geneid | 3099 |
---|---|
ensemblid | ENSG00000159399.10 |
hgncid | 4923 |
symbol | HK2 |
name | hexokinase 2 |
refseq_nuc | NM_000189.5 |
refseq_prot | NP_000180.2 |
ensembl_nuc | ENST00000290573.7 |
ensembl_prot | ENSP00000290573.2 |
mane_status | MANE Select |
chr | chr2 |
start | 74834127 |
end | 74893359 |
strand | + |
ver | v1.2 |
region | chr2:74834127-74893359 |
region5000 | chr2:74829127-74898359 |
regionname0 | HK2_chr2_74834127_74893359 |
regionname5000 | HK2_chr2_74829127_74898359 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 917 | 241 | 33 | 47 | 113 | 15 | 32 | 87 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002 | 0/0 | 917 | 67 | 38 | 4 | 23 | 0 | 2 | 20 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003 | 0/1 | 917 | 61 | 4 | 13 | 33 | 3 | 7 | 26 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004 | 0/0 | 917 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0005 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0006 | 0/0 | 917 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0007 | 0/0 | 917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0008 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0009 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0010 | 0/0 | 917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0011 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0012 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0013 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0014 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0015 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
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 | 0/0 | 2754 | 103 | 11 | 17 | 50 | 8 | 17 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0002 | 1/0 | 2754 | 89 | 5 | 23 | 49 | 5 | 6 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0003 | 0/1 | 2754 | 53 | 3 | 11 | 28 | 3 | 7 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0004 | 0/0 | 2754 | 46 | 24 | 1 | 21 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0005 | 0/0 | 2754 | 17 | 1 | 4 | 7 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0006 | 0/0 | 2754 | 14 | 3 | 1 | 5 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0007 | 0/0 | 2754 | 9 | 7 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0008 | 0/0 | 2754 | 8 | 7 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0009 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0010 | 0/0 | 2754 | 4 | 3 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0011 | 0/0 | 2754 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0012 | 0/0 | 2754 | 3 | 2 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0013 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0014 | 0/0 | 2754 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0015 | 0/0 | 2754 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0016 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0017 | 0/0 | 2754 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0018 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0019 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0020 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0021 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0022 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0023 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0024 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0025 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0026 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0027 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0028 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0029 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0030 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0031 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0032 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0033 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0034 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0035 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0036 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0037 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0038 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0039 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0040 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0041 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0042 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0043 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0044 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0045 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0046 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
c0047 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
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 | 1/0 | 2873 | 90 | 7 | 24 | 48 | 5 | 5 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0002 | 0/0 | 2872 | 78 | 8 | 8 | 41 | 7 | 14 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0003 | 0/0 | 2870 | 58 | 6 | 11 | 33 | 1 | 7 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0004 | 0/0 | 2871 | 19 | 0 | 0 | 17 | 0 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0005 | 0/0 | 2871 | 17 | 0 | 8 | 9 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0006 | 0/0 | 2871 | 16 | 15 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0007 | 0/0 | 2872 | 14 | 3 | 2 | 5 | 1 | 3 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0008 | 0/0 | 2870 | 11 | 0 | 2 | 3 | 2 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0009 | 0/0 | 2871 | 10 | 10 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0010 | 0/0 | 2871 | 10 | 9 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0011 | 0/0 | 2873 | 8 | 2 | 2 | 0 | 1 | 3 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0012 | 0/0 | 2870 | 6 | 5 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0013 | 0/0 | 2871 | 4 | 0 | 0 | 4 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0014 | 0/0 | 2871 | 3 | 0 | 0 | 2 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0015 | 0/0 | 2870 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0016 | 0/0 | 2869 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0017 | 0/0 | 2874 | 3 | 1 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0018 | 0/0 | 2869 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0019 | 0/0 | 2870 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0020 | 0/0 | 2873 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0021 | 0/0 | 2872 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0022 | 0/0 | 2872 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0023 | 0/0 | 2870 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0024 | 0/0 | 2871 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0025 | 0/0 | 2872 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0026 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0027 | 0/0 | 2873 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0028 | 0/0 | 2870 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0029 | 0/0 | 2870 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0030 | 0/0 | 2869 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0031 | 0/0 | 2872 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0032 | 0/0 | 2872 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0033 | 0/0 | 2870 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0034 | 0/0 | 2869 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0035 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0036 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0037 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0038 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0039 | 0/0 | 2870 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0040 | 0/0 | 2872 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0041 | 0/0 | 2870 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0042 | 0/0 | 2870 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0043 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0044 | 0/0 | 2869 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0045 | 0/0 | 2870 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0046 | 0/0 | 2873 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0047 | 0/0 | 2875 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0048 | 0/0 | 2870 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0049 | 0/0 | 2873 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
t0050 | 0/1 | 2870 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0385 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
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 | 0/0 | 2754 | 103 | 11 | 17 | 50 | 8 | 17 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002 | 1/0 | 2754 | 89 | 5 | 23 | 49 | 5 | 6 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005 | 0/0 | 2754 | 17 | 1 | 4 | 7 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006 | 0/0 | 2754 | 14 | 3 | 1 | 5 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0009 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0011 | 0/0 | 2754 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0012 | 0/0 | 2754 | 3 | 2 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0014 | 0/0 | 2754 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0022 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0024 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0030 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0034 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0037 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0039 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004 | 0/0 | 2754 | 46 | 24 | 1 | 21 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007 | 0/0 | 2754 | 9 | 7 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0010 | 0/0 | 2754 | 4 | 3 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0013 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0021 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0023 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0025 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0026 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0035 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0036 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003 | 0/1 | 2754 | 53 | 3 | 11 | 28 | 3 | 7 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0015 | 0/0 | 2754 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0017 | 0/0 | 2754 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0040 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0042 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0044 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0045 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0008 | 0/0 | 2754 | 8 | 7 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0016 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0018 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0041 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0043 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0005c0047 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0006c0046 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0007c0029 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0008c0031 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0009c0019 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0010c0033 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0011c0038 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0012c0032 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0013c0020 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0014c0027 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0015c0028 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5625 | 73 | 8 | 7 | 38 | 7 | 13 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0003 | 0/0 | 5623 | 2 | 0 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0005 | 0/0 | 5624 | 12 | 0 | 6 | 6 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0007 | 0/0 | 5625 | 10 | 2 | 2 | 4 | 0 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0008 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0014 | 0/0 | 5624 | 2 | 0 | 0 | 1 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0040 | 0/0 | 5625 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0001t0041 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0001 | 1/0 | 5626 | 73 | 3 | 20 | 43 | 4 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0011 | 0/0 | 5626 | 7 | 2 | 2 | 0 | 1 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0017 | 0/0 | 5627 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0025 | 0/0 | 5625 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0027 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0036 | 0/0 | 5627 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0046 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0048 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0002t0049 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0001 | 0/0 | 5626 | 4 | 0 | 0 | 1 | 1 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0003 | 0/0 | 5623 | 6 | 0 | 0 | 5 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0005 | 0/0 | 5624 | 2 | 0 | 2 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0007 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0011 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0017 | 0/0 | 5627 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0005t0047 | 0/0 | 5628 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0001 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0003 | 0/0 | 5623 | 6 | 1 | 0 | 3 | 0 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0007 | 0/0 | 5625 | 2 | 0 | 0 | 0 | 1 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0008 | 0/0 | 5623 | 2 | 0 | 1 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0021 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0006t0031 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0009t0015 | 0/0 | 5623 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0009t0034 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0011t0020 | 0/0 | 5626 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0011t0037 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0012t0002 | 0/0 | 5625 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0012t0021 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0012t0022 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0014t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0014t0043 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0022t0001 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0024t0003 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0030t0007 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0034t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0037t0022 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0001c0039t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0004 | 0/0 | 5624 | 17 | 0 | 0 | 17 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0006 | 0/0 | 5624 | 8 | 8 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0009 | 0/0 | 5624 | 5 | 5 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0010 | 0/0 | 5624 | 4 | 4 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0013 | 0/0 | 5624 | 3 | 0 | 0 | 3 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0018 | 0/0 | 5622 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0019 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0023 | 0/0 | 5623 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0026 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0038 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0004t0044 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0006 | 0/0 | 5624 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0010 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0016 | 0/0 | 5622 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0007t0035 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0010t0004 | 0/0 | 5624 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0010t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0010t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0010t0028 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0013t0009 | 0/0 | 5624 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0021t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0023t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0025t0024 | 0/0 | 5624 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0026t0013 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0035t0012 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0002c0036t0004 | 0/0 | 5624 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0003 | 0/0 | 5623 | 41 | 3 | 10 | 23 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0008 | 0/0 | 5623 | 7 | 0 | 1 | 2 | 2 | 2 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0030 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0042 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0003t0050 | 0/1 | 5623 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0015t0001 | 0/0 | 5626 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0017t0003 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0017t0014 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0040t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0042t0033 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0044t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0003c0045t0008 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0008t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0008t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0008t0010 | 0/0 | 5624 | 5 | 4 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0008t0019 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0016t0012 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0018t0024 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0018t0045 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0041t0029 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0004c0043t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0005c0047t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0006c0046t0001 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0007c0029t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0008c0031t0003 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0009c0019t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0010c0033t0002 | 0/0 | 5625 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0011c0038t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0012c0032t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0013c0020t0032 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0014c0027t0039 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
a0015c0028t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | copy fasta | chr2 | 74829127 | 74898359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0014g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0014g0385 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0040g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0041g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0025g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0025g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0027g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0036g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0046g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0048g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0049g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0011g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0017g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0047g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0007g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0008g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0021g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0031g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0034g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0020g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0037g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0002g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0021g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0022g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0014t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0014t0043g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0022t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0024t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0030t0007g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0034t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0037t0022g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0039t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0018g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0019g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0023g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0023g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0026g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0038g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0044g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0035g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0028g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0013t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0013t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0021t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0023t0006g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0025t0024g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0026t0013g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0035t0012g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0036t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0030g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0042g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0050g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0015t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0015t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0017t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0017t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0040t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0042t0033g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0044t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0045t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0019g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0016t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0016t0012g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0018t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0018t0045g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0041t0029g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0043t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0005c0047t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0006c0046t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0007c0029t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0008c0031t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0009c0019t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0010c0033t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0011c0038t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0012c0032t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0013c0020t0032g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0014c0027t0039g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0015c0028t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00099 | hp2 | a0001 | c0001 | t0014 | g0385 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00280 | hp1 | a0001 | c0002 | t0011 | g0325 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00323 | hp1 | a0003 | c0003 | t0003 | g0277 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00323 | hp2 | a0001 | c0006 | t0007 | g0327 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00438 | hp2 | a0003 | c0003 | t0003 | g0063 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00609 | hp2 | a0002 | c0004 | t0013 | g0098 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00639 | hp1 | a0001 | c0039 | t0001 | g0056 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00639 | hp2 | a0003 | c0003 | t0003 | g0087 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0270 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0282 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0264 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00735 | hp1 | a0004 | c0008 | t0010 | g0346 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00738 | hp2 | a0004 | c0041 | t0029 | g0263 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0205 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01069 | hp2 | a0001 | c0005 | t0005 | g0043 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01070 | hp2 | a0003 | c0003 | t0003 | g0085 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0086 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01099 | hp1 | a0003 | c0044 | t0001 | g0077 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01106 | hp1 | a0001 | c0002 | t0011 | g0192 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01109 | hp1 | a0002 | c0025 | t0024 | g0267 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01168 | hp1 | a0001 | c0005 | t0017 | g0084 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0159 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01169 | hp1 | a0001 | c0006 | t0008 | g0251 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01169 | hp2 | a0001 | c0005 | t0047 | g0015 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01175 | hp1 | a0007 | c0029 | t0001 | g0090 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01243 | hp1 | a0002 | c0007 | t0006 | g0106 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01243 | hp2 | a0002 | c0035 | t0012 | g0343 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01255 | hp1 | a0003 | c0042 | t0033 | g0371 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01255 | hp2 | a0003 | c0003 | t0003 | g0059 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01256 | hp2 | a0003 | c0003 | t0008 | g0384 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0374 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01257 | hp2 | a0002 | c0004 | t0023 | g0243 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0375 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0166 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01261 | hp2 | a0001 | c0014 | t0001 | g0078 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01346 | hp2 | a0001 | c0001 | t0041 | g0147 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01358 | hp2 | a0003 | c0003 | t0003 | g0134 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0206 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01496 | hp1 | a0001 | c0002 | t0011 | g0295 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01515 | hp2 | a0003 | c0003 | t0008 | g0307 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01516 | hp1 | a0003 | c0003 | t0008 | g0236 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0215 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0216 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01884 | hp1 | a0004 | c0043 | t0012 | g0177 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01884 | hp2 | a0004 | c0008 | t0019 | g0189 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01891 | hp1 | a0014 | c0027 | t0039 | g0382 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01891 | hp2 | a0004 | c0008 | t0010 | g0349 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0378 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01952 | hp2 | a0003 | c0003 | t0003 | g0377 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01978 | hp1 | a0001 | c0005 | t0005 | g0068 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01978 | hp2 | a0001 | c0002 | t0027 | g0066 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02015 | hp1 | a0003 | c0003 | t0008 | g0260 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02027 | hp1 | a0001 | c0002 | t0049 | g0290 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02040 | hp1 | a0002 | c0004 | t0004 | g0362 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02040 | hp2 | a0003 | c0045 | t0008 | g0261 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02055 | hp1 | a0001 | c0012 | t0022 | g0332 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02055 | hp2 | a0001 | c0009 | t0015 | g0356 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02056 | hp1 | a0003 | c0017 | t0003 | g0224 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02083 | hp2 | a0003 | c0003 | t0003 | g0016 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02132 | hp1 | a0001 | c0006 | t0003 | g0142 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02132 | hp2 | a0001 | c0006 | t0001 | g0046 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02135 | hp2 | a0002 | c0007 | t0035 | g0007 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02145 | hp1 | a0001 | c0006 | t0021 | g0109 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02145 | hp2 | a0003 | c0040 | t0001 | g0071 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02257 | hp1 | a0002 | c0004 | t0018 | g0317 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02258 | hp1 | a0001 | c0002 | t0011 | g0304 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0114 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02280 | hp1 | a0001 | c0011 | t0037 | g0244 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02280 | hp2 | a0002 | c0004 | t0018 | g0230 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0376 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02300 | hp2 | a0010 | c0033 | t0002 | g0157 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02451 | hp1 | a0002 | c0010 | t0028 | g0338 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02451 | hp2 | a0002 | c0004 | t0006 | g0357 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02602 | hp2 | a0001 | c0012 | t0002 | g0369 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02615 | hp1 | a0002 | c0004 | t0009 | g0337 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02615 | hp2 | a0004 | c0008 | t0010 | g0350 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02622 | hp1 | a0001 | c0037 | t0022 | g0360 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02622 | hp2 | a0002 | c0004 | t0006 | g0231 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02630 | hp1 | a0002 | c0004 | t0038 | g0348 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02630 | hp2 | a0002 | c0010 | t0006 | g0232 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02647 | hp2 | a0002 | c0007 | t0016 | g0200 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02683 | hp2 | a0003 | c0003 | t0003 | g0154 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0367 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02698 | hp2 | a0003 | c0003 | t0042 | g0020 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02717 | hp2 | a0002 | c0004 | t0010 | g0246 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02723 | hp1 | a0002 | c0007 | t0016 | g0223 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02723 | hp2 | a0002 | c0013 | t0009 | g0319 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02738 | hp1 | a0001 | c0006 | t0003 | g0239 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02738 | hp2 | a0006 | c0046 | t0001 | g0165 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02809 | hp1 | a0001 | c0006 | t0031 | g0321 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02818 | hp1 | a0002 | c0004 | t0009 | g0318 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02818 | hp2 | a0002 | c0004 | t0006 | g0289 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02886 | hp1 | a0004 | c0008 | t0006 | g0105 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02886 | hp2 | a0002 | c0007 | t0010 | g0248 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02895 | hp1 | a0002 | c0023 | t0006 | g0370 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02896 | hp1 | a0002 | c0007 | t0006 | g0101 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02896 | hp2 | a0002 | c0004 | t0010 | g0004 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02897 | hp2 | a0002 | c0004 | t0010 | g0004 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02922 | hp1 | a0002 | c0004 | t0010 | g0097 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02922 | hp2 | a0002 | c0004 | t0009 | g0226 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02965 | hp1 | a0002 | c0004 | t0044 | g0100 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02965 | hp2 | a0001 | c0011 | t0020 | g0345 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0322 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02976 | hp2 | a0001 | c0009 | t0015 | g0233 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03041 | hp1 | a0002 | c0004 | t0006 | g0247 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03041 | hp2 | a0004 | c0018 | t0045 | g0245 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03098 | hp1 | a0004 | c0008 | t0010 | g0111 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03098 | hp2 | a0003 | c0003 | t0003 | g0288 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03130 | hp1 | a0002 | c0021 | t0006 | g0214 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03130 | hp2 | a0002 | c0004 | t0006 | g0359 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03139 | hp1 | a0002 | c0004 | t0023 | g0227 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03139 | hp2 | a0002 | c0004 | t0006 | g0358 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03209 | hp1 | a0004 | c0018 | t0024 | g0222 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0353 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03225 | hp1 | a0004 | c0008 | t0009 | g0212 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03225 | hp2 | a0002 | c0004 | t0019 | g0339 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03239 | hp1 | a0001 | c0002 | t0011 | g0372 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03239 | hp2 | a0001 | c0005 | t0003 | g0095 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03453 | hp1 | a0008 | c0031 | t0003 | g0203 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03486 | hp1 | a0003 | c0003 | t0003 | g0201 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0373 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03490 | hp1 | a0001 | c0006 | t0007 | g0306 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03490 | hp2 | a0001 | c0001 | t0007 | g0249 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03491 | hp1 | a0002 | c0010 | t0004 | g0058 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03491 | hp2 | a0003 | c0003 | t0008 | g0305 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03516 | hp1 | a0004 | c0008 | t0010 | g0347 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03516 | hp2 | a0002 | c0007 | t0016 | g0123 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03540 | hp1 | a0002 | c0004 | t0006 | g0092 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03540 | hp2 | a0002 | c0013 | t0009 | g0320 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03579 | hp1 | a0013 | c0020 | t0032 | g0336 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03654 | hp2 | a0001 | c0006 | t0003 | g0162 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03669 | hp1 | a0001 | c0006 | t0008 | g0253 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03669 | hp2 | a0001 | c0002 | t0036 | g0010 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03688 | hp1 | a0001 | c0005 | t0001 | g0030 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03688 | hp2 | a0002 | c0036 | t0004 | g0012 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03704 | hp2 | a0003 | c0003 | t0008 | g0383 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0158 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03834 | hp1 | a0001 | c0001 | t0007 | g0386 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03942 | hp1 | a0001 | c0002 | t0011 | g0266 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0217 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04115 | hp2 | a0001 | c0001 | t0040 | g0164 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0311 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04184 | hp2 | a0001 | c0005 | t0001 | g0088 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04199 | hp1 | a0001 | c0002 | t0046 | g0163 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04228 | hp1 | a0001 | c0005 | t0011 | g0294 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18522 | hp2 | a0002 | c0010 | t0009 | g0335 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0185 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18612 | hp2 | a0001 | c0022 | t0001 | g0187 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18747 | hp2 | a0003 | c0003 | t0003 | g0167 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18906 | hp1 | a0002 | c0004 | t0009 | g0323 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18939 | hp1 | a0001 | c0002 | t0005 | g0330 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18940 | hp1 | a0002 | c0004 | t0004 | g0138 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18940 | hp2 | a0003 | c0015 | t0001 | g0064 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18941 | hp1 | a0002 | c0004 | t0004 | g0174 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18943 | hp2 | a0003 | c0003 | t0003 | g0333 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0139 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18946 | hp1 | a0002 | c0026 | t0013 | g0257 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18950 | hp2 | a0002 | c0004 | t0004 | g0293 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18951 | hp2 | a0005 | c0047 | t0005 | g0220 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18954 | hp1 | a0002 | c0004 | t0013 | g0254 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0329 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18957 | hp2 | a0002 | c0004 | t0004 | g0315 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18959 | hp1 | a0003 | c0003 | t0030 | g0259 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18960 | hp2 | a0001 | c0005 | t0003 | g0081 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18961 | hp1 | a0002 | c0004 | t0004 | g0151 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18962 | hp1 | a0001 | c0001 | t0014 | g0256 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18962 | hp2 | a0001 | c0002 | t0025 | g0028 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18964 | hp1 | a0003 | c0015 | t0001 | g0021 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18966 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18968 | hp1 | a0002 | c0004 | t0004 | g0013 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18968 | hp2 | a0001 | c0005 | t0003 | g0180 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18969 | hp1 | a0002 | c0004 | t0004 | g0128 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0308 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18971 | hp1 | a0002 | c0004 | t0004 | g0210 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0269 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18977 | hp1 | a0001 | c0006 | t0003 | g0026 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18979 | hp1 | a0002 | c0004 | t0004 | g0364 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18979 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0291 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18980 | hp2 | a0003 | c0003 | t0008 | g0099 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18985 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18986 | hp1 | a0003 | c0003 | t0003 | g0169 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18987 | hp1 | a0002 | c0004 | t0004 | g0168 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0144 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18994 | hp2 | a0003 | c0003 | t0003 | g0285 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18998 | hp1 | a0003 | c0003 | t0003 | g0268 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18999 | hp1 | a0003 | c0017 | t0014 | g0250 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18999 | hp2 | a0002 | c0004 | t0004 | g0238 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0379 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19002 | hp2 | a0001 | c0034 | t0002 | g0365 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19004 | hp1 | a0002 | c0004 | t0004 | g0024 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19006 | hp1 | a0001 | c0006 | t0003 | g0034 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19006 | hp2 | a0003 | c0003 | t0003 | g0381 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19007 | hp1 | a0001 | c0005 | t0003 | g0022 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19011 | hp1 | a0001 | c0005 | t0003 | g0312 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0036 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19012 | hp1 | a0001 | c0005 | t0003 | g0309 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19030 | hp1 | a0001 | c0014 | t0043 | g0342 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19030 | hp2 | a0001 | c0009 | t0034 | g0183 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19043 | hp1 | a0001 | c0006 | t0003 | g0355 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19043 | hp2 | a0004 | c0016 | t0012 | g0344 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19054 | hp1 | a0003 | c0003 | t0005 | g0122 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19054 | hp2 | a0001 | c0002 | t0017 | g0014 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19056 | hp1 | a0002 | c0004 | t0004 | g0275 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19057 | hp2 | a0002 | c0004 | t0004 | g0017 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19058 | hp1 | a0001 | c0005 | t0001 | g0143 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19060 | hp1 | a0001 | c0002 | t0048 | g0175 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19065 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19066 | hp1 | a0002 | c0004 | t0004 | g0331 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19070 | hp2 | a0001 | c0002 | t0025 | g0057 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19077 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19078 | hp2 | a0002 | c0004 | t0013 | g0184 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19081 | hp1 | a0002 | c0004 | t0026 | g0366 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19085 | hp2 | a0003 | c0003 | t0003 | g0152 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19086 | hp1 | a0003 | c0003 | t0003 | g0284 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19086 | hp2 | a0001 | c0005 | t0007 | g0252 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19091 | hp2 | a0002 | c0004 | t0004 | g0198 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19240 | hp1 | a0015 | c0028 | t0001 | g0172 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19240 | hp2 | a0002 | c0004 | t0009 | g0115 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20129 | hp1 | a0009 | c0019 | t0001 | g0113 | AFR | ASW | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20129 | hp2 | a0004 | c0016 | t0012 | g0351 | AFR | ASW | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0262 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0368 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20805 | hp1 | a0001 | c0005 | t0001 | g0094 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0153 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | GIH | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20905 | hp2 | a0003 | c0003 | t0003 | g0019 | SAS | GIH | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01123 | hp1 | a0003 | c0003 | t0003 | g0240 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02109 | hp2 | a0011 | c0038 | t0012 | g0110 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02486 | hp1 | a0001 | c0011 | t0020 | g0096 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02486 | hp2 | a0001 | c0030 | t0007 | g0387 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02559 | hp1 | a0001 | c0005 | t0017 | g0047 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02559 | hp2 | a0002 | c0004 | t0006 | g0108 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03471 | hp1 | a0001 | c0024 | t0003 | g0182 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03471 | hp2 | a0001 | c0002 | t0011 | g0334 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG06807 | hp2 | a0001 | c0012 | t0021 | g0352 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20300 | hp1 | a0002 | c0007 | t0009 | g0324 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20300 | hp2 | a0001 | c0009 | t0015 | g0354 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA21309 | hp1 | a0012 | c0032 | t0006 | g0102 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA21309 | hp2 | a0002 | c0007 | t0012 | g0103 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0050 | g0302 | REF | REF | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0027 | REF | REF | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834632
|
C | G | 1 | a0005 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.52C>G | p.Gln18Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 506/5626 | 52/2754 | 18/917 | chr2 | 74834632 | ||
chr2:74854392
|
A | G | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.163A>G | p.Thr55Ala | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/18 | 617/5626 | 163/2754 | 55/917 | chr2 | 74854392 | ||
chr2:74872350
|
A | T | 2 | a0003a0004 | 75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
missense_variant | MODERATE | c.426A>T | p.Gln142His | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/18 | 880/5626 | 426/2754 | 142/917 | chr2 | 74872350 | ||
chr2:74874425
|
G | A | 1 | a0007 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.851G>A | p.Gly284Asp | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/18 | 1305/5626 | 851/2754 | 284/917 | chr2 | 74874425 | ||
chr2:74877252
|
G | A | 1 | a0009 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.962G>A | p.Gly321Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1416/5626 | 962/2754 | 321/917 | chr2 | 74877252 | ||
chr2:74877252
|
G | C | 1 | a0008 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.962G>C | p.Gly321Ala | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1416/5626 | 962/2754 | 321/917 | chr2 | 74877252 | ||
chr2:74878815
|
G | T | 2 | a0014a0015 | 2 | HG01891.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1159G>T | p.Ala387Ser | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/18 | 1613/5626 | 1159/2754 | 387/917 | chr2 | 74878815 | ||
chr2:74880329
|
C | T | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1330C>T | p.Arg444Cys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1784/5626 | 1330/2754 | 444/917 | chr2 | 74880329 | ||
chr2:74880392
|
G | C | 2 | a0012a0013 | 2 | HG03579.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1393G>C | p.Asp465His | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1847/5626 | 1393/2754 | 465/917 | chr2 | 74880392 | ||
chr2:74880489
|
G | A | 1 | a0010 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1490G>A | p.Arg497Gln | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1944/5626 | 1490/2754 | 497/917 | chr2 | 74880489 | ||
chr2:74882147
|
G | T | 1 | a0011 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1747G>T | p.Ala583Ser | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/18 | 2201/5626 | 1747/2754 | 583/917 | chr2 | 74882147 | ||
chr2:74889400
|
G | A | 6 | a0002a0004a0008others(3): Show | 85 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(82): Show |
missense_variant | MODERATE | c.2531G>A | p.Arg844Lys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/18 | 2985/5626 | 2531/2754 | 844/917 | chr2 | 74889400 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74873855
|
C | T | 1 | a0001c0039 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.603C>T | p.Ile201Ile | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/18 | 1057/5626 | 603/2754 | 201/917 | chr2 | 74873855 | ||
chr2:74874327
|
T | C | 26 | a0001c0009a0001c0011a0001c0012others(23): Show | 141 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
synonymous_variant | LOW | c.753T>C | p.Asp251Asp | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/18 | 1207/5626 | 753/2754 | 251/917 | chr2 | 74874327 | ||
chr2:74877202
|
G | A | 1 | a0001c0030 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.912G>A | p.Glu304Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1366/5626 | 912/2754 | 304/917 | chr2 | 74877202 | ||
chr2:74878760
|
C | T | 1 | a0003c0045 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.1104C>T | p.Cys368Cys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/18 | 1558/5626 | 1104/2754 | 368/917 | chr2 | 74878760 | ||
chr2:74880289
|
C | T | 1 | a0002c0026 | 1 | NA18946.hp1 | synonymous_variant | LOW | c.1290C>T | p.Thr430Thr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1744/5626 | 1290/2754 | 430/917 | chr2 | 74880289 | ||
chr2:74880544
|
C | T | 1 | a0004c0018 | 2 | HG03041.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1545C>T | p.Tyr515Tyr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1999/5626 | 1545/2754 | 515/917 | chr2 | 74880544 | ||
chr2:74881739
|
T | C | 1 | a0001c0034 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.1599T>C | p.Leu533Leu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/18 | 2053/5626 | 1599/2754 | 533/917 | chr2 | 74881739 | ||
chr2:74886350
|
C | T | 1 | a0001c0037 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1992C>T | p.Thr664Thr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 14/18 | 2446/5626 | 1992/2754 | 664/917 | chr2 | 74886350 | ||
chr2:74886530
|
C | T | 25 | a0001c0001a0001c0009a0001c0011others(22): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
synonymous_variant | LOW | c.2076C>T | p.Asn692Asn | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/18 | 2530/5626 | 2076/2754 | 692/917 | chr2 | 74886530 | ||
chr2:74886662
|
C | G | 25 | a0001c0001a0001c0006a0001c0012others(22): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
synonymous_variant | LOW | c.2208C>G | p.Pro736Pro | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/18 | 2662/5626 | 2208/2754 | 736/917 | chr2 | 74886662 | ||
chr2:74887981
|
A | G | 25 | a0001c0001a0001c0005a0001c0006others(22): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
synonymous_variant | LOW | c.2298A>G | p.Leu766Leu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/18 | 2752/5626 | 2298/2754 | 766/917 | chr2 | 74887981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834191
|
G | C | 1 | a0002c0004t0026 | 1 | NA19081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-390G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 390 | chr2 | 74834191 | |||||
chr2:74834212
|
G | A | 1 | a0001c0002t0027 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-369G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 369 | chr2 | 74834212 | |||||
chr2:74834331
|
C | T | 1 | a0003c0003t0050 | 1 | homoSapiens_chm13v2.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-250C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | chr2 | 74834331 | ||||||
chr2:74834348
|
G | C | 27 | a0001c0001t0007a0001c0001t0008a0001c0001t0014others(24): Show | 59 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-233G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 233 | chr2 | 74834348 | |||||
chr2:74834442
|
T | C | 1 | a0002c0007t0035 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-139T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 139 | chr2 | 74834442 | |||||
chr2:74834525
|
C | T | 1 | a0003c0003t0050 | 1 | homoSapiens_chm13v2.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 56 | chr2 | 74834525 | |||||
chr2:74891058
|
C | A | 1 | a0001c0002t0036 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 117 | chr2 | 74891058 | |||||
chr2:74891195
|
A | G | 7 | a0002c0004t0004a0002c0004t0013a0002c0004t0026others(4): Show | 25 | HG00609.hp2 HG02040.hp1 HG02135.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*254A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 254 | chr2 | 74891195 | |||||
chr2:74891203
|
T | G | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(68): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*262T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 262 | chr2 | 74891203 | |||||
chr2:74891342
|
A | C | 1 | a0001c0002t0049 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 401 | chr2 | 74891342 | |||||
chr2:74891480
|
T | C | 1 | a0001c0002t0036 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 539 | chr2 | 74891480 | |||||
chr2:74891493
|
C | A | 25 | a0001c0001t0006a0001c0011t0037a0002c0004t0004others(22): Show | 56 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 552 | chr2 | 74891493 | |||||
chr2:74891558
|
G | C | 1 | a0001c0014t0043 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 617 | chr2 | 74891558 | |||||
chr2:74891610
|
C | T | 65 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(62): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*669C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 669 | chr2 | 74891610 | |||||
chr2:74891625
|
C | T | 6 | a0001c0006t0021a0001c0006t0031a0001c0012t0021others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*684C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 684 | chr2 | 74891625 | |||||
chr2:74891662
|
G | A | 3 | a0001c0006t0021a0001c0006t0031a0001c0012t0021 | 3 | HG02145.hp1 HG02809.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*721G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 721 | chr2 | 74891662 | |||||
chr2:74891729
|
T | C | 67 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(64): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*788T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 788 | chr2 | 74891729 | |||||
chr2:74891757
|
G | GA | 86 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(83): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*817dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 818 | INFO_REALIGN_3_PRIME | chr2 | 74891757 | ||||
chr2:74891786
|
TAATG | T | 86 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(83): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*850_*853delAATG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 850 | INFO_REALIGN_3_PRIME | chr2 | 74891786 | ||||
chr2:74891814
|
T | C | 1 | a0001c0002t0046 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 873 | chr2 | 74891814 | |||||
chr2:74891892
|
G | C | 1 | a0002c0004t0038 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*951G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 951 | chr2 | 74891892 | |||||
chr2:74891992
|
C | T | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1051C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1051 | chr2 | 74891992 | |||||
chr2:74892046
|
C | T | 3 | a0002c0025t0024a0004c0018t0024a0004c0018t0045 | 3 | HG01109.hp1 HG03041.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1105C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1105 | chr2 | 74892046 | |||||
chr2:74892264
|
T | C | 1 | a0001c0001t0040 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1323 | chr2 | 74892264 | |||||
chr2:74892371
|
A | G | 9 | a0001c0014t0043a0002c0004t0018a0002c0004t0044others(6): Show | 13 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1430A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1430 | chr2 | 74892371 | |||||
chr2:74892394
|
G | A | 1 | a0001c0009t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1453 | chr2 | 74892394 | |||||
chr2:74892738
|
C | T | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1797C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1797 | chr2 | 74892738 | |||||
chr2:74892742
|
T | G | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1801 | chr2 | 74892742 | |||||
chr2:74892862
|
C | T | 1 | a0003c0003t0042 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1921 | chr2 | 74892862 | |||||
chr2:74892961
|
G | A | 1 | a0001c0001t0041 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2020 | chr2 | 74892961 | |||||
chr2:74893032
|
C | CT | 38 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(35): Show | 90 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2107dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2108 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | ||||
chr2:74893032
|
C | CTT | 18 | a0001c0001t0002a0001c0001t0007a0001c0001t0040others(15): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2106_*2107dupTT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2108 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | ||||
chr2:74893032
|
CT | C | 6 | a0001c0002t0025a0001c0009t0034a0002c0004t0018others(3): Show | 10 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2107delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2107 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | ||||
chr2:74893131
|
T | C | 1 | a0001c0009t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2190 | chr2 | 74893131 | |||||
chr2:74893249
|
G | A | 1 | a0001c0009t0015 | 3 | HG02055.hp2 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2308G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2308 | chr2 | 74893249 | |||||
chr2:74893254
|
C | T | 2 | a0002c0004t0018a0002c0007t0016 | 5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2313C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2313 | chr2 | 74893254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834686
|
G | A | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+43G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834686 | ||||||
chr2:74834746
|
C | G | 296 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0124others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.63+103C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834746 | ||||||
chr2:74834762
|
AAAAGTTT others(73): Show |
A | 6 | a0001c0001t0007g0006a0001c0001t0007g0386a0001c0001t0014g0385others(3): Show | 7 | HG00099.hp2 HG01256.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+121_63+200delAA others(78): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74834762 | |||||
chr2:74834773
|
C | T | 1 | a0014c0027t0039g0382 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834773 | ||||||
chr2:74834783
|
A | C | 3 | a0001c0002t0001g0379a0001c0002t0001g0380a0003c0003t0003g0381 | 3 | NA18961.hp2 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.63+140A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834783 | ||||||
chr2:74834870
|
C | T | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+227C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834870 | ||||||
chr2:74835102
|
G | A | 2 | a0001c0011t0020g0096a0002c0004t0010g0097 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.63+459G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835102 | ||||||
chr2:74835169
|
G | C | 2 | a0002c0004t0013g0098a0003c0003t0008g0099 | 2 | HG00609.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.63+526G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835169 | ||||||
chr2:74835335
|
C | T | 5 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+692C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835335 | ||||||
chr2:74835377
|
C | T | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.63+734C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835377 | ||||||
chr2:74835398
|
C | T | 1 | a0003c0003t0003g0373 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+755C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835398 | ||||||
chr2:74835459
|
C | T | 2 | a0001c0002t0011g0372a0003c0042t0033g0371 | 2 | HG01255.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.63+816C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835459 | ||||||
chr2:74835472
|
A | C | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.63+829A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835472 | ||||||
chr2:74835603
|
G | C | 8 | a0001c0001t0002g0107a0001c0002t0001g0104a0002c0004t0044g0100others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+960G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835603 | ||||||
chr2:74835629
|
G | A | 3 | a0001c0006t0021g0109a0002c0004t0006g0108a0002c0004t0010g0004 | 4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+986G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835629 | ||||||
chr2:74835652
|
C | T | 2 | a0001c0001t0002g0368a0001c0012t0002g0369 | 2 | HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.63+1009C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835652 | ||||||
chr2:74835743
|
G | A | 294 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0124others(291): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.63+1100G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835743 | ||||||
chr2:74836083
|
A | G | 5 | a0001c0001t0002g0361a0001c0001t0002g0363a0001c0034t0002g0365others(2): Show | 5 | HG02015.hp2 HG02040.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1440A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836083 | ||||||
chr2:74836475
|
A | G | 25 | a0001c0001t0002g0367a0001c0001t0006g0353a0001c0006t0003g0355others(22): Show | 26 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+1832A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836475 | ||||||
chr2:74836528
|
C | A | 1 | a0001c0001t0002g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+1885C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836528 | ||||||
chr2:74836637
|
T | C | 3 | a0001c0006t0021g0109a0002c0004t0006g0108a0002c0004t0010g0004 | 4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1994T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836637 | ||||||
chr2:74836704
|
A | G | 3 | a0001c0006t0021g0109a0002c0004t0006g0108a0002c0004t0010g0004 | 4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2061A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836704 | ||||||
chr2:74836738
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.63+2095A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836738 | ||||||
chr2:74836817
|
T | A | 6 | a0001c0001t0002g0112a0001c0014t0043g0342a0002c0004t0001g0114others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2174T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836817 | ||||||
chr2:74836883
|
C | T | 1 | a0001c0001t0002g0340 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.63+2240C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836883 | ||||||
chr2:74836963
|
A | G | 1 | a0002c0004t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+2320A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836963 | ||||||
chr2:74837052
|
C | T | 1 | a0002c0004t0019g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+2409C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837052 | ||||||
chr2:74837102
|
T | A | 1 | a0002c0004t0009g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.63+2459T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837102 | ||||||
chr2:74837106
|
G | A | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.63+2463G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837106 | ||||||
chr2:74837235
|
CG | C | 76 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(73): Show | 76 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.63+2593delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837235 | ||||||
chr2:74837246
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+2603A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837246 | ||||||
chr2:74837265
|
T | C | 77 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(74): Show | 77 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.63+2622T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837265 | ||||||
chr2:74837346
|
G | A | 7 | a0001c0002t0001g0118a0001c0002t0001g0119a0001c0002t0001g0120others(4): Show | 7 | HG00408.hp1 NA18946.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2703G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837346 | ||||||
chr2:74837583
|
C | T | 4 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2940C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837583 | ||||||
chr2:74837584
|
G | T | 6 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2941G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837584 | ||||||
chr2:74837648
|
C | G | 9 | a0001c0001t0002g0093a0001c0006t0021g0109a0001c0037t0022g0360others(6): Show | 10 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+3005C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837648 | ||||||
chr2:74837672
|
C | CT | 77 | a0001c0001t0002g0112a0001c0001t0002g0287a0001c0001t0002g0292others(74): Show | 80 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.63+3051dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | |||||
chr2:74837672
|
C | CTT | 10 | a0001c0001t0002g0107a0001c0002t0011g0334a0001c0012t0022g0332others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+3050_63+3051dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | |||||
chr2:74837672
|
CT | C | 81 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(78): Show | 82 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.63+3051delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | |||||
chr2:74837704
|
T | C | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+3061T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837704 | ||||||
chr2:74837738
|
C | T | 1 | a0001c0002t0001g0286 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.63+3095C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837738 | ||||||
chr2:74837821
|
G | A | 281 | a0001c0001t0002g0011a0001c0001t0002g0093a0001c0001t0002g0107others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+3178G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837821 | ||||||
chr2:74837954
|
G | A | 2 | a0001c0002t0001g0179a0001c0005t0003g0180 | 2 | NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.63+3311G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837954 | ||||||
chr2:74837964
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+3321G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837964 | ||||||
chr2:74838204
|
G | C | 1 | a0001c0001t0002g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.63+3561G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838204 | ||||||
chr2:74838265
|
G | A | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+3622G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838265 | ||||||
chr2:74838328
|
G | A | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+3685G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838328 | ||||||
chr2:74838336
|
A | C | 71 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(68): Show | 71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+3693A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838336 | ||||||
chr2:74838345
|
C | T | 5 | a0001c0001t0002g0080a0001c0002t0001g0079a0001c0002t0001g0082others(2): Show | 5 | NA18959.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3702C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838345 | ||||||
chr2:74838346
|
T | C | 139 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0176others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.63+3703T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838346 | ||||||
chr2:74838402
|
T | TCCAAAGC others(11): Show |
3 | a0001c0001t0002g0112a0004c0008t0010g0111a0011c0038t0012g0110 | 3 | HG02109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3780_63+3797dup others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838402 | |||||
chr2:74838518
|
G | A | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+3875G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838518 | ||||||
chr2:74838523
|
G | A | 281 | a0001c0001t0002g0011a0001c0001t0002g0093a0001c0001t0002g0107others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+3880G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838523 | ||||||
chr2:74838537
|
A | AT | 44 | a0001c0001t0002g0093a0001c0001t0002g0255a0001c0001t0007g0241others(41): Show | 45 | HG00609.hp2 HG00673.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+3913dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838537 | |||||
chr2:74838537
|
AT | A | 45 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0181others(42): Show | 48 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.63+3913delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838537 | |||||
chr2:74838601
|
C | G | 81 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0188others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.63+3958C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838601 | ||||||
chr2:74838625
|
A | G | 281 | a0001c0001t0002g0011a0001c0001t0002g0093a0001c0001t0002g0107others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+3982A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838625 | ||||||
chr2:74838631
|
C | T | 2 | a0001c0001t0002g0107a0003c0003t0003g0240 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.63+3988C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838631 | ||||||
chr2:74838639
|
C | T | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG00423.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.63+3996C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838639 | ||||||
chr2:74838653
|
C | G | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4010C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838653 | ||||||
chr2:74838773
|
C | T | 71 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(68): Show | 71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+4130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838773 | ||||||
chr2:74838853
|
T | C | 6 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4210T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838853 | ||||||
chr2:74839026
|
A | T | 71 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(68): Show | 71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+4383A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839026 | ||||||
chr2:74839234
|
A | G | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4591A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839234 | ||||||
chr2:74839241
|
T | C | 4 | a0001c0001t0002g0112a0002c0004t0001g0114a0004c0008t0010g0111others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+4598T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839241 | ||||||
chr2:74839341
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.63+4698C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839341 | ||||||
chr2:74839347
|
G | A | 3 | a0001c0001t0005g0116a0001c0002t0001g0127a0002c0004t0004g0128 | 3 | HG02165.hp2 NA18969.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.63+4704G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839347 | ||||||
chr2:74839473
|
T | C | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4830T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839473 | ||||||
chr2:74839659
|
A | AT | 27 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0107others(24): Show | 27 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.63+5031dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | |||||
chr2:74839659
|
A | ATT | 13 | a0001c0006t0003g0355a0001c0009t0034g0183a0001c0011t0020g0345others(10): Show | 13 | HG01257.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+5030_63+5031dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | |||||
chr2:74839659
|
A | ATTT | 23 | a0001c0001t0002g0255a0001c0001t0007g0185a0001c0001t0007g0249others(20): Show | 23 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+5029_63+5031dup others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | |||||
chr2:74839659
|
AT | A | 9 | a0001c0001t0002g0093a0001c0006t0021g0109a0001c0037t0022g0360others(6): Show | 10 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+5031delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | |||||
chr2:74839828
|
T | TTGTA | 72 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(69): Show | 72 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.63+5186_63+5187ins others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839828 | |||||
chr2:74839883
|
A | G | 1 | a0003c0003t0003g0285 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.63+5240A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839883 | ||||||
chr2:74839951
|
C | CT | 34 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0107others(31): Show | 34 | HG00438.hp2 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+5330dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | |||||
chr2:74839951
|
CT | C | 63 | a0001c0001t0002g0018a0001c0001t0002g0093a0001c0001t0002g0181others(60): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.63+5330delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | |||||
chr2:74839951
|
CTT | C | 18 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0002t0001g0186others(15): Show | 18 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+5329_63+5330del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | |||||
chr2:74840009
|
A | G | 72 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125others(69): Show | 72 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.63+5366A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840009 | ||||||
chr2:74840059
|
C | T | 1 | a0015c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+5416C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840059 | ||||||
chr2:74840116
|
C | A | 1 | a0001c0009t0034g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+5473C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840116 | ||||||
chr2:74840116
|
C | T | 1 | a0001c0001t0007g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.63+5473C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840116 | ||||||
chr2:74840238
|
C | T | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+5595C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840238 | ||||||
chr2:74840248
|
C | T | 1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.63+5605C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840248 | ||||||
chr2:74840258
|
A | AT | 7 | a0001c0001t0002g0008a0001c0001t0002g0199a0001c0002t0001g0161others(4): Show | 7 | HG01175.hp1 HG02055.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+5631dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840258 | |||||
chr2:74840350
|
G | A | 45 | a0001c0001t0002g0018a0001c0001t0002g0287a0001c0001t0002g0296others(42): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.63+5707G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840350 | ||||||
chr2:74840372
|
A | G | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+5729A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840372 | ||||||
chr2:74840458
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+5815G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840458 | ||||||
chr2:74840502
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+5859G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840502 | ||||||
chr2:74840505
|
G | C | 1 | a0001c0002t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+5862G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840505 | ||||||
chr2:74840627
|
A | G | 31 | a0001c0001t0002g0255a0001c0001t0007g0185a0001c0001t0007g0241others(28): Show | 31 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+5984A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840627 | ||||||
chr2:74840634
|
A | G | 1 | a0001c0001t0005g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.63+5991A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840634 | ||||||
chr2:74840649
|
C | T | 72 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0190others(69): Show | 73 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.63+6006C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840649 | ||||||
chr2:74840664
|
A | G | 6 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6021A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840664 | ||||||
chr2:74840692
|
C | A | 8 | a0001c0001t0002g0188a0001c0009t0034g0183a0001c0014t0043g0342others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6049C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840692 | ||||||
chr2:74840698
|
T | C | 4 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6055T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840698 | ||||||
chr2:74840711
|
C | CA | 11 | a0001c0001t0002g0072a0001c0001t0002g0202a0001c0001t0005g0270others(8): Show | 11 | HG00642.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+6086dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | |||||
chr2:74840711
|
CA | C | 207 | a0001c0001t0002g0011a0001c0001t0002g0060a0001c0001t0002g0061others(204): Show | 208 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.63+6086delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | |||||
chr2:74840711
|
CAA | C | 60 | a0001c0001t0002g0018a0001c0001t0002g0112a0001c0001t0002g0170others(57): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.63+6085_63+6086del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | |||||
chr2:74840711
|
CAAAAA | C | 5 | a0001c0001t0002g0093a0001c0006t0021g0109a0002c0004t0006g0092others(2): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6082_63+6086del others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | |||||
chr2:74840714
|
A | C | 1 | a0001c0002t0001g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+6071A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840714 | ||||||
chr2:74840754
|
C | A | 16 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0002t0011g0334others(13): Show | 16 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+6111C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840754 | ||||||
chr2:74840803
|
C | T | 1 | a0001c0024t0003g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+6160C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840803 | ||||||
chr2:74840834
|
G | T | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+6191G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840834 | ||||||
chr2:74840878
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0007g0322a0001c0006t0031g0321a0002c0004t0009g0337others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6252_63+6261dup others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
C | CAAAAAAA others(4): Show |
6 | a0001c0002t0011g0334a0002c0004t0009g0115a0002c0004t0009g0318others(3): Show | 6 | HG02257.hp1 HG02818.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6251_63+6261dup others(11): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0007g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+6250_63+6261dup others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CA | C | 169 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(166): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.63+6261delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CAA | C | 16 | a0001c0001t0002g0093a0001c0001t0007g0249a0001c0002t0017g0014others(13): Show | 17 | HG00323.hp2 HG01169.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+6260_63+6261del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CAAA | C | 18 | a0001c0001t0002g0255a0001c0001t0007g0185a0001c0001t0007g0241others(15): Show | 18 | HG00609.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6259_63+6261del others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CAAAA | C | 6 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6258_63+6261del others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CAAAAAAA others(4): Show |
C | 4 | a0002c0004t0038g0348a0003c0003t0003g0373a0004c0008t0010g0349others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6251_63+6261del others(11): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840878
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0132a0001c0001t0005g0159a0001c0002t0001g0129others(2): Show | 5 | HG00140.hp1 HG00741.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6249_63+6261del others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | |||||
chr2:74840904
|
A | AAAAG | 18 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0001t0002g0361others(15): Show | 18 | HG00438.hp1 HG01106.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | ||||||
chr2:74840904
|
A | AAAG | 37 | a0001c0001t0002g0107a0001c0001t0002g0176a0001c0001t0002g0221others(34): Show | 38 | HG00099.hp1 HG00544.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | ||||||
chr2:74840904
|
A | AAG | 18 | a0001c0001t0002g0181a0001c0001t0002g0188a0001c0001t0002g0190others(15): Show | 18 | HG01106.hp1 HG01516.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | ||||||
chr2:74840904
|
A | AG | 14 | a0001c0001t0002g0112a0001c0001t0002g0193a0001c0001t0002g0195others(11): Show | 14 | HG00408.hp2 HG01884.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+6262dupG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840904 | |||||
chr2:74840904
|
A | G | 6 | a0002c0004t0004g0198a0002c0004t0010g0097a0002c0004t0038g0348others(3): Show | 6 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6261A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | ||||||
chr2:74840955
|
C | T | 6 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6312C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840955 | ||||||
chr2:74840986
|
C | T | 70 | a0001c0001t0002g0112a0001c0001t0002g0176a0001c0001t0002g0190others(67): Show | 71 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+6343C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840986 | ||||||
chr2:74841039
|
C | G | 4 | a0002c0004t0038g0348a0003c0003t0003g0373a0004c0008t0010g0349others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6396C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841039 | ||||||
chr2:74841272
|
G | A | 7 | a0001c0001t0002g0272a0001c0001t0003g0276a0001c0001t0005g0035others(4): Show | 7 | HG00423.hp2 NA18961.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6629G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841272 | ||||||
chr2:74841369
|
C | G | 1 | a0001c0002t0001g0083 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.63+6726C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841369 | ||||||
chr2:74841405
|
C | G | 1 | a0001c0002t0001g0326 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.63+6762C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841405 | ||||||
chr2:74841458
|
G | C | 1 | a0003c0003t0008g0384 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.63+6815G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841458 | ||||||
chr2:74841666
|
C | T | 5 | a0001c0001t0002g0188a0002c0007t0016g0200a0003c0003t0003g0201others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7023C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841666 | ||||||
chr2:74841715
|
C | T | 168 | a0001c0001t0002g0018a0001c0001t0002g0107a0001c0001t0002g0112others(165): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.63+7072C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841715 | ||||||
chr2:74841717
|
C | G | 2 | a0001c0024t0003g0182a0002c0007t0016g0123 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.63+7074C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841717 | ||||||
chr2:74841978
|
C | T | 66 | a0001c0001t0002g0112a0001c0001t0002g0176a0001c0001t0002g0190others(63): Show | 67 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.63+7335C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841978 | ||||||
chr2:74842021
|
A | T | 6 | a0001c0001t0002g0080a0001c0002t0001g0079a0001c0002t0001g0082others(3): Show | 6 | NA18959.hp2 NA18960.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+7378A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842021 | ||||||
chr2:74842052
|
A | C | 1 | a0001c0002t0001g0376 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.63+7409A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842052 | ||||||
chr2:74842115
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+7472T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842115 | ||||||
chr2:74842232
|
A | G | 1 | a0001c0014t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.63+7589A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842232 | ||||||
chr2:74842237
|
AT | A | 8 | a0001c0001t0002g0221a0001c0024t0003g0182a0002c0004t0006g0247others(5): Show | 8 | HG02717.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+7603delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74842237 | |||||
chr2:74842298
|
A | G | 15 | a0001c0009t0034g0183a0001c0012t0021g0352a0001c0014t0043g0342others(12): Show | 15 | HG00639.hp1 HG01243.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+7655A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842298 | ||||||
chr2:74842413
|
C | T | 4 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0155others(1): Show | 4 | HG01496.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+7770C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842413 | ||||||
chr2:74842473
|
A | G | 1 | a0001c0002t0001g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.63+7830A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842473 | ||||||
chr2:74842728
|
G | A | 1 | a0003c0003t0003g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.63+8085G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842728 | ||||||
chr2:74842782
|
G | A | 1 | a0004c0016t0012g0344 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+8139G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842782 | ||||||
chr2:74843089
|
G | A | 65 | a0001c0001t0002g0170a0001c0001t0002g0204a0001c0001t0002g0207others(62): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.63+8446G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843089 | ||||||
chr2:74843115
|
C | T | 5 | a0001c0001t0002g0188a0002c0007t0016g0200a0003c0003t0003g0201others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8472C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843115 | ||||||
chr2:74843136
|
C | A | 67 | a0001c0001t0002g0112a0001c0001t0002g0176a0001c0001t0002g0190others(64): Show | 68 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+8493C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843136 | ||||||
chr2:74843278
|
C | A | 5 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(2): Show | 5 | HG00735.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8635C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843278 | ||||||
chr2:74843281
|
TC | T | 5 | a0001c0011t0020g0345a0002c0023t0006g0370a0004c0008t0010g0346others(2): Show | 5 | HG00735.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8640delC | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74843281 | |||||
chr2:74843440
|
C | T | 89 | a0001c0001t0002g0112a0001c0001t0002g0176a0001c0001t0002g0188others(86): Show | 90 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.63+8797C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843440 | ||||||
chr2:74843547
|
G | A | 7 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0002t0001g0179others(4): Show | 7 | HG00408.hp2 NA18943.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+8904G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843547 | ||||||
chr2:74843548
|
C | T | 1 | a0001c0014t0043g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+8905C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843548 | ||||||
chr2:74843883
|
T | C | 253 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0037others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.63+9240T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843883 | ||||||
chr2:74844068
|
GC | G | 6 | a0001c0001t0002g0107a0001c0002t0001g0104a0002c0004t0044g0100others(3): Show | 6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9428delC | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74844068 | |||||
chr2:74844090
|
C | T | 3 | a0001c0002t0001g0379a0001c0002t0001g0380a0003c0003t0003g0381 | 3 | NA18961.hp2 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.63+9447C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844090 | ||||||
chr2:74844224
|
ATGT | A | 81 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0037others(78): Show | 82 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.63+9585_63+9587del others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74844224 | |||||
chr2:74844494
|
T | C | 1 | a0006c0046t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-9799T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844494 | ||||||
chr2:74844564
|
T | C | 17 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0195others(14): Show | 17 | HG00438.hp1 HG01106.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-9729T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844564 | ||||||
chr2:74844590
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64-9703C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844590 | ||||||
chr2:74844634
|
T | C | 63 | a0001c0001t0002g0176a0001c0001t0002g0190a0001c0001t0002g0191others(60): Show | 64 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.64-9659T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844634 | ||||||
chr2:74844674
|
C | A | 1 | a0001c0002t0011g0295 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.64-9619C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844674 | ||||||
chr2:74844738
|
G | A | 5 | a0001c0001t0002g0093a0001c0006t0021g0109a0002c0004t0006g0092others(2): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9555G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844738 | ||||||
chr2:74844750
|
G | T | 16 | a0001c0001t0007g0249a0001c0002t0001g0262a0001c0005t0011g0294others(13): Show | 16 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-9543G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844750 | ||||||
chr2:74844823
|
C | G | 1 | a0001c0002t0001g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64-9470C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844823 | ||||||
chr2:74844962
|
G | T | 2 | a0003c0003t0003g0139a0003c0003t0003g0169 | 2 | NA18944.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.64-9331G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844962 | ||||||
chr2:74845239
|
A | G | 2 | a0001c0002t0046g0163a0006c0046t0001g0165 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-9054A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845239 | ||||||
chr2:74845335
|
C | G | 1 | a0001c0001t0007g0249 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-8958C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845335 | ||||||
chr2:74845567
|
A | G | 5 | a0001c0005t0017g0084a0001c0005t0047g0015a0003c0003t0003g0085others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8726A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845567 | ||||||
chr2:74845695
|
C | A | 1 | a0001c0001t0002g0140 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.64-8598C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845695 | ||||||
chr2:74845796
|
T | C | 69 | a0001c0001t0002g0112a0001c0001t0002g0176a0001c0001t0002g0190others(66): Show | 70 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-8497T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845796 | ||||||
chr2:74845802
|
G | A | 2 | a0001c0001t0002g0221a0004c0018t0024g0222 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64-8491G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845802 | ||||||
chr2:74845805
|
G | C | 1 | a0002c0004t0006g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-8488G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845805 | ||||||
chr2:74845819
|
C | A | 1 | a0004c0008t0010g0346 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-8474C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845819 | ||||||
chr2:74845821
|
G | T | 6 | a0001c0001t0002g0107a0001c0002t0001g0104a0002c0004t0044g0100others(3): Show | 6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8472G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845821 | ||||||
chr2:74845942
|
T | G | 6 | a0001c0001t0002g0107a0001c0002t0001g0104a0002c0004t0044g0100others(3): Show | 6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8351T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845942 | ||||||
chr2:74846041
|
C | T | 16 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(13): Show | 16 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-8252C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846041 | ||||||
chr2:74846124
|
A | G | 2 | a0001c0024t0003g0182a0002c0007t0016g0123 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-8169A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846124 | ||||||
chr2:74846276
|
T | C | 1 | a0001c0002t0017g0014 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.64-8017T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846276 | ||||||
chr2:74846318
|
C | CT | 256 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0037others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.64-7967dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74846318 | |||||
chr2:74846331
|
C | T | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.64-7962C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846331 | ||||||
chr2:74846420
|
C | G | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-7873C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846420 | ||||||
chr2:74846455
|
G | A | 248 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0037others(245): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.64-7838G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846455 | ||||||
chr2:74846928
|
G | T | 81 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0033others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-7365G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846928 | ||||||
chr2:74847078
|
C | T | 2 | a0001c0011t0037g0244a0004c0018t0045g0245 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.64-7215C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847078 | ||||||
chr2:74847282
|
T | C | 1 | a0003c0003t0003g0373 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-7011T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847282 | ||||||
chr2:74847497
|
G | T | 15 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(12): Show | 15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-6796G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847497 | ||||||
chr2:74847511
|
C | T | 1 | a0001c0014t0043g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-6782C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847511 | ||||||
chr2:74847548
|
C | T | 9 | a0001c0001t0002g0221a0001c0011t0020g0345a0001c0037t0022g0360others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-6745C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847548 | ||||||
chr2:74847626
|
G | A | 9 | a0001c0001t0002g0221a0001c0011t0020g0345a0001c0037t0022g0360others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-6667G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847626 | ||||||
chr2:74847662
|
G | A | 17 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(14): Show | 17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-6631G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847662 | ||||||
chr2:74847704
|
C | T | 5 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-6589C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847704 | ||||||
chr2:74847711
|
TAAAC | T | 67 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(64): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.64-6577_64-6574del others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74847711 | |||||
chr2:74847766
|
T | A | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-6527T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847766 | ||||||
chr2:74847799
|
C | T | 1 | a0001c0001t0002g0340 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.64-6494C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847799 | ||||||
chr2:74847805
|
A | C | 60 | a0001c0001t0002g0107a0001c0001t0002g0132a0001c0001t0002g0140others(57): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.64-6488A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847805 | ||||||
chr2:74847840
|
T | C | 90 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0131others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.64-6453T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847840 | ||||||
chr2:74847974
|
C | G | 5 | a0001c0001t0006g0353a0001c0011t0037g0244a0002c0007t0010g0248others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6319C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847974 | ||||||
chr2:74848055
|
G | A | 15 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(12): Show | 15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-6238G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848055 | ||||||
chr2:74848128
|
G | A | 143 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0093others(140): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.64-6165G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848128 | ||||||
chr2:74848275
|
A | G | 304 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0038others(301): Show | 310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.64-6018A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848275 | ||||||
chr2:74848304
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-5989T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848304 | ||||||
chr2:74848405
|
A | G | 85 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0093others(82): Show | 87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5888A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848405 | ||||||
chr2:74848465
|
C | T | 2 | a0002c0007t0012g0103a0002c0025t0024g0267 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-5828C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848465 | ||||||
chr2:74848469
|
ATTAAT | A | 85 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0093others(82): Show | 87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5821_64-5817del others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74848469 | |||||
chr2:74848486
|
TTA | T | 85 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0093others(82): Show | 87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5805_64-5804del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74848486 | |||||
chr2:74849047
|
A | G | 2 | a0001c0001t0002g0170a0001c0011t0020g0096 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.64-5246A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849047 | ||||||
chr2:74849054
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.64-5239G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849054 | ||||||
chr2:74849252
|
C | T | 1 | a0002c0004t0018g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-5041C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849252 | ||||||
chr2:74849340
|
A | G | 1 | a0001c0002t0001g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-4953A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849340 | ||||||
chr2:74849443
|
C | T | 7 | a0001c0037t0022g0360a0002c0004t0006g0092a0002c0004t0038g0348others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-4850C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849443 | ||||||
chr2:74849662
|
A | C | 222 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.64-4631A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849662 | ||||||
chr2:74849721
|
G | C | 2 | a0001c0012t0022g0332a0002c0004t0001g0114 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-4572G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849721 | ||||||
chr2:74849754
|
A | C | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-4539A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849754 | ||||||
chr2:74849828
|
C | T | 6 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4465C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849828 | ||||||
chr2:74849869
|
G | A | 1 | a0001c0001t0007g0249 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-4424G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849869 | ||||||
chr2:74849927
|
C | T | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-4366C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849927 | ||||||
chr2:74849943
|
T | C | 2 | a0001c0012t0022g0332a0002c0004t0001g0114 | 2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-4350T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849943 | ||||||
chr2:74849973
|
A | C | 182 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(179): Show | 183 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.64-4320A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849973 | ||||||
chr2:74850067
|
C | T | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-4226C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850067 | ||||||
chr2:74850105
|
T | C | 37 | a0001c0001t0002g0107a0001c0001t0002g0132a0001c0001t0002g0287others(34): Show | 38 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.64-4188T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850105 | ||||||
chr2:74850185
|
C | A | 4 | a0002c0004t0006g0092a0002c0004t0023g0227a0002c0004t0038g0348others(1): Show | 4 | HG02630.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-4108C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850185 | ||||||
chr2:74850320
|
T | G | 1 | a0009c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-3973T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850320 | ||||||
chr2:74850413
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0150a0001c0001t0002g0341others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3880C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850413 | ||||||
chr2:74850414
|
G | A | 1 | a0014c0027t0039g0382 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-3879G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850414 | ||||||
chr2:74850468
|
T | C | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-3825T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850468 | ||||||
chr2:74850518
|
C | T | 9 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(6): Show | 9 | HG01243.hp1 HG02896.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-3775C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850518 | ||||||
chr2:74850550
|
A | G | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-3743A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850550 | ||||||
chr2:74850628
|
T | C | 2 | a0001c0002t0046g0163a0003c0017t0014g0250 | 2 | HG04199.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.64-3665T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850628 | ||||||
chr2:74850657
|
C | G | 1 | a0001c0001t0002g0190 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-3636C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850657 | ||||||
chr2:74850787
|
G | A | 1 | a0001c0001t0002g0340 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.64-3506G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850787 | ||||||
chr2:74850812
|
C | T | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-3481C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850812 | ||||||
chr2:74850996
|
A | ACTGTTTC others(10): Show |
84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-3284_64-3268dup others(17): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74850996 | |||||
chr2:74851074
|
G | T | 88 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0093others(85): Show | 88 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.64-3219G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851074 | ||||||
chr2:74851129
|
C | T | 1 | a0002c0007t0016g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-3164C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851129 | ||||||
chr2:74851162
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.64-3131C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851162 | ||||||
chr2:74851253
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG00544.hp1 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.64-3040C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851253 | ||||||
chr2:74851526
|
C | T | 10 | a0001c0001t0002g0052a0001c0002t0001g0032a0001c0002t0001g0042others(7): Show | 10 | HG00642.hp1 HG01109.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-2767C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851526 | ||||||
chr2:74851546
|
G | C | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-2747G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851546 | ||||||
chr2:74851627
|
C | T | 1 | a0003c0003t0003g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-2666C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851627 | ||||||
chr2:74851632
|
G | A | 1 | a0001c0006t0003g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.64-2661G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851632 | ||||||
chr2:74851644
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-2649C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851644 | ||||||
chr2:74851666
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0207a0003c0003t0003g0205others(1): Show | 4 | HG00140.hp2 HG00741.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2627G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851666 | ||||||
chr2:74851678
|
C | T | 1 | a0001c0001t0007g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-2615C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851678 | ||||||
chr2:74851828
|
A | G | 1 | a0001c0002t0001g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-2465A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851828 | ||||||
chr2:74851842
|
A | C | 1 | a0002c0004t0006g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-2451A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851842 | ||||||
chr2:74852031
|
C | T | 4 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0137others(1): Show | 4 | NA18941.hp2 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2262C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852031 | ||||||
chr2:74852219
|
A | T | 40 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(37): Show | 40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.64-2074A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852219 | ||||||
chr2:74852292
|
A | G | 183 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(180): Show | 184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.64-2001A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852292 | ||||||
chr2:74852334
|
A | G | 12 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-1959A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852334 | ||||||
chr2:74852521
|
C | A | 5 | a0001c0002t0001g0118a0001c0002t0001g0119a0001c0002t0001g0120others(2): Show | 5 | NA18946.hp2 NA18953.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-1772C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852521 | ||||||
chr2:74852552
|
A | G | 9 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1741A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852552 | ||||||
chr2:74852582
|
G | T | 1 | a0001c0001t0005g0270 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.64-1711G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852582 | ||||||
chr2:74852689
|
A | T | 7 | a0001c0001t0002g0023a0001c0001t0002g0093a0001c0001t0002g0112others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1604A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852689 | ||||||
chr2:74852698
|
A | C | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-1595A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852698 | ||||||
chr2:74852897
|
T | C | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-1396T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852897 | ||||||
chr2:74852911
|
C | T | 7 | a0001c0001t0002g0221a0001c0011t0020g0345a0002c0007t0016g0200others(4): Show | 7 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1382C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852911 | ||||||
chr2:74853149
|
A | G | 2 | a0001c0001t0002g0131a0001c0006t0002g0009 | 2 | NA18947.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.64-1144A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853149 | ||||||
chr2:74853195
|
A | G | 12 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1098A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853195 | ||||||
chr2:74853247
|
T | C | 84 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-1046T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853247 | ||||||
chr2:74853254
|
C | A | 3 | a0001c0012t0022g0332a0002c0004t0001g0114a0002c0025t0024g0267 | 3 | HG01109.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-1039C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853254 | ||||||
chr2:74853280
|
G | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(38): Show | 41 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-1013G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853280 | ||||||
chr2:74853323
|
C | A | 84 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-970C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853323 | ||||||
chr2:74853393
|
T | C | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-900T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853393 | ||||||
chr2:74853518
|
A | AAAC | 42 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(39): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-730_64-728dupCA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853518
|
A | AAACAAC | 10 | a0001c0001t0002g0048a0001c0001t0002g0052a0001c0002t0001g0075others(7): Show | 10 | HG00423.hp1 HG01123.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-733_64-728dupCA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853518
|
AAAC | A | 71 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0038others(68): Show | 71 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-730_64-728delCA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853518
|
AAACAAC | A | 18 | a0001c0001t0002g0204a0001c0001t0002g0207a0001c0002t0001g0041others(15): Show | 18 | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-733_64-728delCA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853518
|
AAACAACA others(2): Show |
A | 120 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0107others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.64-736_64-728delCA others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853518
|
AAACAACA others(5): Show |
A | 106 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0093others(103): Show | 109 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.64-739_64-728delCA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | |||||
chr2:74853688
|
T | C | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-605T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853688 | ||||||
chr2:74853696
|
C | CA | 44 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.64-585dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853696 | |||||
chr2:74853770
|
CT | C | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-520delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853770 | |||||
chr2:74853785
|
A | G | 16 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0196others(13): Show | 16 | HG00099.hp1 HG00544.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-508A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853785 | ||||||
chr2:74853828
|
A | G | 1 | a0003c0003t0003g0377 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.64-465A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853828 | ||||||
chr2:74853874
|
C | T | 1 | a0001c0022t0001g0187 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64-419C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853874 | ||||||
chr2:74853946
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64-347C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853946 | ||||||
chr2:74853947
|
T | G | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64-346T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853947 | ||||||
chr2:74854007
|
C | T | 2 | a0002c0004t0004g0174a0002c0004t0004g0198 | 2 | NA18941.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.64-286C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854007 | ||||||
chr2:74854008
|
G | A | 2 | a0001c0001t0002g0080a0001c0006t0003g0034 | 2 | NA18987.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.64-285G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854008 | ||||||
chr2:74854140
|
G | A | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-153G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854140 | ||||||
chr2:74854458
|
A | G | 1 | a0004c0008t0019g0189 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.226+3A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854458 | ||||||
chr2:74854556
|
C | T | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.226+101C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854556 | ||||||
chr2:74854795
|
C | T | 2 | a0001c0001t0002g0131a0001c0006t0002g0009 | 2 | NA18947.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.226+340C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854795 | ||||||
chr2:74854844
|
C | T | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.226+389C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854844 | ||||||
chr2:74854864
|
G | A | 1 | a0003c0003t0003g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.226+409G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854864 | ||||||
chr2:74854878
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+423C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854878 | ||||||
chr2:74855008
|
A | T | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.226+553A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855008 | ||||||
chr2:74855089
|
T | C | 173 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(170): Show | 174 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.226+634T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855089 | ||||||
chr2:74855432
|
T | A | 1 | a0001c0002t0001g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.226+977T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855432 | ||||||
chr2:74855488
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.226+1033G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855488 | ||||||
chr2:74855600
|
G | A | 6 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+1145G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855600 | ||||||
chr2:74855623
|
T | C | 2 | a0002c0004t0006g0231a0002c0010t0006g0232 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.226+1168T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855623 | ||||||
chr2:74855647
|
T | C | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0002t0001g0137others(2): Show | 5 | NA18941.hp2 NA18975.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+1192T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855647 | ||||||
chr2:74855707
|
G | A | 1 | a0001c0001t0002g0368 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.226+1252G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855707 | ||||||
chr2:74855717
|
G | A | 6 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+1262G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855717 | ||||||
chr2:74855768
|
G | A | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+1313G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855768 | ||||||
chr2:74855834
|
G | A | 2 | a0003c0003t0003g0029a0003c0003t0003g0329 | 2 | NA18954.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.226+1379G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855834 | ||||||
chr2:74855845
|
G | A | 1 | a0001c0001t0005g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.226+1390G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855845 | ||||||
chr2:74855846
|
G | A | 15 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0196others(12): Show | 15 | HG00544.hp1 HG01255.hp2 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.226+1391G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855846 | ||||||
chr2:74855849
|
G | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+1394G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855849 | ||||||
chr2:74855863
|
C | T | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+1408C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855863 | ||||||
chr2:74855931
|
A | G | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+1476A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855931 | ||||||
chr2:74855987
|
G | A | 8 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(5): Show | 8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+1532G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855987 | ||||||
chr2:74856070
|
C | T | 1 | a0001c0002t0001g0121 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.226+1615C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856070 | ||||||
chr2:74856127
|
T | G | 1 | a0001c0002t0001g0378 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.226+1672T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856127 | ||||||
chr2:74856131
|
G | A | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+1676G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856131 | ||||||
chr2:74856174
|
TG | T | 12 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.226+1722delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74856174 | |||||
chr2:74856185
|
T | C | 1 | a0001c0006t0021g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.226+1730T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856185 | ||||||
chr2:74856458
|
C | T | 4 | a0001c0001t0002g0130a0001c0001t0002g0150a0001c0001t0002g0341others(1): Show | 4 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2003C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856458 | ||||||
chr2:74856462
|
C | T | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+2007C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856462 | ||||||
chr2:74856748
|
C | A | 167 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(164): Show | 168 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.226+2293C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856748 | ||||||
chr2:74856803
|
G | C | 4 | a0001c0001t0002g0188a0001c0012t0021g0352a0004c0008t0019g0189others(1): Show | 4 | HG01884.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2348G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856803 | ||||||
chr2:74856864
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226+2409C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856864 | ||||||
chr2:74856911
|
G | C | 1 | a0002c0035t0012g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226+2456G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856911 | ||||||
chr2:74857177
|
C | T | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2722C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857177 | ||||||
chr2:74857216
|
G | T | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2761G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857216 | ||||||
chr2:74857219
|
T | A | 3 | a0001c0012t0022g0332a0002c0004t0001g0114a0002c0025t0024g0267 | 3 | HG01109.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.226+2764T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857219 | ||||||
chr2:74857425
|
C | A | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2970C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857425 | ||||||
chr2:74857526
|
A | G | 1 | a0004c0016t0012g0344 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226+3071A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857526 | ||||||
chr2:74857614
|
C | A | 1 | a0001c0037t0022g0360 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.226+3159C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857614 | ||||||
chr2:74857743
|
A | C | 7 | a0001c0001t0002g0221a0001c0011t0020g0345a0002c0007t0016g0200others(4): Show | 7 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+3288A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857743 | ||||||
chr2:74857770
|
A | T | 1 | a0001c0001t0002g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.226+3315A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857770 | ||||||
chr2:74857778
|
A | T | 1 | a0006c0046t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.226+3323A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857778 | ||||||
chr2:74858036
|
C | T | 223 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(220): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.226+3581C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858036 | ||||||
chr2:74858057
|
T | C | 40 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(37): Show | 40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.226+3602T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858057 | ||||||
chr2:74858147
|
A | T | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+3692A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858147 | ||||||
chr2:74858153
|
G | A | 2 | a0001c0002t0001g0326a0001c0002t0017g0014 | 2 | NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.226+3698G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858153 | ||||||
chr2:74858235
|
CAGAACCT others(264): Show |
C | 1 | a0002c0004t0019g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.226+3783_226+4053d others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74858235 | |||||
chr2:74858332
|
C | T | 1 | a0002c0004t0023g0243 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.226+3877C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858332 | ||||||
chr2:74858440
|
A | C | 179 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(176): Show | 180 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.226+3985A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858440 | ||||||
chr2:74858452
|
A | G | 2 | a0001c0037t0022g0360a0002c0035t0012g0343 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.226+3997A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858452 | ||||||
chr2:74858490
|
C | T | 1 | a0001c0009t0034g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226+4035C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858490 | ||||||
chr2:74858491
|
G | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+4036G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858491 | ||||||
chr2:74858886
|
C | T | 1 | a0004c0018t0024g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226+4431C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858886 | ||||||
chr2:74858889
|
AG | A | 84 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(81): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+4438delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74858889 | |||||
chr2:74858929
|
T | G | 1 | a0001c0006t0003g0239 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.226+4474T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858929 | ||||||
chr2:74858974
|
A | G | 2 | a0001c0005t0017g0047a0002c0010t0004g0058 | 2 | HG02559.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.226+4519A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858974 | ||||||
chr2:74859035
|
G | A | 37 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(34): Show | 37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.226+4580G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859035 | ||||||
chr2:74859054
|
A | G | 79 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0140others(76): Show | 83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.226+4599A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859054 | ||||||
chr2:74859081
|
T | G | 2 | a0001c0012t0021g0352a0004c0016t0012g0351 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.226+4626T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859081 | ||||||
chr2:74859399
|
A | T | 1 | a0001c0002t0001g0300 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+4944A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859399 | ||||||
chr2:74859435
|
C | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+4980C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859435 | ||||||
chr2:74859458
|
G | A | 6 | a0002c0004t0006g0092a0002c0004t0023g0227a0002c0004t0038g0348others(3): Show | 6 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+5003G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859458 | ||||||
chr2:74859476
|
G | A | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+5021G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859476 | ||||||
chr2:74859512
|
C | T | 1 | a0003c0003t0003g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226+5057C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859512 | ||||||
chr2:74859547
|
G | A | 3 | a0001c0002t0001g0301a0001c0002t0001g0314a0003c0003t0008g0383 | 3 | HG01069.hp1 HG01071.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.226+5092G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859547 | ||||||
chr2:74859585
|
C | T | 1 | a0001c0002t0001g0281 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226+5130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859585 | ||||||
chr2:74859621
|
C | T | 40 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(37): Show | 40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.226+5166C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859621 | ||||||
chr2:74859622
|
G | A | 87 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(84): Show | 88 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.226+5167G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859622 | ||||||
chr2:74859665
|
C | A | 1 | a0001c0002t0001g0300 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5210C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859665 | ||||||
chr2:74859666
|
A | C | 1 | a0001c0002t0001g0300 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5211A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859666 | ||||||
chr2:74859952
|
C | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(38): Show | 41 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.226+5497C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859952 | ||||||
chr2:74859994
|
T | C | 1 | a0003c0003t0003g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.226+5539T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859994 | ||||||
chr2:74860007
|
T | A | 1 | a0001c0002t0001g0300 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5552T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860007 | ||||||
chr2:74860133
|
A | G | 2 | a0001c0002t0001g0326a0001c0002t0017g0014 | 2 | NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.226+5678A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860133 | ||||||
chr2:74860134
|
A | T | 2 | a0001c0001t0002g0037a0003c0003t0003g0036 | 2 | NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.226+5679A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860134 | ||||||
chr2:74860189
|
C | T | 85 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(82): Show | 86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.226+5734C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860189 | ||||||
chr2:74860206
|
G | A | 85 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(82): Show | 86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.226+5751G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860206 | ||||||
chr2:74860231
|
T | A | 2 | a0001c0009t0015g0354a0001c0009t0015g0356 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226+5776T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860231 | ||||||
chr2:74860290
|
A | G | 1 | a0002c0004t0018g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.226+5835A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860290 | ||||||
chr2:74860332
|
T | A | 1 | a0001c0002t0001g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.226+5877T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860332 | ||||||
chr2:74860363
|
C | T | 94 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0140others(91): Show | 98 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.226+5908C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860363 | ||||||
chr2:74860416
|
C | T | 1 | a0002c0007t0016g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.226+5961C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860416 | ||||||
chr2:74860463
|
A | G | 8 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(5): Show | 8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6008A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860463 | ||||||
chr2:74860534
|
T | C | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.226+6079T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860534 | ||||||
chr2:74860535
|
C | A | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+6080C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860535 | ||||||
chr2:74860575
|
G | A | 12 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.226+6120G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860575 | ||||||
chr2:74860614
|
G | C | 8 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(5): Show | 8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6159G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860614 | ||||||
chr2:74860652
|
C | T | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.226+6197C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860652 | ||||||
chr2:74860726
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.226+6271G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860726 | ||||||
chr2:74860747
|
C | T | 8 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(5): Show | 8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6292C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860747 | ||||||
chr2:74860821
|
C | T | 1 | a0003c0003t0003g0240 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.226+6366C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860821 | ||||||
chr2:74860823
|
C | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0093others(90): Show | 93 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.226+6368C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860823 | ||||||
chr2:74860963
|
C | T | 7 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0001t0002g0221others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+6508C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860963 | ||||||
chr2:74861029
|
G | A | 1 | a0003c0003t0003g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.226+6574G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861029 | ||||||
chr2:74861054
|
G | A | 85 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(82): Show | 86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.227-6582G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861054 | ||||||
chr2:74861083
|
A | T | 2 | a0001c0037t0022g0360a0002c0035t0012g0343 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-6553A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861083 | ||||||
chr2:74861335
|
G | A | 6 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0149others(3): Show | 6 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-6301G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861335 | ||||||
chr2:74861638
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.227-5998C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861638 | ||||||
chr2:74861679
|
G | T | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.227-5957G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861679 | ||||||
chr2:74861704
|
G | A | 37 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(34): Show | 37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.227-5932G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861704 | ||||||
chr2:74861783
|
A | T | 2 | a0001c0012t0022g0332a0002c0025t0024g0267 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.227-5853A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861783 | ||||||
chr2:74861925
|
G | A | 1 | a0013c0020t0032g0336 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.227-5711G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861925 | ||||||
chr2:74862092
|
C | A | 100 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(97): Show | 101 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.227-5544C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862092 | ||||||
chr2:74862099
|
G | A | 106 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(103): Show | 107 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.227-5537G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862099 | ||||||
chr2:74862327
|
A | G | 53 | a0001c0001t0002g0107a0001c0001t0002g0132a0001c0001t0002g0204others(50): Show | 54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-5309A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862327 | ||||||
chr2:74862442
|
A | G | 234 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(231): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.227-5194A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862442 | ||||||
chr2:74862522
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-5114A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862522 | ||||||
chr2:74862560
|
CATGGAAG others(9): Show |
C | 1 | a0001c0012t0022g0332 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.227-5075_227-5060d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862560 | ||||||
chr2:74862562
|
T | C | 130 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(127): Show | 131 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.227-5074T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862562 | ||||||
chr2:74862624
|
G | A | 3 | a0001c0002t0001g0104a0002c0004t0044g0100a0004c0008t0006g0105 | 3 | HG01192.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.227-5012G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862624 | ||||||
chr2:74862674
|
T | G | 181 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(178): Show | 182 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.227-4962T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862674 | ||||||
chr2:74862758
|
G | A | 1 | a0003c0003t0050g0302 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.227-4878G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862758 | ||||||
chr2:74862823
|
G | A | 89 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(86): Show | 90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4813G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862823 | ||||||
chr2:74863028
|
G | A | 89 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(86): Show | 90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4608G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863028 | ||||||
chr2:74863215
|
GTGTTT | G | 3 | a0001c0001t0002g0211a0001c0002t0049g0290a0002c0004t0004g0210 | 3 | HG02027.hp1 HG02056.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.227-4419_227-4415d others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74863215 | |||||
chr2:74863273
|
T | C | 4 | a0001c0011t0020g0345a0002c0007t0016g0200a0004c0008t0010g0346others(1): Show | 4 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-4363T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863273 | ||||||
chr2:74863454
|
T | C | 1 | a0002c0007t0010g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-4182T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863454 | ||||||
chr2:74863572
|
G | A | 89 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(86): Show | 90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4064G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863572 | ||||||
chr2:74863632
|
G | A | 1 | a0003c0003t0003g0284 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.227-4004G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863632 | ||||||
chr2:74863638
|
C | T | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3998C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863638 | ||||||
chr2:74863639
|
G | A | 37 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0131others(34): Show | 37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.227-3997G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863639 | ||||||
chr2:74863653
|
A | C | 1 | a0001c0014t0043g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227-3983A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863653 | ||||||
chr2:74863771
|
T | A | 1 | a0001c0002t0001g0194 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.227-3865T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863771 | ||||||
chr2:74863789
|
G | T | 2 | a0002c0004t0006g0289a0002c0007t0016g0223 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.227-3847G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863789 | ||||||
chr2:74863827
|
C | A | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.227-3809C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863827 | ||||||
chr2:74864074
|
G | A | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3562G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864074 | ||||||
chr2:74864145
|
C | G | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0033others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3491C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864145 | ||||||
chr2:74864238
|
G | A | 14 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.227-3398G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864238 | ||||||
chr2:74864514
|
GT | G | 136 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(133): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.227-3112delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74864514 | |||||
chr2:74864567
|
C | T | 96 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0140others(93): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.227-3069C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864567 | ||||||
chr2:74864568
|
G | A | 1 | a0002c0021t0006g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.227-3068G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864568 | ||||||
chr2:74864612
|
T | A | 1 | a0002c0007t0010g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-3024T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864612 | ||||||
chr2:74864679
|
G | A | 136 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(133): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.227-2957G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864679 | ||||||
chr2:74864779
|
A | T | 177 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0018others(174): Show | 178 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.227-2857A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864779 | ||||||
chr2:74864823
|
T | C | 12 | a0001c0001t0007g0316a0001c0001t0007g0322a0001c0006t0031g0321others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2813T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864823 | ||||||
chr2:74864850
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.227-2786C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864850 | ||||||
chr2:74864865
|
C | T | 1 | a0003c0003t0042g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.227-2771C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864865 | ||||||
chr2:74864959
|
GCTGCTGA others(2314): Show |
G | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.227-2675_227-355de others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74864959 | |||||
chr2:74865004
|
G | A | 4 | a0001c0001t0002g0211a0001c0002t0001g0055a0001c0002t0049g0290others(1): Show | 4 | HG02027.hp1 HG02056.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-2632G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865004 | ||||||
chr2:74865048
|
G | A | 1 | a0004c0016t0012g0344 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.227-2588G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865048 | ||||||
chr2:74865413
|
C | T | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.227-2223C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865413 | ||||||
chr2:74865434
|
C | T | 8 | a0001c0024t0003g0182a0002c0004t0009g0323a0002c0004t0019g0339others(5): Show | 8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-2202C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865434 | ||||||
chr2:74865441
|
C | T | 1 | a0002c0007t0016g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.227-2195C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865441 | ||||||
chr2:74865647
|
A | G | 17 | a0001c0001t0002g0188a0001c0001t0007g0316a0001c0001t0007g0322others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-1989A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865647 | ||||||
chr2:74865706
|
T | A | 1 | a0002c0035t0012g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227-1930T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865706 | ||||||
chr2:74865732
|
C | T | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.227-1904C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865732 | ||||||
chr2:74865845
|
C | T | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1791C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865845 | ||||||
chr2:74865869
|
C | G | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-1767C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865869 | ||||||
chr2:74865881
|
T | C | 16 | a0001c0001t0002g0170a0001c0001t0002g0221a0001c0001t0006g0353others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.227-1755T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865881 | ||||||
chr2:74866062
|
G | A | 2 | a0001c0037t0022g0360a0002c0035t0012g0343 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-1574G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866062 | ||||||
chr2:74866070
|
C | T | 6 | a0001c0011t0020g0345a0001c0037t0022g0360a0002c0007t0016g0200others(3): Show | 6 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-1566C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866070 | ||||||
chr2:74866074
|
G | A | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1562G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866074 | ||||||
chr2:74866120
|
C | T | 6 | a0001c0011t0020g0345a0001c0037t0022g0360a0002c0007t0016g0200others(3): Show | 6 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-1516C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866120 | ||||||
chr2:74866243
|
T | G | 1 | a0001c0001t0002g0298 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.227-1393T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866243 | ||||||
chr2:74866283
|
A | G | 10 | a0001c0001t0002g0074a0001c0001t0002g0272a0001c0001t0003g0276others(7): Show | 10 | HG00423.hp2 HG02083.hp2 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.227-1353A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866283 | ||||||
chr2:74866304
|
G | C | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1332G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866304 | ||||||
chr2:74866341
|
A | G | 83 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-1295A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866341 | ||||||
chr2:74866344
|
C | G | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.227-1292C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866344 | ||||||
chr2:74866503
|
G | C | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1133G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866503 | ||||||
chr2:74866504
|
C | T | 1 | a0001c0001t0005g0141 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.227-1132C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866504 | ||||||
chr2:74866509
|
C | T | 1 | a0001c0030t0007g0387 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.227-1127C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866509 | ||||||
chr2:74866649
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-987G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866649 | ||||||
chr2:74866686
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.227-950T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866686 | ||||||
chr2:74866854
|
T | A | 79 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(76): Show | 80 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-782T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866854 | ||||||
chr2:74866886
|
G | A | 102 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(99): Show | 103 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.227-750G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866886 | ||||||
chr2:74866998
|
C | T | 79 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(76): Show | 80 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-638C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866998 | ||||||
chr2:74867092
|
G | A | 4 | a0001c0011t0020g0345a0002c0007t0016g0200a0004c0008t0010g0346others(1): Show | 4 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-544G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867092 | ||||||
chr2:74867131
|
C | T | 76 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(73): Show | 77 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.227-505C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867131 | ||||||
chr2:74867174
|
G | A | 6 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0006t0021g0109others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-462G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867174 | ||||||
chr2:74867176
|
C | G | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-460C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867176 | ||||||
chr2:74867188
|
T | C | 77 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-448T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867188 | ||||||
chr2:74867196
|
A | G | 2 | a0001c0037t0022g0360a0002c0035t0012g0343 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-440A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867196 | ||||||
chr2:74867219
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.227-417C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867219 | ||||||
chr2:74867294
|
G | A | 107 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0044others(104): Show | 108 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.227-342G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867294 | ||||||
chr2:74867310
|
G | C | 3 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376 | 3 | HG01257.hp1 HG01258.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.227-326G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867310 | ||||||
chr2:74867399
|
T | TAA | 13 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.227-228_227-227dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74867399 | |||||
chr2:74867577
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.227-59C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867577 | ||||||
chr2:74867619
|
C | T | 1 | a0003c0003t0003g0154 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.227-17C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867619 | ||||||
chr2:74867853
|
C | G | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.375+69C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74867853 | ||||||
chr2:74867976
|
G | GTA | 42 | a0001c0001t0002g0107a0001c0001t0002g0132a0001c0001t0002g0204others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.375+193_375+194dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74867976 | |||||
chr2:74868044
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.375+260T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868044 | ||||||
chr2:74868052
|
C | T | 3 | a0001c0006t0007g0306a0001c0006t0007g0327a0003c0003t0008g0305 | 3 | HG00323.hp2 HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.375+268C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868052 | ||||||
chr2:74868096
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.375+312C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868096 | ||||||
chr2:74868164
|
T | C | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.375+380T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868164 | ||||||
chr2:74868293
|
C | T | 1 | a0001c0002t0001g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.375+509C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868293 | ||||||
chr2:74868682
|
G | A | 39 | a0001c0001t0002g0131a0001c0001t0002g0170a0001c0001t0002g0181others(36): Show | 39 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.375+898G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868682 | ||||||
chr2:74868706
|
C | T | 11 | a0001c0001t0002g0221a0001c0009t0034g0183a0001c0024t0003g0182others(8): Show | 11 | HG01243.hp1 HG02896.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.375+922C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868706 | ||||||
chr2:74868717
|
A | G | 1 | a0001c0005t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.375+933A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868717 | ||||||
chr2:74868765
|
A | C | 15 | a0001c0001t0002g0221a0001c0002t0001g0005a0001c0002t0011g0334others(12): Show | 16 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.375+981A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868765 | ||||||
chr2:74868817
|
C | A | 5 | a0001c0011t0020g0345a0002c0007t0016g0200a0004c0008t0010g0346others(2): Show | 5 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+1033C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868817 | ||||||
chr2:74868888
|
A | G | 10 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+1104A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868888 | ||||||
chr2:74868901
|
G | C | 45 | a0001c0001t0002g0131a0001c0001t0002g0170a0001c0001t0002g0181others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.375+1117G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868901 | ||||||
chr2:74868935
|
T | C | 10 | a0001c0001t0002g0170a0001c0001t0006g0353a0001c0009t0015g0354others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+1151T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868935 | ||||||
chr2:74869027
|
A | G | 1 | a0003c0003t0008g0307 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.375+1243A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869027 | ||||||
chr2:74869120
|
TA | T | 10 | a0001c0001t0002g0125a0001c0001t0002g0170a0001c0009t0015g0354others(7): Show | 10 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.375+1347delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74869120 | |||||
chr2:74869373
|
T | C | 5 | a0001c0011t0037g0244a0001c0037t0022g0360a0002c0035t0012g0343others(2): Show | 5 | HG01243.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.375+1589T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869373 | ||||||
chr2:74869595
|
C | A | 2 | a0001c0022t0001g0187a0003c0003t0005g0122 | 2 | NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.375+1811C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869595 | ||||||
chr2:74869616
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.375+1832C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869616 | ||||||
chr2:74869617
|
G | A | 4 | a0001c0002t0001g0104a0002c0004t0006g0247a0002c0035t0012g0343others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+1833G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869617 | ||||||
chr2:74869626
|
G | A | 4 | a0001c0002t0001g0104a0002c0004t0006g0247a0002c0035t0012g0343others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+1842G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869626 | ||||||
chr2:74869724
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.375+1940G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869724 | ||||||
chr2:74869861
|
T | C | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.375+2077T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869861 | ||||||
chr2:74869878
|
A | G | 5 | a0001c0001t0002g0107a0001c0001t0005g0141a0002c0004t0019g0339others(2): Show | 5 | HG02257.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+2094A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869878 | ||||||
chr2:74869881
|
G | A | 2 | a0003c0003t0003g0029a0003c0003t0003g0329 | 2 | NA18954.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.375+2097G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869881 | ||||||
chr2:74869982
|
G | GTCTTT | 3 | a0002c0004t0018g0230a0002c0004t0018g0317a0004c0043t0012g0177 | 3 | HG01884.hp1 HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.375+2200_375+2204d others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74869982 | |||||
chr2:74869989
|
T | C | 2 | a0001c0011t0037g0244a0009c0019t0001g0113 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.375+2205T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869989 | ||||||
chr2:74869991
|
C | T | 2 | a0001c0011t0037g0244a0009c0019t0001g0113 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.375+2207C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869991 | ||||||
chr2:74870001
|
C | CT | 8 | a0001c0001t0002g0008a0001c0001t0002g0023a0001c0001t0002g0149others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+2235dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | |||||
chr2:74870001
|
CT | C | 177 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0045others(174): Show | 179 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.375+2235delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | |||||
chr2:74870001
|
CTT | C | 8 | a0001c0002t0001g0215a0001c0002t0001g0216a0004c0008t0006g0105others(5): Show | 8 | HG00735.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+2234_375+2235d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | |||||
chr2:74870063
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.376-2237C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870063 | ||||||
chr2:74870078
|
G | A | 2 | a0001c0002t0001g0039a0001c0002t0048g0175 | 2 | NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.376-2222G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870078 | ||||||
chr2:74870146
|
C | A | 1 | a0002c0021t0006g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-2154C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870146 | ||||||
chr2:74870177
|
T | G | 1 | a0003c0003t0003g0036 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.376-2123T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870177 | ||||||
chr2:74870270
|
G | A | 2 | a0002c0004t0010g0097a0002c0021t0006g0214 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.376-2030G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870270 | ||||||
chr2:74870428
|
C | T | 1 | a0001c0012t0022g0332 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.376-1872C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870428 | ||||||
chr2:74870477
|
T | TTGCTTTT others(156): Show |
2 | a0002c0013t0009g0319a0002c0013t0009g0320 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.376-1807_376-1806i others(165): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | |||||
chr2:74870477
|
T | TTGCTTTT others(156): Show |
13 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(10): Show | 13 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-1807_376-1806i others(165): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | |||||
chr2:74870477
|
T | TTGCTTTT others(157): Show |
1 | a0008c0031t0003g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.376-1807_376-1806i others(166): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | |||||
chr2:74870554
|
C | CT | 18 | a0001c0001t0002g0126a0001c0001t0002g0190a0001c0001t0002g0199others(15): Show | 18 | HG00423.hp2 HG00741.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.376-1725dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | |||||
chr2:74870554
|
CT | C | 21 | a0001c0001t0002g0080a0001c0001t0002g0211a0001c0001t0002g0340others(18): Show | 21 | HG00423.hp1 HG00735.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.376-1725delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | |||||
chr2:74870554
|
CTTT | C | 72 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(69): Show | 73 | HG00323.hp2 HG00609.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.376-1727_376-1725d others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | |||||
chr2:74870558
|
T | C | 48 | a0001c0009t0034g0183a0001c0011t0020g0096a0001c0011t0020g0345others(45): Show | 49 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.376-1742T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870558 | ||||||
chr2:74870559
|
T | C | 2 | a0002c0004t0018g0230a0002c0004t0018g0317 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.376-1741T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870559 | ||||||
chr2:74870597
|
A | G | 4 | a0001c0011t0020g0096a0001c0011t0020g0345a0002c0004t0006g0247others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-1703A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870597 | ||||||
chr2:74870686
|
G | A | 1 | a0001c0005t0007g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.376-1614G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870686 | ||||||
chr2:74871010
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.376-1290C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871010 | ||||||
chr2:74871056
|
G | A | 279 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.376-1244G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871056 | ||||||
chr2:74871239
|
G | T | 1 | a0003c0003t0003g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.376-1061G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871239 | ||||||
chr2:74871510
|
G | A | 1 | a0001c0014t0043g0342 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376-790G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871510 | ||||||
chr2:74871573
|
T | A | 1 | a0001c0001t0002g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.376-727T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871573 | ||||||
chr2:74871766
|
G | C | 1 | a0002c0004t0006g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.376-534G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871766 | ||||||
chr2:74871780
|
G | A | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376-520G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871780 | ||||||
chr2:74871803
|
A | G | 2 | a0003c0003t0008g0236a0003c0003t0008g0305 | 2 | HG01516.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.376-497A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871803 | ||||||
chr2:74871827
|
C | A | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-473C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871827 | ||||||
chr2:74871827
|
C | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0149 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.376-473C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871827 | ||||||
chr2:74871959
|
C | T | 1 | a0002c0036t0004g0012 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376-341C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871959 | ||||||
chr2:74872095
|
G | A | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.376-205G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872095 | ||||||
chr2:74872110
|
C | G | 47 | a0001c0011t0020g0096a0001c0011t0020g0345a0001c0011t0037g0244others(44): Show | 48 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.376-190C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872110 | ||||||
chr2:74872197
|
T | G | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.376-103T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872197 | ||||||
chr2:74872254
|
T | C | 76 | a0002c0004t0018g0317a0003c0003t0002g0291a0003c0003t0003g0016others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.376-46T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872254 | ||||||
chr2:74872567
|
G | A | 56 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0037others(53): Show | 57 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.495+148G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872567 | ||||||
chr2:74872571
|
G | C | 1 | a0002c0004t0006g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.495+152G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872571 | ||||||
chr2:74872705
|
A | G | 76 | a0001c0011t0037g0244a0003c0003t0002g0291a0003c0003t0003g0016others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+286A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872705 | ||||||
chr2:74872745
|
T | C | 76 | a0001c0011t0037g0244a0003c0003t0002g0291a0003c0003t0003g0016others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+326T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872745 | ||||||
chr2:74872981
|
A | G | 23 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(20): Show | 23 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.496-295A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872981 | ||||||
chr2:74872991
|
C | G | 7 | a0002c0004t0018g0317a0004c0008t0006g0105a0004c0008t0010g0111others(4): Show | 7 | HG00735.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-285C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872991 | ||||||
chr2:74873174
|
C | T | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-102C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74873174 | ||||||
chr2:74873223
|
G | T | 1 | a0004c0041t0029g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.496-53G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74873223 | ||||||
chr2:74873380
|
G | A | 2 | a0001c0009t0034g0183a0002c0025t0024g0267 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.591+9G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873380 | ||||||
chr2:74873381
|
G | A | 3 | a0001c0011t0020g0096a0001c0011t0020g0345a0002c0004t0009g0318 | 3 | HG02486.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.591+10G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873381 | ||||||
chr2:74873687
|
A | C | 7 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(4): Show | 7 | HG00735.hp1 HG00738.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-157A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873687 | ||||||
chr2:74873724
|
GA | G | 4 | a0002c0004t0010g0097a0002c0004t0018g0230a0002c0004t0018g0317others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-119delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873724 | ||||||
chr2:74873730
|
G | A | 1 | a0004c0041t0029g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.592-114G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873730 | ||||||
chr2:74873746
|
A | AAGAAGGA others(5): Show |
42 | a0001c0011t0020g0096a0001c0011t0020g0345a0001c0012t0021g0352others(39): Show | 43 | HG00609.hp2 HG00738.hp2 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.592-96_592-95insAA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873746
|
A | AAGAAGGA others(8): Show |
7 | a0002c0004t0009g0115a0004c0008t0006g0105a0004c0008t0010g0111others(4): Show | 7 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-96_592-95insAA others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873746
|
A | AAGG | 7 | a0001c0014t0043g0342a0002c0004t0010g0097a0002c0004t0023g0243others(4): Show | 7 | HG01257.hp2 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-77_592-75dupGA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873746
|
A | AAGGAGG | 94 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(91): Show | 94 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.592-80_592-75dupGA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873746
|
A | AAGGAGGA others(5): Show |
2 | a0002c0004t0004g0362a0002c0004t0026g0366 | 2 | HG02040.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.592-86_592-75dupGA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873746
|
A | AAGGAGGA others(8): Show |
1 | a0002c0010t0006g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.592-89_592-75dupGA others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | |||||
chr2:74873992
|
G | A | 1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.691+49G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74873992 | ||||||
chr2:74874069
|
C | A | 1 | a0001c0006t0031g0321 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691+126C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874069 | ||||||
chr2:74874228
|
G | A | 1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.692-38G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874228 | ||||||
chr2:74874237
|
G | A | 36 | a0001c0012t0021g0352a0001c0022t0001g0187a0002c0004t0004g0013others(33): Show | 36 | HG00609.hp2 HG02040.hp1 HG02451.hp2 others(33): Show |
intron_variant | MODIFIER | c.692-29G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874237 | ||||||
chr2:74874517
|
G | A | 1 | a0001c0005t0003g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.875+68G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874517 | ||||||
chr2:74874518
|
C | A | 1 | a0001c0005t0003g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.875+69C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874518 | ||||||
chr2:74874523
|
G | C | 1 | a0001c0002t0001g0076 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.875+74G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874523 | ||||||
chr2:74874632
|
G | A | 3 | a0001c0006t0007g0306a0001c0006t0007g0327a0008c0031t0003g0203 | 3 | HG00323.hp2 HG03453.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.875+183G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874632 | ||||||
chr2:74874766
|
G | A | 1 | a0001c0024t0003g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.875+317G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874766 | ||||||
chr2:74874793
|
G | A | 1 | a0004c0041t0029g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.875+344G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874793 | ||||||
chr2:74875003
|
A | G | 72 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(69): Show | 73 | HG00323.hp2 HG00609.hp2 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.875+554A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875003 | ||||||
chr2:74875049
|
A | G | 95 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.875+600A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875049 | ||||||
chr2:74875112
|
C | G | 27 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(24): Show | 27 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.875+663C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875112 | ||||||
chr2:74875206
|
G | C | 4 | a0001c0009t0034g0183a0002c0004t0001g0114a0002c0004t0044g0100others(1): Show | 4 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+757G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875206 | ||||||
chr2:74875209
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.875+760C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875209 | ||||||
chr2:74875226
|
CTG | C | 5 | a0001c0002t0001g0083a0001c0002t0001g0119a0001c0002t0001g0120others(2): Show | 5 | NA18953.hp2 NA18957.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+779_875+780del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875226 | |||||
chr2:74875308
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.875+859C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875308 | ||||||
chr2:74875327
|
G | GT | 213 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0018others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.875+897dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | |||||
chr2:74875327
|
G | GTT | 31 | a0001c0001t0002g0008a0001c0001t0002g0023a0001c0001t0002g0044others(28): Show | 31 | HG00735.hp1 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.875+896_875+897dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | |||||
chr2:74875327
|
G | T | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.875+878G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875327 | ||||||
chr2:74875327
|
GT | G | 11 | a0001c0002t0001g0039a0001c0009t0015g0233a0001c0009t0015g0354others(8): Show | 11 | HG01257.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+897delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | |||||
chr2:74875365
|
G | C | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+916G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875365 | ||||||
chr2:74875379
|
T | A | 1 | a0002c0004t0004g0293 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.875+930T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875379 | ||||||
chr2:74875397
|
T | C | 154 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(151): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.875+948T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875397 | ||||||
chr2:74875435
|
TCTCCTAC others(5): Show |
T | 3 | a0003c0003t0003g0059a0003c0003t0008g0384a0003c0044t0001g0077 | 3 | HG01099.hp1 HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.875+989_875+1000de others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875435 | |||||
chr2:74875473
|
C | T | 1 | a0001c0024t0003g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.875+1024C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875473 | ||||||
chr2:74875567
|
G | A | 1 | a0002c0021t0006g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.875+1118G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875567 | ||||||
chr2:74875571
|
C | T | 32 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(29): Show | 32 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.875+1122C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875571 | ||||||
chr2:74875656
|
G | T | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+1207G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875656 | ||||||
chr2:74875821
|
C | T | 6 | a0001c0011t0020g0096a0001c0011t0020g0345a0002c0004t0006g0247others(3): Show | 6 | HG02486.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-1345C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875821 | ||||||
chr2:74875837
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0011g0334 | 4 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.876-1329C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875837 | ||||||
chr2:74875949
|
C | T | 1 | a0003c0003t0003g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.876-1217C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875949 | ||||||
chr2:74876090
|
T | A | 1 | a0004c0041t0029g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876-1076T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876090 | ||||||
chr2:74876139
|
G | A | 1 | a0009c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.876-1027G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876139 | ||||||
chr2:74876195
|
C | T | 55 | a0003c0003t0003g0016a0003c0003t0003g0029a0003c0003t0003g0031others(52): Show | 55 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.876-971C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876195 | ||||||
chr2:74876248
|
A | G | 1 | a0004c0041t0029g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876-918A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876248 | ||||||
chr2:74876296
|
C | T | 51 | a0001c0009t0015g0233a0001c0009t0015g0354a0001c0009t0015g0356others(48): Show | 52 | HG00609.hp2 HG01257.hp2 HG02040.hp1 others(49): Show |
intron_variant | MODIFIER | c.876-870C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876296 | ||||||
chr2:74876462
|
C | A | 1 | a0001c0002t0049g0290 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.876-704C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876462 | ||||||
chr2:74876515
|
C | A | 1 | a0003c0015t0001g0064 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.876-651C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876515 | ||||||
chr2:74876561
|
G | A | 4 | a0001c0001t0002g0341a0001c0006t0007g0306a0001c0006t0007g0327others(1): Show | 4 | HG00323.hp2 HG00738.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.876-605G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876561 | ||||||
chr2:74876605
|
C | G | 1 | a0001c0011t0020g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.876-561C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876605 | ||||||
chr2:74876671
|
G | A | 1 | a0004c0008t0010g0349 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.876-495G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876671 | ||||||
chr2:74876704
|
C | T | 2 | a0002c0004t0001g0114a0002c0004t0044g0100 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.876-462C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876704 | ||||||
chr2:74876762
|
A | G | 2 | a0003c0003t0003g0201a0003c0003t0003g0288 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.876-404A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876762 | ||||||
chr2:74876807
|
A | C | 1 | a0003c0003t0003g0373 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.876-359A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876807 | ||||||
chr2:74876825
|
A | G | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-341A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876825 | ||||||
chr2:74876868
|
C | T | 45 | a0001c0001t0002g0003a0001c0001t0002g0037a0001c0001t0002g0048others(42): Show | 45 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.876-298C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876868 | ||||||
chr2:74876889
|
C | A | 7 | a0001c0009t0034g0183a0002c0004t0001g0114a0002c0004t0044g0100others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-277C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876889 | ||||||
chr2:74876892
|
G | T | 1 | a0001c0001t0002g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.876-274G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876892 | ||||||
chr2:74876911
|
T | C | 2 | a0001c0022t0001g0187a0002c0004t0004g0315 | 2 | NA18612.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.876-255T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876911 | ||||||
chr2:74876939
|
T | A | 7 | a0001c0009t0034g0183a0002c0004t0001g0114a0002c0004t0044g0100others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-227T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876939 | ||||||
chr2:74876992
|
A | G | 79 | a0001c0009t0034g0183a0001c0011t0020g0096a0001c0011t0020g0345others(76): Show | 79 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.876-174A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876992 | ||||||
chr2:74877091
|
A | G | 79 | a0001c0009t0034g0183a0001c0011t0020g0096a0001c0011t0020g0345others(76): Show | 79 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.876-75A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74877091 | ||||||
chr2:74877115
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0002g0221a0001c0006t0003g0355 | 3 | HG03453.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.876-51G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74877115 | ||||||
chr2:74877342
|
C | G | 1 | a0002c0004t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1031+21C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877342 | ||||||
chr2:74877403
|
C | T | 1 | a0008c0031t0003g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1031+82C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877403 | ||||||
chr2:74877443
|
A | G | 75 | a0001c0009t0034g0183a0001c0011t0037g0244a0002c0004t0001g0114others(72): Show | 75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1031+122A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877443 | ||||||
chr2:74877448
|
G | A | 68 | a0001c0011t0037g0244a0002c0013t0009g0319a0002c0013t0009g0320others(65): Show | 68 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1031+127G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877448 | ||||||
chr2:74877500
|
T | A | 1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1031+179T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877500 | ||||||
chr2:74877501
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0023a0001c0001t0002g0149 | 3 | HG03831.hp1 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1031+180C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877501 | ||||||
chr2:74877543
|
A | G | 1 | a0003c0003t0003g0277 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1031+222A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877543 | ||||||
chr2:74877546
|
G | A | 2 | a0001c0002t0001g0380a0001c0005t0001g0143 | 2 | NA18961.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1031+225G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877546 | ||||||
chr2:74877620
|
G | A | 5 | a0001c0009t0015g0233a0001c0009t0015g0354a0001c0009t0015g0356others(2): Show | 5 | HG01257.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1031+299G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877620 | ||||||
chr2:74877719
|
C | A | 1 | a0002c0004t0044g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1031+398C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877719 | ||||||
chr2:74877752
|
C | T | 2 | a0002c0013t0009g0319a0002c0013t0009g0320 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1031+431C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877752 | ||||||
chr2:74877800
|
C | T | 1 | a0003c0003t0003g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1031+479C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877800 | ||||||
chr2:74877818
|
G | A | 67 | a0001c0011t0037g0244a0002c0013t0009g0319a0002c0013t0009g0320others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1031+497G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877818 | ||||||
chr2:74877836
|
G | A | 1 | a0003c0003t0003g0146 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1031+515G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877836 | ||||||
chr2:74877890
|
C | G | 1 | a0003c0003t0008g0307 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1031+569C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877890 | ||||||
chr2:74877920
|
A | G | 4 | a0002c0004t0010g0097a0002c0004t0018g0230a0002c0004t0018g0317others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031+599A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877920 | ||||||
chr2:74877963
|
T | A | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1031+642T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877963 | ||||||
chr2:74877985
|
T | G | 2 | a0001c0002t0001g0075a0001c0002t0001g0197 | 2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1031+664T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877985 | ||||||
chr2:74878124
|
C | A | 1 | a0001c0037t0022g0360 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032-564C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878124 | ||||||
chr2:74878165
|
A | T | 1 | a0001c0002t0001g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1032-523A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878165 | ||||||
chr2:74878235
|
G | A | 1 | a0015c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1032-453G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878235 | ||||||
chr2:74878302
|
G | A | 2 | a0002c0013t0009g0319a0002c0013t0009g0320 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1032-386G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878302 | ||||||
chr2:74878334
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1032-354G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878334 | ||||||
chr2:74878377
|
A | T | 1 | a0001c0001t0006g0353 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1032-311A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878377 | ||||||
chr2:74878380
|
A | G | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1032-308A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878380 | ||||||
chr2:74878381
|
G | A | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1032-307G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878381 | ||||||
chr2:74878404
|
C | T | 12 | a0001c0006t0021g0109a0001c0006t0031g0321a0001c0037t0022g0360others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1032-284C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878404 | ||||||
chr2:74878413
|
C | CTG | 4 | a0001c0001t0002g0093a0001c0001t0002g0112a0001c0002t0011g0192others(1): Show | 4 | HG01106.hp1 HG02738.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032-250_1032-249d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878413
|
CTG | C | 7 | a0001c0001t0002g0052a0001c0001t0002g0170a0001c0002t0001g0153others(4): Show | 7 | HG01433.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-250_1032-249d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878413
|
CTGTG | C | 120 | a0001c0001t0002g0018a0001c0001t0002g0023a0001c0001t0002g0038others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1032-252_1032-249d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878413
|
CTGTGTG | C | 58 | a0003c0003t0003g0016a0003c0003t0003g0029a0003c0003t0003g0031others(55): Show | 58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1032-254_1032-249d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878413
|
CTGTGTGT others(1): Show |
C | 7 | a0003c0003t0003g0062a0004c0008t0006g0105a0004c0008t0010g0111others(4): Show | 7 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-256_1032-249d others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878413
|
CTGTGTGT others(9): Show |
C | 2 | a0001c0001t0002g0008a0001c0001t0002g0149 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1032-264_1032-249d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | |||||
chr2:74878420
|
TGTGTGTG others(31): Show |
T | 2 | a0002c0013t0009g0319a0002c0013t0009g0320 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1032-256_1032-219d others(40): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878420 | |||||
chr2:74878432
|
T | TGTGTGTG others(21): Show |
2 | a0002c0004t0010g0097a0002c0021t0006g0214 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1032-246_1032-245i others(30): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878432 | |||||
chr2:74878438
|
T | C | 3 | a0001c0014t0001g0078a0001c0039t0001g0056a0003c0003t0002g0291 | 3 | HG00639.hp1 HG01261.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1032-250T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878438 | ||||||
chr2:74878441
|
G | A | 16 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1032-247G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878441 | ||||||
chr2:74878453
|
G | A | 3 | a0003c0003t0003g0240a0003c0003t0008g0383a0003c0003t0050g0302 | 3 | HG01123.hp1 HG03704.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1032-235G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878453 | ||||||
chr2:74878457
|
G | A | 2 | a0001c0001t0002g0298a0001c0001t0007g0264 | 2 | HG00673.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1032-231G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878457 | ||||||
chr2:74878458
|
C | T | 1 | a0002c0004t0004g0331 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1032-230C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878458 | ||||||
chr2:74878459
|
G | A | 1 | a0002c0004t0018g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1032-229G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878459 | ||||||
chr2:74878561
|
A | G | 3 | a0002c0023t0006g0370a0014c0027t0039g0382a0015c0028t0001g0172 | 3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1032-127A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878561 | ||||||
chr2:74878579
|
C | T | 4 | a0001c0009t0034g0183a0002c0004t0001g0114a0002c0004t0044g0100others(1): Show | 4 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032-109C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878579 | ||||||
chr2:74878583
|
G | A | 3 | a0002c0023t0006g0370a0014c0027t0039g0382a0015c0028t0001g0172 | 3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1032-105G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878583 | ||||||
chr2:74878671
|
A | G | 383 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(380): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1032-17A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878671 | ||||||
chr2:74879026
|
G | T | 2 | a0002c0004t0010g0097a0002c0021t0006g0214 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1265+105G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879026 | ||||||
chr2:74879193
|
G | A | 3 | a0004c0008t0009g0212a0004c0016t0012g0344a0004c0016t0012g0351 | 3 | HG03225.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1265+272G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879193 | ||||||
chr2:74879208
|
C | T | 1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1265+287C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879208 | ||||||
chr2:74879314
|
T | C | 150 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1265+393T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879314 | ||||||
chr2:74879542
|
T | C | 2 | a0004c0018t0024g0222a0004c0018t0045g0245 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1265+621T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879542 | ||||||
chr2:74879543
|
C | T | 1 | a0001c0001t0007g0322 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1265+622C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879543 | ||||||
chr2:74879547
|
T | C | 3 | a0001c0005t0003g0022a0001c0005t0003g0081a0001c0005t0003g0180 | 3 | NA18960.hp2 NA18968.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1265+626T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879547 | ||||||
chr2:74879785
|
A | G | 3 | a0001c0006t0007g0306a0001c0006t0007g0327a0008c0031t0003g0203 | 3 | HG00323.hp2 HG03453.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1266-480A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879785 | ||||||
chr2:74879899
|
C | G | 1 | a0001c0002t0048g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1266-366C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879899 | ||||||
chr2:74879921
|
G | T | 195 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1266-344G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879921 | ||||||
chr2:74879933
|
A | T | 5 | a0001c0001t0002g0237a0001c0002t0001g0005a0001c0002t0001g0104others(2): Show | 6 | HG01192.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266-332A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879933 | ||||||
chr2:74879997
|
T | G | 1 | a0002c0004t0023g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1266-268T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879997 | ||||||
chr2:74880074
|
G | A | 15 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(12): Show | 15 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-191G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880074 | ||||||
chr2:74880119
|
C | G | 24 | a0001c0006t0007g0306a0001c0006t0007g0327a0001c0006t0021g0109others(21): Show | 24 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1266-146C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880119 | ||||||
chr2:74880240
|
T | G | 57 | a0003c0003t0002g0291a0003c0003t0003g0016a0003c0003t0003g0029others(54): Show | 57 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1266-25T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880240 | ||||||
chr2:74880247
|
C | T | 6 | a0001c0002t0001g0215a0001c0002t0001g0216a0002c0007t0010g0248others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266-18C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880247 | ||||||
chr2:74880677
|
G | A | 3 | a0002c0007t0016g0123a0002c0007t0016g0200a0002c0007t0016g0223 | 3 | HG02647.hp2 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1570+108G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880677 | ||||||
chr2:74880747
|
G | A | 1 | a0002c0004t0019g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1570+178G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880747 | ||||||
chr2:74880748
|
T | C | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1570+179T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880748 | ||||||
chr2:74880889
|
G | A | 1 | a0002c0025t0024g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1570+320G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880889 | ||||||
chr2:74881071
|
T | TTTA | 272 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1570+506_1570+508d others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 74881071 | |||||
chr2:74881085
|
A | G | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1570+516A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881085 | ||||||
chr2:74881094
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0124a0001c0001t0002g0176others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1570+525C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881094 | ||||||
chr2:74881182
|
C | T | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1571-529C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881182 | ||||||
chr2:74881312
|
A | T | 2 | a0001c0006t0021g0109a0001c0006t0031g0321 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1571-399A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881312 | ||||||
chr2:74881463
|
C | T | 5 | a0004c0008t0010g0111a0004c0008t0010g0346a0004c0008t0010g0347others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571-248C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881463 | ||||||
chr2:74881464
|
G | A | 2 | a0002c0004t0010g0004a0002c0004t0010g0246 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1571-247G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881464 | ||||||
chr2:74881570
|
T | A | 2 | a0001c0006t0007g0306a0001c0006t0007g0327 | 2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1571-141T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881570 | ||||||
chr2:74881617
|
A | G | 71 | a0001c0011t0020g0096a0001c0011t0020g0345a0001c0011t0037g0244others(68): Show | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1571-94A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881617 | ||||||
chr2:74881936
|
C | G | 1 | a0002c0004t0004g0024 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1719+77C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/17 | chr2 | 74881936 | ||||||
chr2:74882051
|
G | A | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1720-69G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/17 | chr2 | 74882051 | ||||||
chr2:74882310
|
G | T | 2 | a0004c0018t0024g0222a0004c0018t0045g0245 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1839+71G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882310 | ||||||
chr2:74882461
|
T | C | 2 | a0001c0009t0034g0183a0002c0025t0024g0267 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1839+222T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882461 | ||||||
chr2:74882473
|
T | A | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1839+234T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882473 | ||||||
chr2:74882604
|
C | CATATATA others(41): Show |
1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1839+365_1839+366i others(50): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882604 | ||||||
chr2:74882605
|
T | A | 1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1839+366T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882605 | ||||||
chr2:74882605
|
T | TTA | 10 | a0001c0002t0001g0049a0001c0002t0027g0066a0002c0013t0009g0319others(7): Show | 10 | HG00735.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1839+381_1839+382d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATA | 8 | a0002c0004t0044g0100a0002c0007t0012g0103a0004c0008t0006g0105others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1839+379_1839+382d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(3): Show |
1 | a0002c0004t0004g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1839+373_1839+382d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(5): Show |
7 | a0002c0004t0001g0114a0002c0007t0006g0101a0002c0007t0006g0106others(4): Show | 7 | HG00738.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+371_1839+382d others(14): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(7): Show |
6 | a0001c0006t0002g0009a0002c0004t0004g0024a0002c0007t0009g0324others(3): Show | 6 | HG03041.hp2 HG03209.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839+369_1839+382d others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0131a0001c0001t0007g0264 | 2 | HG00673.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1839+367_1839+382d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(11): Show |
3 | a0001c0006t0007g0327a0013c0020t0032g0336a0014c0027t0039g0382 | 3 | HG00323.hp2 HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(20): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(13): Show |
3 | a0001c0001t0002g0237a0001c0006t0007g0306a0002c0023t0006g0370 | 3 | HG02717.hp1 HG02895.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(22): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(15): Show |
7 | a0001c0001t0002g0148a0002c0004t0013g0098a0003c0003t0003g0029others(4): Show | 7 | HG00609.hp2 HG02300.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(24): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(17): Show |
20 | a0001c0001t0002g0037a0001c0001t0002g0191a0001c0001t0008g0311others(17): Show | 20 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(26): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(19): Show |
29 | a0001c0001t0002g0003a0001c0001t0002g0054a0001c0001t0002g0072others(26): Show | 30 | HG00438.hp2 HG01099.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(28): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(21): Show |
19 | a0001c0001t0002g0011a0001c0001t0002g0080a0001c0001t0002g0211others(16): Show | 19 | HG00544.hp2 HG01256.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(30): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(23): Show |
12 | a0001c0001t0002g0048a0001c0001t0002g0181a0001c0001t0002g0193others(9): Show | 12 | HG00408.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(32): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(25): Show |
17 | a0001c0001t0002g0074a0001c0001t0002g0140a0001c0001t0002g0229others(14): Show | 17 | HG00099.hp1 HG00673.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(34): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(27): Show |
7 | a0001c0001t0002g0221a0001c0001t0002g0368a0001c0001t0005g0116others(4): Show | 7 | HG01255.hp2 HG02280.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(36): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(29): Show |
12 | a0001c0001t0002g0208a0001c0001t0002g0272a0001c0002t0001g0300others(9): Show | 12 | HG00423.hp2 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(38): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(31): Show |
13 | a0001c0001t0002g0287a0001c0001t0007g0322a0001c0005t0005g0043others(10): Show | 13 | HG00741.hp1 HG01069.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(40): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(33): Show |
11 | a0001c0001t0002g0052a0001c0001t0002g0060a0001c0001t0002g0093others(8): Show | 12 | HG00140.hp2 HG00408.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(42): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(35): Show |
28 | a0001c0001t0002g0033a0001c0001t0002g0061a0001c0001t0002g0107others(25): Show | 28 | HG00609.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(44): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(37): Show |
14 | a0001c0001t0002g0018a0001c0001t0002g0045a0001c0001t0002g0130others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(46): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(39): Show |
13 | a0001c0001t0002g0008a0001c0001t0002g0038a0001c0001t0002g0112others(10): Show | 13 | HG02027.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(48): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(41): Show |
9 | a0001c0001t0002g0044a0001c0001t0002g0150a0001c0001t0002g0170others(6): Show | 9 | HG01123.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(50): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(43): Show |
2 | a0001c0001t0002g0023a0002c0004t0006g0247 | 2 | HG03041.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(52): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(45): Show |
7 | a0001c0001t0002g0126a0001c0001t0002g0155a0001c0001t0002g0341others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(54): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(47): Show |
1 | a0002c0004t0004g0238 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(56): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTATATAT others(53): Show |
1 | a0001c0001t0002g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(62): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882605
|
T | TTTATATA others(28): Show |
1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1839+367_1839+368i others(37): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | |||||
chr2:74882621
|
A | ATATATAT others(49): Show |
1 | a0002c0004t0006g0359 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(58): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882621 | ||||||
chr2:74882629
|
T | G | 1 | a0001c0006t0003g0034 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1839+390T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882629 | ||||||
chr2:74882683
|
G | A | 47 | a0001c0011t0020g0096a0001c0011t0020g0345a0001c0011t0037g0244others(44): Show | 48 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.1839+444G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882683 | ||||||
chr2:74882912
|
C | G | 1 | a0001c0022t0001g0187 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1839+673C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882912 | ||||||
chr2:74883055
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1839+816G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883055 | ||||||
chr2:74883144
|
T | A | 116 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1839+905T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883144 | ||||||
chr2:74883161
|
T | C | 219 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1839+922T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883161 | ||||||
chr2:74883225
|
C | G | 1 | a0001c0001t0002g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1839+986C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883225 | ||||||
chr2:74883328
|
C | T | 213 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1839+1089C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883328 | ||||||
chr2:74883377
|
G | C | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1839+1138G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883377 | ||||||
chr2:74883501
|
C | G | 6 | a0004c0008t0006g0105a0004c0008t0010g0111a0004c0008t0010g0346others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+1262C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883501 | ||||||
chr2:74883784
|
G | A | 7 | a0001c0006t0003g0162a0001c0006t0008g0253a0003c0003t0003g0134others(4): Show | 7 | HG00741.hp1 HG01261.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+1545G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883784 | ||||||
chr2:74883930
|
A | G | 262 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1840-1564A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883930 | ||||||
chr2:74883975
|
T | C | 261 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1840-1519T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883975 | ||||||
chr2:74884007
|
T | C | 265 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1840-1487T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884007 | ||||||
chr2:74884041
|
C | G | 261 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1840-1453C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884041 | ||||||
chr2:74884234
|
G | A | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1840-1260G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884234 | ||||||
chr2:74884234
|
G | C | 2 | a0001c0009t0034g0183a0002c0025t0024g0267 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-1260G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884234 | ||||||
chr2:74884308
|
C | T | 220 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0018others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1840-1186C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884308 | ||||||
chr2:74884359
|
A | G | 275 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1840-1135A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884359 | ||||||
chr2:74884547
|
G | A | 1 | a0002c0007t0016g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1840-947G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884547 | ||||||
chr2:74884822
|
C | T | 2 | a0001c0009t0034g0183a0002c0025t0024g0267 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-672C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884822 | ||||||
chr2:74884823
|
G | A | 192 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1840-671G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884823 | ||||||
chr2:74884915
|
C | T | 24 | a0002c0004t0001g0114a0002c0004t0009g0318a0002c0004t0010g0097others(21): Show | 24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-579C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884915 | ||||||
chr2:74884953
|
G | T | 5 | a0001c0009t0034g0183a0002c0023t0006g0370a0002c0025t0024g0267others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1840-541G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884953 | ||||||
chr2:74885044
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1840-450T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885044 | ||||||
chr2:74885144
|
G | A | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1840-350G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885144 | ||||||
chr2:74885245
|
C | T | 2 | a0002c0007t0012g0103a0011c0038t0012g0110 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1840-249C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885245 | ||||||
chr2:74885377
|
G | C | 3 | a0001c0002t0001g0186a0001c0002t0001g0265a0001c0002t0001g0286 | 3 | NA18982.hp1 NA18990.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1840-117G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885377 | ||||||
chr2:74885383
|
G | A | 24 | a0002c0004t0001g0114a0002c0004t0009g0318a0002c0004t0010g0097others(21): Show | 24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-111G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885383 | ||||||
chr2:74885385
|
G | A | 1 | a0015c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1840-109G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885385 | ||||||
chr2:74885714
|
C | T | 24 | a0002c0004t0001g0114a0002c0004t0009g0318a0002c0004t0010g0097others(21): Show | 24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1935+125C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885714 | ||||||
chr2:74885737
|
A | T | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+148A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885737 | ||||||
chr2:74885738
|
C | G | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+149C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885738 | ||||||
chr2:74885743
|
T | G | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+154T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885743 | ||||||
chr2:74885845
|
A | AAC | 38 | a0001c0001t0002g0011a0001c0001t0002g0045a0001c0001t0002g0048others(35): Show | 40 | HG00280.hp2 HG00423.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1935+296_1935+297d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACAC | 36 | a0001c0001t0002g0074a0001c0001t0002g0126a0001c0001t0002g0176others(33): Show | 36 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1935+294_1935+297d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACAC | 7 | a0001c0001t0002g0140a0001c0002t0001g0129a0001c0002t0001g0153others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+292_1935+297d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(1): Show |
7 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0006t0008g0251others(4): Show | 7 | HG01169.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+290_1935+297d others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(3): Show |
15 | a0001c0002t0011g0266a0001c0011t0037g0244a0002c0004t0006g0108others(12): Show | 15 | HG00609.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1935+288_1935+297d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(5): Show |
12 | a0001c0009t0034g0183a0002c0004t0004g0017a0002c0004t0004g0174others(9): Show | 12 | HG01109.hp1 HG03130.hp1 HG03130.hp2 others(9): Show |
intron_variant | MODIFIER | c.1935+286_1935+297d others(14): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(7): Show |
8 | a0001c0009t0015g0233a0001c0009t0015g0354a0001c0009t0015g0356others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1935+284_1935+297d others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(9): Show |
7 | a0002c0004t0004g0013a0002c0004t0004g0024a0002c0004t0004g0138others(4): Show | 7 | HG02040.hp1 NA18940.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+282_1935+297d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(11): Show |
3 | a0002c0004t0004g0168a0002c0004t0004g0275a0002c0004t0010g0246 | 3 | HG02717.hp2 NA18987.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1935+280_1935+297d others(20): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(13): Show |
3 | a0002c0004t0023g0243a0002c0004t0026g0366a0002c0007t0035g0007 | 3 | HG01257.hp2 HG02135.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1935+278_1935+297d others(22): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(15): Show |
1 | a0002c0004t0004g0364 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1935+276_1935+297d others(24): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(17): Show |
1 | a0002c0004t0004g0128 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1935+274_1935+297d others(26): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
A | AACACACA others(19): Show |
1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1935+272_1935+297d others(28): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
AAC | A | 17 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0072others(14): Show | 17 | HG00609.hp1 HG00741.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1935+296_1935+297d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
AACAC | A | 6 | a0001c0001t0005g0035a0001c0001t0005g0328a0001c0001t0014g0256others(3): Show | 6 | HG01346.hp1 HG01361.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+294_1935+297d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
AACACAC | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0249a0004c0008t0010g0346 | 4 | HG00735.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+292_1935+297d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885845
|
AACACACA others(3): Show |
A | 3 | a0001c0006t0003g0355a0001c0024t0003g0182a0002c0023t0006g0370 | 3 | HG02895.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1935+288_1935+297d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | |||||
chr2:74885885
|
C | A | 2 | a0004c0008t0010g0346a0004c0018t0045g0245 | 2 | HG00735.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1935+296C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885885 | ||||||
chr2:74885885
|
C | CACACAA | 13 | a0002c0004t0001g0114a0002c0004t0009g0318a0002c0004t0044g0100others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1935+297_1935+298i others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | |||||
chr2:74885885
|
C | CACACACA others(3): Show |
2 | a0002c0004t0010g0097a0004c0008t0019g0189 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1935+297_1935+298i others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | |||||
chr2:74885885
|
C | CACACACA others(7): Show |
3 | a0004c0008t0010g0111a0004c0008t0010g0347a0004c0008t0010g0349 | 3 | HG01891.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1935+297_1935+298i others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | |||||
chr2:74885885
|
C | CACACACA others(9): Show |
1 | a0004c0008t0010g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1935+297_1935+298i others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | |||||
chr2:74885923
|
A | G | 217 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1935+334A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885923 | ||||||
chr2:74885930
|
T | C | 4 | a0001c0005t0017g0084a0001c0005t0047g0015a0001c0039t0001g0056others(1): Show | 4 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+341T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885930 | ||||||
chr2:74885973
|
T | C | 3 | a0002c0023t0006g0370a0014c0027t0039g0382a0015c0028t0001g0172 | 3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1936-321T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885973 | ||||||
chr2:74885987
|
G | A | 2 | a0001c0009t0034g0183a0004c0043t0012g0177 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1936-307G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885987 | ||||||
chr2:74886210
|
T | C | 2 | a0003c0003t0003g0085a0003c0003t0003g0086 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1936-84T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74886210 | ||||||
chr2:74886445
|
G | A | 190 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2036-45G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 14/17 | chr2 | 74886445 | ||||||
chr2:74886765
|
C | T | 1 | a0002c0004t0006g0247 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2219+92C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886765 | ||||||
chr2:74886772
|
C | T | 1 | a0001c0009t0034g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2219+99C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886772 | ||||||
chr2:74886776
|
A | G | 78 | a0001c0006t0001g0046a0001c0006t0002g0009a0001c0006t0003g0026others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2219+103A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886776 | ||||||
chr2:74886861
|
C | T | 1 | a0009c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219+188C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886861 | ||||||
chr2:74887030
|
C | T | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2219+357C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887030 | ||||||
chr2:74887214
|
C | T | 3 | a0001c0001t0002g0204a0001c0001t0007g0386a0001c0012t0002g0369 | 3 | HG02602.hp2 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2219+541C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887214 | ||||||
chr2:74887229
|
G | A | 2 | a0004c0018t0024g0222a0004c0018t0045g0245 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2219+556G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887229 | ||||||
chr2:74887245
|
T | G | 50 | a0001c0011t0037g0244a0001c0012t0021g0352a0002c0004t0001g0114others(47): Show | 51 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.2219+572T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887245 | ||||||
chr2:74887413
|
C | A | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2220-490C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887413 | ||||||
chr2:74887434
|
ATGGGGGC | A | 84 | a0001c0001t0041g0147a0001c0005t0003g0022a0001c0005t0003g0081others(81): Show | 84 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2220-468_2220-462d others(9): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887434 | ||||||
chr2:74887442
|
C | A | 84 | a0001c0001t0041g0147a0001c0005t0003g0022a0001c0005t0003g0081others(81): Show | 84 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2220-461C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887442 | ||||||
chr2:74887523
|
T | G | 87 | a0001c0001t0041g0147a0001c0002t0001g0025a0001c0002t0001g0133others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2220-380T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887523 | ||||||
chr2:74887603
|
C | T | 104 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(101): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.2220-300C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887603 | ||||||
chr2:74887712
|
A | G | 85 | a0001c0001t0041g0147a0001c0005t0003g0022a0001c0005t0003g0081others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2220-191A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887712 | ||||||
chr2:74888183
|
T | G | 2 | a0014c0027t0039g0382a0015c0028t0001g0172 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2375+125T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888183 | ||||||
chr2:74888252
|
C | T | 196 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2375+194C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888252 | ||||||
chr2:74888256
|
A | C | 69 | a0001c0011t0037g0244a0002c0004t0001g0114a0002c0004t0004g0013others(66): Show | 70 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2375+198A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888256 | ||||||
chr2:74888343
|
C | T | 1 | a0001c0012t0021g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2375+285C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888343 | ||||||
chr2:74888365
|
A | G | 1 | a0001c0009t0034g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2375+307A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888365 | ||||||
chr2:74888560
|
G | A | 57 | a0001c0011t0037g0244a0002c0004t0001g0114a0002c0004t0004g0013others(54): Show | 57 | HG00609.hp2 HG00738.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.2375+502G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888560 | ||||||
chr2:74888591
|
T | C | 1 | a0002c0004t0004g0315 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2375+533T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888591 | ||||||
chr2:74888599
|
T | C | 197 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2375+541T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888599 | ||||||
chr2:74888638
|
T | A | 1 | a0001c0002t0001g0002 | 2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2375+580T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888638 | ||||||
chr2:74888659
|
T | C | 3 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0025g0028 | 3 | NA18962.hp2 NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2376-586T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888659 | ||||||
chr2:74888873
|
T | G | 1 | a0002c0023t0006g0370 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2376-372T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888873 | ||||||
chr2:74888887
|
G | A | 39 | a0002c0004t0001g0114a0002c0004t0004g0013a0002c0004t0004g0017others(36): Show | 39 | HG00609.hp2 HG02040.hp1 HG02135.hp2 others(36): Show |
intron_variant | MODIFIER | c.2376-358G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888887 | ||||||
chr2:74889140
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2376-105T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74889140 | ||||||
chr2:74889500
|
C | T | 281 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2609+22C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889500 | ||||||
chr2:74889613
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0133 | 2 | HG00544.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2609+135T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889613 | ||||||
chr2:74889658
|
C | G | 1 | a0015c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2609+180C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889658 | ||||||
chr2:74889699
|
A | G | 1 | a0001c0001t0007g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2609+221A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889699 | ||||||
chr2:74889848
|
T | TGGCTGGC others(129): Show |
1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2609+372_2609+507d others(138): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 74889848 | |||||
chr2:74890016
|
T | C | 1 | a0001c0002t0001g0025 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2609+538T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890016 | ||||||
chr2:74890065
|
A | G | 11 | a0002c0004t0010g0004a0002c0004t0010g0097a0002c0004t0010g0246others(8): Show | 12 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609+587A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890065 | ||||||
chr2:74890377
|
G | A | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2610-420G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890377 | ||||||
chr2:74890426
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2610-371C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890426 | ||||||
chr2:74890604
|
G | A | 3 | a0001c0009t0015g0233a0001c0009t0015g0354a0001c0009t0015g0356 | 3 | HG02055.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2610-193G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890604 | ||||||
chr2:74890668
|
T | C | 1 | a0002c0004t0023g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2610-129T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890668 | ||||||
chr2:74890733
|
G | A | 2 | a0001c0002t0001g0215a0001c0002t0001g0216 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2610-64G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890733 |