geneid | 6498 |
---|---|
ensemblid | ENSG00000136603.15 |
hgncid | 10897 |
symbol | SKIL |
name | SKI like proto-oncogene |
refseq_nuc | NM_005414.5 |
refseq_prot | NP_005405.2 |
ensembl_nuc | ENST00000259119.9 |
ensembl_prot | ENSP00000259119.4 |
mane_status | MANE Select |
chr | chr3 |
start | 170357715 |
end | 170396835 |
strand | + |
ver | v1.2 |
region | chr3:170357715-170396835 |
region5000 | chr3:170352715-170401835 |
regionname0 | SKIL_chr3_170357715_170396835 |
regionname5000 | SKIL_chr3_170352715_170401835 |
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 | 0/1 | 684 | 233 | 34 | 52 | 115 | 7 | 24 | 86 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002 | 1/0 | 684 | 118 | 57 | 17 | 33 | 1 | 9 | 25 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0003 | 0/0 | 684 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0004 | 0/0 | 684 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0005 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0006 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0007 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0008 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0009 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0010 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
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 | 0/1 | 2055 | 221 | 34 | 52 | 103 | 7 | 24 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0002 | 1/0 | 2055 | 116 | 55 | 17 | 33 | 1 | 9 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0003 | 0/0 | 2055 | 12 | 0 | 0 | 12 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0004 | 0/0 | 2055 | 2 | 0 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0005 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0006 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0007 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0008 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0009 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0010 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0011 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0012 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
c0013 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
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 | 5096 | 65 | 12 | 9 | 36 | 1 | 7 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0002 | 0/0 | 5098 | 34 | 1 | 9 | 22 | 2 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0003 | 0/0 | 5095 | 21 | 0 | 13 | 3 | 2 | 3 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0004 | 0/0 | 5095 | 21 | 1 | 5 | 11 | 0 | 4 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0005 | 1/0 | 5101 | 19 | 3 | 7 | 3 | 0 | 5 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0006 | 0/0 | 5092 | 15 | 0 | 1 | 13 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0007 | 0/1 | 5096 | 15 | 0 | 4 | 10 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0008 | 0/0 | 5099 | 14 | 5 | 2 | 5 | 1 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0009 | 0/0 | 5097 | 9 | 2 | 0 | 6 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0010 | 0/0 | 5102 | 8 | 2 | 2 | 3 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0011 | 0/0 | 5104 | 7 | 7 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0012 | 0/0 | 5098 | 7 | 1 | 2 | 0 | 0 | 4 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0013 | 0/0 | 5100 | 6 | 5 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0014 | 0/0 | 5097 | 6 | 0 | 1 | 5 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0015 | 0/0 | 5101 | 5 | 0 | 0 | 5 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0016 | 0/0 | 5095 | 5 | 3 | 1 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0017 | 0/0 | 5101 | 3 | 2 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0018 | 0/0 | 5093 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0019 | 0/0 | 5101 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0020 | 0/0 | 5102 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0021 | 0/0 | 5100 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0022 | 0/0 | 5097 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0023 | 0/0 | 5097 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0024 | 0/0 | 5098 | 3 | 0 | 0 | 3 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0025 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0026 | 0/0 | 5103 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0027 | 0/0 | 5100 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0028 | 0/0 | 5101 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0029 | 0/0 | 5102 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0030 | 0/0 | 5102 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0031 | 0/0 | 5103 | 2 | 1 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0032 | 0/0 | 5104 | 2 | 1 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0033 | 0/0 | 5102 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0034 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0035 | 0/0 | 5105 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0036 | 0/0 | 5097 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0037 | 0/0 | 5099 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0038 | 0/0 | 5101 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0039 | 0/0 | 5097 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0040 | 0/0 | 5096 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0041 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0042 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0043 | 0/0 | 5095 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0044 | 0/0 | 5091 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0045 | 0/0 | 5092 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0046 | 0/0 | 5092 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0047 | 0/0 | 5091 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0048 | 0/0 | 5100 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0049 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0050 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0051 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0052 | 0/0 | 5101 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0053 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0054 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0055 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0056 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0057 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0058 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0059 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0060 | 0/0 | 5099 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0061 | 0/0 | 5095 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0062 | 0/0 | 5095 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0063 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0064 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0065 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0066 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0067 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0068 | 0/0 | 5100 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0069 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0070 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0071 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0072 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0073 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0074 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0075 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0076 | 0/0 | 5095 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0077 | 0/0 | 5095 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0078 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0079 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0080 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0081 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0082 | 0/0 | 5100 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0083 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0084 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0085 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0086 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0087 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0088 | 0/0 | 5100 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
t0089 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
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 | 6 | 0 | 1 | 3 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0002 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0003 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
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 | 0/1 | 2055 | 221 | 34 | 52 | 103 | 7 | 24 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003 | 0/0 | 2055 | 12 | 0 | 0 | 12 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002 | 1/0 | 2055 | 116 | 55 | 17 | 33 | 1 | 9 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0008 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0009 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0003c0004 | 0/0 | 2055 | 2 | 0 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0004c0005 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0005c0006 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0006c0007 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0007c0012 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0008c0011 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0009c0010 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0010c0013 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7150 | 61 | 12 | 8 | 33 | 1 | 7 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0002 | 0/0 | 7152 | 33 | 0 | 9 | 22 | 2 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0003 | 0/0 | 7149 | 21 | 0 | 13 | 3 | 2 | 3 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0004 | 0/0 | 7149 | 19 | 1 | 5 | 10 | 0 | 3 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0007 | 0/1 | 7150 | 12 | 0 | 4 | 7 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0008 | 0/0 | 7153 | 14 | 5 | 2 | 5 | 1 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0009 | 0/0 | 7151 | 8 | 2 | 0 | 5 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0012 | 0/0 | 7152 | 5 | 1 | 0 | 0 | 0 | 4 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0014 | 0/0 | 7151 | 4 | 0 | 1 | 3 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0016 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0021 | 0/0 | 7154 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0022 | 0/0 | 7151 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0023 | 0/0 | 7151 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0024 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0036 | 0/0 | 7151 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0037 | 0/0 | 7153 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0038 | 0/0 | 7155 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0039 | 0/0 | 7151 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0040 | 0/0 | 7150 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0060 | 0/0 | 7153 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0061 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0062 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0063 | 0/0 | 7150 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0064 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0065 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0067 | 0/0 | 7151 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0068 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0069 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0070 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0071 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0072 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0073 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0074 | 0/0 | 7151 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0075 | 0/0 | 7148 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0077 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0078 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0079 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0083 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0084 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0085 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0086 | 0/0 | 7151 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0001t0087 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0004 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0007 | 0/0 | 7150 | 3 | 0 | 0 | 3 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0014 | 0/0 | 7151 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0024 | 0/0 | 7152 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0043 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0076 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0081 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0001c0003t0082 | 0/0 | 7154 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0002 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0005 | 1/0 | 7155 | 19 | 3 | 7 | 3 | 0 | 5 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0006 | 0/0 | 7146 | 15 | 0 | 1 | 13 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0010 | 0/0 | 7156 | 8 | 2 | 2 | 3 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0011 | 0/0 | 7158 | 7 | 7 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0013 | 0/0 | 7154 | 6 | 5 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0015 | 0/0 | 7155 | 5 | 0 | 0 | 5 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0016 | 0/0 | 7149 | 4 | 3 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0017 | 0/0 | 7155 | 3 | 2 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0018 | 0/0 | 7147 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0019 | 0/0 | 7155 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0020 | 0/0 | 7156 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0025 | 0/0 | 7157 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0026 | 0/0 | 7157 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0027 | 0/0 | 7154 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0028 | 0/0 | 7155 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0029 | 0/0 | 7156 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0030 | 0/0 | 7156 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0031 | 0/0 | 7157 | 2 | 1 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0032 | 0/0 | 7158 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0033 | 0/0 | 7156 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0034 | 0/0 | 7157 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0035 | 0/0 | 7159 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0041 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0042 | 0/0 | 7157 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0044 | 0/0 | 7145 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0045 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0046 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0047 | 0/0 | 7145 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0049 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0051 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0052 | 0/0 | 7155 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0053 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0054 | 0/0 | 7155 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0055 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0056 | 0/0 | 7155 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0057 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0058 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0059 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0088 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0002t0089 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0008t0050 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0002c0009t0032 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0003c0004t0004 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0003c0004t0080 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0004c0005t0012 | 0/0 | 7152 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0005c0006t0001 | 0/0 | 7150 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0006c0007t0048 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0007c0012t0009 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0008c0011t0001 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0009c0010t0001 | 0/0 | 7150 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
a0010c0013t0066 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | copy fasta | chr3 | 170352715 | 170401835 |
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 | 3 | 0 | 1 | 1 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0002 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0012g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0014g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0016g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0021g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0022g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0022g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0023g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0023g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0023g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0024g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0036g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0036g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0037g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0037g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0038g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0038g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0039g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0040g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0040g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0060g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0061g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0062g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0063g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0064g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0065g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0067g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0068g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0069g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0070g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0071g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0072g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0073g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0074g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0075g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0077g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0078g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0079g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0083g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0084g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0085g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0086g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0001t0087g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0014g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0024g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0024g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0043g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0076g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0081g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0001c0003t0082g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0015g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0015g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0016g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0016g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0017g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0017g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0017g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0018g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0018g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0018g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0020g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0020g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0025g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0025g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0026g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0026g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0027g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0027g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0028g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0028g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0029g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0029g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0030g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0030g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0031g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0031g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0032g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0033g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0033g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0034g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0035g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0035g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0041g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0042g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0044g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0045g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0046g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0047g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0049g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0051g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0052g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0053g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0054g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0055g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0056g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0057g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0058g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0059g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0088g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0002t0089g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0008t0050g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0002c0009t0032g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0003c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0003c0004t0080g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0004c0005t0012g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0004c0005t0012g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0005c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0005c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0006c0007t0048g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0007c0012t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0008c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0009c0010t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
a0010c0013t0066g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | GBR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0157 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00323 | hp2 | a0001 | c0001 | t0075 | g0234 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00423 | hp1 | a0001 | c0001 | t0072 | g0086 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00423 | hp2 | a0001 | c0001 | t0084 | g0060 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00438 | hp2 | a0001 | c0003 | t0007 | g0077 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00558 | hp2 | a0002 | c0002 | t0006 | g0258 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00609 | hp2 | a0001 | c0001 | t0085 | g0001 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00621 | hp1 | a0008 | c0011 | t0001 | g0114 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00639 | hp1 | a0001 | c0001 | t0036 | g0104 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00673 | hp1 | a0001 | c0001 | t0008 | g0088 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00673 | hp2 | a0001 | c0001 | t0040 | g0055 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00735 | hp1 | a0001 | c0001 | t0063 | g0165 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00735 | hp2 | a0001 | c0001 | t0073 | g0076 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01069 | hp1 | a0002 | c0002 | t0005 | g0017 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01070 | hp1 | a0001 | c0001 | t0038 | g0152 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01071 | hp1 | a0002 | c0002 | t0005 | g0256 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01081 | hp2 | a0002 | c0002 | t0005 | g0249 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01099 | hp1 | a0002 | c0002 | t0010 | g0017 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01106 | hp2 | a0002 | c0002 | t0005 | g0257 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01109 | hp1 | a0001 | c0001 | t0037 | g0072 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01109 | hp2 | a0001 | c0001 | t0037 | g0113 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01168 | hp2 | a0002 | c0002 | t0026 | g0305 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01169 | hp2 | a0002 | c0002 | t0026 | g0306 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01175 | hp1 | a0002 | c0002 | t0032 | g0253 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01243 | hp1 | a0009 | c0010 | t0001 | g0171 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01243 | hp2 | a0002 | c0002 | t0013 | g0272 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0330 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01256 | hp1 | a0001 | c0001 | t0023 | g0108 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01257 | hp2 | a0004 | c0005 | t0012 | g0071 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01258 | hp1 | a0004 | c0005 | t0012 | g0075 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01358 | hp1 | a0002 | c0002 | t0017 | g0304 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01358 | hp2 | a0001 | c0001 | t0070 | g0106 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0090 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01361 | hp2 | a0002 | c0002 | t0010 | g0016 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01433 | hp2 | a0002 | c0002 | t0016 | g0026 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01496 | hp2 | a0002 | c0002 | t0005 | g0242 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01884 | hp2 | a0002 | c0002 | t0034 | g0295 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01891 | hp2 | a0002 | c0002 | t0031 | g0003 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0190 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01928 | hp2 | a0002 | c0002 | t0005 | g0255 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01952 | hp1 | a0001 | c0001 | t0014 | g0057 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01952 | hp2 | a0001 | c0001 | t0060 | g0194 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01978 | hp1 | a0002 | c0002 | t0018 | g0318 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02040 | hp1 | a0001 | c0003 | t0004 | g0084 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02055 | hp1 | a0002 | c0002 | t0013 | g0296 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02055 | hp2 | a0002 | c0002 | t0088 | g0309 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02056 | hp1 | a0002 | c0002 | t0029 | g0260 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02071 | hp1 | a0002 | c0002 | t0005 | g0245 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02071 | hp2 | a0002 | c0002 | t0018 | g0314 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02074 | hp2 | a0002 | c0002 | t0010 | g0248 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02080 | hp2 | a0002 | c0002 | t0029 | g0264 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02135 | hp2 | a0002 | c0002 | t0005 | g0213 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02145 | hp1 | a0002 | c0002 | t0053 | g0282 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02148 | hp2 | a0001 | c0001 | t0007 | g0059 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02257 | hp1 | a0002 | c0002 | t0020 | g0283 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02257 | hp2 | a0001 | c0001 | t0074 | g0007 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02258 | hp1 | a0001 | c0001 | t0067 | g0139 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02258 | hp2 | a0002 | c0002 | t0011 | g0273 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02273 | hp2 | a0001 | c0001 | t0065 | g0094 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0002 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02280 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02293 | hp2 | a0002 | c0002 | t0006 | g0326 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02451 | hp1 | a0002 | c0002 | t0041 | g0331 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02451 | hp2 | a0002 | c0002 | t0011 | g0269 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02572 | hp1 | a0002 | c0002 | t0013 | g0274 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02572 | hp2 | a0002 | c0002 | t0020 | g0278 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02615 | hp1 | a0002 | c0002 | t0034 | g0018 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02622 | hp1 | a0002 | c0002 | t0058 | g0027 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02622 | hp2 | a0002 | c0002 | t0035 | g0004 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02630 | hp1 | a0002 | c0002 | t0027 | g0298 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02630 | hp2 | a0002 | c0002 | t0010 | g0292 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02647 | hp2 | a0002 | c0002 | t0005 | g0288 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02698 | hp1 | a0001 | c0001 | t0086 | g0034 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02698 | hp2 | a0001 | c0001 | t0036 | g0038 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02717 | hp1 | a0002 | c0002 | t0019 | g0212 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02723 | hp1 | a0002 | c0002 | t0059 | g0028 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02723 | hp2 | a0001 | c0001 | t0021 | g0041 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02738 | hp1 | a0003 | c0004 | t0080 | g0227 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02809 | hp1 | a0002 | c0002 | t0016 | g0022 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02809 | hp2 | a0002 | c0002 | t0011 | g0268 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02818 | hp1 | a0002 | c0002 | t0054 | g0294 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02818 | hp2 | a0002 | c0002 | t0016 | g0025 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02886 | hp1 | a0002 | c0002 | t0035 | g0018 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02886 | hp2 | a0002 | c0002 | t0005 | g0289 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02896 | hp1 | a0002 | c0002 | t0005 | g0290 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02896 | hp2 | a0002 | c0002 | t0025 | g0303 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02897 | hp2 | a0002 | c0002 | t0017 | g0299 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02922 | hp1 | a0002 | c0002 | t0011 | g0271 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02922 | hp2 | a0002 | c0002 | t0051 | g0334 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02965 | hp1 | a0001 | c0001 | t0087 | g0065 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02965 | hp2 | a0002 | c0002 | t0033 | g0293 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02970 | hp1 | a0002 | c0009 | t0032 | g0287 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02976 | hp1 | a0002 | c0008 | t0050 | g0019 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02976 | hp2 | a0002 | c0002 | t0011 | g0267 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03041 | hp1 | a0001 | c0001 | t0022 | g0042 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03041 | hp2 | a0006 | c0007 | t0048 | g0310 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03098 | hp1 | a0002 | c0002 | t0055 | g0291 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03098 | hp2 | a0001 | c0001 | t0022 | g0078 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03139 | hp1 | a0002 | c0002 | t0011 | g0004 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03139 | hp2 | a0001 | c0001 | t0071 | g0040 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03209 | hp1 | a0001 | c0001 | t0068 | g0196 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03209 | hp2 | a0002 | c0002 | t0030 | g0285 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03225 | hp1 | a0002 | c0002 | t0020 | g0277 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03239 | hp2 | a0002 | c0002 | t0056 | g0244 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03453 | hp1 | a0002 | c0002 | t0011 | g0004 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03453 | hp2 | a0002 | c0002 | t0049 | g0019 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03486 | hp1 | a0002 | c0002 | t0027 | g0307 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03486 | hp2 | a0002 | c0002 | t0033 | g0332 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03490 | hp1 | a0001 | c0001 | t0012 | g0049 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03491 | hp1 | a0001 | c0001 | t0062 | g0151 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03491 | hp2 | a0002 | c0002 | t0005 | g0241 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03492 | hp1 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0070 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03516 | hp1 | a0002 | c0002 | t0057 | g0023 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03540 | hp2 | a0002 | c0002 | t0013 | g0270 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03579 | hp1 | a0002 | c0002 | t0013 | g0297 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03654 | hp2 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03669 | hp2 | a0001 | c0001 | t0083 | g0035 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03688 | hp1 | a0001 | c0001 | t0012 | g0073 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0180 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0182 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03710 | hp2 | a0002 | c0002 | t0010 | g0016 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0315 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03831 | hp2 | a0010 | c0013 | t0066 | g0137 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03834 | hp1 | a0002 | c0002 | t0005 | g0251 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0239 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04115 | hp1 | a0003 | c0004 | t0004 | g0223 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04204 | hp1 | a0002 | c0002 | t0031 | g0250 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04204 | hp2 | a0001 | c0001 | t0012 | g0074 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG04228 | hp2 | a0001 | c0001 | t0038 | g0141 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18522 | hp1 | a0002 | c0002 | t0025 | g0302 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18522 | hp2 | a0002 | c0002 | t0019 | g0276 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18612 | hp1 | a0002 | c0002 | t0010 | g0246 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18939 | hp1 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18939 | hp2 | a0002 | c0002 | t0015 | g0263 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18942 | hp1 | a0001 | c0001 | t0024 | g0217 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18942 | hp2 | a0001 | c0003 | t0024 | g0046 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18948 | hp1 | a0001 | c0001 | t0077 | g0221 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18949 | hp2 | a0002 | c0002 | t0006 | g0325 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18950 | hp1 | a0001 | c0001 | t0008 | g0185 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18950 | hp2 | a0002 | c0002 | t0006 | g0323 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18951 | hp2 | a0002 | c0002 | t0044 | g0311 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18953 | hp2 | a0002 | c0002 | t0006 | g0316 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18964 | hp2 | a0002 | c0002 | t0006 | g0317 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18967 | hp1 | a0001 | c0001 | t0008 | g0177 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18967 | hp2 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18969 | hp1 | a0002 | c0002 | t0006 | g0319 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18969 | hp2 | a0001 | c0003 | t0014 | g0173 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18971 | hp1 | a0001 | c0001 | t0040 | g0048 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18971 | hp2 | a0005 | c0006 | t0001 | g0135 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18973 | hp1 | a0001 | c0001 | t0014 | g0174 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18973 | hp2 | a0002 | c0002 | t0015 | g0265 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18975 | hp1 | a0002 | c0002 | t0006 | g0329 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18978 | hp2 | a0001 | c0001 | t0061 | g0132 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18979 | hp1 | a0002 | c0002 | t0005 | g0240 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18981 | hp1 | a0002 | c0002 | t0006 | g0313 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18982 | hp1 | a0002 | c0002 | t0006 | g0324 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18982 | hp2 | a0002 | c0002 | t0052 | g0254 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18983 | hp1 | a0001 | c0003 | t0024 | g0052 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18984 | hp1 | a0001 | c0001 | t0016 | g0031 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18984 | hp2 | a0001 | c0003 | t0076 | g0082 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18991 | hp1 | a0001 | c0003 | t0007 | g0176 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18991 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18993 | hp1 | a0001 | c0003 | t0007 | g0175 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18993 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18994 | hp2 | a0002 | c0002 | t0006 | g0328 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19000 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19004 | hp2 | a0002 | c0002 | t0046 | g0322 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19006 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19006 | hp2 | a0002 | c0002 | t0015 | g0261 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19007 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19009 | hp2 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19010 | hp1 | a0001 | c0001 | t0023 | g0062 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19010 | hp2 | a0001 | c0001 | t0023 | g0191 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19011 | hp1 | a0001 | c0003 | t0014 | g0202 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19011 | hp2 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19030 | hp1 | a0001 | c0001 | t0069 | g0047 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19030 | hp2 | a0001 | c0001 | t0064 | g0181 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19043 | hp1 | a0002 | c0002 | t0016 | g0024 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19043 | hp2 | a0002 | c0002 | t0017 | g0301 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19054 | hp2 | a0001 | c0003 | t0082 | g0134 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19056 | hp2 | a0001 | c0003 | t0043 | g0083 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19057 | hp2 | a0002 | c0002 | t0010 | g0247 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19065 | hp1 | a0002 | c0002 | t0015 | g0262 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19066 | hp1 | a0001 | c0001 | t0079 | g0058 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19066 | hp2 | a0002 | c0002 | t0006 | g0321 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19067 | hp1 | a0002 | c0002 | t0018 | g0327 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19068 | hp2 | a0002 | c0002 | t0015 | g0259 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19070 | hp2 | a0007 | c0012 | t0009 | g0001 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19075 | hp1 | a0002 | c0002 | t0006 | g0333 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19080 | hp1 | a0001 | c0001 | t0078 | g0066 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19080 | hp2 | a0002 | c0002 | t0006 | g0312 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19081 | hp2 | a0002 | c0002 | t0045 | g0266 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19087 | hp1 | a0005 | c0006 | t0001 | g0153 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19087 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19088 | hp1 | a0001 | c0003 | t0081 | g0006 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19089 | hp1 | a0002 | c0002 | t0047 | g0320 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19240 | hp1 | a0002 | c0002 | t0089 | g0308 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0101 | EUR | TSI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20752 | hp2 | a0002 | c0002 | t0042 | g0300 | EUR | TSI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20905 | hp1 | a0002 | c0002 | t0005 | g0243 | SAS | GIH | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02109 | hp1 | a0002 | c0002 | t0019 | g0279 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02109 | hp2 | a0001 | c0001 | t0022 | g0007 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02486 | hp2 | a0002 | c0002 | t0030 | g0284 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG02559 | hp2 | a0001 | c0001 | t0021 | g0064 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03471 | hp1 | a0002 | c0002 | t0013 | g0275 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG03471 | hp2 | a0002 | c0002 | t0028 | g0281 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG06807 | hp1 | a0001 | c0001 | t0021 | g0039 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20300 | hp1 | a0002 | c0002 | t0028 | g0280 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
NA21309 | hp2 | a0002 | c0002 | t0010 | g0286 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0081 | REF | REF | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0005 | g0252 | REF | REF | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:170360444
|
C | T | 8 | a0001a0003a0004others(5): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
missense_variant | MODERATE | c.113C>T | p.Ala38Val | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 795/7155 | 113/2055 | 38/684 | chr3 | 170360444 | ||
chr3:170360534
|
A | G | 1 | a0010 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.203A>G | p.His68Arg | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 885/7155 | 203/2055 | 68/684 | chr3 | 170360534 | ||
chr3:170360536
|
G | C | 1 | a0006 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.205G>C | p.Val69Leu | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 887/7155 | 205/2055 | 69/684 | chr3 | 170360536 | ||
chr3:170360905
|
A | G | 1 | a0005 | 2 | NA18971.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.574A>G | p.Ile192Val | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1256/7155 | 574/2055 | 192/684 | chr3 | 170360905 | ||
chr3:170360929
|
G | C | 1 | a0009 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.598G>C | p.Asp200His | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1280/7155 | 598/2055 | 200/684 | chr3 | 170360929 | ||
chr3:170381326
|
C | G | 1 | a0007 | 1 | NA19070.hp2 | stop_gained | HIGH | c.1181C>G | p.Ser394* | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/7 | 1863/7155 | 1181/2055 | 394/684 | chr3 | 170381326 | ||
chr3:170384760
|
G | A | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1424G>A | p.Arg475His | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/7 | 2106/7155 | 1424/2055 | 475/684 | chr3 | 170384760 | ||
chr3:170390318
|
G | A | 1 | a0003 | 2 | HG02738.hp1 HG04115.hp1 |
missense_variant | MODERATE | c.1525G>A | p.Val509Ile | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/7 | 2207/7155 | 1525/2055 | 509/684 | chr3 | 170390318 | ||
chr3:170392359
|
T | A | 1 | a0004 | 2 | HG01257.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.1997T>A | p.Met666Lys | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2679/7155 | 1997/2055 | 666/684 | chr3 | 170392359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:170360628
|
C | T | 1 | a0002c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.297C>T | p.Ser99Ser | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 979/7155 | 297/2055 | 99/684 | chr3 | 170360628 | ||
chr3:170360682
|
G | A | 1 | a0002c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.351G>A | p.Ser117Ser | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1033/7155 | 351/2055 | 117/684 | chr3 | 170360682 | ||
chr3:170361039
|
A | G | 1 | a0001c0003 | 12 | HG00438.hp2 HG02040.hp1 NA18942.hp2 others(9): Show |
synonymous_variant | LOW | c.708A>G | p.Pro236Pro | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1390/7155 | 708/2055 | 236/684 | chr3 | 170361039 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:170357742
|
A | ACGG | 5 | a0002c0002t0017a0002c0002t0025a0002c0002t0026others(2): Show | 9 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-642_-640dupCGG | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/7 | 2574 | INFO_REALIGN_3_PRIME | chr3 | 170357742 | ||||
chr3:170359722
|
A | G | 1 | a0002c0002t0089 | 1 | NA19240.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-610A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | chr3 | 170359722 | ||||||
chr3:170359731
|
G | A | 1 | a0001c0003t0043 | 1 | NA19056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-601G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 601 | chr3 | 170359731 | |||||
chr3:170359883
|
A | G | 1 | a0002c0002t0088 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-449A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 449 | chr3 | 170359883 | |||||
chr3:170359925
|
A | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
5_prime_UTR_variant | MODIFIER | c.-407A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 407 | chr3 | 170359925 | |||||
chr3:170359987
|
T | G | 6 | a0002c0002t0006a0002c0002t0018a0002c0002t0044others(3): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-345T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 345 | chr3 | 170359987 | |||||
chr3:170360033
|
T | A | 1 | a0006c0007t0048 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-299T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 299 | chr3 | 170360033 | |||||
chr3:170360110
|
C | T | 1 | a0001c0001t0087 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-222C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 222 | chr3 | 170360110 | |||||
chr3:170360146
|
A | G | 1 | a0001c0001t0086 | 1 | HG02698.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-186A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | chr3 | 170360146 | ||||||
chr3:170360215
|
A | G | 1 | a0001c0001t0085 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-117A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 117 | chr3 | 170360215 | |||||
chr3:170392481
|
G | C | 1 | a0006c0007t0048 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 64 | chr3 | 170392481 | |||||
chr3:170392544
|
T | G | 2 | a0002c0002t0049a0002c0008t0050 | 2 | HG02976.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*127T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 127 | chr3 | 170392544 | |||||
chr3:170392630
|
TA | T | 2 | a0001c0001t0023a0002c0002t0047 | 4 | HG01256.hp1 NA19010.hp1 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*220delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 220 | INFO_REALIGN_3_PRIME | chr3 | 170392630 | ||||
chr3:170392630
|
TAA | T | 23 | a0001c0001t0004a0001c0001t0007a0001c0001t0014others(20): Show | 61 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*220delAA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 219 | INFO_REALIGN_3_PRIME | chr3 | 170392630 | ||||
chr3:170392659
|
A | G | 1 | a0001c0001t0074 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 242 | chr3 | 170392659 | |||||
chr3:170392741
|
T | A | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 324 | chr3 | 170392741 | |||||
chr3:170392886
|
T | C | 1 | a0002c0002t0057 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 469 | chr3 | 170392886 | |||||
chr3:170392895
|
C | T | 1 | a0001c0001t0073 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 478 | chr3 | 170392895 | |||||
chr3:170393012
|
C | T | 2 | a0001c0001t0022a0001c0001t0074 | 4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*595C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 595 | chr3 | 170393012 | |||||
chr3:170393020
|
C | T | 2 | a0001c0001t0040a0001c0001t0084 | 3 | HG00423.hp2 HG00673.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 603 | chr3 | 170393020 | |||||
chr3:170393061
|
C | G | 1 | a0002c0002t0056 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 644 | chr3 | 170393061 | |||||
chr3:170393115
|
T | G | 2 | a0002c0002t0058a0002c0002t0059 | 2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 698 | chr3 | 170393115 | |||||
chr3:170393143
|
A | G | 1 | a0002c0002t0055 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 726 | chr3 | 170393143 | |||||
chr3:170393151
|
A | G | 1 | a0001c0001t0072 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*734A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 734 | chr3 | 170393151 | |||||
chr3:170393164
|
TTTTG | T | 6 | a0002c0002t0006a0002c0002t0018a0002c0002t0044others(3): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*756delTTGT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 753 | INFO_REALIGN_3_PRIME | chr3 | 170393164 | ||||
chr3:170393184
|
G | A | 1 | a0001c0001t0060 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 767 | chr3 | 170393184 | |||||
chr3:170393278
|
A | G | 6 | a0002c0002t0011a0002c0002t0013a0002c0002t0033others(3): Show | 20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*861A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 861 | chr3 | 170393278 | |||||
chr3:170393443
|
C | T | 1 | a0001c0001t0071 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1026 | chr3 | 170393443 | |||||
chr3:170393522
|
A | G | 2 | a0001c0001t0083a0001c0001t0086 | 2 | HG02698.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1105 | chr3 | 170393522 | |||||
chr3:170393564
|
A | T | 1 | a0001c0001t0070 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1147 | chr3 | 170393564 | |||||
chr3:170393578
|
A | G | 1 | a0001c0001t0069 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1161 | chr3 | 170393578 | |||||
chr3:170394115
|
A | AT | 4 | a0002c0002t0010a0002c0002t0020a0002c0002t0029others(1): Show | 15 | HG01099.hp1 HG01361.hp2 HG02056.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1729dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
A | ATT | 4 | a0002c0002t0031a0002c0002t0033a0002c0002t0053others(1): Show | 6 | HG01891.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1728_*1729dupTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
A | ATTT | 5 | a0002c0002t0032a0002c0002t0034a0002c0002t0049others(2): Show | 6 | HG01175.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1727_*1729dupTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
A | ATTTT | 4 | a0002c0002t0011a0002c0002t0035a0002c0002t0089others(1): Show | 11 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1729dupTTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
A | T | 2 | a0001c0001t0068a0002c0002t0088 | 2 | HG02055.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1698A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1698 | chr3 | 170394115 | |||||
chr3:170394115
|
ATT | A | 4 | a0001c0001t0021a0001c0001t0024a0001c0003t0024others(1): Show | 9 | HG01358.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1728_*1729delTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1728 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
ATTT | A | 11 | a0001c0001t0008a0001c0001t0014a0001c0001t0060others(8): Show | 30 | HG00423.hp2 HG00673.hp1 HG01361.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1727_*1729delTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1727 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
ATTTT | A | 31 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(28): Show | 122 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1729delTTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1726 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
ATTTTT | A | 17 | a0001c0001t0001a0001c0001t0012a0001c0001t0016others(14): Show | 87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1725_*1729delTTTT others(1): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1725 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
ATTTTTT | A | 3 | a0001c0001t0003a0001c0001t0061a0001c0001t0062 | 23 | HG00140.hp1 HG00280.hp1 HG01168.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1729delTTTT others(2): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1724 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394115
|
ATTTTTTT others(7): Show |
A | 2 | a0002c0002t0058a0002c0002t0059 | 2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716_*1729delTTTT others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1716 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | ||||
chr3:170394155
|
G | A | 1 | a0002c0002t0020 | 3 | HG02257.hp1 HG02572.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1738 | chr3 | 170394155 | |||||
chr3:170394191
|
A | G | 2 | a0001c0001t0022a0001c0001t0074 | 4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1774A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1774 | chr3 | 170394191 | |||||
chr3:170394193
|
C | G | 2 | a0002c0002t0058a0002c0002t0059 | 2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1776C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1776 | chr3 | 170394193 | |||||
chr3:170394251
|
C | T | 2 | a0002c0002t0030a0002c0002t0055 | 3 | HG02486.hp2 HG03098.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1834C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1834 | chr3 | 170394251 | |||||
chr3:170394355
|
A | G | 1 | a0001c0001t0069 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1938 | chr3 | 170394355 | |||||
chr3:170394519
|
T | G | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*2102T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2102 | chr3 | 170394519 | |||||
chr3:170394584
|
G | A | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2167G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2167 | chr3 | 170394584 | |||||
chr3:170394712
|
C | T | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2295 | chr3 | 170394712 | |||||
chr3:170394744
|
A | G | 1 | a0002c0002t0042 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2327 | chr3 | 170394744 | |||||
chr3:170394894
|
A | G | 1 | a0002c0002t0046 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2477A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2477 | chr3 | 170394894 | |||||
chr3:170395037
|
T | G | 1 | a0002c0002t0052 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2620T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2620 | chr3 | 170395037 | |||||
chr3:170395070
|
A | G | 3 | a0002c0002t0049a0002c0002t0051a0002c0008t0050 | 3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2653A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2653 | chr3 | 170395070 | |||||
chr3:170395166
|
T | G | 3 | a0001c0001t0061a0002c0002t0015a0002c0002t0029 | 8 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2749T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2749 | chr3 | 170395166 | |||||
chr3:170395185
|
C | T | 1 | a0001c0001t0079 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2768C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2768 | chr3 | 170395185 | |||||
chr3:170395268
|
T | C | 1 | a0001c0001t0065 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2851T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2851 | chr3 | 170395268 | |||||
chr3:170395310
|
G | A | 2 | a0001c0001t0022a0001c0001t0074 | 4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2893G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2893 | chr3 | 170395310 | |||||
chr3:170395359
|
C | T | 1 | a0001c0003t0081 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2942C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2942 | chr3 | 170395359 | |||||
chr3:170395486
|
A | C | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3069A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3069 | chr3 | 170395486 | |||||
chr3:170395499
|
C | T | 1 | a0001c0001t0073 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3082C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3082 | chr3 | 170395499 | |||||
chr3:170395529
|
A | G | 1 | a0001c0001t0062 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3112A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3112 | chr3 | 170395529 | |||||
chr3:170395689
|
T | A | 1 | a0002c0002t0045 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3272T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3272 | chr3 | 170395689 | |||||
chr3:170395693
|
G | A | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*3276G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3276 | chr3 | 170395693 | |||||
chr3:170395745
|
G | A | 1 | a0001c0001t0063 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3328G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3328 | chr3 | 170395745 | |||||
chr3:170395813
|
G | A | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*3396G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3396 | chr3 | 170395813 | |||||
chr3:170395918
|
A | AT | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*3511dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3512 | INFO_REALIGN_3_PRIME | chr3 | 170395918 | ||||
chr3:170395918
|
A | ATT | 5 | a0001c0001t0012a0001c0001t0037a0001c0001t0039others(2): Show | 12 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3510_*3511dupTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3512 | INFO_REALIGN_3_PRIME | chr3 | 170395918 | ||||
chr3:170395998
|
T | C | 1 | a0001c0001t0064 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3581T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3581 | chr3 | 170395998 | |||||
chr3:170396010
|
GT | G | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | 199 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*3609delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3609 | INFO_REALIGN_3_PRIME | chr3 | 170396010 | ||||
chr3:170396042
|
G | A | 1 | a0001c0001t0067 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3625 | chr3 | 170396042 | |||||
chr3:170396290
|
A | C | 40 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(37): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*3873A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3873 | chr3 | 170396290 | |||||
chr3:170396344
|
T | C | 1 | a0002c0002t0033 | 2 | HG02965.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3927T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3927 | chr3 | 170396344 | |||||
chr3:170396375
|
A | G | 3 | a0001c0001t0078a0001c0001t0079a0002c0002t0019 | 5 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3958A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3958 | chr3 | 170396375 | |||||
chr3:170396432
|
A | G | 1 | a0002c0002t0026 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4015A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4015 | chr3 | 170396432 | |||||
chr3:170396446
|
T | C | 6 | a0002c0002t0015a0002c0002t0019a0002c0002t0020others(3): Show | 16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4029T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4029 | chr3 | 170396446 | |||||
chr3:170396622
|
A | G | 1 | a0002c0002t0059 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4205A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4205 | chr3 | 170396622 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:170357913
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(242): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-634+150G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170357913 | ||||||
chr3:170358043
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0009g0020 | 2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-634+280G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358043 | ||||||
chr3:170358045
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(234): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-634+282C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358045 | ||||||
chr3:170358136
|
C | G | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-634+373C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358136 | ||||||
chr3:170358142
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0016g0031 | 3 | NA18948.hp2 NA18984.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-634+379C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358142 | ||||||
chr3:170358218
|
C | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(325): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-634+455C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358218 | ||||||
chr3:170358227
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-634+464G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358227 | ||||||
chr3:170358357
|
C | T | 1 | a0001c0001t0008g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-634+594C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358357 | ||||||
chr3:170358458
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0007g0015 | 2 | HG00741.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-634+695C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358458 | ||||||
chr3:170358495
|
G | T | 3 | a0002c0002t0049g0019a0002c0002t0051g0334a0002c0008t0050g0019 | 3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-634+732G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358495 | ||||||
chr3:170358514
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-634+751G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358514 | ||||||
chr3:170358531
|
C | T | 1 | a0002c0002t0006g0333 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-634+768C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358531 | ||||||
chr3:170358588
|
C | T | 1 | a0002c0002t0033g0332 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-634+825C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358588 | ||||||
chr3:170358783
|
C | T | 24 | a0001c0001t0004g0014a0001c0001t0004g0216a0001c0001t0004g0219others(21): Show | 25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-633-916C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358783 | ||||||
chr3:170358808
|
T | C | 1 | a0002c0002t0006g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-633-891T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358808 | ||||||
chr3:170359314
|
G | A | 7 | a0002c0002t0015g0259a0002c0002t0015g0261a0002c0002t0015g0262others(4): Show | 7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-633-385G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359314 | ||||||
chr3:170359442
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-633-257A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359442 | ||||||
chr3:170359571
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-633-128C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359571 | ||||||
chr3:170359597
|
A | G | 1 | a0001c0001t0003g0215 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-633-102A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359597 | ||||||
chr3:170359598
|
G | A | 3 | a0001c0001t0003g0215a0001c0001t0083g0035a0001c0001t0086g0034 | 3 | HG01168.hp1 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-633-101G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359598 | ||||||
chr3:170359598
|
G | GA | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-633-88dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 170359598 | |||||
chr3:170359598
|
GA | G | 22 | a0002c0002t0005g0330a0002c0002t0006g0258a0002c0002t0006g0312others(19): Show | 22 | HG00558.hp2 HG01255.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-633-88delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 170359598 | |||||
chr3:170361452
|
T | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+23T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361452 | ||||||
chr3:170361530
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1098+101A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361530 | ||||||
chr3:170361594
|
T | A | 9 | a0002c0002t0011g0267a0002c0002t0011g0268a0002c0002t0011g0269others(6): Show | 9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+165T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361594 | ||||||
chr3:170361742
|
CT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1098+329delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170361742 | |||||
chr3:170361873
|
C | T | 1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1098+444C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361873 | ||||||
chr3:170361909
|
T | G | 16 | a0002c0002t0015g0259a0002c0002t0015g0261a0002c0002t0015g0262others(13): Show | 16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+480T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361909 | ||||||
chr3:170362028
|
A | G | 1 | a0002c0002t0013g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1098+599A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362028 | ||||||
chr3:170362364
|
G | A | 2 | a0001c0001t0008g0036a0001c0001t0008g0037 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1098+935G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362364 | ||||||
chr3:170362462
|
A | C | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+1033A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362462 | ||||||
chr3:170362498
|
C | A | 1 | a0001c0001t0036g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1098+1069C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362498 | ||||||
chr3:170362511
|
AAAAC | A | 3 | a0001c0001t0002g0195a0002c0002t0041g0331a0002c0002t0089g0308 | 3 | HG02451.hp1 NA19060.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1098+1093_1098+109 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170362511 | |||||
chr3:170362544
|
CAATG | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1098+1120_1098+112 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170362544 | |||||
chr3:170362709
|
G | C | 3 | a0002c0002t0006g0312a0002c0002t0006g0333a0002c0002t0044g0311 | 3 | NA18951.hp2 NA19075.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1098+1280G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362709 | ||||||
chr3:170362778
|
A | G | 12 | a0001c0001t0002g0013a0001c0001t0002g0186a0001c0001t0002g0187others(9): Show | 12 | HG01433.hp1 HG01928.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+1349A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362778 | ||||||
chr3:170362964
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(260): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1098+1535C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362964 | ||||||
chr3:170363281
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1098+1852C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363281 | ||||||
chr3:170363545
|
G | T | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+2116G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363545 | ||||||
chr3:170363546
|
C | T | 24 | a0001c0001t0004g0014a0001c0001t0004g0216a0001c0001t0004g0219others(21): Show | 25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+2117C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363546 | ||||||
chr3:170363682
|
G | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+2253G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363682 | ||||||
chr3:170363901
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1098+2472G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363901 | ||||||
chr3:170363983
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1098+2554C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363983 | ||||||
chr3:170364004
|
G | T | 4 | a0002c0002t0005g0017a0002c0002t0005g0256a0002c0002t0005g0257others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+2575G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364004 | ||||||
chr3:170364137
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+2708G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364137 | ||||||
chr3:170364263
|
C | G | 1 | a0002c0002t0010g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1098+2834C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364263 | ||||||
chr3:170364311
|
CT | C | 48 | a0001c0001t0068g0196a0002c0002t0005g0003a0002c0002t0005g0017others(45): Show | 49 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+2911delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364311
|
CTTTTTT | C | 16 | a0001c0001t0001g0032a0001c0001t0001g0179a0001c0001t0001g0198others(13): Show | 16 | HG00558.hp2 HG01884.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+2906_1098+291 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364311
|
CTTTTTTT | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1098+2905_1098+291 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364311
|
CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0001g0045a0001c0001t0002g0043a0001c0001t0002g0044others(10): Show | 13 | HG01168.hp1 HG02165.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2904_1098+291 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364311
|
CTTTTTTT others(5): Show |
C | 19 | a0002c0002t0011g0004a0002c0002t0011g0268a0002c0002t0011g0269others(16): Show | 20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+2900_1098+291 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364311
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0011g0267 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+2899_1098+291 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | |||||
chr3:170364354
|
G | C | 6 | a0002c0002t0027g0298a0002c0002t0027g0307a0002c0002t0049g0019others(3): Show | 6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+2925G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364354 | ||||||
chr3:170364393
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1098+2964A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364393 | ||||||
chr3:170364412
|
C | G | 1 | a0001c0001t0008g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1098+2983C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364412 | ||||||
chr3:170364422
|
C | T | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1098+2993C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364422 | ||||||
chr3:170364497
|
G | A | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+3068G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364497 | ||||||
chr3:170364706
|
A | G | 1 | a0001c0003t0014g0173 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1098+3277A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364706 | ||||||
chr3:170364773
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+3344A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364773 | ||||||
chr3:170364877
|
G | T | 1 | a0002c0002t0015g0265 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1098+3448G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364877 | ||||||
chr3:170364887
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(335): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1098+3458C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364887 | ||||||
chr3:170364935
|
T | A | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1098+3506T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364935 | ||||||
chr3:170365095
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+3666C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365095 | ||||||
chr3:170365165
|
CAA | C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+3737_1098+373 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365165 | ||||||
chr3:170365512
|
A | G | 7 | a0002c0002t0015g0259a0002c0002t0015g0261a0002c0002t0015g0262others(4): Show | 7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+4083A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365512 | ||||||
chr3:170365752
|
C | CTTT | 7 | a0002c0002t0011g0268a0002c0002t0027g0298a0002c0002t0027g0307others(4): Show | 7 | HG02630.hp1 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+4342_1098+434 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTT | 7 | a0002c0002t0017g0301a0002c0002t0017g0304a0002c0002t0025g0302others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+4340_1098+434 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(4): Show |
1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1098+4334_1098+434 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0068g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1098+4333_1098+434 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0088g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1098+4332_1098+434 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(8): Show |
5 | a0002c0002t0011g0267a0002c0002t0011g0269a0002c0002t0011g0271others(2): Show | 5 | HG01243.hp2 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+4330_1098+434 others(19): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(9): Show |
5 | a0002c0002t0011g0004a0002c0002t0011g0273a0002c0002t0013g0274others(2): Show | 6 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+4329_1098+434 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(10): Show |
6 | a0002c0002t0013g0275a0002c0002t0013g0296a0002c0002t0013g0297others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4328_1098+434 others(21): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(14): Show |
3 | a0002c0002t0006g0316a0002c0002t0006g0317a0002c0002t0045g0266 | 3 | NA18953.hp2 NA18964.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1098+4324_1098+434 others(25): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(15): Show |
6 | a0002c0002t0006g0319a0002c0002t0006g0321a0002c0002t0006g0323others(3): Show | 6 | HG01978.hp1 NA18950.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(26): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(18): Show |
1 | a0002c0002t0006g0324 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(29): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(19): Show |
3 | a0002c0002t0006g0258a0002c0002t0006g0325a0002c0002t0044g0311 | 3 | HG00558.hp2 NA18949.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(30): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(20): Show |
4 | a0002c0002t0006g0326a0002c0002t0006g0329a0002c0002t0006g0333others(1): Show | 4 | HG02293.hp2 NA18975.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(31): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(21): Show |
1 | a0002c0002t0006g0328 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(32): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
C | CTTTTTTT others(24): Show |
1 | a0002c0002t0006g0312 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(35): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
CTTT | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0172a0001c0001t0001g0184others(3): Show | 6 | HG00544.hp1 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4342_1098+434 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
CTTTT | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+4341_1098+434 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365752
|
CTTTTT | C | 145 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0067others(142): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1098+4340_1098+434 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | |||||
chr3:170365794
|
C | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+4365C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365794 | ||||||
chr3:170365796
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+4367C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365796 | ||||||
chr3:170365797
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0037g0113 | 2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1098+4368C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365797 | ||||||
chr3:170365816
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1098+4387C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365816 | ||||||
chr3:170365841
|
C | G | 51 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(48): Show | 52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1098+4412C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365841 | ||||||
chr3:170365941
|
A | G | 5 | a0001c0003t0004g0084a0001c0003t0007g0175a0001c0003t0007g0176others(2): Show | 5 | HG02040.hp1 NA18984.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+4512A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365941 | ||||||
chr3:170366019
|
G | A | 2 | a0001c0001t0001g0115a0008c0011t0001g0114 | 2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1098+4590G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366019 | ||||||
chr3:170366055
|
C | CT | 8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0172others(5): Show | 8 | HG00597.hp2 HG00609.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+4644dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366055 | |||||
chr3:170366055
|
CT | C | 8 | a0001c0001t0001g0116a0001c0001t0002g0085a0001c0001t0003g0117others(5): Show | 8 | HG00323.hp1 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+4644delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366055 | |||||
chr3:170366056
|
T | C | 1 | a0002c0002t0042g0300 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1098+4627T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366056 | ||||||
chr3:170366170
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1098+4741A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366170 | ||||||
chr3:170366365
|
C | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+4936C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366365 | ||||||
chr3:170366388
|
C | T | 4 | a0001c0001t0007g0080a0001c0001t0007g0081a0001c0001t0083g0035others(1): Show | 4 | HG01069.hp2 HG02698.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+4959C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366388 | ||||||
chr3:170366415
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0037g0113 | 2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1098+4986C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366415 | ||||||
chr3:170366479
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5050G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366479 | ||||||
chr3:170366547
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1098+5118A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366547 | ||||||
chr3:170366552
|
C | A | 8 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+5123C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366552 | ||||||
chr3:170366688
|
C | CACACACA others(7): Show |
1 | a0002c0002t0016g0022 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | |||||
chr3:170366688
|
C | CACACACA others(5): Show |
8 | a0002c0002t0016g0024a0002c0002t0016g0025a0002c0002t0016g0026others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | |||||
chr3:170366688
|
C | CACACACA others(3): Show |
1 | a0002c0002t0017g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | |||||
chr3:170366690
|
C | CACACACA others(13): Show |
1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(24): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366690 | |||||
chr3:170366690
|
C | CAG | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+5262_1098+526 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366690 | |||||
chr3:170366692
|
C | CACACACA others(9): Show |
2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | |||||
chr3:170366692
|
C | CACACAGA others(7): Show |
2 | a0001c0001t0001g0119a0001c0001t0002g0214 | 2 | HG03669.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | |||||
chr3:170366692
|
C | CAGACACA others(3): Show |
7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0009g0079others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+5264_1098+526 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | |||||
chr3:170366694
|
C | CACAGACA others(5): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0121 | 4 | HG00639.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366694 | |||||
chr3:170366694
|
C | G | 1 | a0002c0002t0005g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1098+5265C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366694 | ||||||
chr3:170366696
|
G | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0116a0001c0001t0001g0118others(41): Show | 45 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1098+5267G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366696 | ||||||
chr3:170366696
|
G | GACAC | 5 | a0001c0001t0069g0047a0001c0001t0072g0086a0002c0002t0005g0288others(2): Show | 5 | HG00423.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+5283_1098+528 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACAC | 4 | a0002c0002t0010g0292a0002c0002t0030g0284a0002c0002t0030g0285others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+5281_1098+528 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(1): Show |
10 | a0002c0002t0013g0275a0002c0002t0026g0305a0002c0002t0026g0306others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+5279_1098+528 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(3): Show |
35 | a0002c0002t0005g0290a0002c0002t0011g0004a0002c0002t0011g0267others(32): Show | 36 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+5277_1098+528 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(5): Show |
4 | a0001c0001t0068g0196a0002c0002t0005g0330a0002c0002t0019g0276others(1): Show | 4 | HG01255.hp2 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+5275_1098+528 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(3): Show |
10 | a0001c0001t0002g0085a0001c0001t0002g0103a0001c0001t0002g0105others(7): Show | 11 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(5): Show |
200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(197): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(7): Show |
7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01981.hp1 HG02970.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366696
|
G | GACACACA others(11): Show |
1 | a0001c0001t0004g0087 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1098+5274_1098+527 others(22): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | |||||
chr3:170366700
|
C | G | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1098+5271C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366700 | ||||||
chr3:170366716
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(240): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1098+5287T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366716 | ||||||
chr3:170366777
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5348C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366777 | ||||||
chr3:170367036
|
GTTTAC | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0197 | 3 | NA19056.hp1 NA19057.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1098+5610_1098+561 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367036 | |||||
chr3:170367059
|
C | G | 24 | a0001c0001t0004g0014a0001c0001t0004g0216a0001c0001t0004g0219others(21): Show | 25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+5630C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367059 | ||||||
chr3:170367091
|
T | A | 6 | a0002c0002t0027g0298a0002c0002t0027g0307a0002c0002t0049g0019others(3): Show | 6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+5662T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367091 | ||||||
chr3:170367137
|
C | G | 2 | a0002c0002t0015g0263a0002c0002t0029g0264 | 2 | HG02080.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1098+5708C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367137 | ||||||
chr3:170367149
|
A | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1098+5720A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367149 | ||||||
chr3:170367175
|
G | C | 2 | a0001c0001t0002g0103a0001c0001t0036g0104 | 2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1098+5746G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367175 | ||||||
chr3:170367244
|
G | T | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+5815G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367244 | ||||||
chr3:170367343
|
G | T | 2 | a0002c0002t0026g0305a0002c0002t0026g0306 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1098+5914G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367343 | ||||||
chr3:170367430
|
C | G | 5 | a0001c0003t0004g0084a0001c0003t0007g0175a0001c0003t0007g0176others(2): Show | 5 | HG02040.hp1 NA18984.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+6001C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367430 | ||||||
chr3:170367463
|
CT | C | 9 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+6049delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367463 | |||||
chr3:170367464
|
T | C | 1 | a0002c0002t0010g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1098+6035T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367464 | ||||||
chr3:170367476
|
TTTA | T | 26 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0131others(23): Show | 26 | HG00323.hp1 HG00558.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.1098+6048_1098+605 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367476 | ||||||
chr3:170367477
|
TTA | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1098+6049_1098+605 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367477 | ||||||
chr3:170367478
|
TA | T | 3 | a0002c0002t0041g0331a0002c0002t0058g0027a0002c0002t0059g0028 | 3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+6052delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367478 | |||||
chr3:170367479
|
A | T | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+6050A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367479 | ||||||
chr3:170367481
|
A | G | 3 | a0002c0002t0049g0019a0002c0002t0051g0334a0002c0008t0050g0019 | 3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+6052A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367481 | ||||||
chr3:170367623
|
C | T | 1 | a0001c0001t0009g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1098+6194C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367623 | ||||||
chr3:170367624
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1098+6195A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367624 | ||||||
chr3:170367780
|
T | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1098+6351T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367780 | ||||||
chr3:170367979
|
C | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+6550C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367979 | ||||||
chr3:170368144
|
A | G | 1 | a0001c0001t0007g0211 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1098+6715A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368144 | ||||||
chr3:170368222
|
G | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1098+6793G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368222 | ||||||
chr3:170368308
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1098+6879A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368308 | ||||||
chr3:170368349
|
A | AT | 14 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(11): Show | 14 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+6927dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170368349 | |||||
chr3:170368395
|
A | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+6966A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368395 | ||||||
chr3:170368402
|
T | C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+6973T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368402 | ||||||
chr3:170368432
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+7003A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368432 | ||||||
chr3:170368674
|
GACAA | G | 7 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0169others(4): Show | 7 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+7250_1098+725 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170368674 | |||||
chr3:170368694
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1098+7265G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368694 | ||||||
chr3:170368946
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0133 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1098+7517G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368946 | ||||||
chr3:170369082
|
A | AT | 16 | a0002c0002t0005g0257a0002c0002t0017g0301a0002c0002t0025g0302others(13): Show | 16 | HG01106.hp2 HG01169.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+7677dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | |||||
chr3:170369082
|
A | ATT | 6 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(3): Show | 6 | HG01358.hp1 HG01433.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+7676_1098+767 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | |||||
chr3:170369082
|
AT | A | 22 | a0002c0002t0005g0241a0002c0002t0006g0258a0002c0002t0006g0312others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+7677delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | |||||
chr3:170369082
|
ATTTTTTT | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1098+7671_1098+767 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | |||||
chr3:170369082
|
ATTTTTTT others(1): Show |
A | 9 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0012g0049others(6): Show | 9 | HG00639.hp2 HG02280.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+7670_1098+767 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | |||||
chr3:170369274
|
AAAAC | A | 4 | a0002c0002t0005g0017a0002c0002t0005g0256a0002c0002t0005g0257others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+7849_1098+785 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369274 | |||||
chr3:170369324
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+7895G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369324 | ||||||
chr3:170369456
|
C | T | 11 | a0001c0001t0008g0182a0001c0001t0012g0049a0001c0001t0012g0050others(8): Show | 11 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+8027C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369456 | ||||||
chr3:170369461
|
A | AGGCAATC others(9): Show |
1 | a0002c0002t0005g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1098+8033_1098+804 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369461 | |||||
chr3:170369482
|
A | G | 1 | a0002c0002t0005g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1098+8053A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369482 | ||||||
chr3:170369487
|
C | T | 1 | a0002c0002t0031g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1098+8058C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369487 | ||||||
chr3:170369645
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+8216G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369645 | ||||||
chr3:170370055
|
T | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+8626T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370055 | ||||||
chr3:170370119
|
G | C | 1 | a0001c0001t0008g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+8690G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370119 | ||||||
chr3:170370156
|
G | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+8727G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370156 | ||||||
chr3:170370224
|
G | C | 24 | a0001c0001t0004g0014a0001c0001t0004g0216a0001c0001t0004g0219others(21): Show | 25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+8795G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370224 | ||||||
chr3:170370233
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1098+8804C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370233 | ||||||
chr3:170370320
|
A | G | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1098+8891A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370320 | ||||||
chr3:170370404
|
A | G | 1 | a0002c0002t0005g0249 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1098+8975A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370404 | ||||||
chr3:170370421
|
C | CAG | 53 | a0001c0001t0001g0061a0001c0001t0002g0013a0001c0001t0002g0015others(50): Show | 54 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1098+9009_1098+901 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370421 | |||||
chr3:170370432
|
A | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+9003A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370432 | ||||||
chr3:170370438
|
A | C | 8 | a0002c0002t0005g0245a0002c0002t0017g0299a0002c0002t0017g0301others(5): Show | 8 | HG01358.hp1 HG02071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+9009A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370438 | ||||||
chr3:170370439
|
G | C | 2 | a0002c0002t0005g0245a0002c0002t0010g0246 | 2 | HG02071.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1098+9010G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | ||||||
chr3:170370439
|
G | GA | 24 | a0001c0001t0002g0008a0001c0001t0002g0044a0001c0001t0002g0112others(21): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | ||||||
chr3:170370439
|
G | GAGC | 38 | a0001c0001t0002g0085a0001c0001t0002g0091a0001c0001t0002g0092others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | ||||||
chr3:170370439
|
G | GAGCC | 8 | a0001c0001t0002g0103a0001c0001t0002g0195a0001c0001t0004g0216others(5): Show | 8 | HG00642.hp2 HG00741.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | ||||||
chr3:170370439
|
G | GC | 16 | a0001c0001t0001g0033a0001c0001t0001g0120a0001c0001t0001g0121others(13): Show | 16 | HG00639.hp2 HG01175.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1098+9026dupC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | |||||
chr3:170370439
|
GC | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+9026delC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | |||||
chr3:170370439
|
GCC | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(52): Show | 59 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+9025_1098+902 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | |||||
chr3:170370439
|
GCCC | G | 17 | a0001c0001t0063g0165a0001c0001t0068g0196a0002c0002t0005g0290others(14): Show | 17 | HG00735.hp1 HG01433.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1098+9024_1098+902 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | |||||
chr3:170370439
|
GCCCC | G | 26 | a0002c0002t0011g0004a0002c0002t0011g0267a0002c0002t0011g0268others(23): Show | 27 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1098+9023_1098+902 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | |||||
chr3:170370440
|
C | A | 29 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0169others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1098+9011C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370440 | ||||||
chr3:170370440
|
C | G | 24 | a0001c0001t0002g0008a0001c0001t0002g0044a0001c0001t0002g0112others(21): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1098+9011C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370440 | ||||||
chr3:170370441
|
C | A | 3 | a0002c0002t0015g0263a0002c0002t0015g0265a0002c0002t0029g0264 | 3 | HG02080.hp2 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1098+9012C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370441 | ||||||
chr3:170370441
|
C | G | 31 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0169others(28): Show | 31 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1098+9012C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370441 | ||||||
chr3:170370442
|
C | G | 3 | a0002c0002t0015g0263a0002c0002t0015g0265a0002c0002t0029g0264 | 3 | HG02080.hp2 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1098+9013C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370442 | ||||||
chr3:170370442
|
C | T | 1 | a0002c0002t0005g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1098+9013C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370442 | ||||||
chr3:170370443
|
C | G | 1 | a0002c0002t0013g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1098+9014C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370443 | ||||||
chr3:170370443
|
C | T | 1 | a0002c0002t0005g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1098+9014C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370443 | ||||||
chr3:170370449
|
C | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+9020C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370449 | ||||||
chr3:170370450
|
C | A | 1 | a0002c0002t0020g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+9021C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370450 | ||||||
chr3:170370451
|
C | A | 6 | a0001c0001t0004g0014a0001c0001t0004g0219a0001c0001t0004g0220others(3): Show | 7 | NA18747.hp1 NA18942.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+9022C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370451 | ||||||
chr3:170370453
|
C | T | 2 | a0002c0002t0015g0261a0002c0002t0015g0262 | 2 | NA19006.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1098+9024C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370453 | ||||||
chr3:170370456
|
G | C | 1 | a0001c0001t0077g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1098+9027G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370456 | ||||||
chr3:170370492
|
A | G | 1 | a0001c0001t0021g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1098+9063A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370492 | ||||||
chr3:170370660
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1098+9231C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370660 | ||||||
chr3:170370819
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1098+9390C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370819 | ||||||
chr3:170370855
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1098+9426G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370855 | ||||||
chr3:170371008
|
A | G | 6 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0328others(3): Show | 6 | HG00558.hp2 NA18951.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+9579A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371008 | ||||||
chr3:170371025
|
T | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+9596T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371025 | ||||||
chr3:170371191
|
G | A | 1 | a0002c0002t0052g0254 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1098+9762G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371191 | ||||||
chr3:170371327
|
C | T | 1 | a0001c0001t0007g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1098+9898C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371327 | ||||||
chr3:170371351
|
A | T | 1 | a0002c0002t0019g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1099-9893A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371351 | ||||||
chr3:170371379
|
C | T | 6 | a0001c0001t0003g0117a0001c0001t0003g0127a0001c0001t0003g0149others(3): Show | 6 | HG01261.hp1 HG01981.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-9865C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371379 | ||||||
chr3:170371536
|
A | G | 1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-9708A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371536 | ||||||
chr3:170371567
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-9677T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371567 | ||||||
chr3:170372105
|
ATTAAG | A | 9 | a0002c0002t0006g0313a0002c0002t0006g0315a0002c0002t0006g0317others(6): Show | 9 | HG02071.hp2 HG03831.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-9136_1099-913 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372105 | |||||
chr3:170372218
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-9026A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372218 | ||||||
chr3:170372586
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1099-8658A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372586 | ||||||
chr3:170372599
|
C | G | 1 | a0002c0002t0005g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1099-8645C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372599 | ||||||
chr3:170372615
|
G | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-8629G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372615 | ||||||
chr3:170372767
|
T | C | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099-8477T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372767 | ||||||
chr3:170372895
|
A | G | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-8349A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372895 | ||||||
chr3:170372944
|
C | T | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-8300C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372944 | ||||||
chr3:170372973
|
T | C | 6 | a0002c0002t0027g0298a0002c0002t0027g0307a0002c0002t0049g0019others(3): Show | 6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-8271T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372973 | ||||||
chr3:170372988
|
A | AT | 78 | a0001c0001t0001g0138a0001c0001t0002g0008a0001c0001t0002g0013others(75): Show | 79 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1099-8239dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372988 | |||||
chr3:170372988
|
A | ATT | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(184): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1099-8240_1099-823 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372988 | |||||
chr3:170372988
|
A | T | 2 | a0002c0002t0026g0305a0002c0002t0026g0306 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1099-8256A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372988 | ||||||
chr3:170373049
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0003g0117a0001c0001t0003g0127others(5): Show | 8 | HG01070.hp1 HG01261.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-8195G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373049 | ||||||
chr3:170373066
|
C | T | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-8178C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373066 | ||||||
chr3:170373205
|
C | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-8039C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373205 | ||||||
chr3:170373214
|
T | C | 1 | a0001c0001t0003g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099-8030T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373214 | ||||||
chr3:170373260
|
G | A | 1 | a0005c0006t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1099-7984G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373260 | ||||||
chr3:170373325
|
C | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-7919C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373325 | ||||||
chr3:170373387
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1099-7857C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373387 | ||||||
chr3:170373422
|
T | TC | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-7820dupC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170373422 | |||||
chr3:170373545
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1099-7699T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373545 | ||||||
chr3:170373701
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-7543A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373701 | ||||||
chr3:170373722
|
CAAAAAAA others(4): Show |
C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-7510_1099-750 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170373722 | |||||
chr3:170373741
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1099-7503A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373741 | ||||||
chr3:170373796
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1099-7448C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373796 | ||||||
chr3:170373856
|
T | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-7388T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373856 | ||||||
chr3:170373884
|
A | G | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-7360A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373884 | ||||||
chr3:170373958
|
C | G | 8 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-7286C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373958 | ||||||
chr3:170374047
|
A | T | 1 | a0001c0001t0036g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1099-7197A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374047 | ||||||
chr3:170374060
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-7184G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374060 | ||||||
chr3:170374114
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(278): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1099-7130C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374114 | ||||||
chr3:170374265
|
AG | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1099-6977delG | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170374265 | |||||
chr3:170374269
|
A | C | 51 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(48): Show | 52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1099-6975A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374269 | ||||||
chr3:170374293
|
G | A | 2 | a0004c0005t0012g0071a0004c0005t0012g0075 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1099-6951G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374293 | ||||||
chr3:170374451
|
A | G | 1 | a0001c0001t0014g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1099-6793A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374451 | ||||||
chr3:170374919
|
A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-6325A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374919 | ||||||
chr3:170375020
|
A | T | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-6224A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375020 | ||||||
chr3:170375175
|
T | G | 2 | a0002c0002t0016g0022a0002c0002t0057g0023 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1099-6069T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375175 | ||||||
chr3:170375271
|
A | C | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-5973A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375271 | ||||||
chr3:170375296
|
A | G | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-5948A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375296 | ||||||
chr3:170375340
|
T | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-5904T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375340 | ||||||
chr3:170375363
|
G | T | 4 | a0001c0001t0022g0007a0001c0001t0022g0042a0001c0001t0022g0078others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-5881G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375363 | ||||||
chr3:170375364
|
C | A | 4 | a0001c0001t0022g0007a0001c0001t0022g0042a0001c0001t0022g0078others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-5880C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375364 | ||||||
chr3:170375364
|
C | G | 1 | a0001c0001t0023g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1099-5880C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375364 | ||||||
chr3:170375365
|
T | A | 1 | a0001c0001t0023g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1099-5879T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375365 | ||||||
chr3:170375459
|
G | C | 1 | a0001c0001t0009g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1099-5785G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375459 | ||||||
chr3:170375542
|
A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5702A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375542 | ||||||
chr3:170375569
|
A | G | 6 | a0002c0002t0027g0298a0002c0002t0027g0307a0002c0002t0049g0019others(3): Show | 6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-5675A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375569 | ||||||
chr3:170375592
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-5652C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375592 | ||||||
chr3:170375731
|
C | T | 2 | a0002c0002t0027g0298a0002c0002t0027g0307 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1099-5513C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375731 | ||||||
chr3:170375751
|
A | AT | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1099-5485dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170375751 | |||||
chr3:170375800
|
G | A | 1 | a0001c0001t0040g0055 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1099-5444G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375800 | ||||||
chr3:170375917
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5327T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375917 | ||||||
chr3:170375972
|
A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5272A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375972 | ||||||
chr3:170376042
|
C | CT | 16 | a0001c0001t0002g0091a0001c0001t0002g0192a0001c0001t0004g0220others(13): Show | 16 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-5179dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | |||||
chr3:170376042
|
CT | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(121): Show | 128 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1099-5179delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | |||||
chr3:170376042
|
CTT | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0032others(22): Show | 27 | HG00639.hp2 HG01884.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099-5180_1099-517 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | |||||
chr3:170376042
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0009t0032g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-5192_1099-517 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | |||||
chr3:170376101
|
G | A | 2 | a0002c0002t0027g0298a0002c0002t0027g0307 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1099-5143G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376101 | ||||||
chr3:170376197
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-5047A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376197 | ||||||
chr3:170376274
|
G | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-4970G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376274 | ||||||
chr3:170376340
|
C | A | 1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-4904C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376340 | ||||||
chr3:170376371
|
A | G | 1 | a0001c0001t0004g0230 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-4873A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376371 | ||||||
chr3:170376402
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-4842G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376402 | ||||||
chr3:170376471
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4773T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376471 | ||||||
chr3:170376472
|
G | T | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4772G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376472 | ||||||
chr3:170376473
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4771T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376473 | ||||||
chr3:170376529
|
C | A | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099-4715C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376529 | ||||||
chr3:170376603
|
T | C | 1 | a0002c0002t0005g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1099-4641T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376603 | ||||||
chr3:170376692
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4552T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376692 | ||||||
chr3:170376787
|
G | T | 3 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0169 | 3 | HG00597.hp2 HG00609.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1099-4457G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376787 | ||||||
chr3:170376795
|
CA | C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-4446delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376795 | |||||
chr3:170376872
|
G | T | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-4372G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376872 | ||||||
chr3:170376875
|
T | C | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1099-4369T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376875 | ||||||
chr3:170376936
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4308A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376936 | ||||||
chr3:170377025
|
C | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4219C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377025 | ||||||
chr3:170377120
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1099-4124T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377120 | ||||||
chr3:170377125
|
C | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4119C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377125 | ||||||
chr3:170377147
|
A | G | 2 | a0001c0001t0004g0229a0001c0001t0075g0234 | 2 | HG00323.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1099-4097A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377147 | ||||||
chr3:170377231
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-4013G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377231 | ||||||
chr3:170377245
|
T | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-3999T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377245 | ||||||
chr3:170377357
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1099-3887T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377357 | ||||||
chr3:170377398
|
C | CT | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1099-3831dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377398 | |||||
chr3:170377493
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(278): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1099-3751T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377493 | ||||||
chr3:170377542
|
C | CT | 31 | a0001c0001t0001g0033a0001c0001t0001g0148a0001c0001t0001g0197others(28): Show | 31 | HG00597.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1099-3678dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | |||||
chr3:170377542
|
CT | C | 15 | a0001c0001t0001g0030a0001c0001t0001g0144a0001c0001t0004g0225others(12): Show | 15 | HG01169.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-3678delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | |||||
chr3:170377542
|
CTTTTTTT others(6): Show |
C | 3 | a0002c0002t0019g0212a0002c0002t0019g0276a0002c0002t0019g0279 | 3 | HG02109.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-3690_1099-367 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | |||||
chr3:170377631
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1099-3613C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377631 | ||||||
chr3:170377639
|
T | A | 1 | a0002c0002t0006g0328 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1099-3605T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377639 | ||||||
chr3:170377652
|
G | A | 1 | a0002c0002t0017g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1099-3592G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377652 | ||||||
chr3:170377696
|
C | CT | 3 | a0001c0001t0002g0043a0001c0001t0002g0100a0001c0001t0002g0195 | 3 | NA18994.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1099-3547dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377696 | |||||
chr3:170377936
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-3308C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377936 | ||||||
chr3:170378110
|
C | T | 3 | a0002c0002t0020g0277a0002c0002t0020g0278a0002c0002t0020g0283 | 3 | HG02257.hp1 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1099-3134C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378110 | ||||||
chr3:170378126
|
C | T | 131 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(128): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1099-3118C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378126 | ||||||
chr3:170378169
|
G | A | 1 | a0002c0002t0005g0255 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1099-3075G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378169 | ||||||
chr3:170378184
|
CCCTG | C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-3056_1099-305 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378184 | |||||
chr3:170378303
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1099-2941G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378303 | ||||||
chr3:170378315
|
G | C | 4 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0025g0302others(1): Show | 4 | HG02896.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-2929G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378315 | ||||||
chr3:170378364
|
T | G | 1 | a0001c0001t0002g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1099-2880T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378364 | ||||||
chr3:170378509
|
C | T | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-2735C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378509 | ||||||
chr3:170378549
|
C | CTT | 24 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0315others(21): Show | 24 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-2694_1099-269 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378549 | |||||
chr3:170378551
|
C | T | 26 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0315others(23): Show | 26 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-2693C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378551 | ||||||
chr3:170378553
|
C | CTTTTTT | 15 | a0001c0001t0001g0116a0001c0001t0001g0154a0001c0001t0001g0172others(12): Show | 15 | HG00323.hp1 HG01069.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-2681_1099-267 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | |||||
chr3:170378553
|
C | CTTTTTTT | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(200): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1099-2682_1099-267 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | |||||
chr3:170378553
|
C | CTTTTTTT others(1): Show |
13 | a0001c0001t0001g0021a0001c0001t0001g0131a0001c0001t0001g0148others(10): Show | 13 | HG01175.hp2 HG01192.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1099-2683_1099-267 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | |||||
chr3:170378553
|
C | T | 27 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(24): Show | 27 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-2691C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378553 | ||||||
chr3:170378583
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1099-2661G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378583 | ||||||
chr3:170378668
|
C | T | 1 | a0002c0002t0019g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-2576C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378668 | ||||||
chr3:170378692
|
C | T | 1 | a0001c0001t0004g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1099-2552C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378692 | ||||||
chr3:170378705
|
C | G | 8 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-2539C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378705 | ||||||
chr3:170378708
|
T | C | 11 | a0001c0001t0008g0182a0001c0001t0012g0049a0001c0001t0012g0050others(8): Show | 11 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2536T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378708 | ||||||
chr3:170378835
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-2409A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378835 | ||||||
chr3:170378849
|
TTTTA | T | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(323): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1099-2363_1099-236 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378849 | |||||
chr3:170378849
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0120a0001c0001t0068g0196a0002c0002t0088g0309 | 3 | HG00639.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-2367_1099-236 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378849 | |||||
chr3:170378881
|
A | T | 9 | a0001c0001t0071g0040a0002c0002t0016g0022a0002c0002t0016g0024others(6): Show | 9 | HG01433.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-2363A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378881 | ||||||
chr3:170378881
|
ATTTT | A | 12 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0004g0014others(9): Show | 13 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-2358_1099-235 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378881 | |||||
chr3:170378885
|
T | A | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1099-2359T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378885 | ||||||
chr3:170379002
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1099-2242G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379002 | ||||||
chr3:170379073
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1099-2171C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379073 | ||||||
chr3:170379077
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(278): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1099-2167G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379077 | ||||||
chr3:170379136
|
C | T | 8 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0070others(5): Show | 8 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-2108C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379136 | ||||||
chr3:170379230
|
G | A | 7 | a0001c0001t0001g0033a0002c0002t0027g0298a0002c0002t0027g0307others(4): Show | 7 | HG02145.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-2014G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379230 | ||||||
chr3:170379265
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1099-1979A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379265 | ||||||
chr3:170379267
|
T | C | 1 | a0001c0001t0021g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1099-1977T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379267 | ||||||
chr3:170379484
|
C | CCT | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(261): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-1759_1099-175 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170379484 | |||||
chr3:170379667
|
C | T | 2 | a0002c0002t0028g0281a0002c0002t0053g0282 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1099-1577C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379667 | ||||||
chr3:170379685
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1099-1559C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379685 | ||||||
chr3:170379690
|
C | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1099-1554C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379690 | ||||||
chr3:170379724
|
C | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(277): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1099-1520C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379724 | ||||||
chr3:170379818
|
G | A | 74 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1099-1426G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379818 | ||||||
chr3:170379855
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0093a0001c0001t0008g0177 | 4 | NA18951.hp1 NA18953.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1389G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379855 | ||||||
chr3:170379893
|
C | T | 1 | a0001c0001t0004g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1099-1351C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379893 | ||||||
chr3:170379906
|
A | G | 1 | a0002c0002t0010g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1099-1338A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379906 | ||||||
chr3:170379938
|
C | T | 4 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0169others(1): Show | 4 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1306C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379938 | ||||||
chr3:170379946
|
T | C | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1099-1298T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379946 | ||||||
chr3:170380050
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-1194A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380050 | ||||||
chr3:170380054
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1099-1190C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380054 | ||||||
chr3:170380067
|
T | C | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-1177T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380067 | ||||||
chr3:170380212
|
G | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-1032G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380212 | ||||||
chr3:170380395
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1099-849C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380395 | ||||||
chr3:170380494
|
A | G | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-750A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380494 | ||||||
chr3:170380567
|
C | T | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-677C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380567 | ||||||
chr3:170380600
|
G | A | 7 | a0002c0002t0015g0259a0002c0002t0015g0261a0002c0002t0015g0262others(4): Show | 7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-644G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380600 | ||||||
chr3:170380603
|
A | C | 1 | a0001c0003t0014g0202 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1099-641A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380603 | ||||||
chr3:170380651
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1099-593A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380651 | ||||||
chr3:170380655
|
A | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(266): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1099-589A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380655 | ||||||
chr3:170380659
|
T | A | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-585T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380659 | ||||||
chr3:170380704
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1099-540A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380704 | ||||||
chr3:170380892
|
A | G | 1 | a0001c0001t0063g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1099-352A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380892 | ||||||
chr3:170380995
|
A | AT | 41 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0116others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-230dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | |||||
chr3:170380995
|
A | ATT | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(196): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1099-231_1099-230d others(4): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | |||||
chr3:170380995
|
A | ATTT | 30 | a0001c0001t0001g0167a0001c0001t0001g0210a0001c0001t0002g0013others(27): Show | 30 | HG00558.hp1 HG00673.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1099-232_1099-230d others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | |||||
chr3:170381047
|
T | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-197T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170381047 | ||||||
chr3:170381201
|
A | G | 1 | a0002c0002t0056g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-43A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170381201 | ||||||
chr3:170381380
|
C | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1196+39C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381380 | ||||||
chr3:170381430
|
A | G | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1196+89A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381430 | ||||||
chr3:170381430
|
ATTAT | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(93): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1196+100_1196+103d others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170381430 | |||||
chr3:170381564
|
C | T | 1 | a0001c0001t0084g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196+223C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381564 | ||||||
chr3:170381590
|
G | A | 6 | a0002c0002t0005g0240a0002c0002t0005g0249a0002c0002t0005g0255others(3): Show | 6 | HG01081.hp2 HG01928.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+249G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381590 | ||||||
chr3:170381605
|
T | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(298): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1196+264T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381605 | ||||||
chr3:170381628
|
T | A | 1 | a0001c0001t0064g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1196+287T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381628 | ||||||
chr3:170381725
|
G | T | 1 | a0003c0004t0004g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1196+384G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381725 | ||||||
chr3:170381819
|
T | C | 1 | a0001c0003t0076g0082 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1196+478T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381819 | ||||||
chr3:170381877
|
C | T | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1196+536C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381877 | ||||||
chr3:170381945
|
G | C | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1196+604G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381945 | ||||||
chr3:170381965
|
C | T | 19 | a0002c0002t0011g0004a0002c0002t0011g0267a0002c0002t0011g0268others(16): Show | 20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1196+624C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381965 | ||||||
chr3:170381971
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1196+630A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381971 | ||||||
chr3:170382036
|
C | T | 17 | a0002c0002t0011g0004a0002c0002t0011g0267a0002c0002t0011g0268others(14): Show | 18 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1196+695C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382036 | ||||||
chr3:170382168
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1196+827G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382168 | ||||||
chr3:170382261
|
TTTGAAA | T | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+922_1196+927d others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382261 | |||||
chr3:170382269
|
A | C | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+928A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382269 | ||||||
chr3:170382413
|
A | AT | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1196+1091dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382413 | |||||
chr3:170382413
|
A | ATT | 7 | a0001c0001t0001g0032a0001c0001t0001g0119a0001c0001t0001g0131others(4): Show | 7 | HG02622.hp1 HG02723.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1196+1090_1196+109 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382413 | |||||
chr3:170382416
|
T | TA | 129 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(126): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1196+1075_1196+107 others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382416 | ||||||
chr3:170382417
|
T | A | 1 | a0001c0001t0007g0080 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1196+1076T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382417 | ||||||
chr3:170382556
|
G | T | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1215G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382556 | ||||||
chr3:170382557
|
C | A | 20 | a0002c0002t0011g0004a0002c0002t0011g0267a0002c0002t0011g0268others(17): Show | 21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1196+1216C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382557 | ||||||
chr3:170382659
|
G | A | 7 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(4): Show | 7 | HG01433.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+1318G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382659 | ||||||
chr3:170382688
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(318): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1196+1347T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382688 | ||||||
chr3:170382718
|
A | AT | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1196+1395dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382718 | |||||
chr3:170382718
|
A | ATT | 16 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0168others(13): Show | 16 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1196+1394_1196+139 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382718 | |||||
chr3:170382749
|
C | T | 1 | a0002c0002t0053g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1196+1408C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382749 | ||||||
chr3:170382875
|
C | T | 5 | a0002c0002t0006g0316a0002c0002t0006g0319a0002c0002t0045g0266others(2): Show | 5 | NA18953.hp2 NA18969.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1534C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382875 | ||||||
chr3:170383028
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1197-1505T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383028 | ||||||
chr3:170383058
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1197-1475T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383058 | ||||||
chr3:170383078
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1197-1455G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383078 | ||||||
chr3:170383116
|
G | C | 1 | a0001c0001t0001g0207 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1197-1417G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383116 | ||||||
chr3:170383252
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1197-1281G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383252 | ||||||
chr3:170383330
|
A | C | 7 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(4): Show | 7 | HG01433.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197-1203A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383330 | ||||||
chr3:170383475
|
T | C | 16 | a0002c0002t0015g0259a0002c0002t0015g0261a0002c0002t0015g0262others(13): Show | 16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1197-1058T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383475 | ||||||
chr3:170383646
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1197-887G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383646 | ||||||
chr3:170383649
|
G | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1197-884G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383649 | ||||||
chr3:170383912
|
G | T | 1 | a0001c0001t0009g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1197-621G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383912 | ||||||
chr3:170384037
|
C | CA | 29 | a0001c0001t0001g0033a0001c0001t0001g0138a0001c0001t0004g0225others(26): Show | 30 | HG01192.hp2 HG01255.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1197-481dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170384037 | |||||
chr3:170384037
|
CA | C | 32 | a0001c0001t0001g0129a0001c0001t0001g0198a0001c0001t0001g0199others(29): Show | 32 | HG00558.hp2 HG01433.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1197-481delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170384037 | |||||
chr3:170384920
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0067g0139 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1429+155T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384920 | ||||||
chr3:170384961
|
A | G | 6 | a0001c0001t0003g0117a0001c0001t0003g0127a0001c0001t0003g0149others(3): Show | 6 | HG01261.hp1 HG01981.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1429+196A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384961 | ||||||
chr3:170384991
|
C | T | 2 | a0002c0002t0010g0286a0002c0009t0032g0287 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1429+226C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384991 | ||||||
chr3:170385134
|
C | T | 8 | a0001c0001t0012g0049a0001c0001t0012g0050a0001c0001t0012g0070others(5): Show | 8 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+369C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385134 | ||||||
chr3:170385171
|
G | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1429+406G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385171 | ||||||
chr3:170385257
|
A | AT | 23 | a0001c0001t0001g0033a0001c0001t0001g0131a0001c0001t0001g0148others(20): Show | 23 | HG01106.hp2 HG01175.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1429+509dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170385257 | |||||
chr3:170385258
|
T | A | 1 | a0001c0001t0014g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1429+493T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385258 | ||||||
chr3:170385536
|
A | G | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+771A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385536 | ||||||
chr3:170385595
|
G | A | 4 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0228others(1): Show | 4 | HG01192.hp2 HG01993.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+830G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385595 | ||||||
chr3:170385804
|
T | C | 131 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(128): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1429+1039T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385804 | ||||||
chr3:170385954
|
C | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1429+1189C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385954 | ||||||
chr3:170386035
|
G | A | 1 | a0002c0002t0013g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1429+1270G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386035 | ||||||
chr3:170386123
|
T | G | 1 | a0002c0002t0020g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1429+1358T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386123 | ||||||
chr3:170386123
|
T | TTTTG | 4 | a0001c0001t0004g0087a0001c0001t0008g0090a0001c0001t0065g0094others(1): Show | 4 | HG01361.hp1 HG01934.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1379_1429+138 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170386123 | |||||
chr3:170386143
|
G | T | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1429+1378G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386143 | ||||||
chr3:170386225
|
G | C | 131 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(128): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1429+1460G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386225 | ||||||
chr3:170386287
|
C | T | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+1522C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386287 | ||||||
chr3:170386318
|
C | T | 1 | a0002c0002t0006g0326 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1429+1553C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386318 | ||||||
chr3:170386319
|
G | A | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+1554G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386319 | ||||||
chr3:170386382
|
G | A | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1429+1617G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386382 | ||||||
chr3:170386390
|
A | C | 2 | a0002c0002t0010g0286a0002c0009t0032g0287 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1429+1625A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386390 | ||||||
chr3:170386429
|
C | T | 1 | a0002c0002t0020g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1429+1664C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386429 | ||||||
chr3:170386469
|
C | G | 1 | a0010c0013t0066g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1429+1704C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386469 | ||||||
chr3:170386552
|
T | G | 2 | a0001c0001t0002g0189a0001c0001t0008g0185 | 2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1429+1787T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386552 | ||||||
chr3:170386618
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1429+1853C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386618 | ||||||
chr3:170386648
|
T | C | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+1883T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386648 | ||||||
chr3:170386658
|
CAG | C | 11 | a0001c0001t0008g0036a0001c0001t0008g0037a0001c0001t0008g0051others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1429+1894_1429+189 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386658 | ||||||
chr3:170386842
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1429+2077T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386842 | ||||||
chr3:170386944
|
A | G | 2 | a0001c0001t0002g0189a0001c0001t0008g0185 | 2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1429+2179A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386944 | ||||||
chr3:170387056
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1429+2291C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387056 | ||||||
chr3:170387057
|
G | A | 5 | a0002c0002t0016g0022a0002c0002t0016g0024a0002c0002t0016g0025others(2): Show | 5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+2292G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387057 | ||||||
chr3:170387281
|
A | G | 2 | a0001c0001t0001g0138a0010c0013t0066g0137 | 2 | HG01255.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1429+2516A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387281 | ||||||
chr3:170387337
|
T | C | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+2572T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387337 | ||||||
chr3:170387349
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1429+2584C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387349 | ||||||
chr3:170387445
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1429+2680C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387445 | ||||||
chr3:170387504
|
T | TTGCATGT others(17): Show |
1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-2717_1430-271 others(28): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387504 | |||||
chr3:170387521
|
ACTT | A | 49 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(46): Show | 50 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1430-2698_1430-269 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387521 | |||||
chr3:170387590
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1430-2633C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387590 | ||||||
chr3:170387591
|
G | A | 1 | a0002c0002t0010g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1430-2632G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387591 | ||||||
chr3:170387645
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1430-2578C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387645 | ||||||
chr3:170387699
|
G | A | 6 | a0002c0002t0027g0298a0002c0002t0027g0307a0002c0002t0049g0019others(3): Show | 6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1430-2524G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387699 | ||||||
chr3:170387719
|
C | T | 1 | a0001c0001t0072g0086 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1430-2504C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387719 | ||||||
chr3:170387759
|
T | TAA | 20 | a0002c0002t0011g0004a0002c0002t0011g0267a0002c0002t0011g0268others(17): Show | 21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1430-2450_1430-244 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | |||||
chr3:170387759
|
T | TAAAAAAA others(2): Show |
119 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0120others(116): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1430-2457_1430-244 others(13): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | |||||
chr3:170387759
|
T | TAAAAAAA others(3): Show |
64 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1430-2458_1430-244 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | |||||
chr3:170387759
|
T | TAAAAAAA others(4): Show |
67 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 69 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1430-2459_1430-244 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | |||||
chr3:170387759
|
T | TAAAAAAA others(5): Show |
8 | a0002c0002t0006g0316a0002c0002t0006g0321a0002c0002t0006g0325others(5): Show | 8 | HG01978.hp1 NA18949.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.1430-2460_1430-244 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | |||||
chr3:170387760
|
A | AAAAAAAA others(3): Show |
1 | a0005c0006t0001g0135 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1430-2454_1430-245 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387760 | |||||
chr3:170387775
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(83): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1430-2448T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387775 | ||||||
chr3:170387851
|
G | A | 1 | a0001c0001t0008g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1430-2372G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387851 | ||||||
chr3:170387859
|
G | A | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-2364G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387859 | ||||||
chr3:170387888
|
C | G | 1 | a0002c0002t0025g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2335C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387888 | ||||||
chr3:170387889
|
C | G | 1 | a0002c0002t0025g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2334C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387889 | ||||||
chr3:170387890
|
C | T | 1 | a0002c0002t0025g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2333C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387890 | ||||||
chr3:170387921
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1430-2302G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387921 | ||||||
chr3:170387933
|
C | CA | 153 | a0001c0001t0001g0021a0001c0001t0001g0179a0001c0001t0002g0008others(150): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1430-2266dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | |||||
chr3:170387933
|
C | CAA | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 125 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1430-2267_1430-226 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | |||||
chr3:170387933
|
C | CAAA | 30 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1430-2268_1430-226 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | |||||
chr3:170388111
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1430-2112C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388111 | ||||||
chr3:170388302
|
T | C | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-1921T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388302 | ||||||
chr3:170388303
|
C | G | 6 | a0001c0001t0004g0014a0001c0001t0004g0219a0001c0001t0004g0220others(3): Show | 7 | NA18747.hp1 NA18942.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1430-1920C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388303 | ||||||
chr3:170388348
|
G | GGTT | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1430-1871_1430-186 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388348 | |||||
chr3:170388361
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1430-1862T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388361 | ||||||
chr3:170388526
|
G | A | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1430-1697G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388526 | ||||||
chr3:170388579
|
T | G | 1 | a0001c0001t0002g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1430-1644T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388579 | ||||||
chr3:170388719
|
C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-1504C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388719 | ||||||
chr3:170388721
|
C | T | 1 | a0002c0002t0010g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1430-1502C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388721 | ||||||
chr3:170388756
|
G | A | 1 | a0001c0001t0038g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1430-1467G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388756 | ||||||
chr3:170388772
|
A | G | 8 | a0002c0002t0017g0299a0002c0002t0017g0301a0002c0002t0017g0304others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-1451A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388772 | ||||||
chr3:170388860
|
G | GTATT | 28 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(25): Show | 28 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1430-1341_1430-133 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388860 | |||||
chr3:170388884
|
T | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(84): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1430-1339T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388884 | ||||||
chr3:170388884
|
T | TTATTTAT others(1): Show |
140 | a0001c0001t0001g0033a0001c0001t0001g0123a0001c0001t0001g0133others(137): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1430-1338_1430-133 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388884 | |||||
chr3:170388884
|
T | TTATTTAT others(5): Show |
13 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0121others(10): Show | 14 | HG00438.hp2 HG00639.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1430-1338_1430-133 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388884 | |||||
chr3:170388911
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1430-1312C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388911 | ||||||
chr3:170388962
|
C | T | 1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1430-1261C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388962 | ||||||
chr3:170389017
|
G | A | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-1206G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389017 | ||||||
chr3:170389018
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0004g0056 | 3 | HG03239.hp1 HG04115.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1430-1205C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389018 | ||||||
chr3:170389084
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1430-1139G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389084 | ||||||
chr3:170389175
|
G | C | 1 | a0001c0001t0004g0087 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1430-1048G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389175 | ||||||
chr3:170389259
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0197 | 3 | NA19056.hp1 NA19057.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1430-964A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389259 | ||||||
chr3:170389267
|
C | A | 9 | a0002c0002t0011g0267a0002c0002t0011g0268a0002c0002t0011g0269others(6): Show | 9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1430-956C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389267 | ||||||
chr3:170389316
|
C | CT | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0002g0103others(7): Show | 10 | HG00642.hp2 HG02071.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1430-892dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170389316 | |||||
chr3:170389400
|
G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-823G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389400 | ||||||
chr3:170389546
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(240): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1430-677C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389546 | ||||||
chr3:170389603
|
C | T | 1 | a0001c0001t0008g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1430-620C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389603 | ||||||
chr3:170389802
|
G | C | 1 | a0001c0001t0007g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1430-421G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389802 | ||||||
chr3:170389872
|
T | C | 1 | a0001c0001t0060g0194 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1430-351T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389872 | ||||||
chr3:170389995
|
C | A | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1430-228C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389995 | ||||||
chr3:170390068
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1430-155T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170390068 | ||||||
chr3:170390543
|
G | T | 1 | a0002c0002t0046g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1671+79G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390543 | ||||||
chr3:170390696
|
A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1671+232A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390696 | ||||||
chr3:170390721
|
C | T | 22 | a0002c0002t0006g0258a0002c0002t0006g0312a0002c0002t0006g0313others(19): Show | 22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1671+257C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390721 | ||||||
chr3:170390778
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1672-258C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390778 | ||||||
chr3:170390804
|
A | T | 1 | a0001c0001t0065g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1672-232A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390804 | ||||||
chr3:170391324
|
C | CT | 6 | a0001c0003t0007g0176a0002c0002t0016g0022a0002c0002t0016g0024others(3): Show | 6 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1896+76dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 170391324 | |||||
chr3:170391391
|
C | T | 1 | a0002c0002t0052g0254 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1896+131C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391391 | ||||||
chr3:170391481
|
A | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1896+221A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391481 | ||||||
chr3:170391615
|
G | A | 1 | a0006c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1896+355G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391615 | ||||||
chr3:170391622
|
G | A | 1 | a0001c0001t0064g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1896+362G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391622 | ||||||
chr3:170391646
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1896+386C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391646 | ||||||
chr3:170391805
|
A | C | 2 | a0001c0001t0068g0196a0002c0002t0088g0309 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1897-454A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391805 | ||||||
chr3:170391825
|
TTA | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(90): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1897-430_1897-429d others(4): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 170391825 | |||||
chr3:170391908
|
A | G | 2 | a0002c0002t0027g0298a0002c0002t0027g0307 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1897-351A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391908 | ||||||
chr3:170392223
|
A | C | 2 | a0002c0002t0058g0027a0002c0002t0059g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1897-36A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170392223 |