geneid | 54801 |
---|---|
ensemblid | ENSG00000147874.11 |
hgncid | 25948 |
symbol | HAUS6 |
name | HAUS augmin like complex subunit 6 |
refseq_nuc | NM_017645.5 |
refseq_prot | NP_060115.3 |
ensembl_nuc | ENST00000380502.8 |
ensembl_prot | ENSP00000369871.3 |
mane_status | MANE Select |
chr | chr9 |
start | 19053141 |
end | 19102904 |
strand | - |
ver | v1.2 |
region | chr9:19053141-19102904 |
region5000 | chr9:19048141-19107904 |
regionname0 | HAUS6_chr9_19053141_19102904 |
regionname5000 | HAUS6_chr9_19048141_19107904 |
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 | 955 | 298 | 64 | 48 | 142 | 10 | 33 | 114 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002 | 0/0 | 955 | 39 | 7 | 7 | 22 | 1 | 2 | 16 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0003 | 0/0 | 955 | 23 | 4 | 7 | 4 | 3 | 5 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0004 | 0/1 | 955 | 9 | 1 | 2 | 0 | 2 | 3 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005 | 0/0 | 955 | 8 | 0 | 0 | 6 | 0 | 2 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006 | 0/0 | 955 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0007 | 0/0 | 955 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0008 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0009 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0010 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0011 | 0/0 | 955 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0012 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0013 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0014 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0015 | 0/0 | 955 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0016 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0017 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0018 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0019 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0020 | 0/0 | 941 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0021 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0022 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0023 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
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 | 2868 | 110 | 11 | 24 | 50 | 5 | 20 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0002 | 1/0 | 2868 | 93 | 7 | 15 | 61 | 3 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0003 | 0/0 | 2868 | 38 | 7 | 7 | 21 | 1 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0004 | 0/0 | 2868 | 31 | 17 | 5 | 7 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0005 | 0/0 | 2868 | 27 | 17 | 1 | 3 | 0 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0006 | 0/0 | 2868 | 23 | 4 | 7 | 4 | 3 | 5 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0007 | 0/0 | 2868 | 15 | 0 | 2 | 13 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0008 | 0/1 | 2868 | 9 | 1 | 2 | 0 | 2 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0009 | 0/0 | 2868 | 6 | 0 | 0 | 6 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0010 | 0/0 | 2868 | 4 | 0 | 0 | 4 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0011 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0012 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0013 | 0/0 | 2868 | 4 | 3 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0014 | 0/0 | 2868 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0015 | 0/0 | 2868 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0016 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0017 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0018 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0019 | 0/0 | 2868 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0020 | 0/0 | 2868 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0021 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0022 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0023 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0024 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0025 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0026 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0027 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0028 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0029 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0030 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0031 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0032 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0033 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0034 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0035 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0036 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0037 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0038 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0039 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0040 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0041 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
c0042 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3456 | 122 | 13 | 25 | 57 | 5 | 22 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0002 | 1/0 | 3456 | 111 | 6 | 17 | 77 | 3 | 7 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0003 | 0/0 | 3457 | 62 | 25 | 14 | 11 | 5 | 7 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0004 | 0/0 | 3456 | 29 | 20 | 1 | 4 | 0 | 4 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0005 | 0/0 | 3456 | 29 | 0 | 5 | 22 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0006 | 0/1 | 3456 | 8 | 1 | 2 | 0 | 2 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0007 | 0/0 | 3457 | 7 | 7 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0008 | 0/0 | 3456 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0009 | 0/0 | 3456 | 3 | 0 | 2 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0010 | 0/0 | 3457 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0011 | 0/0 | 3457 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0012 | 0/0 | 3456 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0013 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0014 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0015 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0016 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0017 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0018 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0019 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0020 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0021 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0022 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0023 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0024 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0025 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0026 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0027 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0028 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0029 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0030 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0031 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
t0032 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
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 | 1/0 | 6 | 0 | 3 | 1 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0025 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
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 | 2868 | 110 | 11 | 24 | 50 | 5 | 20 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002 | 1/0 | 2868 | 93 | 7 | 15 | 61 | 3 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0004 | 0/0 | 2868 | 31 | 17 | 5 | 7 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0005 | 0/0 | 2868 | 27 | 17 | 1 | 3 | 0 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0007 | 0/0 | 2868 | 15 | 0 | 2 | 13 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0010 | 0/0 | 2868 | 4 | 0 | 0 | 4 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0011 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0012 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0019 | 0/0 | 2868 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0020 | 0/0 | 2868 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0024 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0026 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0029 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0031 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0035 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0037 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0003 | 0/0 | 2868 | 38 | 7 | 7 | 21 | 1 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0030 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0003c0006 | 0/0 | 2868 | 23 | 4 | 7 | 4 | 3 | 5 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0004c0008 | 0/1 | 2868 | 9 | 1 | 2 | 0 | 2 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0009 | 0/0 | 2868 | 6 | 0 | 0 | 6 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0023 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0036 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0014 | 0/0 | 2868 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0016 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0007c0013 | 0/0 | 2868 | 4 | 3 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0008c0018 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0009c0021 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0010c0017 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0011c0015 | 0/0 | 2868 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0012c0042 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0013c0041 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0014c0039 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0015c0038 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0016c0027 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0017c0034 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0018c0032 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0019c0025 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0020c0033 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0021c0022 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0022c0028 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0023c0040 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6323 | 106 | 10 | 24 | 48 | 5 | 19 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0001t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0001t0015 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0001t0020 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0001t0029 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002t0002 | 1/0 | 6323 | 88 | 6 | 15 | 57 | 3 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002t0012 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002t0017 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002t0018 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0002t0031 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0004t0003 | 0/0 | 6324 | 31 | 17 | 5 | 7 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0005t0003 | 0/0 | 6324 | 2 | 1 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0005t0004 | 0/0 | 6323 | 20 | 12 | 1 | 3 | 0 | 4 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0005t0008 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0005t0023 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0007t0002 | 0/0 | 6323 | 14 | 0 | 2 | 12 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0007t0024 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0010t0002 | 0/0 | 6323 | 4 | 0 | 0 | 4 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0011t0004 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0012t0004 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0019t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0019t0015 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0020t0001 | 0/0 | 6323 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0024t0021 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0026t0028 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0029t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0031t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0035t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0001c0037t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0003t0005 | 0/0 | 6323 | 27 | 0 | 5 | 20 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0003t0007 | 0/0 | 6324 | 7 | 7 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0003t0009 | 0/0 | 6323 | 3 | 0 | 2 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0003t0032 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0002c0030t0005 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0003c0006t0003 | 0/0 | 6324 | 22 | 4 | 7 | 3 | 3 | 5 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0003c0006t0027 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0004c0008t0006 | 0/1 | 6323 | 8 | 1 | 2 | 0 | 2 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0004c0008t0030 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0009t0001 | 0/0 | 6323 | 5 | 0 | 0 | 5 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0009t0019 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0023t0001 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0005c0036t0002 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0014t0010 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0014t0022 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0014t0025 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0006c0016t0014 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0007c0013t0003 | 0/0 | 6324 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0007c0013t0011 | 0/0 | 6324 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0008c0018t0010 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0009c0021t0003 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0010c0017t0013 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0011c0015t0003 | 0/0 | 6324 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0012c0042t0016 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0013c0041t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0014c0039t0003 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0015c0038t0003 | 0/0 | 6324 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0016c0027t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0017c0034t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0018c0032t0001 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0019c0025t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0020c0033t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0021c0022t0026 | 0/0 | 6324 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0022c0028t0005 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
a0023c0040t0004 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | copy fasta | chr9 | 19048141 | 19107904 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0020g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0029g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0001 | 1/0 | 6 | 0 | 3 | 1 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0031g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0023g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0019t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0019t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0020t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0024t0021g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0026t0028g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0029t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0031t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0035t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0037t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0032g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0030t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0027g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0025 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0030g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0023t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0036t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0016t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0016t0014g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0008c0018t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0008c0018t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0009c0021t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0009c0021t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0010c0017t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0010c0017t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0011c0015t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0011c0015t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0012c0042t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0013c0041t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0014c0039t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0015c0038t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0016c0027t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0017c0034t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0018c0032t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0019c0025t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0020c0033t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0021c0022t0026g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0022c0028t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0023c0040t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00099 | hp2 | a0004 | c0008 | t0006 | g0025 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00140 | hp1 | a0003 | c0006 | t0003 | g0161 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00140 | hp2 | a0002 | c0003 | t0009 | g0313 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00408 | hp1 | a0005 | c0009 | t0001 | g0208 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00408 | hp2 | a0001 | c0031 | t0002 | g0209 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00423 | hp2 | a0001 | c0007 | t0002 | g0168 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00438 | hp2 | a0005 | c0009 | t0001 | g0238 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00544 | hp2 | a0001 | c0007 | t0002 | g0142 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00558 | hp1 | a0001 | c0007 | t0002 | g0152 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00609 | hp2 | a0001 | c0004 | t0003 | g0289 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00621 | hp2 | a0001 | c0002 | t0012 | g0075 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00639 | hp2 | a0002 | c0003 | t0005 | g0358 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00642 | hp2 | a0003 | c0006 | t0003 | g0154 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00733 | hp1 | a0003 | c0006 | t0003 | g0135 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00733 | hp2 | a0002 | c0003 | t0005 | g0355 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00735 | hp2 | a0002 | c0003 | t0009 | g0315 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00741 | hp2 | a0002 | c0003 | t0005 | g0331 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01069 | hp1 | a0001 | c0020 | t0001 | g0018 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01070 | hp2 | a0004 | c0008 | t0006 | g0366 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01074 | hp2 | a0004 | c0008 | t0006 | g0362 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01081 | hp1 | a0001 | c0005 | t0004 | g0132 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01081 | hp2 | a0003 | c0006 | t0003 | g0013 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01106 | hp1 | a0003 | c0006 | t0003 | g0166 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01167 | hp2 | a0002 | c0003 | t0005 | g0341 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01169 | hp2 | a0002 | c0003 | t0005 | g0347 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01192 | hp1 | a0002 | c0003 | t0009 | g0314 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01192 | hp2 | a0001 | c0004 | t0003 | g0300 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01243 | hp2 | a0007 | c0013 | t0003 | g0294 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01257 | hp2 | a0001 | c0004 | t0003 | g0023 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01258 | hp1 | a0001 | c0004 | t0003 | g0023 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01433 | hp1 | a0001 | c0004 | t0003 | g0302 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01516 | hp1 | a0001 | c0004 | t0003 | g0022 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01517 | hp1 | a0001 | c0004 | t0003 | g0022 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01884 | hp2 | a0001 | c0005 | t0004 | g0012 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0106 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01891 | hp2 | a0012 | c0042 | t0016 | g0318 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01928 | hp2 | a0001 | c0007 | t0002 | g0143 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01934 | hp2 | a0001 | c0007 | t0002 | g0144 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01943 | hp1 | a0015 | c0038 | t0003 | g0292 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01981 | hp2 | a0003 | c0006 | t0003 | g0148 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02015 | hp2 | a0002 | c0003 | t0032 | g0353 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02040 | hp2 | a0002 | c0003 | t0005 | g0346 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02055 | hp1 | a0001 | c0011 | t0004 | g0131 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02055 | hp2 | a0010 | c0017 | t0013 | g0172 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02056 | hp1 | a0002 | c0003 | t0005 | g0359 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02129 | hp2 | a0001 | c0002 | t0031 | g0325 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02132 | hp1 | a0003 | c0006 | t0027 | g0164 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02135 | hp1 | a0001 | c0004 | t0003 | g0290 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02145 | hp1 | a0003 | c0006 | t0003 | g0150 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02145 | hp2 | a0006 | c0014 | t0022 | g0124 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02155 | hp1 | a0002 | c0003 | t0005 | g0344 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02155 | hp2 | a0011 | c0015 | t0003 | g0285 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02165 | hp1 | a0002 | c0003 | t0005 | g0007 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02257 | hp1 | a0001 | c0004 | t0003 | g0310 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02258 | hp1 | a0001 | c0026 | t0028 | g0170 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02258 | hp2 | a0001 | c0004 | t0003 | g0301 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02280 | hp1 | a0001 | c0011 | t0004 | g0129 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02280 | hp2 | a0001 | c0005 | t0004 | g0012 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02293 | hp2 | a0003 | c0006 | t0003 | g0155 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02451 | hp1 | a0001 | c0004 | t0003 | g0306 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02451 | hp2 | a0003 | c0006 | t0003 | g0014 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02523 | hp1 | a0020 | c0033 | t0001 | g0226 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0303 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02572 | hp2 | a0001 | c0005 | t0008 | g0328 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02602 | hp1 | a0001 | c0005 | t0004 | g0098 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0309 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02622 | hp1 | a0001 | c0011 | t0004 | g0130 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02622 | hp2 | a0001 | c0004 | t0003 | g0295 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02630 | hp1 | a0001 | c0012 | t0004 | g0101 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02630 | hp2 | a0001 | c0005 | t0004 | g0115 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0304 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02647 | hp2 | a0001 | c0012 | t0004 | g0099 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02683 | hp1 | a0001 | c0005 | t0004 | g0121 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02683 | hp2 | a0001 | c0020 | t0001 | g0018 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02698 | hp1 | a0018 | c0032 | t0001 | g0224 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02717 | hp2 | a0009 | c0021 | t0003 | g0307 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02735 | hp1 | a0002 | c0003 | t0005 | g0330 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02738 | hp1 | a0001 | c0001 | t0029 | g0319 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02809 | hp1 | a0001 | c0002 | t0018 | g0171 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02809 | hp2 | a0001 | c0005 | t0003 | g0297 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02818 | hp1 | a0002 | c0003 | t0007 | g0368 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02818 | hp2 | a0001 | c0005 | t0004 | g0117 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02895 | hp2 | a0007 | c0013 | t0011 | g0324 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02896 | hp2 | a0007 | c0013 | t0011 | g0323 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02897 | hp2 | a0007 | c0013 | t0011 | g0322 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02922 | hp1 | a0006 | c0014 | t0025 | g0126 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02965 | hp1 | a0001 | c0005 | t0004 | g0109 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02965 | hp2 | a0002 | c0003 | t0007 | g0335 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02970 | hp1 | a0001 | c0005 | t0008 | g0326 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02970 | hp2 | a0006 | c0016 | t0014 | g0123 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03017 | hp2 | a0001 | c0005 | t0023 | g0095 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03041 | hp1 | a0002 | c0003 | t0007 | g0334 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03041 | hp2 | a0017 | c0034 | t0001 | g0201 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03098 | hp1 | a0001 | c0004 | t0003 | g0283 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03098 | hp2 | a0001 | c0019 | t0015 | g0119 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03130 | hp1 | a0001 | c0005 | t0004 | g0133 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03130 | hp2 | a0002 | c0003 | t0007 | g0337 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03139 | hp2 | a0001 | c0011 | t0004 | g0128 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03195 | hp1 | a0001 | c0037 | t0001 | g0311 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03195 | hp2 | a0001 | c0012 | t0004 | g0100 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03209 | hp1 | a0002 | c0003 | t0007 | g0333 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03209 | hp2 | a0001 | c0004 | t0003 | g0282 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03225 | hp1 | a0001 | c0005 | t0004 | g0118 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03225 | hp2 | a0001 | c0004 | t0003 | g0299 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03453 | hp1 | a0008 | c0018 | t0010 | g0102 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0215 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0116 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03486 | hp2 | a0010 | c0017 | t0013 | g0173 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03490 | hp1 | a0001 | c0005 | t0003 | g0114 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03491 | hp2 | a0001 | c0005 | t0004 | g0122 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03516 | hp1 | a0001 | c0005 | t0008 | g0329 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03516 | hp2 | a0001 | c0004 | t0003 | g0305 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03540 | hp1 | a0008 | c0018 | t0010 | g0103 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03540 | hp2 | a0003 | c0006 | t0003 | g0151 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03579 | hp1 | a0001 | c0012 | t0004 | g0127 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03654 | hp2 | a0001 | c0005 | t0004 | g0113 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03669 | hp1 | a0004 | c0008 | t0006 | g0363 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03688 | hp1 | a0003 | c0006 | t0003 | g0147 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03688 | hp2 | a0003 | c0006 | t0003 | g0167 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03704 | hp1 | a0004 | c0008 | t0006 | g0365 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03710 | hp1 | a0002 | c0003 | t0005 | g0007 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03831 | hp1 | a0005 | c0023 | t0001 | g0136 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03834 | hp1 | a0003 | c0006 | t0003 | g0165 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03942 | hp1 | a0004 | c0008 | t0030 | g0320 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04115 | hp2 | a0003 | c0006 | t0003 | g0158 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04184 | hp1 | a0021 | c0022 | t0026 | g0169 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04184 | hp2 | a0005 | c0036 | t0002 | g0069 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04228 | hp1 | a0003 | c0006 | t0003 | g0183 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04228 | hp2 | a0011 | c0015 | t0003 | g0284 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0108 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18522 | hp2 | a0003 | c0006 | t0003 | g0160 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18612 | hp2 | a0002 | c0003 | t0005 | g0352 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18747 | hp1 | a0005 | c0009 | t0001 | g0228 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0111 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18939 | hp2 | a0001 | c0004 | t0003 | g0105 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18942 | hp1 | a0001 | c0007 | t0002 | g0156 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18945 | hp1 | a0002 | c0003 | t0005 | g0343 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18945 | hp2 | a0002 | c0003 | t0005 | g0342 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18947 | hp1 | a0002 | c0003 | t0005 | g0345 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18947 | hp2 | a0005 | c0009 | t0001 | g0237 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18953 | hp2 | a0002 | c0003 | t0005 | g0354 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18954 | hp2 | a0005 | c0009 | t0019 | g0202 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18957 | hp1 | a0001 | c0007 | t0002 | g0159 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0104 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18961 | hp2 | a0001 | c0007 | t0002 | g0145 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18963 | hp2 | a0001 | c0004 | t0003 | g0288 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18964 | hp2 | a0001 | c0007 | t0002 | g0137 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18967 | hp1 | a0001 | c0007 | t0002 | g0163 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18971 | hp2 | a0001 | c0007 | t0002 | g0140 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18977 | hp2 | a0001 | c0029 | t0001 | g0227 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18979 | hp2 | a0001 | c0007 | t0002 | g0139 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18980 | hp2 | a0001 | c0035 | t0001 | g0239 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18981 | hp2 | a0001 | c0010 | t0002 | g0008 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0287 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18983 | hp2 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18985 | hp2 | a0001 | c0002 | t0012 | g0031 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18987 | hp1 | a0003 | c0006 | t0003 | g0138 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18990 | hp1 | a0023 | c0040 | t0004 | g0316 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18991 | hp1 | a0001 | c0007 | t0002 | g0153 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18993 | hp2 | a0001 | c0005 | t0004 | g0120 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18994 | hp1 | a0002 | c0003 | t0005 | g0356 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18999 | hp1 | a0002 | c0003 | t0005 | g0361 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19002 | hp2 | a0002 | c0003 | t0005 | g0351 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19004 | hp1 | a0001 | c0002 | t0017 | g0051 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19009 | hp1 | a0001 | c0005 | t0004 | g0107 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19010 | hp1 | a0001 | c0010 | t0002 | g0042 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19010 | hp2 | a0001 | c0007 | t0002 | g0141 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19012 | hp1 | a0002 | c0003 | t0005 | g0349 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19030 | hp1 | a0001 | c0005 | t0008 | g0327 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19030 | hp2 | a0002 | c0003 | t0007 | g0338 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19043 | hp1 | a0001 | c0004 | t0003 | g0024 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19043 | hp2 | a0001 | c0004 | t0003 | g0281 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19062 | hp1 | a0002 | c0003 | t0005 | g0348 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19062 | hp2 | a0001 | c0004 | t0003 | g0291 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19063 | hp1 | a0002 | c0003 | t0005 | g0339 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19066 | hp1 | a0022 | c0028 | t0005 | g0340 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19066 | hp2 | a0016 | c0027 | t0002 | g0071 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19068 | hp1 | a0003 | c0006 | t0003 | g0157 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19070 | hp1 | a0002 | c0030 | t0005 | g0321 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19072 | hp2 | a0002 | c0003 | t0005 | g0360 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19074 | hp1 | a0019 | c0025 | t0002 | g0056 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19079 | hp1 | a0002 | c0003 | t0005 | g0350 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19080 | hp1 | a0001 | c0005 | t0004 | g0134 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19081 | hp2 | a0005 | c0009 | t0001 | g0236 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19083 | hp1 | a0001 | c0019 | t0001 | g0029 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19083 | hp2 | a0002 | c0003 | t0005 | g0357 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19086 | hp1 | a0001 | c0010 | t0002 | g0040 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19086 | hp2 | a0001 | c0001 | t0020 | g0240 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19087 | hp1 | a0001 | c0007 | t0024 | g0162 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19088 | hp1 | a0003 | c0006 | t0003 | g0014 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19089 | hp1 | a0002 | c0003 | t0005 | g0332 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19091 | hp1 | a0001 | c0010 | t0002 | g0008 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0298 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20129 | hp1 | a0002 | c0003 | t0007 | g0336 | AFR | ASW | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20129 | hp2 | a0001 | c0004 | t0003 | g0024 | AFR | ASW | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20752 | hp2 | a0003 | c0006 | t0003 | g0146 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20805 | hp1 | a0003 | c0006 | t0003 | g0013 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20805 | hp2 | a0004 | c0008 | t0006 | g0364 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01123 | hp1 | a0003 | c0006 | t0003 | g0149 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01123 | hp2 | a0001 | c0004 | t0003 | g0286 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02109 | hp1 | a0001 | c0005 | t0004 | g0110 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02109 | hp2 | a0006 | c0016 | t0014 | g0125 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02486 | hp1 | a0001 | c0005 | t0004 | g0112 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02486 | hp2 | a0004 | c0008 | t0006 | g0367 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03471 | hp1 | a0001 | c0004 | t0003 | g0296 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03471 | hp2 | a0014 | c0039 | t0003 | g0308 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG06807 | hp2 | a0006 | c0014 | t0010 | g0277 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20300 | hp2 | a0009 | c0021 | t0003 | g0293 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA21309 | hp1 | a0001 | c0024 | t0021 | g0177 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA21309 | hp2 | a0013 | c0041 | t0001 | g0317 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
homoSapiens_chm13v2 | hp1 | a0004 | c0008 | t0006 | g0025 | REF | REF | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0001 | REF | REF | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056387
|
T | A | 1 | a0020 | 1 | HG02523.hp1 | stop_gained | HIGH | c.2824A>T | p.Lys942* | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3077/6323 | 2824/2868 | 942/955 | chr9 | 19056387 | ||
chr9:19057967
|
A | T | 1 | a0019 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2800T>A | p.Leu934Ile | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 3053/6323 | 2800/2868 | 934/955 | chr9 | 19057967 | ||
chr9:19057987
|
C | T | 1 | a0018 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2780G>A | p.Ser927Asn | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 3033/6323 | 2780/2868 | 927/955 | chr9 | 19057987 | ||
chr9:19058050
|
G | A | 1 | a0017 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2717C>T | p.Ser906Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2970/6323 | 2717/2868 | 906/955 | chr9 | 19058050 | ||
chr9:19058057
|
T | G | 1 | a0016 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2710A>C | p.Lys904Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2963/6323 | 2710/2868 | 904/955 | chr9 | 19058057 | ||
chr9:19058431
|
G | C | 1 | a0010 | 2 | HG02055.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.2336C>G | p.Thr779Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2589/6323 | 2336/2868 | 779/955 | chr9 | 19058431 | ||
chr9:19058485
|
C | A | 1 | a0003 | 23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
missense_variant | MODERATE | c.2282G>T | p.Ser761Ile | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2535/6323 | 2282/2868 | 761/955 | chr9 | 19058485 | ||
chr9:19058571
|
A | T | 1 | a0021 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.2196T>A | p.Phe732Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2449/6323 | 2196/2868 | 732/955 | chr9 | 19058571 | ||
chr9:19058735
|
G | A | 1 | a0008 | 2 | HG03453.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.2032C>T | p.Pro678Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2285/6323 | 2032/2868 | 678/955 | chr9 | 19058735 | ||
chr9:19058745
|
G | C | 2 | a0002a0022 | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
missense_variant | MODERATE | c.2022C>G | p.His674Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2275/6323 | 2022/2868 | 674/955 | chr9 | 19058745 | ||
chr9:19058923
|
G | A | 3 | a0003a0006a0008 | 30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
missense_variant | MODERATE | c.1844C>T | p.Ala615Val | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2097/6323 | 1844/2868 | 615/955 | chr9 | 19058923 | ||
chr9:19060106
|
G | A | 1 | a0016 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1747C>T | p.Arg583Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/17 | 2000/6323 | 1747/2868 | 583/955 | chr9 | 19060106 | ||
chr9:19060199
|
A | T | 1 | a0004 | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
missense_variant | MODERATE | c.1654T>A | p.Ser552Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/17 | 1907/6323 | 1654/2868 | 552/955 | chr9 | 19060199 | ||
chr9:19063097
|
T | G | 1 | a0022 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.1540A>C | p.Lys514Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/17 | 1793/6323 | 1540/2868 | 514/955 | chr9 | 19063097 | ||
chr9:19078259
|
C | A | 1 | a0007 | 4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.1108G>T | p.Val370Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1361/6323 | 1108/2868 | 370/955 | chr9 | 19078259 | ||
chr9:19078276
|
G | C | 1 | a0015 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.1091C>G | p.Thr364Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1344/6323 | 1091/2868 | 364/955 | chr9 | 19078276 | ||
chr9:19080572
|
T | C | 2 | a0009a0014 | 3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.971A>G | p.Gln324Arg | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1224/6323 | 971/2868 | 324/955 | chr9 | 19080572 | ||
chr9:19080579
|
G | A | 1 | a0005 | 8 | HG00408.hp1 HG00438.hp2 HG03831.hp1 others(5): Show |
missense_variant | MODERATE | c.964C>T | p.Arg322Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1217/6323 | 964/2868 | 322/955 | chr9 | 19080579 | ||
chr9:19086739
|
G | C | 1 | a0014 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.694C>G | p.Gln232Glu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/17 | 947/6323 | 694/2868 | 232/955 | chr9 | 19086739 | ||
chr9:19089419
|
T | C | 1 | a0012 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.577A>G | p.Asn193Asp | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/17 | 830/6323 | 577/2868 | 193/955 | chr9 | 19089419 | ||
chr9:19093270
|
C | T | 1 | a0010 | 2 | HG02055.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.337G>A | p.Gly113Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 590/6323 | 337/2868 | 113/955 | chr9 | 19093270 | ||
chr9:19093290
|
C | G | 1 | a0011 | 2 | HG02155.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.317G>C | p.Ser106Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 570/6323 | 317/2868 | 106/955 | chr9 | 19093290 | ||
chr9:19102615
|
G | A | 1 | a0023 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.37C>T | p.His13Tyr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 290/6323 | 37/2868 | 13/955 | chr9 | 19102615 | ||
chr9:19102648
|
T | C | 2 | a0012a0013 | 2 | HG01891.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.4A>G | p.Ser2Gly | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 257/6323 | 4/2868 | 2/955 | chr9 | 19102648 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056376
|
A | G | 1 | a0001c0026 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.2835T>C | p.Asp945Asp | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3088/6323 | 2835/2868 | 945/955 | chr9 | 19056376 | ||
chr9:19058115
|
G | A | 1 | a0008c0018 | 2 | HG03453.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.2652C>T | p.Thr884Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2905/6323 | 2652/2868 | 884/955 | chr9 | 19058115 | ||
chr9:19058427
|
G | A | 16 | a0001c0004a0001c0005a0001c0011others(13): Show | 130 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(127): Show |
synonymous_variant | LOW | c.2340C>T | p.Leu780Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2593/6323 | 2340/2868 | 780/955 | chr9 | 19058427 | ||
chr9:19058708
|
A | G | 1 | a0001c0024 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2059T>C | p.Leu687Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2312/6323 | 2059/2868 | 687/955 | chr9 | 19058708 | ||
chr9:19058715
|
T | G | 1 | a0001c0035 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.2052A>C | p.Ser684Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2305/6323 | 2052/2868 | 684/955 | chr9 | 19058715 | ||
chr9:19058781
|
G | A | 1 | a0001c0010 | 4 | NA18981.hp2 NA19010.hp1 NA19086.hp1 others(1): Show |
synonymous_variant | LOW | c.1986C>T | p.Cys662Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2239/6323 | 1986/2868 | 662/955 | chr9 | 19058781 | ||
chr9:19058823
|
A | G | 3 | a0002c0003a0002c0030a0022c0028 | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
synonymous_variant | LOW | c.1944T>C | p.Phe648Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2197/6323 | 1944/2868 | 648/955 | chr9 | 19058823 | ||
chr9:19063110
|
T | C | 12 | a0001c0001a0001c0019a0001c0020others(9): Show | 128 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
synonymous_variant | LOW | c.1527A>G | p.Leu509Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/17 | 1780/6323 | 1527/2868 | 509/955 | chr9 | 19063110 | ||
chr9:19076669
|
C | T | 1 | a0001c0029 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.1227G>A | p.Ser409Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/17 | 1480/6323 | 1227/2868 | 409/955 | chr9 | 19076669 | ||
chr9:19076675
|
G | C | 13 | a0001c0001a0001c0011a0001c0020others(10): Show | 131 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
synonymous_variant | LOW | c.1221C>G | p.Pro407Pro | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/17 | 1474/6323 | 1221/2868 | 407/955 | chr9 | 19076675 | ||
chr9:19078194
|
T | G | 1 | a0001c0012 | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1173A>C | p.Leu391Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1426/6323 | 1173/2868 | 391/955 | chr9 | 19078194 | ||
chr9:19080601
|
G | C | 1 | a0001c0020 | 2 | HG01069.hp1 HG02683.hp2 |
synonymous_variant | LOW | c.942C>G | p.Val314Val | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1195/6323 | 942/2868 | 314/955 | chr9 | 19080601 | ||
chr9:19087156
|
T | C | 8 | a0001c0004a0001c0037a0004c0008others(5): Show | 51 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(48): Show |
splice_region_variant&synonymous_variant | LOW | c.585A>G | p.Gln195Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/17 | 838/6323 | 585/2868 | 195/955 | chr9 | 19087156 | ||
chr9:19093289
|
A | G | 6 | a0001c0007a0003c0006a0005c0023others(3): Show | 45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
synonymous_variant | LOW | c.318T>C | p.Ser106Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 571/6323 | 318/2868 | 106/955 | chr9 | 19093289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19053213
|
A | G | 1 | a0001c0024t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3130T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3130 | chr9 | 19053213 | |||||
chr9:19053249
|
T | C | 11 | a0001c0005t0023a0002c0003t0005a0002c0003t0007others(8): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3094A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3094 | chr9 | 19053249 | |||||
chr9:19053281
|
T | C | 2 | a0004c0008t0006a0004c0008t0030 | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3062A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3062 | chr9 | 19053281 | |||||
chr9:19053349
|
T | A | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2994A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2994 | chr9 | 19053349 | |||||
chr9:19053377
|
G | A | 1 | a0002c0003t0032 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2966 | chr9 | 19053377 | |||||
chr9:19053420
|
T | G | 1 | a0001c0005t0023 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2923A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2923 | chr9 | 19053420 | |||||
chr9:19053489
|
T | C | 1 | a0001c0002t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2854 | chr9 | 19053489 | |||||
chr9:19053507
|
A | C | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2836 | chr9 | 19053507 | |||||
chr9:19053573
|
A | G | 2 | a0004c0008t0006a0004c0008t0030 | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2770T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2770 | chr9 | 19053573 | |||||
chr9:19053581
|
T | C | 2 | a0004c0008t0006a0004c0008t0030 | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2762A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2762 | chr9 | 19053581 | |||||
chr9:19053772
|
C | A | 5 | a0001c0005t0004a0001c0005t0008a0001c0011t0004others(2): Show | 33 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2571G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2571 | chr9 | 19053772 | |||||
chr9:19053813
|
A | G | 6 | a0002c0003t0005a0002c0003t0007a0002c0003t0009others(3): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2530T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2530 | chr9 | 19053813 | |||||
chr9:19053851
|
G | C | 2 | a0004c0008t0006a0004c0008t0030 | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2492C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2492 | chr9 | 19053851 | |||||
chr9:19053919
|
T | C | 26 | a0001c0004t0003a0001c0005t0003a0001c0005t0004others(23): Show | 145 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2424A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2424 | chr9 | 19053919 | |||||
chr9:19053925
|
T | C | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2418A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2418 | chr9 | 19053925 | |||||
chr9:19054078
|
A | C | 2 | a0006c0014t0010a0008c0018t0010 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2265T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2265 | chr9 | 19054078 | |||||
chr9:19054251
|
C | T | 1 | a0006c0014t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2092G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2092 | chr9 | 19054251 | |||||
chr9:19054340
|
C | G | 1 | a0012c0042t0016 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2003 | chr9 | 19054340 | |||||
chr9:19054389
|
C | T | 28 | a0001c0004t0003a0001c0005t0003a0001c0005t0004others(25): Show | 148 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1954 | chr9 | 19054389 | |||||
chr9:19054423
|
C | A | 50 | a0001c0001t0001a0001c0001t0015a0001c0001t0020others(47): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1920G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1920 | chr9 | 19054423 | |||||
chr9:19054609
|
G | T | 1 | a0001c0024t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1734 | chr9 | 19054609 | |||||
chr9:19054921
|
G | C | 1 | a0005c0009t0019 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1422C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1422 | chr9 | 19054921 | |||||
chr9:19054957
|
A | T | 2 | a0006c0014t0010a0008c0018t0010 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1386 | chr9 | 19054957 | |||||
chr9:19055002
|
A | AT | 1 | a0002c0003t0007 | 7 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1340dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1340 | chr9 | 19055002 | |||||
chr9:19055068
|
C | T | 1 | a0006c0016t0014 | 2 | HG02109.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1275 | chr9 | 19055068 | |||||
chr9:19055071
|
A | G | 1 | a0001c0002t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1272 | chr9 | 19055071 | |||||
chr9:19055092
|
G | A | 1 | a0001c0001t0020 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1251 | chr9 | 19055092 | |||||
chr9:19055142
|
A | T | 2 | a0006c0016t0014a0012c0042t0016 | 3 | HG01891.hp2 HG02109.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1201T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1201 | chr9 | 19055142 | |||||
chr9:19055528
|
A | G | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 815 | chr9 | 19055528 | |||||
chr9:19055967
|
T | C | 36 | a0001c0001t0015a0001c0004t0003a0001c0005t0003others(33): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 376 | chr9 | 19055967 | |||||
chr9:19056100
|
T | A | 1 | a0003c0006t0027 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*243A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 243 | chr9 | 19056100 | |||||
chr9:19056149
|
T | TA | 15 | a0001c0004t0003a0001c0005t0003a0001c0007t0024others(12): Show | 72 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*193dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 193 | chr9 | 19056149 | |||||
chr9:19056160
|
A | G | 1 | a0010c0017t0013 | 2 | HG02055.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 183 | chr9 | 19056160 | |||||
chr9:19056210
|
G | T | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 133 | chr9 | 19056210 | |||||
chr9:19056279
|
A | C | 1 | a0001c0002t0012 | 2 | HG00621.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 64 | chr9 | 19056279 | |||||
chr9:19056325
|
T | G | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 18 | chr9 | 19056325 | |||||
chr9:19102779
|
T | A | 2 | a0001c0001t0029a0004c0008t0030 | 2 | HG02738.hp1 HG03942.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | chr9 | 19102779 | ||||||
chr9:19102830
|
T | C | 9 | a0001c0002t0031a0001c0005t0008a0002c0003t0005others(6): Show | 53 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-179A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 179 | chr9 | 19102830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056484
|
A | G | 1 | a0002c0003t0005g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2807-80T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056484 | ||||||
chr9:19056501
|
T | C | 3 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0283 | 5 | HG01257.hp2 HG01258.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2807-97A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056501 | ||||||
chr9:19056508
|
C | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2807-104G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056508 | ||||||
chr9:19056597
|
CT | C | 8 | a0001c0005t0008g0328a0002c0003t0007g0333a0002c0003t0007g0334others(5): Show | 8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2807-194delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056597 | ||||||
chr9:19056602
|
T | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2807-198A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056602 | ||||||
chr9:19056726
|
G | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0001g0185others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2807-322C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056726 | ||||||
chr9:19056750
|
G | A | 2 | a0006c0016t0014g0123a0006c0016t0014g0125 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2807-346C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056750 | ||||||
chr9:19056756
|
G | A | 149 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(146): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2807-352C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056756 | ||||||
chr9:19056794
|
T | C | 1 | a0005c0009t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2807-390A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056794 | ||||||
chr9:19056858
|
C | T | 22 | a0003c0006t0003g0013a0003c0006t0003g0014a0003c0006t0003g0135others(19): Show | 24 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.2807-454G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056858 | ||||||
chr9:19056926
|
T | TAA | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0273 | 3 | NA18973.hp1 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2807-524_2807-523d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056926 | ||||||
chr9:19057007
|
T | G | 1 | a0022c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2807-603A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057007 | ||||||
chr9:19057010
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2807-606A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057010 | ||||||
chr9:19057043
|
CA | C | 4 | a0001c0012t0004g0099a0001c0012t0004g0100a0001c0012t0004g0101others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2807-640delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057043 | ||||||
chr9:19057085
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2807-681G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057085 | ||||||
chr9:19057156
|
C | A | 2 | a0001c0004t0003g0024a0001c0004t0003g0299 | 3 | HG03225.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2807-752G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057156 | ||||||
chr9:19057423
|
G | A | 2 | a0001c0002t0002g0059a0001c0002t0002g0064 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2806+538C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057423 | ||||||
chr9:19057553
|
T | C | 143 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(140): Show | 151 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.2806+408A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057553 | ||||||
chr9:19057601
|
T | G | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2806+360A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057601 | ||||||
chr9:19057772
|
A | C | 15 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0104others(12): Show | 17 | HG00609.hp2 HG01123.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2806+189T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057772 | ||||||
chr9:19057779
|
T | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2806+182A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057779 | ||||||
chr9:19057854
|
A | G | 1 | a0001c0002t0002g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2806+107T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057854 | ||||||
chr9:19057878
|
C | T | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2806+83G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057878 | ||||||
chr9:19057912
|
G | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2806+49C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057912 | ||||||
chr9:19059157
|
T | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1766-156A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059157 | ||||||
chr9:19059287
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1766-286C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059287 | ||||||
chr9:19059375
|
A | T | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1766-374T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059375 | ||||||
chr9:19059377
|
T | C | 3 | a0006c0014t0022g0124a0006c0016t0014g0123a0006c0016t0014g0125 | 3 | HG02109.hp2 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1766-376A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059377 | ||||||
chr9:19059397
|
T | C | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1766-396A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059397 | ||||||
chr9:19059399
|
A | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18950.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1766-398T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059399 | ||||||
chr9:19059553
|
A | G | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1765+535T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059553 | ||||||
chr9:19059658
|
G | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1765+430C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059658 | ||||||
chr9:19059680
|
G | A | 21 | a0003c0006t0003g0013a0003c0006t0003g0014a0003c0006t0003g0135others(18): Show | 23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1765+408C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059680 | ||||||
chr9:19059702
|
T | G | 1 | a0001c0012t0004g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1765+386A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059702 | ||||||
chr9:19059765
|
T | C | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1765+323A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059765 | ||||||
chr9:19059771
|
T | C | 139 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(136): Show | 147 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1765+317A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059771 | ||||||
chr9:19059867
|
G | C | 23 | a0003c0006t0003g0013a0003c0006t0003g0014a0003c0006t0003g0135others(20): Show | 25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1765+221C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059867 | ||||||
chr9:19059892
|
T | C | 2 | a0006c0016t0014g0123a0006c0016t0014g0125 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1765+196A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059892 | ||||||
chr9:19059896
|
T | A | 2 | a0002c0003t0005g0341a0002c0003t0005g0347 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1765+192A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059896 | ||||||
chr9:19060048
|
C | T | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1765+40G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19060048 | ||||||
chr9:19060233
|
A | G | 2 | a0001c0004t0003g0300a0001c0004t0003g0301 | 2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1630-10T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060233 | ||||||
chr9:19060370
|
C | A | 150 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(147): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1630-147G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060370 | ||||||
chr9:19060371
|
A | G | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1630-148T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060371 | ||||||
chr9:19060372
|
A | T | 40 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(37): Show | 43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1630-149T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060372 | ||||||
chr9:19060410
|
G | C | 1 | a0001c0020t0001g0018 | 2 | HG01069.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1630-187C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060410 | ||||||
chr9:19060417
|
G | C | 10 | a0001c0005t0004g0012a0001c0005t0004g0108a0001c0005t0004g0109others(7): Show | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-194C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060417 | ||||||
chr9:19060425
|
G | A | 150 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(147): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1630-202C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060425 | ||||||
chr9:19060556
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1630-333G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060556 | ||||||
chr9:19060828
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1630-605G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060828 | ||||||
chr9:19060891
|
G | A | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1630-668C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060891 | ||||||
chr9:19060962
|
G | T | 1 | a0001c0020t0001g0018 | 2 | HG01069.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1630-739C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060962 | ||||||
chr9:19061118
|
C | T | 1 | a0003c0006t0003g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1630-895G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061118 | ||||||
chr9:19061159
|
C | T | 138 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(135): Show | 146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1630-936G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061159 | ||||||
chr9:19061249
|
G | A | 1 | a0001c0002t0002g0080 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1630-1026C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061249 | ||||||
chr9:19061250
|
C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1630-1027G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061250 | ||||||
chr9:19061275
|
T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1630-1052A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061275 | ||||||
chr9:19061289
|
C | T | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1630-1066G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061289 | ||||||
chr9:19061360
|
C | T | 138 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(135): Show | 146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1630-1137G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061360 | ||||||
chr9:19061466
|
G | C | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1630-1243C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061466 | ||||||
chr9:19061626
|
C | T | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1629+1382G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061626 | ||||||
chr9:19061640
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1629+1368T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061640 | ||||||
chr9:19061660
|
T | C | 150 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(147): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1629+1348A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061660 | ||||||
chr9:19061661
|
C | T | 138 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(135): Show | 146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1629+1347G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061661 | ||||||
chr9:19061688
|
A | T | 2 | a0008c0018t0010g0102a0008c0018t0010g0103 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1629+1320T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061688 | ||||||
chr9:19061761
|
G | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1629+1247C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061761 | ||||||
chr9:19061767
|
C | T | 3 | a0001c0002t0002g0037a0001c0002t0002g0044a0001c0002t0002g0047 | 3 | NA18980.hp1 NA18993.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1629+1241G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061767 | ||||||
chr9:19061859
|
C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1629+1149G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061859 | ||||||
chr9:19061943
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+1065A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061943 | ||||||
chr9:19061986
|
G | C | 1 | a0004c0008t0006g0365 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1629+1022C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061986 | ||||||
chr9:19062120
|
C | G | 3 | a0009c0021t0003g0293a0009c0021t0003g0307a0014c0039t0003g0308 | 3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1629+888G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062120 | ||||||
chr9:19062168
|
T | C | 3 | a0009c0021t0003g0293a0009c0021t0003g0307a0014c0039t0003g0308 | 3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1629+840A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062168 | ||||||
chr9:19062280
|
A | T | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1629+728T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062280 | ||||||
chr9:19062350
|
A | G | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+658T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062350 | ||||||
chr9:19062355
|
A | G | 33 | a0001c0004t0003g0106a0001c0005t0004g0012a0001c0005t0004g0098others(30): Show | 34 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1629+653T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062355 | ||||||
chr9:19062460
|
G | C | 1 | a0001c0007t0002g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1629+548C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062460 | ||||||
chr9:19062512
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+496A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062512 | ||||||
chr9:19062534
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0216a0001c0001t0001g0241 | 5 | HG03017.hp1 HG03710.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+474C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062534 | ||||||
chr9:19062583
|
C | G | 114 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(111): Show | 120 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1629+425G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062583 | ||||||
chr9:19062609
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0020g0240 | 3 | NA18999.hp2 NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1629+399G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062609 | ||||||
chr9:19062691
|
T | G | 5 | a0002c0003t0007g0334a0002c0003t0007g0335a0002c0003t0007g0336others(2): Show | 5 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+317A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062691 | ||||||
chr9:19062773
|
C | T | 6 | a0001c0001t0001g0214a0001c0001t0001g0248a0001c0001t0001g0249others(3): Show | 6 | HG02257.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629+235G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062773 | ||||||
chr9:19062876
|
T | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1629+132A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062876 | ||||||
chr9:19062885
|
C | G | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+123G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062885 | ||||||
chr9:19062899
|
C | G | 1 | a0001c0001t0001g0021 | 2 | NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1629+109G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062899 | ||||||
chr9:19062944
|
A | G | 167 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(164): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1629+64T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062944 | ||||||
chr9:19063323
|
C | G | 2 | a0001c0002t0002g0034a0001c0002t0002g0060 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1444-130G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063323 | ||||||
chr9:19063368
|
G | A | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1443+146C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063368 | ||||||
chr9:19063369
|
A | AAT | 168 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(165): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1443+143_1443+144d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063369 | ||||||
chr9:19063379
|
G | T | 1 | a0001c0005t0004g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1443+135C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063379 | ||||||
chr9:19063392
|
A | AT | 3 | a0001c0001t0001g0017a0001c0001t0001g0229a0001c0001t0001g0232 | 4 | HG01884.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443+121dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063392 | ||||||
chr9:19063592
|
A | G | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1377-12T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063592 | ||||||
chr9:19063632
|
T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377-52A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063632 | ||||||
chr9:19063767
|
A | G | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1377-187T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063767 | ||||||
chr9:19063848
|
T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1377-268A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063848 | ||||||
chr9:19063931
|
T | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1377-351A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063931 | ||||||
chr9:19063970
|
A | AT | 15 | a0001c0001t0001g0252a0001c0002t0002g0011a0001c0002t0002g0181others(12): Show | 17 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1377-391dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | ||||||
chr9:19063970
|
A | ATT | 6 | a0006c0014t0010g0277a0006c0014t0022g0124a0006c0016t0014g0123others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377-392_1377-391d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | ||||||
chr9:19063970
|
A | ATTT | 78 | a0001c0005t0004g0012a0001c0005t0004g0098a0001c0005t0004g0107others(75): Show | 81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1377-393_1377-391d others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | ||||||
chr9:19063970
|
A | ATTTT | 25 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(22): Show | 27 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1377-394_1377-391d others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | ||||||
chr9:19063972
|
T | TTTA | 43 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(40): Show | 46 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.1377-393_1377-392i others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063972 | ||||||
chr9:19063975
|
T | A | 1 | a0001c0002t0002g0179 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1377-395A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063975 | ||||||
chr9:19063977
|
T | A | 2 | a0001c0005t0003g0297a0006c0014t0025g0126 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1377-397A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063977 | ||||||
chr9:19064036
|
T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1377-456A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064036 | ||||||
chr9:19064053
|
C | T | 1 | a0005c0036t0002g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1377-473G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064053 | ||||||
chr9:19064058
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG00099.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377-478G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064058 | ||||||
chr9:19064070
|
C | A | 140 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(137): Show | 148 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.1377-490G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064070 | ||||||
chr9:19064131
|
G | C | 151 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(148): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1377-551C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064131 | ||||||
chr9:19064192
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1377-612G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064192 | ||||||
chr9:19064299
|
T | C | 2 | a0001c0004t0003g0289a0001c0004t0003g0290 | 2 | HG00609.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1377-719A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064299 | ||||||
chr9:19064359
|
T | C | 1 | a0001c0007t0002g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1377-779A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064359 | ||||||
chr9:19064391
|
G | C | 1 | a0001c0019t0015g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1377-811C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064391 | ||||||
chr9:19064423
|
T | C | 2 | a0008c0018t0010g0102a0008c0018t0010g0103 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1377-843A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064423 | ||||||
chr9:19064691
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1377-1111A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064691 | ||||||
chr9:19064699
|
T | G | 168 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(165): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1377-1119A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064699 | ||||||
chr9:19064735
|
C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1377-1155G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064735 | ||||||
chr9:19065061
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1377-1481G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065061 | ||||||
chr9:19065154
|
G | C | 30 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(27): Show | 32 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1377-1574C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065154 | ||||||
chr9:19065297
|
T | C | 164 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1377-1717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065297 | ||||||
chr9:19065510
|
CA | C | 165 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(162): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1377-1931delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065510 | ||||||
chr9:19065528
|
G | A | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1377-1948C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065528 | ||||||
chr9:19065614
|
G | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377-2034C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065614 | ||||||
chr9:19065705
|
G | A | 1 | a0001c0005t0004g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1377-2125C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065705 | ||||||
chr9:19065713
|
C | T | 2 | a0001c0001t0001g0233a0001c0035t0001g0239 | 2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1377-2133G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065713 | ||||||
chr9:19065714
|
G | A | 2 | a0001c0001t0001g0223a0012c0042t0016g0318 | 2 | HG01891.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1377-2134C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065714 | ||||||
chr9:19065759
|
T | C | 1 | a0001c0002t0002g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1377-2179A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065759 | ||||||
chr9:19065827
|
A | G | 164 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1377-2247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065827 | ||||||
chr9:19065836
|
C | T | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377-2256G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065836 | ||||||
chr9:19065848
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1377-2268T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065848 | ||||||
chr9:19065864
|
T | C | 164 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1377-2284A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065864 | ||||||
chr9:19065935
|
A | AT | 13 | a0001c0001t0001g0027a0001c0001t0001g0246a0001c0001t0001g0255others(10): Show | 13 | HG00544.hp1 HG01175.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377-2356dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065935 | ||||||
chr9:19065935
|
AT | A | 61 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0220others(58): Show | 65 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1377-2356delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065935 | ||||||
chr9:19066048
|
G | A | 36 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(33): Show | 38 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1377-2468C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066048 | ||||||
chr9:19066084
|
G | A | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1377-2504C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066084 | ||||||
chr9:19066102
|
A | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377-2522T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066102 | ||||||
chr9:19066117
|
A | G | 164 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1377-2537T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066117 | ||||||
chr9:19066137
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1377-2557A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066137 | ||||||
chr9:19066150
|
G | T | 3 | a0001c0005t0004g0111a0001c0005t0004g0112a0001c0005t0004g0116 | 3 | HG02486.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1377-2570C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066150 | ||||||
chr9:19066193
|
C | A | 1 | a0001c0002t0002g0015 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1377-2613G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066193 | ||||||
chr9:19066553
|
C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377-2973G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066553 | ||||||
chr9:19066579
|
CCA | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377-3001_1377-300 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066579 | ||||||
chr9:19066582
|
C | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377-3002G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066582 | ||||||
chr9:19066687
|
C | T | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1377-3107G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066687 | ||||||
chr9:19066698
|
G | C | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1377-3118C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066698 | ||||||
chr9:19066811
|
T | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377-3231A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066811 | ||||||
chr9:19066830
|
C | CA | 115 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0247others(112): Show | 119 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1377-3251dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | ||||||
chr9:19066830
|
C | CAA | 7 | a0001c0004t0003g0290a0001c0005t0008g0327a0001c0005t0008g0328others(4): Show | 7 | HG01934.hp2 HG02135.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377-3252_1377-325 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | ||||||
chr9:19066830
|
CAAAAAA | C | 38 | a0001c0005t0023g0095a0002c0003t0005g0007a0002c0003t0005g0330others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1377-3256_1377-325 others(10): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | ||||||
chr9:19067005
|
C | CA | 7 | a0001c0002t0002g0048a0001c0007t0002g0163a0001c0024t0021g0177others(4): Show | 7 | HG02055.hp2 HG02698.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1376+3213dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067005 | ||||||
chr9:19067103
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+3116A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067103 | ||||||
chr9:19067131
|
T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1376+3088A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067131 | ||||||
chr9:19067149
|
T | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+3070A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067149 | ||||||
chr9:19067214
|
C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+3005G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067214 | ||||||
chr9:19067238
|
A | G | 1 | a0001c0005t0004g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1376+2981T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067238 | ||||||
chr9:19067243
|
A | G | 2 | a0001c0026t0028g0170a0013c0041t0001g0317 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1376+2976T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067243 | ||||||
chr9:19067260
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+2959A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067260 | ||||||
chr9:19067320
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1376+2899T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067320 | ||||||
chr9:19067362
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1376+2857G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067362 | ||||||
chr9:19067432
|
T | C | 1 | a0002c0003t0005g0358 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1376+2787A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067432 | ||||||
chr9:19067483
|
G | A | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1376+2736C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067483 | ||||||
chr9:19067510
|
C | T | 2 | a0001c0010t0002g0008a0001c0010t0002g0040 | 3 | NA18981.hp2 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1376+2709G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067510 | ||||||
chr9:19067694
|
G | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1376+2525C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067694 | ||||||
chr9:19067757
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1376+2462G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067757 | ||||||
chr9:19067765
|
C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1376+2454G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067765 | ||||||
chr9:19067775
|
G | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+2444C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067775 | ||||||
chr9:19067835
|
A | G | 165 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(162): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1376+2384T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067835 | ||||||
chr9:19067867
|
T | G | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+2352A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067867 | ||||||
chr9:19067997
|
CA | C | 5 | a0002c0003t0005g0339a0002c0003t0005g0344a0002c0003t0005g0345others(2): Show | 5 | HG02155.hp1 HG03453.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+2221delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067997 | ||||||
chr9:19067998
|
A | C | 2 | a0005c0009t0001g0228a0005c0009t0001g0238 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1376+2221T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067998 | ||||||
chr9:19068053
|
A | G | 166 | a0001c0002t0018g0171a0001c0004t0003g0022a0001c0004t0003g0023others(163): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1376+2166T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068053 | ||||||
chr9:19068132
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1376+2087C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068132 | ||||||
chr9:19068151
|
T | C | 2 | a0001c0001t0001g0257a0018c0032t0001g0224 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1376+2068A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068151 | ||||||
chr9:19068252
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG00323.hp2 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1376+1967G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068252 | ||||||
chr9:19068254
|
CCAGGTCC others(113): Show |
C | 3 | a0002c0003t0005g0332a0002c0003t0005g0360a0022c0028t0005g0340 | 3 | NA19066.hp1 NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1376+1845_1376+196 others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068254 | ||||||
chr9:19068257
|
G | A | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1376+1962C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068257 | ||||||
chr9:19068320
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1376+1899A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068320 | ||||||
chr9:19068320
|
T | G | 45 | a0001c0005t0023g0095a0001c0007t0002g0137a0001c0007t0002g0139others(42): Show | 47 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1376+1899A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068320 | ||||||
chr9:19068374
|
A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1376+1845T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068374 | ||||||
chr9:19068495
|
C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+1724G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068495 | ||||||
chr9:19068507
|
T | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1376+1712A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068507 | ||||||
chr9:19068510
|
C | A | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1376+1709G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068510 | ||||||
chr9:19068581
|
C | T | 121 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(118): Show | 128 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.1376+1638G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068581 | ||||||
chr9:19068667
|
C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+1552G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068667 | ||||||
chr9:19068714
|
T | TA | 83 | a0001c0001t0001g0259a0001c0004t0003g0022a0001c0004t0003g0023others(80): Show | 88 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1376+1504dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068714 | ||||||
chr9:19068804
|
T | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+1415A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068804 | ||||||
chr9:19068845
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1376+1374T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068845 | ||||||
chr9:19068907
|
T | C | 1 | a0001c0007t0002g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1376+1312A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068907 | ||||||
chr9:19068952
|
A | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1376+1267T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068952 | ||||||
chr9:19068966
|
T | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+1253A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068966 | ||||||
chr9:19069017
|
C | T | 1 | a0014c0039t0003g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1376+1202G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069017 | ||||||
chr9:19069120
|
C | T | 1 | a0021c0022t0026g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1376+1099G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069120 | ||||||
chr9:19069411
|
G | A | 112 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(109): Show | 118 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.1376+808C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069411 | ||||||
chr9:19069481
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1376+738C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069481 | ||||||
chr9:19069487
|
G | A | 72 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(69): Show | 76 | HG00609.hp2 HG01081.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.1376+732C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069487 | ||||||
chr9:19069566
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1376+653C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069566 | ||||||
chr9:19069653
|
C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1376+566G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069653 | ||||||
chr9:19069827
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+392T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069827 | ||||||
chr9:19069863
|
C | A | 81 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(78): Show | 86 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1376+356G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069863 | ||||||
chr9:19069913
|
C | T | 118 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(115): Show | 125 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1376+306G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069913 | ||||||
chr9:19069972
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069972 | ||||||
chr9:19070108
|
C | G | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1376+111G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070108 | ||||||
chr9:19070132
|
G | A | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1376+87C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070132 | ||||||
chr9:19070133
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+86G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070133 | ||||||
chr9:19070193
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1376+26T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070193 | ||||||
chr9:19070391
|
C | G | 3 | a0006c0014t0010g0277a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1295-91G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070391 | ||||||
chr9:19070474
|
A | G | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1295-174T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070474 | ||||||
chr9:19070483
|
G | C | 1 | a0004c0008t0006g0364 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1295-183C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070483 | ||||||
chr9:19070488
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-188G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070488 | ||||||
chr9:19070609
|
C | G | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1295-309G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070609 | ||||||
chr9:19070615
|
C | T | 4 | a0001c0002t0002g0030a0001c0002t0002g0038a0001c0002t0002g0039others(1): Show | 4 | NA18963.hp1 NA18986.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295-315G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070615 | ||||||
chr9:19070619
|
C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1295-319G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070619 | ||||||
chr9:19070664
|
T | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-364A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070664 | ||||||
chr9:19071205
|
A | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1295-905T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071205 | ||||||
chr9:19071237
|
A | G | 48 | a0001c0001t0001g0017a0001c0002t0002g0179a0001c0005t0004g0132others(45): Show | 51 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1295-937T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071237 | ||||||
chr9:19071304
|
G | C | 1 | a0002c0030t0005g0321 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1295-1004C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071304 | ||||||
chr9:19071366
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1295-1066G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071366 | ||||||
chr9:19071404
|
A | G | 1 | a0001c0002t0002g0084 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1295-1104T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071404 | ||||||
chr9:19071573
|
C | CT | 46 | a0001c0002t0002g0079a0001c0002t0002g0083a0001c0002t0002g0091others(43): Show | 48 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1295-1274dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | ||||||
chr9:19071573
|
C | CTT | 8 | a0001c0007t0002g0153a0003c0006t0003g0013a0003c0006t0003g0148others(5): Show | 9 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-1275_1295-127 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | ||||||
chr9:19071573
|
CT | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 236 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1295-1274delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | ||||||
chr9:19071617
|
C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1295-1317G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071617 | ||||||
chr9:19071640
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0275 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1295-1340G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071640 | ||||||
chr9:19071654
|
G | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295-1354C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071654 | ||||||
chr9:19071658
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1295-1358G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071658 | ||||||
chr9:19071833
|
G | C | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1295-1533C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071833 | ||||||
chr9:19071925
|
C | T | 1 | a0001c0004t0003g0282 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1295-1625G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071925 | ||||||
chr9:19071979
|
G | A | 1 | a0022c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1295-1679C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071979 | ||||||
chr9:19071996
|
G | C | 2 | a0008c0018t0010g0102a0008c0018t0010g0103 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1295-1696C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071996 | ||||||
chr9:19072014
|
G | GCCAACAT others(7): Show |
8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-1715_1295-171 others(18): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072014 | ||||||
chr9:19072095
|
T | C | 1 | a0001c0005t0004g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-1795A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072095 | ||||||
chr9:19072175
|
A | G | 1 | a0004c0008t0006g0363 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1295-1875T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072175 | ||||||
chr9:19072190
|
C | CA | 156 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0002t0018g0171others(153): Show | 164 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1295-1891dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072190 | ||||||
chr9:19072220
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1295-1920T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072220 | ||||||
chr9:19072248
|
A | C | 153 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0002t0018g0171others(150): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1295-1948T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072248 | ||||||
chr9:19072289
|
G | T | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295-1989C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072289 | ||||||
chr9:19072292
|
C | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0001g0185others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1295-1992G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072292 | ||||||
chr9:19072294
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-1994G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072294 | ||||||
chr9:19072386
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0269 | 3 | NA18957.hp2 NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1295-2086C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072386 | ||||||
chr9:19072423
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1295-2123C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072423 | ||||||
chr9:19072508
|
CA | C | 13 | a0001c0002t0002g0087a0001c0005t0004g0109a0001c0005t0023g0095others(10): Show | 14 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1295-2209delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072508 | ||||||
chr9:19072586
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-2286G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072586 | ||||||
chr9:19072600
|
G | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1295-2300C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072600 | ||||||
chr9:19072629
|
C | G | 2 | a0001c0002t0018g0171a0001c0024t0021g0177 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1295-2329G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072629 | ||||||
chr9:19072747
|
T | C | 1 | a0003c0006t0003g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1295-2447A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072747 | ||||||
chr9:19072926
|
C | G | 112 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0004t0003g0022others(109): Show | 118 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-2626G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072926 | ||||||
chr9:19073025
|
C | A | 1 | a0005c0036t0002g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1295-2725G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073025 | ||||||
chr9:19073034
|
A | C | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1295-2734T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073034 | ||||||
chr9:19073180
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1295-2880A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073180 | ||||||
chr9:19073200
|
G | C | 1 | a0002c0003t0005g0346 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1295-2900C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073200 | ||||||
chr9:19073246
|
T | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-2946A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073246 | ||||||
chr9:19073422
|
G | GA | 111 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(108): Show | 117 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1295-3123dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073422 | ||||||
chr9:19073447
|
T | C | 34 | a0001c0004t0003g0106a0001c0005t0003g0114a0001c0005t0004g0012others(31): Show | 35 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1295-3147A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073447 | ||||||
chr9:19073474
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1294+3128C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073474 | ||||||
chr9:19073642
|
C | A | 10 | a0001c0005t0023g0095a0004c0008t0006g0025a0004c0008t0006g0362others(7): Show | 11 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+2960G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073642 | ||||||
chr9:19073654
|
A | C | 1 | a0001c0005t0004g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1294+2948T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073654 | ||||||
chr9:19073912
|
A | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1294+2690T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073912 | ||||||
chr9:19073922
|
T | G | 1 | a0004c0008t0006g0367 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1294+2680A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073922 | ||||||
chr9:19073970
|
A | G | 10 | a0001c0005t0023g0095a0004c0008t0006g0025a0004c0008t0006g0362others(7): Show | 11 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+2632T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073970 | ||||||
chr9:19074073
|
C | A | 1 | a0011c0015t0003g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1294+2529G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074073 | ||||||
chr9:19074115
|
A | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+2487T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074115 | ||||||
chr9:19074140
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1294+2462C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074140 | ||||||
chr9:19074195
|
C | T | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1294+2407G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074195 | ||||||
chr9:19074220
|
C | T | 3 | a0001c0005t0004g0107a0001c0005t0004g0134a0023c0040t0004g0316 | 3 | NA18990.hp1 NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1294+2382G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074220 | ||||||
chr9:19074244
|
C | CA | 12 | a0002c0003t0005g0342a0002c0003t0005g0349a0002c0003t0005g0354others(9): Show | 13 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1294+2357dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074244 | ||||||
chr9:19074333
|
G | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+2269C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074333 | ||||||
chr9:19074342
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1294+2260C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074342 | ||||||
chr9:19074355
|
T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1294+2247A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074355 | ||||||
chr9:19074364
|
C | T | 1 | a0003c0006t0003g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1294+2238G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074364 | ||||||
chr9:19074416
|
C | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1294+2186G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074416 | ||||||
chr9:19074428
|
G | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+2174C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074428 | ||||||
chr9:19074492
|
G | A | 1 | a0002c0003t0005g0356 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1294+2110C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074492 | ||||||
chr9:19074540
|
A | G | 164 | a0001c0002t0018g0171a0001c0004t0003g0022a0001c0004t0003g0023others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1294+2062T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074540 | ||||||
chr9:19074561
|
T | C | 1 | a0001c0004t0003g0295 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1294+2041A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074561 | ||||||
chr9:19074742
|
A | G | 51 | a0001c0005t0023g0095a0001c0007t0002g0137a0001c0007t0002g0139others(48): Show | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1294+1860T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074742 | ||||||
chr9:19074788
|
A | T | 51 | a0001c0005t0023g0095a0001c0007t0002g0137a0001c0007t0002g0139others(48): Show | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1294+1814T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074788 | ||||||
chr9:19074812
|
C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1294+1790G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074812 | ||||||
chr9:19074822
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1294+1780G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074822 | ||||||
chr9:19075001
|
A | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1294+1601T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075001 | ||||||
chr9:19075327
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1294+1275A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075327 | ||||||
chr9:19075632
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1294+970G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075632 | ||||||
chr9:19075664
|
C | T | 3 | a0002c0003t0005g0342a0002c0003t0005g0349a0002c0003t0005g0354 | 3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1294+938G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075664 | ||||||
chr9:19075675
|
C | T | 1 | a0002c0003t0007g0333 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1294+927G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075675 | ||||||
chr9:19075713
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1294+889C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075713 | ||||||
chr9:19075737
|
C | T | 1 | a0002c0003t0007g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1294+865G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075737 | ||||||
chr9:19075799
|
C | CA | 39 | a0001c0001t0001g0253a0002c0003t0005g0007a0002c0003t0005g0330others(36): Show | 41 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1294+802dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075799 | ||||||
chr9:19075860
|
G | C | 1 | a0001c0004t0003g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1294+742C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075860 | ||||||
chr9:19075915
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+687G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075915 | ||||||
chr9:19075961
|
A | G | 3 | a0001c0004t0003g0310a0010c0017t0013g0172a0010c0017t0013g0173 | 3 | HG02055.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1294+641T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075961 | ||||||
chr9:19075970
|
A | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+632T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075970 | ||||||
chr9:19075975
|
A | AC | 10 | a0001c0001t0001g0242a0001c0001t0001g0260a0001c0001t0001g0268others(7): Show | 10 | HG00423.hp2 HG02273.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294+626_1294+627i others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075975 | ||||||
chr9:19075975
|
A | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1294+627T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075975 | ||||||
chr9:19076012
|
G | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+590C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076012 | ||||||
chr9:19076083
|
G | T | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1294+519C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076083 | ||||||
chr9:19076096
|
A | G | 42 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+506T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076096 | ||||||
chr9:19076102
|
G | A | 42 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+500C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076102 | ||||||
chr9:19076169
|
G | A | 42 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+433C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076169 | ||||||
chr9:19076196
|
CA | C | 125 | a0001c0002t0002g0038a0001c0002t0018g0171a0001c0005t0003g0114others(122): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1294+405delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076196 | ||||||
chr9:19076208
|
A | T | 43 | a0001c0002t0002g0049a0001c0007t0002g0137a0001c0007t0002g0139others(40): Show | 45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1294+394T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076208 | ||||||
chr9:19076313
|
G | A | 2 | a0001c0001t0001g0257a0018c0032t0001g0224 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1294+289C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076313 | ||||||
chr9:19076315
|
C | T | 3 | a0002c0003t0005g0332a0002c0003t0005g0360a0022c0028t0005g0340 | 3 | NA19066.hp1 NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1294+287G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076315 | ||||||
chr9:19076316
|
T | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1294+286A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076316 | ||||||
chr9:19076355
|
A | G | 3 | a0002c0003t0005g0342a0002c0003t0005g0349a0002c0003t0005g0354 | 3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1294+247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076355 | ||||||
chr9:19076465
|
A | T | 1 | a0001c0012t0004g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1294+137T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076465 | ||||||
chr9:19076530
|
G | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0275 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1294+72C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076530 | ||||||
chr9:19076766
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192-62T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076766 | ||||||
chr9:19076792
|
CT | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192-89delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076792 | ||||||
chr9:19076857
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0086 | 4 | HG00597.hp2 NA18964.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-153A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076857 | ||||||
chr9:19076883
|
G | A | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1192-179C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076883 | ||||||
chr9:19077033
|
A | G | 346 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(343): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1192-329T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077033 | ||||||
chr9:19077095
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192-391G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077095 | ||||||
chr9:19077120
|
A | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1192-416T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077120 | ||||||
chr9:19077133
|
C | T | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1192-429G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077133 | ||||||
chr9:19077418
|
C | A | 11 | a0001c0004t0003g0104a0001c0004t0003g0105a0001c0004t0003g0286others(8): Show | 11 | HG00609.hp2 HG01123.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1192-714G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077418 | ||||||
chr9:19077423
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-719A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077423 | ||||||
chr9:19077472
|
C | T | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+704G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077472 | ||||||
chr9:19077490
|
G | A | 1 | a0001c0002t0002g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1191+686C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077490 | ||||||
chr9:19077492
|
G | A | 30 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(27): Show | 32 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1191+684C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077492 | ||||||
chr9:19077505
|
A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1191+671T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077505 | ||||||
chr9:19077516
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0020g0240 | 3 | NA18999.hp2 NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1191+660A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077516 | ||||||
chr9:19077612
|
C | T | 2 | a0001c0001t0001g0027a0001c0037t0001g0311 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1191+564G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077612 | ||||||
chr9:19077621
|
A | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+555T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077621 | ||||||
chr9:19077636
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+540G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077636 | ||||||
chr9:19077824
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1191+352C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077824 | ||||||
chr9:19077872
|
G | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+304C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077872 | ||||||
chr9:19077919
|
G | A | 3 | a0001c0026t0028g0170a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1191+257C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077919 | ||||||
chr9:19077922
|
T | G | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1191+254A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077922 | ||||||
chr9:19078012
|
G | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1191+164C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078012 | ||||||
chr9:19078118
|
C | CA | 7 | a0001c0001t0001g0192a0001c0004t0003g0024a0001c0004t0003g0298others(4): Show | 8 | HG00735.hp1 HG01433.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1191+57dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078118 | ||||||
chr9:19078133
|
A | C | 3 | a0001c0001t0001g0312a0010c0017t0013g0172a0010c0017t0013g0173 | 3 | HG01515.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1191+43T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078133 | ||||||
chr9:19078144
|
G | A | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+32C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078144 | ||||||
chr9:19078402
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0174a0001c0001t0001g0175others(9): Show | 14 | HG00544.hp1 HG00609.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1065-100A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078402 | ||||||
chr9:19078404
|
G | C | 2 | a0003c0006t0003g0158a0003c0006t0003g0165 | 2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1065-102C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078404 | ||||||
chr9:19078509
|
C | T | 1 | a0001c0005t0004g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-207G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078509 | ||||||
chr9:19078517
|
G | A | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0005t0003g0297 | 3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1065-215C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078517 | ||||||
chr9:19078584
|
T | C | 1 | a0001c0002t0002g0087 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1065-282A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078584 | ||||||
chr9:19078645
|
G | A | 3 | a0001c0026t0028g0170a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1065-343C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078645 | ||||||
chr9:19078781
|
G | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1065-479C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078781 | ||||||
chr9:19078801
|
A | T | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1065-499T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078801 | ||||||
chr9:19078845
|
TA | T | 125 | a0001c0002t0002g0037a0001c0002t0002g0041a0001c0002t0002g0043others(122): Show | 132 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.1065-544delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078845 | ||||||
chr9:19078845
|
TAA | T | 29 | a0001c0007t0024g0162a0002c0003t0005g0348a0003c0006t0003g0013others(26): Show | 31 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1065-545_1065-544d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078845 | ||||||
chr9:19078847
|
A | T | 2 | a0001c0004t0003g0281a0001c0004t0003g0282 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1065-545T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078847 | ||||||
chr9:19078937
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065-635T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078937 | ||||||
chr9:19079078
|
C | G | 1 | a0005c0009t0001g0237 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1065-776G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079078 | ||||||
chr9:19079119
|
G | A | 4 | a0001c0012t0004g0099a0001c0012t0004g0100a0001c0012t0004g0101others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065-817C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079119 | ||||||
chr9:19079160
|
G | A | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | HG03654.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1065-858C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079160 | ||||||
chr9:19079164
|
C | CA | 9 | a0001c0001t0001g0191a0001c0001t0001g0235a0001c0001t0001g0246others(6): Show | 9 | HG01175.hp1 HG02055.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065-863dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079164 | ||||||
chr9:19079164
|
CA | C | 31 | a0001c0005t0004g0122a0001c0007t0024g0162a0003c0006t0003g0013others(28): Show | 34 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1065-863delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079164 | ||||||
chr9:19079201
|
T | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-899A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079201 | ||||||
chr9:19079377
|
G | A | 71 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(68): Show | 75 | HG00609.hp2 HG01081.hp1 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.1065-1075C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079377 | ||||||
chr9:19079506
|
C | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1064+973G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079506 | ||||||
chr9:19079550
|
T | C | 1 | a0001c0002t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1064+929A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079550 | ||||||
chr9:19079678
|
G | A | 4 | a0001c0012t0004g0099a0001c0012t0004g0100a0001c0012t0004g0101others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064+801C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079678 | ||||||
chr9:19079720
|
T | C | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064+759A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079720 | ||||||
chr9:19079766
|
G | C | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0005t0003g0297 | 3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1064+713C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079766 | ||||||
chr9:19079800
|
G | A | 1 | a0001c0005t0003g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1064+679C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079800 | ||||||
chr9:19079828
|
G | A | 28 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(25): Show | 30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1064+651C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079828 | ||||||
chr9:19079831
|
A | C | 29 | a0001c0005t0023g0095a0001c0007t0024g0162a0003c0006t0003g0013others(26): Show | 31 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1064+648T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079831 | ||||||
chr9:19079851
|
A | G | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+628T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079851 | ||||||
chr9:19079890
|
A | G | 2 | a0002c0003t0005g0332a0002c0003t0005g0360 | 2 | NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1064+589T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079890 | ||||||
chr9:19079891
|
G | A | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064+588C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079891 | ||||||
chr9:19079941
|
G | A | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1064+538C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079941 | ||||||
chr9:19080038
|
G | A | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1064+441C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080038 | ||||||
chr9:19080056
|
C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1064+423G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080056 | ||||||
chr9:19080125
|
G | C | 1 | a0001c0029t0001g0227 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1064+354C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080125 | ||||||
chr9:19080138
|
C | A | 3 | a0001c0002t0002g0033a0001c0002t0002g0035a0001c0002t0002g0077 | 3 | NA18948.hp2 NA18967.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1064+341G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080138 | ||||||
chr9:19080161
|
C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+318G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080161 | ||||||
chr9:19080174
|
C | CA | 47 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0192others(44): Show | 49 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1064+304dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | ||||||
chr9:19080174
|
C | CAA | 58 | a0001c0001t0001g0253a0001c0001t0001g0263a0001c0004t0003g0022others(55): Show | 62 | HG01081.hp1 HG01192.hp2 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.1064+303_1064+304d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | ||||||
chr9:19080174
|
C | CAAA | 14 | a0001c0001t0001g0246a0001c0004t0003g0286a0001c0004t0003g0288others(11): Show | 14 | HG00609.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1064+302_1064+304d others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | ||||||
chr9:19080174
|
CA | C | 8 | a0001c0001t0001g0174a0001c0001t0001g0197a0001c0001t0001g0220others(5): Show | 8 | HG01516.hp2 HG02970.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064+304delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | ||||||
chr9:19080328
|
A | G | 3 | a0010c0017t0013g0172a0010c0017t0013g0173a0012c0042t0016g0318 | 3 | HG01891.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1064+151T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080328 | ||||||
chr9:19080354
|
A | G | 165 | a0001c0001t0001g0019a0001c0001t0020g0240a0001c0002t0018g0171others(162): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1064+125T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080354 | ||||||
chr9:19080388
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1064+91G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080388 | ||||||
chr9:19080708
|
A | G | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0005t0003g0297 | 3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.871-36T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080708 | ||||||
chr9:19080752
|
T | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-80A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080752 | ||||||
chr9:19080799
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.871-127C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080799 | ||||||
chr9:19080824
|
C | T | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.871-152G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080824 | ||||||
chr9:19080844
|
G | C | 1 | a0001c0005t0008g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.871-172C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080844 | ||||||
chr9:19080863
|
G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.871-191C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080863 | ||||||
chr9:19080880
|
C | T | 4 | a0001c0011t0004g0128a0001c0011t0004g0129a0001c0011t0004g0130others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-208G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080880 | ||||||
chr9:19080933
|
G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.871-261C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080933 | ||||||
chr9:19080986
|
C | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-314G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080986 | ||||||
chr9:19080987
|
G | A | 1 | a0001c0002t0002g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.871-315C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080987 | ||||||
chr9:19081096
|
CG | C | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.871-425delC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081096 | ||||||
chr9:19081117
|
C | T | 39 | a0001c0001t0001g0019a0001c0001t0020g0240a0002c0003t0005g0007others(36): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-445G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081117 | ||||||
chr9:19081136
|
G | A | 1 | a0001c0011t0004g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.871-464C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081136 | ||||||
chr9:19081196
|
T | C | 1 | a0001c0004t0003g0304 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-524A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081196 | ||||||
chr9:19081223
|
G | A | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.871-551C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081223 | ||||||
chr9:19081224
|
T | C | 1 | a0001c0010t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.871-552A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081224 | ||||||
chr9:19081276
|
G | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-604C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081276 | ||||||
chr9:19081313
|
T | A | 39 | a0001c0001t0001g0019a0001c0001t0020g0240a0002c0003t0005g0007others(36): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-641A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081313 | ||||||
chr9:19081511
|
C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-839G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081511 | ||||||
chr9:19081622
|
T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-950A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081622 | ||||||
chr9:19081730
|
T | C | 14 | a0001c0005t0003g0114a0001c0005t0004g0098a0001c0005t0004g0121others(11): Show | 14 | HG01081.hp1 HG02572.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-1058A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081730 | ||||||
chr9:19081869
|
G | A | 1 | a0001c0004t0003g0300 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.870+1004C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081869 | ||||||
chr9:19081899
|
TACTAA | T | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+969_870+973del others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081899 | ||||||
chr9:19081922
|
G | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.870+951C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081922 | ||||||
chr9:19081995
|
G | C | 4 | a0001c0005t0008g0326a0001c0005t0008g0327a0001c0005t0008g0328others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+878C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081995 | ||||||
chr9:19082121
|
T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.870+752A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082121 | ||||||
chr9:19082434
|
GT | G | 58 | a0001c0005t0003g0114a0001c0005t0004g0012a0001c0005t0004g0098others(55): Show | 61 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.870+438delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082434 | ||||||
chr9:19082434
|
GTT | G | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.870+437_870+438del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082434 | ||||||
chr9:19082578
|
G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.870+295C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082578 | ||||||
chr9:19082639
|
G | A | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+234C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082639 | ||||||
chr9:19082656
|
G | A | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.870+217C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082656 | ||||||
chr9:19082678
|
G | A | 1 | a0003c0006t0003g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.870+195C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082678 | ||||||
chr9:19082743
|
T | C | 38 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(35): Show | 41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.870+130A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082743 | ||||||
chr9:19082755
|
AAAAAAAC | A | 78 | a0001c0002t0018g0171a0001c0004t0003g0022a0001c0004t0003g0023others(75): Show | 83 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.870+111_870+117del others(7): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082755 | ||||||
chr9:19082834
|
G | A | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.870+39C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082834 | ||||||
chr9:19083057
|
A | C | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.700-14T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083057 | ||||||
chr9:19083122
|
T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.700-79A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083122 | ||||||
chr9:19083128
|
C | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-85G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083128 | ||||||
chr9:19083277
|
A | C | 1 | a0003c0006t0003g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700-234T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083277 | ||||||
chr9:19083449
|
C | G | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.700-406G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083449 | ||||||
chr9:19083585
|
G | A | 29 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(26): Show | 31 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.700-542C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083585 | ||||||
chr9:19083618
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.700-575G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083618 | ||||||
chr9:19083695
|
G | A | 37 | a0001c0005t0023g0095a0002c0003t0005g0007a0002c0003t0005g0330others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.700-652C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083695 | ||||||
chr9:19083698
|
A | G | 4 | a0001c0004t0003g0281a0001c0004t0003g0282a0001c0004t0003g0296others(1): Show | 4 | HG03209.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-655T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083698 | ||||||
chr9:19083728
|
G | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0187 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.700-685C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083728 | ||||||
chr9:19083733
|
C | T | 21 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(18): Show | 23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.700-690G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083733 | ||||||
chr9:19083756
|
C | T | 7 | a0001c0007t0002g0141a0001c0007t0002g0142a0001c0007t0002g0143others(4): Show | 7 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-713G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083756 | ||||||
chr9:19083757
|
G | A | 1 | a0001c0004t0003g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-714C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083757 | ||||||
chr9:19083759
|
G | A | 1 | a0003c0006t0003g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.700-716C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083759 | ||||||
chr9:19083812
|
A | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(107): Show | 122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.700-769T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083812 | ||||||
chr9:19083813
|
A | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG04115.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.700-770T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083813 | ||||||
chr9:19083817
|
AT | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.700-775delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083817 | ||||||
chr9:19083818
|
T | A | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0004t0003g0301others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-775A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083818 | ||||||
chr9:19083852
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.700-809T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083852 | ||||||
chr9:19083943
|
A | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.700-900T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083943 | ||||||
chr9:19083974
|
C | T | 1 | a0001c0002t0002g0035 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.700-931G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083974 | ||||||
chr9:19083978
|
C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.700-935G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083978 | ||||||
chr9:19084051
|
C | CA | 134 | a0001c0002t0002g0033a0001c0002t0002g0074a0001c0002t0012g0031others(131): Show | 141 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.700-1009dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084051 | ||||||
chr9:19084051
|
C | CAA | 11 | a0001c0004t0003g0024a0002c0003t0007g0338a0003c0006t0003g0150others(8): Show | 13 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.700-1010_700-1009d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084051 | ||||||
chr9:19084118
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.700-1075G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084118 | ||||||
chr9:19084177
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700-1134T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084177 | ||||||
chr9:19084250
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.700-1207T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084250 | ||||||
chr9:19084345
|
T | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-1302A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084345 | ||||||
chr9:19084407
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(111): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.700-1364C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084407 | ||||||
chr9:19084446
|
T | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(158): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.700-1403A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084446 | ||||||
chr9:19084504
|
T | C | 3 | a0001c0026t0028g0170a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.700-1461A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084504 | ||||||
chr9:19084531
|
A | G | 37 | a0001c0005t0023g0095a0002c0003t0005g0007a0002c0003t0005g0330others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.700-1488T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084531 | ||||||
chr9:19084551
|
G | C | 6 | a0001c0005t0004g0107a0001c0005t0004g0113a0001c0005t0004g0120others(3): Show | 6 | HG03654.hp2 NA18990.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.700-1508C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084551 | ||||||
chr9:19084569
|
T | TG | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.700-1527dupC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084569 | ||||||
chr9:19084582
|
C | T | 1 | a0002c0003t0005g0351 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.700-1539G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084582 | ||||||
chr9:19084635
|
CT | C | 72 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(69): Show | 78 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.700-1593delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084635 | ||||||
chr9:19084679
|
C | A | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.700-1636G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084679 | ||||||
chr9:19084788
|
A | G | 5 | a0001c0004t0003g0287a0001c0004t0003g0288a0001c0004t0003g0289others(2): Show | 5 | HG00609.hp2 HG02135.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1745T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084788 | ||||||
chr9:19084799
|
CT | C | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.700-1757delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084799 | ||||||
chr9:19084958
|
C | T | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.699+1776G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084958 | ||||||
chr9:19085035
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.699+1699G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085035 | ||||||
chr9:19085442
|
C | T | 1 | a0001c0001t0020g0240 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.699+1292G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085442 | ||||||
chr9:19085465
|
T | C | 2 | a0002c0003t0005g0343a0002c0003t0005g0350 | 2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.699+1269A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085465 | ||||||
chr9:19085466
|
G | A | 3 | a0006c0014t0022g0124a0006c0016t0014g0123a0006c0016t0014g0125 | 3 | HG02109.hp2 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.699+1268C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085466 | ||||||
chr9:19085615
|
C | CA | 35 | a0001c0002t0002g0179a0001c0004t0003g0106a0001c0005t0003g0114others(32): Show | 36 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.699+1118dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085615 | ||||||
chr9:19085615
|
CA | C | 88 | a0001c0001t0001g0229a0001c0002t0002g0036a0001c0002t0002g0091others(85): Show | 94 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.699+1118delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085615 | ||||||
chr9:19085908
|
G | A | 1 | a0002c0030t0005g0321 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.699+826C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085908 | ||||||
chr9:19085991
|
T | A | 1 | a0001c0002t0002g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.699+743A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | ||||||
chr9:19085991
|
T | TA | 47 | a0001c0001t0001g0262a0001c0004t0003g0022a0001c0004t0003g0023others(44): Show | 51 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.699+742dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | ||||||
chr9:19085991
|
TA | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0174a0001c0001t0001g0217others(5): Show | 9 | HG01884.hp1 HG02717.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+742delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | ||||||
chr9:19085992
|
A | T | 2 | a0002c0003t0007g0333a0003c0006t0003g0135 | 2 | HG00733.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.699+742T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085992 | ||||||
chr9:19086034
|
G | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0091a0001c0005t0023g0095 | 3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.699+700C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086034 | ||||||
chr9:19086143
|
C | T | 45 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(42): Show | 49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.699+591G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086143 | ||||||
chr9:19086147
|
A | G | 40 | a0001c0002t0002g0036a0001c0002t0002g0091a0001c0005t0023g0095others(37): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.699+587T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086147 | ||||||
chr9:19086165
|
G | C | 1 | a0001c0002t0002g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.699+569C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086165 | ||||||
chr9:19086188
|
G | T | 1 | a0002c0003t0009g0313 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.699+546C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086188 | ||||||
chr9:19086288
|
G | A | 3 | a0001c0002t0002g0076a0001c0002t0002g0096a0001c0002t0002g0097 | 3 | HG02056.hp2 NA18988.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.699+446C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086288 | ||||||
chr9:19086322
|
G | A | 50 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(47): Show | 54 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.699+412C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086322 | ||||||
chr9:19086712
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.699+22G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086712 | ||||||
chr9:19086787
|
T | C | 1 | a0001c0002t0002g0085 | 1 | NA18991.hp2 | splice_region_variant&intron_variant | LOW | c.651-5A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086787 | ||||||
chr9:19086811
|
C | T | 1 | a0003c0006t0003g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.651-29G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086811 | ||||||
chr9:19086870
|
C | G | 1 | a0008c0018t0010g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.651-88G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086870 | ||||||
chr9:19086968
|
T | C | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.650+123A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086968 | ||||||
chr9:19086981
|
C | T | 72 | a0001c0005t0003g0114a0001c0005t0004g0012a0001c0005t0004g0098others(69): Show | 75 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.650+110G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086981 | ||||||
chr9:19087198
|
G | A | 37 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(34): Show | 40 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.585-42C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087198 | ||||||
chr9:19087205
|
T | C | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-49A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087205 | ||||||
chr9:19087240
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.585-84A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087240 | ||||||
chr9:19087252
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.585-96C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087252 | ||||||
chr9:19087272
|
G | A | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-116C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087272 | ||||||
chr9:19087273
|
C | T | 2 | a0002c0003t0005g0343a0002c0003t0005g0350 | 2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.585-117G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087273 | ||||||
chr9:19087373
|
G | A | 1 | a0001c0035t0001g0239 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.585-217C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087373 | ||||||
chr9:19087400
|
G | A | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.585-244C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087400 | ||||||
chr9:19087431
|
A | G | 92 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(89): Show | 98 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.585-275T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087431 | ||||||
chr9:19087597
|
G | C | 2 | a0001c0007t0002g0143a0001c0007t0002g0144 | 2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.585-441C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087597 | ||||||
chr9:19087634
|
G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585-478C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087634 | ||||||
chr9:19087685
|
C | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585-529G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087685 | ||||||
chr9:19087755
|
A | T | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.585-599T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087755 | ||||||
chr9:19087846
|
C | CA | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 133 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.585-691dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | ||||||
chr9:19087846
|
C | CAA | 22 | a0001c0001t0001g0019a0001c0001t0001g0196a0001c0001t0001g0207others(19): Show | 23 | HG00597.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.585-692_585-691dup others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | ||||||
chr9:19087846
|
CA | C | 105 | a0001c0002t0002g0058a0001c0002t0002g0059a0001c0002t0002g0096others(102): Show | 110 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.585-691delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | ||||||
chr9:19087864
|
A | G | 47 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(44): Show | 51 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-708T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087864 | ||||||
chr9:19087895
|
C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585-739G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087895 | ||||||
chr9:19087910
|
G | C | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-754C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087910 | ||||||
chr9:19088014
|
A | T | 2 | a0004c0008t0006g0362a0004c0008t0006g0366 | 2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.585-858T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088014 | ||||||
chr9:19088034
|
T | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.585-878A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088034 | ||||||
chr9:19088073
|
G | C | 4 | a0006c0014t0010g0277a0010c0017t0013g0172a0010c0017t0013g0173others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-917C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088073 | ||||||
chr9:19088098
|
C | T | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.585-942G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088098 | ||||||
chr9:19088127
|
T | C | 47 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(44): Show | 51 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-971A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088127 | ||||||
chr9:19088193
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.585-1037A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088193 | ||||||
chr9:19088308
|
C | A | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.584+1104G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088308 | ||||||
chr9:19088377
|
C | A | 4 | a0007c0013t0003g0294a0007c0013t0011g0322a0007c0013t0011g0323others(1): Show | 4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+1035G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088377 | ||||||
chr9:19088409
|
C | G | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+1003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088409 | ||||||
chr9:19088415
|
C | CA | 71 | a0001c0001t0015g0215a0001c0002t0002g0036a0001c0002t0002g0048others(68): Show | 75 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.584+996dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088415 | ||||||
chr9:19088588
|
C | A | 26 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(23): Show | 28 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+824G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088588 | ||||||
chr9:19088713
|
C | CA | 6 | a0001c0001t0001g0246a0001c0001t0001g0261a0001c0002t0002g0033others(3): Show | 6 | HG01175.hp1 HG03017.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+698dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088713 | ||||||
chr9:19088740
|
T | A | 4 | a0007c0013t0003g0294a0007c0013t0011g0322a0007c0013t0011g0323others(1): Show | 4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+672A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088740 | ||||||
chr9:19088773
|
G | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.584+639C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088773 | ||||||
chr9:19088822
|
G | A | 26 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(23): Show | 28 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+590C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088822 | ||||||
chr9:19088824
|
G | GC | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.584+587dupG | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088824 | ||||||
chr9:19089100
|
G | C | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.584+312C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089100 | ||||||
chr9:19089198
|
G | T | 1 | a0001c0004t0003g0283 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.584+214C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089198 | ||||||
chr9:19089222
|
G | T | 37 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.584+190C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089222 | ||||||
chr9:19089267
|
AAAG | A | 24 | a0001c0002t0002g0077a0001c0007t0024g0162a0001c0031t0002g0209others(21): Show | 26 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+142_584+144del others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089267 | ||||||
chr9:19089277
|
A | T | 1 | a0001c0002t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.584+135T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089277 | ||||||
chr9:19089295
|
A | G | 46 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(43): Show | 50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.584+117T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089295 | ||||||
chr9:19089309
|
G | A | 37 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.584+103C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089309 | ||||||
chr9:19089377
|
A | C | 28 | a0001c0007t0024g0162a0003c0006t0003g0013a0003c0006t0003g0014others(25): Show | 30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.584+35T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089377 | ||||||
chr9:19089642
|
A | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0091a0001c0005t0023g0095 | 3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.437-83T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089642 | ||||||
chr9:19089645
|
T | G | 37 | a0001c0005t0003g0114a0001c0005t0004g0012a0001c0005t0004g0098others(34): Show | 38 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.437-86A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089645 | ||||||
chr9:19089658
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.437-99T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089658 | ||||||
chr9:19089742
|
A | G | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437-183T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089742 | ||||||
chr9:19089749
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0275 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.437-190C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089749 | ||||||
chr9:19089767
|
C | T | 37 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.437-208G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089767 | ||||||
chr9:19089773
|
T | A | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-214A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089773 | ||||||
chr9:19089856
|
A | G | 1 | a0001c0005t0004g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.437-297T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089856 | ||||||
chr9:19089877
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-318C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089877 | ||||||
chr9:19089961
|
T | G | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-402A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089961 | ||||||
chr9:19090233
|
CAG | C | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-676_437-675del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090233 | ||||||
chr9:19090240
|
T | C | 42 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0141others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.437-681A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090240 | ||||||
chr9:19090304
|
G | C | 1 | a0003c0006t0003g0154 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.437-745C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090304 | ||||||
chr9:19090319
|
G | A | 1 | a0003c0006t0003g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.437-760C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090319 | ||||||
chr9:19090322
|
A | G | 3 | a0002c0003t0005g0342a0002c0003t0005g0349a0002c0003t0005g0354 | 3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.437-763T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090322 | ||||||
chr9:19090388
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-829C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090388 | ||||||
chr9:19090416
|
A | G | 168 | a0001c0001t0001g0257a0001c0002t0002g0036a0001c0002t0002g0091others(165): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.437-857T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090416 | ||||||
chr9:19090423
|
G | A | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.437-864C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090423 | ||||||
chr9:19090433
|
C | T | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.437-874G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090433 | ||||||
chr9:19090457
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.437-898T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090457 | ||||||
chr9:19090538
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.437-979C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090538 | ||||||
chr9:19090580
|
A | G | 1 | a0001c0004t0003g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.437-1021T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090580 | ||||||
chr9:19090674
|
T | C | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.437-1115A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090674 | ||||||
chr9:19090755
|
T | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.437-1196A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090755 | ||||||
chr9:19090898
|
T | C | 6 | a0001c0001t0001g0203a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | NA18950.hp2 NA18960.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-1339A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090898 | ||||||
chr9:19090957
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.437-1398G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090957 | ||||||
chr9:19090973
|
T | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.437-1414A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090973 | ||||||
chr9:19091072
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.437-1513C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091072 | ||||||
chr9:19091107
|
T | C | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-1548A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091107 | ||||||
chr9:19091113
|
A | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0091a0001c0005t0023g0095 | 3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.437-1554T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091113 | ||||||
chr9:19091255
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.437-1696C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091255 | ||||||
chr9:19091259
|
C | T | 40 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(37): Show | 43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.437-1700G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091259 | ||||||
chr9:19091277
|
G | C | 1 | a0001c0007t0002g0156 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.437-1718C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091277 | ||||||
chr9:19091287
|
G | A | 1 | a0001c0004t0003g0105 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.437-1728C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091287 | ||||||
chr9:19091294
|
C | T | 1 | a0001c0002t0002g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.437-1735G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091294 | ||||||
chr9:19091296
|
T | A | 1 | a0001c0002t0002g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.437-1737A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091296 | ||||||
chr9:19091301
|
G | GA | 6 | a0001c0002t0012g0031a0001c0004t0003g0306a0001c0004t0003g0309others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1743dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091301 | ||||||
chr9:19091301
|
GA | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 121 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.437-1743delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091301 | ||||||
chr9:19091318
|
A | G | 5 | a0001c0005t0004g0133a0001c0005t0008g0326a0001c0005t0008g0327others(2): Show | 5 | HG02572.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-1759T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091318 | ||||||
chr9:19091375
|
C | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+1796G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091375 | ||||||
chr9:19091389
|
C | T | 91 | a0001c0002t0002g0036a0001c0002t0002g0091a0001c0002t0018g0171others(88): Show | 97 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.436+1782G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091389 | ||||||
chr9:19091488
|
T | C | 5 | a0001c0004t0003g0282a0007c0013t0003g0294a0007c0013t0011g0322others(2): Show | 5 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+1683A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091488 | ||||||
chr9:19091573
|
G | C | 1 | a0003c0006t0003g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.436+1598C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091573 | ||||||
chr9:19091587
|
G | A | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.436+1584C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091587 | ||||||
chr9:19091628
|
T | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+1543A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091628 | ||||||
chr9:19091634
|
A | G | 40 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(37): Show | 43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+1537T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091634 | ||||||
chr9:19091767
|
T | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.436+1404A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091767 | ||||||
chr9:19091807
|
G | A | 2 | a0001c0005t0004g0107a0001c0005t0004g0134 | 2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.436+1364C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091807 | ||||||
chr9:19091973
|
A | AT | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+1197dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091973 | ||||||
chr9:19091975
|
T | A | 2 | a0001c0005t0004g0117a0001c0005t0004g0118 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.436+1196A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091975 | ||||||
chr9:19092032
|
A | G | 45 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(42): Show | 48 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.436+1139T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092032 | ||||||
chr9:19092110
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0273 | 3 | NA18973.hp1 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.436+1061G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092110 | ||||||
chr9:19092192
|
T | C | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+979A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092192 | ||||||
chr9:19092291
|
T | TA | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.436+879dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092291 | ||||||
chr9:19092298
|
A | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.436+873T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092298 | ||||||
chr9:19092301
|
A | C | 88 | a0001c0004t0003g0296a0001c0007t0002g0137a0001c0007t0002g0139others(85): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.436+870T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092301 | ||||||
chr9:19092303
|
A | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+868T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092303 | ||||||
chr9:19092378
|
G | C | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.436+793C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092378 | ||||||
chr9:19092405
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18950.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.436+766G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092405 | ||||||
chr9:19092406
|
G | A | 1 | a0003c0006t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436+765C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092406 | ||||||
chr9:19092434
|
G | A | 4 | a0001c0005t0003g0114a0001c0005t0004g0098a0001c0005t0004g0121others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+737C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092434 | ||||||
chr9:19092472
|
G | A | 1 | a0002c0003t0005g0348 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.436+699C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092472 | ||||||
chr9:19092597
|
A | G | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+574T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092597 | ||||||
chr9:19092598
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436+573T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092598 | ||||||
chr9:19092616
|
C | CG | 16 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0015g0215others(13): Show | 17 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.436+554dupC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092616 | ||||||
chr9:19092618
|
G | GA | 56 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0197others(53): Show | 56 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.436+552dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | ||||||
chr9:19092618
|
G | GGA | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0005t0004g0115others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+552_436+553ins others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | ||||||
chr9:19092618
|
GA | G | 7 | a0001c0001t0001g0193a0001c0001t0001g0211a0001c0001t0001g0212others(4): Show | 7 | HG01891.hp2 HG01928.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+552delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | ||||||
chr9:19092618
|
GAAAA | G | 33 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(30): Show | 35 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.436+549_436+552del others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | ||||||
chr9:19092618
|
GAAAAA | G | 8 | a0002c0003t0005g0341a0004c0008t0006g0025a0004c0008t0006g0362others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+548_436+552del others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | ||||||
chr9:19092623
|
A | G | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.436+548T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092623 | ||||||
chr9:19092644
|
C | G | 1 | a0023c0040t0004g0316 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.436+527G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092644 | ||||||
chr9:19092649
|
C | T | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+522G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092649 | ||||||
chr9:19092650
|
G | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG00735.hp1 HG01433.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.436+521C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092650 | ||||||
chr9:19092703
|
A | C | 40 | a0001c0002t0018g0171a0002c0003t0005g0007a0002c0003t0005g0330others(37): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.436+468T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092703 | ||||||
chr9:19092788
|
G | C | 1 | a0001c0007t0002g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.436+383C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092788 | ||||||
chr9:19092795
|
G | C | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+376C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092795 | ||||||
chr9:19092803
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436+368A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092803 | ||||||
chr9:19092862
|
T | C | 3 | a0004c0008t0006g0025a0004c0008t0006g0364a0004c0008t0006g0367 | 4 | HG00099.hp2 HG02486.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+309A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092862 | ||||||
chr9:19092886
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0204a0001c0001t0001g0210others(4): Show | 8 | HG01167.hp1 HG01361.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+285A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092886 | ||||||
chr9:19092916
|
C | CA | 48 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0190others(45): Show | 51 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.436+254dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(6): Show |
1 | a0002c0003t0005g0360 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.436+242_436+254dup others(13): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(7): Show |
1 | a0022c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.436+241_436+254dup others(14): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(8): Show |
18 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0339others(15): Show | 20 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.436+240_436+254dup others(15): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(9): Show |
9 | a0002c0003t0005g0331a0002c0003t0005g0332a0002c0003t0005g0349others(6): Show | 9 | HG00741.hp2 HG02015.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+239_436+254dup others(16): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(10): Show |
6 | a0002c0003t0005g0355a0002c0003t0005g0356a0002c0003t0007g0335others(3): Show | 6 | HG00733.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+238_436+254dup others(17): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092916
|
C | CAAAAAAA others(11): Show |
2 | a0002c0003t0007g0333a0002c0003t0007g0338 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+254_436+255ins others(18): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | ||||||
chr9:19092983
|
G | C | 2 | a0001c0005t0004g0107a0001c0005t0004g0134 | 2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.436+188C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092983 | ||||||
chr9:19093019
|
C | G | 88 | a0001c0002t0018g0171a0001c0007t0002g0137a0001c0007t0002g0139others(85): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.436+152G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093019 | ||||||
chr9:19093050
|
G | C | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.436+121C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093050 | ||||||
chr9:19093051
|
G | A | 1 | a0001c0012t0004g0127 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+120C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093051 | ||||||
chr9:19093100
|
G | A | 43 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(40): Show | 45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+71C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093100 | ||||||
chr9:19093120
|
C | A | 5 | a0001c0004t0003g0306a0001c0004t0003g0309a0009c0021t0003g0293others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+51G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093120 | ||||||
chr9:19093343
|
A | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-40T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093343 | ||||||
chr9:19093414
|
C | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.304-111G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093414 | ||||||
chr9:19093528
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-225C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093528 | ||||||
chr9:19093651
|
T | A | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.304-348A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093651 | ||||||
chr9:19093740
|
A | C | 1 | a0019c0025t0002g0056 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.304-437T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093740 | ||||||
chr9:19093763
|
G | T | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.304-460C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093763 | ||||||
chr9:19093787
|
C | T | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-484G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093787 | ||||||
chr9:19093791
|
C | G | 1 | a0002c0003t0007g0333 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.304-488G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093791 | ||||||
chr9:19093833
|
C | G | 37 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(34): Show | 39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.303+484G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093833 | ||||||
chr9:19093960
|
A | G | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+357T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093960 | ||||||
chr9:19094217
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+100C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19094217 | ||||||
chr9:19094283
|
A | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+34T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19094283 | ||||||
chr9:19094424
|
C | G | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.225-29G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094424 | ||||||
chr9:19094434
|
C | T | 1 | a0001c0005t0004g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.225-39G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094434 | ||||||
chr9:19094516
|
G | A | 1 | a0004c0008t0006g0365 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225-121C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094516 | ||||||
chr9:19094519
|
C | T | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-124G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094519 | ||||||
chr9:19094520
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-125C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094520 | ||||||
chr9:19094621
|
G | A | 39 | a0001c0002t0002g0279a0001c0002t0002g0280a0002c0003t0005g0007others(36): Show | 41 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.225-226C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094621 | ||||||
chr9:19094638
|
A | G | 1 | a0011c0015t0003g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.225-243T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094638 | ||||||
chr9:19094752
|
C | G | 3 | a0001c0026t0028g0170a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.225-357G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094752 | ||||||
chr9:19094800
|
A | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG00323.hp2 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.225-405T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094800 | ||||||
chr9:19095058
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.225-663A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095058 | ||||||
chr9:19095086
|
C | T | 9 | a0001c0004t0003g0104a0001c0004t0003g0105a0001c0004t0003g0287others(6): Show | 9 | HG00609.hp2 HG02135.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-691G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095086 | ||||||
chr9:19095112
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.225-717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095112 | ||||||
chr9:19095119
|
C | A | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-724G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095119 | ||||||
chr9:19095146
|
T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225-751A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095146 | ||||||
chr9:19095161
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-766C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095161 | ||||||
chr9:19095210
|
G | C | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-815C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095210 | ||||||
chr9:19095235
|
T | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-840A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095235 | ||||||
chr9:19095273
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225-878T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095273 | ||||||
chr9:19095312
|
T | C | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-917A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095312 | ||||||
chr9:19095313
|
T | G | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-918A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095313 | ||||||
chr9:19095365
|
G | A | 38 | a0002c0003t0005g0007a0002c0003t0005g0330a0002c0003t0005g0331others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.225-970C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095365 | ||||||
chr9:19095504
|
C | CA | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.225-1110dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095504 | ||||||
chr9:19095504
|
CA | C | 11 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(8): Show | 12 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.225-1110delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095504 | ||||||
chr9:19095565
|
A | G | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+1109T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095565 | ||||||
chr9:19095682
|
T | C | 1 | a0001c0002t0012g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.224+992A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095682 | ||||||
chr9:19095754
|
T | C | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224+920A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095754 | ||||||
chr9:19095851
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.224+823A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095851 | ||||||
chr9:19095881
|
G | A | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.224+793C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095881 | ||||||
chr9:19095994
|
C | T | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+680G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095994 | ||||||
chr9:19096042
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.224+632C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096042 | ||||||
chr9:19096066
|
C | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.224+608G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096066 | ||||||
chr9:19096070
|
A | C | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.224+604T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096070 | ||||||
chr9:19096442
|
A | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.224+232T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096442 | ||||||
chr9:19096458
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.224+216T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096458 | ||||||
chr9:19096552
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.224+122C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096552 | ||||||
chr9:19096564
|
C | CA | 15 | a0001c0002t0002g0050a0001c0002t0002g0054a0001c0002t0002g0076others(12): Show | 15 | HG00140.hp1 HG00423.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.224+109dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
C | CAAA | 33 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(30): Show | 36 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.224+107_224+109dup others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
C | CAAAAA | 20 | a0001c0004t0003g0106a0001c0005t0003g0114a0001c0005t0004g0012others(17): Show | 21 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.224+105_224+109dup others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
C | CAAAAAA | 10 | a0001c0005t0004g0098a0001c0005t0004g0116a0001c0005t0004g0117others(7): Show | 10 | HG02602.hp1 HG02818.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+104_224+109dup others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
CA | C | 16 | a0001c0001t0001g0178a0001c0002t0002g0078a0001c0002t0012g0031others(13): Show | 16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.224+109delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
CAA | C | 6 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(3): Show | 6 | NA18951.hp2 NA18985.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+108_224+109del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
CAAA | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.224+107_224+109del others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
CAAAA | C | 9 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0272others(6): Show | 10 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+106_224+109del others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096564
|
CAAAAAAA others(6): Show |
C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.224+97_224+109delT others(12): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | ||||||
chr9:19096578
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.224+96T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096578 | ||||||
chr9:19096598
|
T | C | 14 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0078others(11): Show | 19 | HG00597.hp2 HG00621.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.224+76A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096598 | ||||||
chr9:19096646
|
T | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.224+28A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096646 | ||||||
chr9:19096816
|
A | G | 1 | a0001c0004t0003g0022 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.129-47T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096816 | ||||||
chr9:19096834
|
A | T | 42 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.129-65T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096834 | ||||||
chr9:19096956
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.129-187G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096956 | ||||||
chr9:19096981
|
A | G | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-212T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096981 | ||||||
chr9:19096997
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0269 | 3 | NA18957.hp2 NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.129-228A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096997 | ||||||
chr9:19096998
|
G | A | 4 | a0001c0011t0004g0128a0001c0011t0004g0129a0001c0011t0004g0130others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-229C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096998 | ||||||
chr9:19097025
|
A | C | 3 | a0001c0026t0028g0170a0008c0018t0010g0102a0008c0018t0010g0103 | 3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.129-256T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097025 | ||||||
chr9:19097035
|
A | T | 1 | a0001c0002t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.129-266T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097035 | ||||||
chr9:19097117
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129-348C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097117 | ||||||
chr9:19097124
|
T | A | 1 | a0006c0014t0022g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.129-355A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097124 | ||||||
chr9:19097153
|
G | A | 1 | a0003c0006t0027g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.129-384C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097153 | ||||||
chr9:19097166
|
A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0205 | 2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.129-397T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097166 | ||||||
chr9:19097235
|
C | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129-466G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097235 | ||||||
chr9:19097252
|
G | C | 1 | a0008c0018t0010g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.129-483C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097252 | ||||||
chr9:19097320
|
G | A | 161 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(158): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.129-551C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097320 | ||||||
chr9:19097355
|
C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129-586G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097355 | ||||||
chr9:19097379
|
A | C | 45 | a0001c0007t0002g0137a0001c0007t0002g0139a0001c0007t0002g0140others(42): Show | 47 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.129-610T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097379 | ||||||
chr9:19097398
|
T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-629A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097398 | ||||||
chr9:19097464
|
G | A | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.129-695C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097464 | ||||||
chr9:19097489
|
A | C | 10 | a0001c0002t0002g0009a0001c0002t0002g0026a0001c0002t0002g0052others(7): Show | 11 | HG02015.hp1 HG03831.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-720T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097489 | ||||||
chr9:19097506
|
T | C | 1 | a0001c0002t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.129-737A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097506 | ||||||
chr9:19097576
|
G | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.129-807C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097576 | ||||||
chr9:19097767
|
T | TA | 42 | a0001c0005t0004g0121a0001c0005t0004g0122a0001c0007t0002g0137others(39): Show | 44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.129-999dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097767 | ||||||
chr9:19097775
|
A | C | 39 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(36): Show | 42 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.129-1006T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097775 | ||||||
chr9:19097780
|
A | AT | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.129-1012_129-1011i others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097780 | ||||||
chr9:19097953
|
T | C | 5 | a0001c0004t0003g0287a0001c0004t0003g0288a0001c0004t0003g0289others(2): Show | 5 | HG00609.hp2 HG02135.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-1184A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097953 | ||||||
chr9:19098111
|
G | A | 1 | a0003c0006t0003g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.129-1342C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098111 | ||||||
chr9:19098162
|
C | T | 1 | a0001c0005t0004g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.129-1393G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098162 | ||||||
chr9:19098165
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129-1396C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098165 | ||||||
chr9:19098221
|
A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129-1452T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098221 | ||||||
chr9:19098259
|
G | A | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129-1490C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098259 | ||||||
chr9:19098267
|
A | G | 163 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(160): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.129-1498T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098267 | ||||||
chr9:19098357
|
G | A | 2 | a0002c0003t0005g0330a0002c0003t0005g0331 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-1588C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098357 | ||||||
chr9:19098401
|
G | A | 38 | a0001c0037t0001g0311a0002c0003t0005g0007a0002c0003t0005g0330others(35): Show | 40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.129-1632C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098401 | ||||||
chr9:19098436
|
C | CA | 106 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(103): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.129-1668dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | ||||||
chr9:19098436
|
C | CAA | 7 | a0001c0001t0001g0006a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 9 | HG00544.hp1 HG00609.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.129-1669_129-1668d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | ||||||
chr9:19098436
|
CA | C | 110 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0004t0003g0022others(107): Show | 116 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.129-1668delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | ||||||
chr9:19098470
|
A | T | 16 | a0001c0002t0002g0030a0001c0002t0002g0037a0001c0002t0002g0038others(13): Show | 17 | HG00423.hp1 HG02523.hp2 NA18950.hp1 others(14): Show |
intron_variant | MODIFIER | c.129-1701T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098470 | ||||||
chr9:19098478
|
C | G | 8 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(5): Show | 9 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.129-1709G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098478 | ||||||
chr9:19098507
|
C | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-1738G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098507 | ||||||
chr9:19098508
|
C | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-1739G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098508 | ||||||
chr9:19098613
|
G | C | 1 | a0001c0005t0004g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129-1844C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098613 | ||||||
chr9:19098642
|
A | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129-1873T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098642 | ||||||
chr9:19098649
|
C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129-1880G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098649 | ||||||
chr9:19098714
|
A | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(278): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.129-1945T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098714 | ||||||
chr9:19098729
|
T | TA | 274 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(271): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.129-1961dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098729 | ||||||
chr9:19098772
|
C | G | 8 | a0001c0037t0001g0311a0002c0003t0007g0333a0002c0003t0007g0334others(5): Show | 8 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-2003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098772 | ||||||
chr9:19098947
|
GGGAGGC | G | 38 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(35): Show | 41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.129-2184_129-2179d others(8): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098947 | ||||||
chr9:19098957
|
G | C | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.129-2188C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098957 | ||||||
chr9:19098969
|
G | A | 124 | a0001c0004t0003g0022a0001c0004t0003g0023a0001c0004t0003g0024others(121): Show | 131 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.129-2200C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098969 | ||||||
chr9:19099017
|
CA | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.129-2249delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099017 | ||||||
chr9:19099052
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.129-2283A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099052 | ||||||
chr9:19099065
|
G | T | 16 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0001g0185others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.129-2296C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099065 | ||||||
chr9:19099067
|
G | T | 1 | a0001c0002t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.129-2298C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099067 | ||||||
chr9:19099090
|
A | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129-2321T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099090 | ||||||
chr9:19099144
|
T | C | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129-2375A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099144 | ||||||
chr9:19099171
|
G | GT | 10 | a0001c0002t0002g0026a0001c0002t0002g0030a0001c0002t0002g0032others(7): Show | 10 | HG02258.hp1 HG03453.hp1 HG03540.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-2403dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099171 | ||||||
chr9:19099171
|
GT | G | 66 | a0001c0004t0003g0024a0001c0004t0003g0281a0001c0004t0003g0282others(63): Show | 69 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.129-2403delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099171 | ||||||
chr9:19099225
|
G | A | 2 | a0002c0003t0005g0330a0002c0003t0005g0331 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-2456C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099225 | ||||||
chr9:19099226
|
G | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-2457C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099226 | ||||||
chr9:19099228
|
G | A | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.129-2459C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099228 | ||||||
chr9:19099244
|
G | T | 4 | a0001c0012t0004g0099a0001c0012t0004g0100a0001c0012t0004g0101others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2475C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099244 | ||||||
chr9:19099461
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.129-2692G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099461 | ||||||
chr9:19099503
|
T | A | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129-2734A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099503 | ||||||
chr9:19099560
|
G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-2791C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099560 | ||||||
chr9:19099653
|
G | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+2871C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099653 | ||||||
chr9:19099764
|
C | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+2760G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099764 | ||||||
chr9:19099774
|
G | C | 1 | a0003c0006t0003g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128+2750C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099774 | ||||||
chr9:19099807
|
T | C | 1 | a0001c0012t0004g0127 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.128+2717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099807 | ||||||
chr9:19099807
|
T | G | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128+2717A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099807 | ||||||
chr9:19099820
|
C | T | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.128+2704G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099820 | ||||||
chr9:19099821
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.128+2703C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099821 | ||||||
chr9:19099968
|
T | A | 7 | a0004c0008t0006g0025a0004c0008t0006g0362a0004c0008t0006g0363others(4): Show | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+2556A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099968 | ||||||
chr9:19100020
|
C | T | 36 | a0002c0003t0005g0007a0002c0003t0005g0332a0002c0003t0005g0339others(33): Show | 38 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.128+2504G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100020 | ||||||
chr9:19100062
|
G | A | 6 | a0001c0005t0004g0132a0001c0005t0004g0133a0001c0005t0008g0326others(3): Show | 6 | HG01081.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+2462C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100062 | ||||||
chr9:19100098
|
G | A | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.128+2426C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100098 | ||||||
chr9:19100254
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18953.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.128+2270G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100254 | ||||||
chr9:19100307
|
A | C | 2 | a0010c0017t0013g0172a0010c0017t0013g0173 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.128+2217T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100307 | ||||||
chr9:19100485
|
G | C | 1 | a0001c0037t0001g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.128+2039C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100485 | ||||||
chr9:19100519
|
T | C | 2 | a0001c0005t0023g0095a0001c0007t0002g0168 | 2 | HG00423.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.128+2005A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100519 | ||||||
chr9:19100547
|
G | A | 1 | a0001c0005t0004g0134 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.128+1977C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100547 | ||||||
chr9:19100901
|
G | A | 1 | a0021c0022t0026g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.128+1623C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100901 | ||||||
chr9:19101040
|
A | G | 1 | a0003c0006t0003g0135 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128+1484T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101040 | ||||||
chr9:19101051
|
T | C | 41 | a0001c0002t0002g0028a0001c0002t0018g0171a0001c0007t0002g0137others(38): Show | 43 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.128+1473A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101051 | ||||||
chr9:19101082
|
A | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.128+1442T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101082 | ||||||
chr9:19101087
|
C | T | 2 | a0001c0004t0003g0281a0001c0004t0003g0282 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.128+1437G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101087 | ||||||
chr9:19101223
|
G | A | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.128+1301C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101223 | ||||||
chr9:19101342
|
G | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128+1182C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101342 | ||||||
chr9:19101352
|
A | G | 121 | a0001c0002t0002g0028a0001c0004t0003g0022a0001c0004t0003g0023others(118): Show | 127 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.128+1172T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101352 | ||||||
chr9:19101368
|
G | A | 1 | a0013c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.128+1156C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101368 | ||||||
chr9:19101449
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128+1075G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101449 | ||||||
chr9:19101574
|
T | C | 2 | a0001c0002t0002g0096a0001c0002t0002g0097 | 2 | NA18988.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.128+950A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101574 | ||||||
chr9:19101660
|
G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128+864C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101660 | ||||||
chr9:19101718
|
G | A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.128+806C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101718 | ||||||
chr9:19101773
|
G | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.128+751C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101773 | ||||||
chr9:19101896
|
G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128+628C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101896 | ||||||
chr9:19101912
|
C | A | 3 | a0001c0002t0002g0278a0001c0002t0002g0279a0001c0002t0002g0280 | 3 | HG02015.hp1 NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.128+612G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101912 | ||||||
chr9:19101932
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.128+592G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101932 | ||||||
chr9:19102202
|
AC | A | 38 | a0001c0001t0001g0312a0001c0004t0003g0022a0001c0004t0003g0023others(35): Show | 41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.128+321delG | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102202 | ||||||
chr9:19102234
|
C | T | 1 | a0001c0002t0002g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.128+290G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102234 | ||||||
chr9:19102345
|
T | G | 50 | a0001c0002t0031g0325a0001c0005t0008g0326a0001c0005t0008g0327others(47): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.128+179A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102345 |