
chr10:7786777
|
C | T | 2 | a0001c0001t0006g0135a0001c0001t0006g0136 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.114+1043G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786777 | ||||||
chr10:7786786
|
T | A | 3 | a0001c0001t0002g0132a0001c0001t0021g0133a0001c0001t0021g0134 | 3 | HG01192.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1034A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786786 | ||||||
chr10:7786787
|
A | C | 3 | a0001c0001t0002g0132a0001c0001t0021g0133a0001c0001t0021g0134 | 3 | HG01192.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1033T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786787 | ||||||
chr10:7786789
|
T | C | 96 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(93): Show | 125 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.114+1031A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786789 | ||||||
chr10:7786838
|
T | C | 1 | a0001c0001t0048g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.114+982A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786838 | ||||||
chr10:7786894
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.114+926G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786894 | ||||||
chr10:7787004
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114+816A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787004 | ||||||
chr10:7787055
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0037others(52): Show | 72 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+765C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787055 | ||||||
chr10:7787074
|
T | C | 61 | a0001c0001t0002g0273a0001c0001t0002g0303a0001c0001t0002g0321others(58): Show | 78 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.114+746A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787074 | ||||||
chr10:7787081
|
GC | G | 95 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(92): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.114+738delG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787081 | ||||||
chr10:7787147
|
A | G | 1 | a0001c0001t0060g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114+673T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787147 | ||||||
chr10:7787368
|
T | C | 1 | a0001c0001t0005g0324 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.114+452A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787368 | ||||||
chr10:7787468
|
G | T | 1 | a0001c0001t0004g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.114+352C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787468 | ||||||
chr10:7787475
|
A | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0035others(318): Show | 415 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.114+345T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787475 | ||||||
chr10:7787521
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.114+299T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787521 | ||||||
chr10:7787565
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.114+255T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787565 | ||||||
chr10:7787585
|
C | T | 1 | a0001c0001t0006g0082 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.114+235G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787585 | ||||||
chr10:7787761
|
C | G | 1 | a0001c0001t0080g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+59G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787761 | ||||||
chr10:7787796
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0020others(40): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.114+24G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787796 |