geneid | 7994 |
---|---|
ensemblid | ENSG00000083168.11 |
hgncid | 13013 |
symbol | KAT6A |
name | lysine acetyltransferase 6A |
refseq_nuc | NM_006766.5 |
refseq_prot | NP_006757.2 |
ensembl_nuc | ENST00000265713.8 |
ensembl_prot | ENSP00000265713.2 |
mane_status | MANE Select |
chr | chr8 |
start | 41929479 |
end | 42051987 |
strand | - |
ver | v1.2 |
region | chr8:41929479-42051987 |
region5000 | chr8:41924479-42056987 |
regionname0 | KAT6A_chr8_41929479_42051987 |
regionname5000 | KAT6A_chr8_41924479_42056987 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2004 | 286 | 71 | 49 | 123 | 10 | 31 | 94 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002 | 0/0 | 2004 | 72 | 7 | 16 | 42 | 0 | 7 | 37 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0003 | 0/0 | 2003 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0004 | 0/0 | 2004 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0005 | 0/0 | 2004 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0006 | 0/0 | 2004 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0007 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0008 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0009 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0010 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0011 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 6015 | 209 | 19 | 35 | 121 | 6 | 26 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0002 | 0/0 | 6015 | 71 | 7 | 16 | 41 | 0 | 7 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0003 | 0/0 | 6015 | 52 | 31 | 13 | 0 | 3 | 5 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0004 | 0/0 | 6015 | 9 | 9 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0005 | 0/0 | 6015 | 6 | 6 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0006 | 0/0 | 6012 | 4 | 0 | 0 | 4 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0007 | 0/0 | 6015 | 3 | 3 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0008 | 0/0 | 6015 | 3 | 2 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0009 | 0/0 | 6015 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0010 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0011 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0012 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0013 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0014 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0015 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0016 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0017 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0018 | 0/0 | 6015 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0019 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0020 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0021 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0022 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
c0023 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
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 | 3131 | 51 | 2 | 13 | 34 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0002 | 1/0 | 3139 | 49 | 0 | 9 | 36 | 1 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0003 | 0/1 | 3131 | 38 | 1 | 7 | 22 | 1 | 6 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0004 | 0/0 | 3141 | 13 | 1 | 5 | 0 | 2 | 5 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0005 | 0/0 | 3131 | 9 | 0 | 1 | 6 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0006 | 0/0 | 3144 | 9 | 0 | 0 | 7 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0007 | 0/0 | 3139 | 8 | 7 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0008 | 0/0 | 3130 | 6 | 0 | 0 | 6 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0009 | 0/0 | 3140 | 6 | 0 | 1 | 3 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0010 | 0/0 | 3140 | 6 | 2 | 1 | 1 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0011 | 0/0 | 3139 | 6 | 0 | 2 | 3 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0012 | 0/0 | 3142 | 5 | 5 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0013 | 0/0 | 3131 | 5 | 0 | 1 | 3 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0014 | 0/0 | 3139 | 5 | 0 | 0 | 5 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0015 | 0/0 | 3134 | 4 | 0 | 2 | 0 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0016 | 0/0 | 3143 | 4 | 4 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0017 | 0/0 | 3141 | 4 | 3 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0018 | 0/0 | 3131 | 4 | 0 | 2 | 1 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0019 | 0/0 | 3134 | 4 | 0 | 0 | 4 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0020 | 0/0 | 3141 | 4 | 4 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0021 | 0/0 | 3134 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0022 | 0/0 | 3131 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0023 | 0/0 | 3139 | 3 | 2 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0024 | 0/0 | 3131 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0025 | 0/0 | 3151 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0026 | 0/0 | 3134 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0027 | 0/0 | 3139 | 2 | 1 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0028 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0029 | 0/0 | 3134 | 2 | 0 | 1 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0030 | 0/0 | 3131 | 2 | 1 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0031 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0032 | 0/0 | 3144 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0033 | 0/0 | 3132 | 2 | 1 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0034 | 0/0 | 3131 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0035 | 0/0 | 3140 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0036 | 0/0 | 3133 | 2 | 0 | 1 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0037 | 0/0 | 3146 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0038 | 0/0 | 3132 | 2 | 1 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0039 | 0/0 | 3132 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0040 | 0/0 | 3133 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0041 | 0/0 | 3133 | 2 | 0 | 1 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0042 | 0/0 | 3145 | 2 | 0 | 0 | 0 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0043 | 0/0 | 3132 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0044 | 0/0 | 3143 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0045 | 0/0 | 3139 | 2 | 1 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0046 | 0/0 | 3140 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0047 | 0/0 | 3141 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0048 | 0/0 | 3142 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0049 | 0/0 | 3142 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0050 | 0/0 | 3140 | 2 | 0 | 1 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0051 | 0/0 | 3139 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0052 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0053 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0054 | 0/0 | 3155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0055 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0056 | 0/0 | 3131 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0057 | 0/0 | 3151 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0058 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0059 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0060 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0061 | 0/0 | 3123 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0062 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0063 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0064 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0065 | 0/0 | 3133 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0066 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0067 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0068 | 0/0 | 3143 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0069 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0070 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0071 | 0/0 | 3139 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0072 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0073 | 0/0 | 3130 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0074 | 0/0 | 3143 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0075 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0076 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0077 | 0/0 | 3140 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0078 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0079 | 0/0 | 3131 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0080 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0081 | 0/0 | 3140 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0082 | 0/0 | 3133 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0083 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0084 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0085 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0086 | 0/0 | 3142 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0087 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0088 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0089 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0090 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0091 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0092 | 0/0 | 3134 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0093 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0094 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0095 | 0/0 | 3131 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0096 | 0/0 | 3142 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0097 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0098 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0099 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0100 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0101 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0102 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0103 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0104 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0105 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0106 | 0/0 | 3142 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0107 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0108 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0109 | 0/0 | 3140 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0110 | 0/0 | 3139 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0111 | 0/0 | 3138 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0112 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0113 | 0/0 | 3139 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0114 | 0/0 | 3139 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0115 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0116 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0117 | 0/0 | 3144 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0118 | 0/0 | 3130 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0119 | 0/0 | 3140 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
t0120 | 0/0 | 3139 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 6015 | 209 | 19 | 35 | 121 | 6 | 26 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003 | 0/0 | 6015 | 52 | 31 | 13 | 0 | 3 | 5 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004 | 0/0 | 6015 | 9 | 9 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0005 | 0/0 | 6015 | 6 | 6 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0008 | 0/0 | 6015 | 3 | 2 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0012 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0016 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0017 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0019 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0020 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0021 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0022 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002 | 0/0 | 6015 | 71 | 7 | 16 | 41 | 0 | 7 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0011 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0003c0006 | 0/0 | 6012 | 4 | 0 | 0 | 4 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0004c0007 | 0/0 | 6015 | 3 | 3 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0005c0009 | 0/0 | 6015 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0006c0010 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0007c0014 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0008c0018 | 0/0 | 6015 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0009c0015 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0010c0013 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0011c0023 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9145 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0002 | 1/0 | 9153 | 49 | 0 | 9 | 36 | 1 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0003 | 0/1 | 9145 | 37 | 1 | 7 | 22 | 0 | 6 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0005 | 0/0 | 9145 | 9 | 0 | 1 | 6 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0006 | 0/0 | 9158 | 9 | 0 | 0 | 7 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0007 | 0/0 | 9153 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0008 | 0/0 | 9144 | 6 | 0 | 0 | 6 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0009 | 0/0 | 9154 | 5 | 0 | 0 | 3 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0010 | 0/0 | 9154 | 5 | 2 | 1 | 1 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0011 | 0/0 | 9153 | 6 | 0 | 2 | 3 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0013 | 0/0 | 9145 | 4 | 0 | 1 | 2 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0014 | 0/0 | 9153 | 5 | 0 | 0 | 5 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0022 | 0/0 | 9145 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0024 | 0/0 | 9145 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0025 | 0/0 | 9165 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0027 | 0/0 | 9153 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0029 | 0/0 | 9148 | 2 | 0 | 1 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0033 | 0/0 | 9146 | 2 | 1 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0034 | 0/0 | 9145 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0036 | 0/0 | 9147 | 2 | 0 | 1 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0038 | 0/0 | 9146 | 2 | 1 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0039 | 0/0 | 9146 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0040 | 0/0 | 9147 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0041 | 0/0 | 9147 | 2 | 0 | 1 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0042 | 0/0 | 9159 | 2 | 0 | 0 | 0 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0043 | 0/0 | 9146 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0044 | 0/0 | 9157 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0047 | 0/0 | 9155 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0048 | 0/0 | 9156 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0049 | 0/0 | 9156 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0050 | 0/0 | 9154 | 2 | 0 | 1 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0051 | 0/0 | 9153 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0053 | 0/0 | 9167 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0054 | 0/0 | 9169 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0055 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0056 | 0/0 | 9145 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0059 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0061 | 0/0 | 9137 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0065 | 0/0 | 9147 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0066 | 0/0 | 9147 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0070 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0072 | 0/0 | 9143 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0077 | 0/0 | 9154 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0080 | 0/0 | 9158 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0081 | 0/0 | 9154 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0083 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0084 | 0/0 | 9147 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0085 | 0/0 | 9155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0092 | 0/0 | 9148 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0094 | 0/0 | 9158 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0096 | 0/0 | 9156 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0097 | 0/0 | 9154 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0100 | 0/0 | 9158 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0101 | 0/0 | 9147 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0109 | 0/0 | 9154 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0110 | 0/0 | 9153 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0111 | 0/0 | 9152 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0112 | 0/0 | 9156 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0113 | 0/0 | 9153 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0114 | 0/0 | 9153 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0115 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0116 | 0/0 | 9154 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0118 | 0/0 | 9144 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0001t0120 | 0/0 | 9153 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0004 | 0/0 | 9155 | 13 | 1 | 5 | 0 | 2 | 5 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0007 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0016 | 0/0 | 9157 | 4 | 4 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0017 | 0/0 | 9155 | 3 | 3 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0023 | 0/0 | 9153 | 3 | 2 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0027 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0028 | 0/0 | 9155 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0031 | 0/0 | 9156 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0035 | 0/0 | 9154 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0037 | 0/0 | 9160 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0045 | 0/0 | 9153 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0046 | 0/0 | 9154 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0057 | 0/0 | 9165 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0060 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0068 | 0/0 | 9157 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0069 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0071 | 0/0 | 9153 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0074 | 0/0 | 9157 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0075 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0076 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0087 | 0/0 | 9164 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0090 | 0/0 | 9155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0091 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0103 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0105 | 0/0 | 9156 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0106 | 0/0 | 9156 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0107 | 0/0 | 9154 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0003t0108 | 0/0 | 9155 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004t0012 | 0/0 | 9156 | 4 | 4 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004t0032 | 0/0 | 9158 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004t0063 | 0/0 | 9158 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004t0067 | 0/0 | 9140 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0004t0086 | 0/0 | 9156 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0005t0020 | 0/0 | 9155 | 4 | 4 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0005t0062 | 0/0 | 9158 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0005t0088 | 0/0 | 9155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0008t0007 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0008t0012 | 0/0 | 9156 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0008t0017 | 0/0 | 9155 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0012t0045 | 0/0 | 9153 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0016t0102 | 0/0 | 9155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0017t0003 | 0/0 | 9145 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0019t0007 | 0/0 | 9153 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0020t0073 | 0/0 | 9144 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0021t0013 | 0/0 | 9145 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0001c0022t0058 | 0/0 | 9164 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0001 | 0/0 | 9145 | 48 | 2 | 11 | 33 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0015 | 0/0 | 9148 | 4 | 0 | 2 | 0 | 0 | 2 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0018 | 0/0 | 9145 | 4 | 0 | 2 | 1 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0019 | 0/0 | 9148 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0021 | 0/0 | 9148 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0026 | 0/0 | 9148 | 2 | 2 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0030 | 0/0 | 9145 | 2 | 1 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0064 | 0/0 | 9149 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0078 | 0/0 | 9145 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0079 | 0/0 | 9145 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0082 | 0/0 | 9147 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0093 | 0/0 | 9145 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0002t0095 | 0/0 | 9145 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0002c0011t0001 | 0/0 | 9145 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0003c0006t0019 | 0/0 | 9145 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0003c0006t0089 | 0/0 | 9145 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0003c0006t0098 | 0/0 | 9144 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0004c0007t0007 | 0/0 | 9153 | 3 | 3 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0005c0009t0009 | 0/0 | 9154 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0005c0009t0048 | 0/0 | 9156 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0006c0010t0052 | 0/0 | 9159 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0006c0010t0104 | 0/0 | 9148 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0007c0014t0047 | 0/0 | 9155 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0008c0018t0117 | 0/0 | 9158 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0009c0015t0099 | 0/0 | 9155 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0010c0013t0119 | 0/0 | 9154 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
a0011c0023t0010 | 0/0 | 9154 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | copy fasta | chr8 | 41924479 | 42056987 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0009g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0011g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0014g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0014g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0014g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0022g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0022g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0024g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0024g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0025g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0027g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0029g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0029g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0033g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0033g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0034g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0034g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0036g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0036g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0038g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0038g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0039g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0039g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0040g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0040g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0041g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0041g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0042g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0042g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0043g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0043g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0044g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0044g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0047g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0048g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0049g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0049g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0050g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0050g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0051g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0051g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0053g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0054g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0055g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0056g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0059g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0061g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0065g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0066g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0070g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0072g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0077g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0080g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0081g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0083g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0084g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0085g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0092g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0094g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0096g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0097g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0100g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0101g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0109g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0110g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0111g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0112g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0113g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0114g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0115g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0116g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0118g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0001t0120g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0016g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0017g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0023g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0023g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0027g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0028g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0028g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0031g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0031g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0035g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0035g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0037g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0037g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0045g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0046g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0046g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0057g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0060g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0068g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0069g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0071g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0074g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0075g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0076g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0087g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0090g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0091g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0103g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0105g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0106g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0107g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0003t0108g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0032g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0032g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0063g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0067g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0004t0086g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0020g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0020g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0020g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0062g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0005t0088g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0008t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0008t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0008t0017g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0012t0045g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0016t0102g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0017t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0019t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0020t0073g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0021t0013g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0001c0022t0058g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0015g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0015g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0015g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0015g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0018g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0018g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0018g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0019g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0019g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0021g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0021g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0021g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0026g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0026g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0030g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0030g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0064g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0078g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0079g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0082g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0093g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0002t0095g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0002c0011t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0003c0006t0019g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0003c0006t0019g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0003c0006t0089g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0003c0006t0098g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0004c0007t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0004c0007t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0004c0007t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0005c0009t0009g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0005c0009t0048g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0006c0010t0052g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0006c0010t0104g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0007c0014t0047g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0008c0018t0117g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0009c0015t0099g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0010c0013t0119g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
a0011c0023t0010g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0111 | g0278 | EUR | GBR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00099 | hp2 | a0001 | c0001 | t0061 | g0058 | EUR | GBR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00323 | hp1 | a0001 | c0001 | t0056 | g0089 | EUR | FIN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | FIN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00438 | hp2 | a0001 | c0001 | t0034 | g0109 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00544 | hp1 | a0001 | c0001 | t0039 | g0055 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00639 | hp2 | a0001 | c0001 | t0050 | g0256 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0196 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00642 | hp2 | a0002 | c0002 | t0030 | g0337 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00673 | hp1 | a0001 | c0001 | t0034 | g0048 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00673 | hp2 | a0001 | c0001 | t0100 | g0201 | EAS | CHS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00735 | hp1 | a0002 | c0002 | t0015 | g0357 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00735 | hp2 | a0001 | c0001 | t0051 | g0282 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG00741 | hp2 | a0001 | c0003 | t0004 | g0199 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01070 | hp1 | a0001 | c0003 | t0046 | g0148 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01070 | hp2 | a0002 | c0002 | t0018 | g0007 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01071 | hp1 | a0002 | c0002 | t0018 | g0007 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01071 | hp2 | a0001 | c0001 | t0112 | g0221 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0314 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0319 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01099 | hp1 | a0001 | c0001 | t0010 | g0284 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0320 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01106 | hp1 | a0001 | c0003 | t0023 | g0150 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01109 | hp1 | a0001 | c0001 | t0038 | g0053 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01167 | hp1 | a0001 | c0003 | t0046 | g0184 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01167 | hp2 | a0001 | c0008 | t0017 | g0131 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01168 | hp1 | a0001 | c0003 | t0107 | g0189 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01192 | hp2 | a0001 | c0003 | t0045 | g0192 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01243 | hp2 | a0001 | c0003 | t0071 | g0158 | AMR | PUR | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01255 | hp1 | a0001 | c0003 | t0105 | g0193 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0051 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01258 | hp1 | a0001 | c0001 | t0051 | g0271 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01261 | hp1 | a0001 | c0001 | t0041 | g0113 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01346 | hp2 | a0001 | c0003 | t0004 | g0194 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0205 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01361 | hp2 | a0001 | c0003 | t0004 | g0186 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01516 | hp1 | a0001 | c0017 | t0003 | g0033 | EUR | IBS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01516 | hp2 | a0001 | c0003 | t0004 | g0180 | EUR | IBS | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01891 | hp1 | a0001 | c0005 | t0020 | g0121 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01891 | hp2 | a0001 | c0003 | t0087 | g0174 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01934 | hp1 | a0001 | c0001 | t0029 | g0065 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01934 | hp2 | a0001 | c0001 | t0116 | g0265 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01943 | hp2 | a0001 | c0001 | t0048 | g0258 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01975 | hp1 | a0002 | c0002 | t0015 | g0348 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01975 | hp2 | a0001 | c0001 | t0049 | g0270 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01978 | hp1 | a0008 | c0018 | t0117 | g0214 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01978 | hp2 | a0001 | c0003 | t0108 | g0182 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0309 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01981 | hp2 | a0001 | c0001 | t0036 | g0036 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01993 | hp1 | a0001 | c0001 | t0049 | g0230 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0322 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02004 | hp2 | a0001 | c0003 | t0004 | g0185 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02027 | hp1 | a0002 | c0002 | t0018 | g0304 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02027 | hp2 | a0001 | c0001 | t0115 | g0242 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0361 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02040 | hp2 | a0001 | c0021 | t0013 | g0067 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02055 | hp1 | a0001 | c0001 | t0077 | g0094 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02055 | hp2 | a0001 | c0003 | t0037 | g0145 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02071 | hp2 | a0002 | c0002 | t0019 | g0336 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02074 | hp2 | a0001 | c0001 | t0014 | g0263 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02083 | hp2 | a0001 | c0001 | t0013 | g0057 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02135 | hp1 | a0001 | c0001 | t0022 | g0088 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02145 | hp1 | a0001 | c0001 | t0066 | g0106 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02145 | hp2 | a0001 | c0005 | t0062 | g0116 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02148 | hp2 | a0005 | c0009 | t0048 | g0262 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02155 | hp1 | a0001 | c0001 | t0039 | g0047 | EAS | CDX | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CDX | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CDX | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02165 | hp2 | a0001 | c0001 | t0022 | g0061 | EAS | CDX | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02257 | hp1 | a0001 | c0004 | t0063 | g0132 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02257 | hp2 | a0001 | c0001 | t0025 | g0016 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02258 | hp1 | a0001 | c0001 | t0025 | g0017 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02258 | hp2 | a0001 | c0005 | t0020 | g0120 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02280 | hp1 | a0001 | c0020 | t0073 | g0167 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02280 | hp2 | a0001 | c0003 | t0017 | g0296 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02293 | hp2 | a0005 | c0009 | t0009 | g0212 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02300 | hp1 | a0001 | c0001 | t0011 | g0248 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02451 | hp1 | a0001 | c0003 | t0035 | g0293 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02451 | hp2 | a0009 | c0015 | t0099 | g0142 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02572 | hp1 | a0001 | c0004 | t0012 | g0122 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02572 | hp2 | a0001 | c0001 | t0081 | g0090 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02615 | hp1 | a0001 | c0001 | t0054 | g0014 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02615 | hp2 | a0004 | c0007 | t0007 | g0178 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02630 | hp1 | a0001 | c0004 | t0012 | g0128 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02630 | hp2 | a0001 | c0003 | t0075 | g0147 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02647 | hp1 | a0001 | c0001 | t0033 | g0060 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02647 | hp2 | a0001 | c0003 | t0016 | g0162 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02683 | hp2 | a0001 | c0003 | t0004 | g0198 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02698 | hp1 | a0001 | c0001 | t0011 | g0240 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02698 | hp2 | a0001 | c0001 | t0092 | g0034 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02717 | hp1 | a0001 | c0001 | t0055 | g0015 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02717 | hp2 | a0001 | c0003 | t0017 | g0161 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02723 | hp1 | a0001 | c0016 | t0102 | g0170 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02723 | hp2 | a0001 | c0003 | t0016 | g0179 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02735 | hp1 | a0001 | c0001 | t0113 | g0219 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02738 | hp1 | a0002 | c0002 | t0015 | g0363 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02738 | hp2 | a0010 | c0013 | t0119 | g0218 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02809 | hp1 | a0001 | c0003 | t0060 | g0165 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02809 | hp2 | a0001 | c0003 | t0023 | g0164 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02818 | hp1 | a0001 | c0004 | t0032 | g0126 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02818 | hp2 | a0001 | c0003 | t0076 | g0173 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02886 | hp1 | a0001 | c0004 | t0086 | g0133 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02886 | hp2 | a0002 | c0002 | t0030 | g0338 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02896 | hp1 | a0004 | c0007 | t0007 | g0166 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02896 | hp2 | a0001 | c0004 | t0067 | g0124 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02922 | hp1 | a0001 | c0003 | t0027 | g0175 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02922 | hp2 | a0001 | c0008 | t0012 | g0130 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02965 | hp1 | a0001 | c0005 | t0020 | g0119 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02965 | hp2 | a0001 | c0003 | t0031 | g0160 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02970 | hp1 | a0004 | c0007 | t0007 | g0177 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02976 | hp1 | a0002 | c0002 | t0078 | g0340 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02976 | hp2 | a0001 | c0003 | t0031 | g0156 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03017 | hp1 | a0002 | c0002 | t0018 | g0310 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03017 | hp2 | a0001 | c0001 | t0120 | g0239 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03041 | hp1 | a0001 | c0003 | t0023 | g0151 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03041 | hp2 | a0001 | c0004 | t0012 | g0125 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03098 | hp1 | a0001 | c0001 | t0083 | g0171 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03098 | hp2 | a0001 | c0001 | t0059 | g0203 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03130 | hp1 | a0001 | c0004 | t0032 | g0123 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03130 | hp2 | a0002 | c0002 | t0026 | g0341 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03139 | hp1 | a0001 | c0003 | t0028 | g0294 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03139 | hp2 | a0001 | c0001 | t0085 | g0172 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03209 | hp1 | a0006 | c0010 | t0104 | g0169 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03209 | hp2 | a0002 | c0002 | t0093 | g0342 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03225 | hp1 | a0001 | c0001 | t0053 | g0018 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03239 | hp2 | a0011 | c0023 | t0010 | g0298 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03453 | hp1 | a0001 | c0004 | t0012 | g0127 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03453 | hp2 | a0001 | c0003 | t0074 | g0152 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03486 | hp1 | a0001 | c0022 | t0058 | g0115 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03486 | hp2 | a0001 | c0003 | t0037 | g0146 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03490 | hp1 | a0001 | c0003 | t0004 | g0188 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03490 | hp2 | a0001 | c0001 | t0010 | g0253 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03492 | hp1 | a0001 | c0003 | t0004 | g0190 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03516 | hp1 | a0001 | c0001 | t0038 | g0154 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03516 | hp2 | a0002 | c0002 | t0026 | g0343 | AFR | ESN | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03540 | hp1 | a0001 | c0005 | t0088 | g0117 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0351 | AFR | GWD | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03579 | hp1 | a0001 | c0003 | t0017 | g0295 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03579 | hp2 | a0001 | c0003 | t0091 | g0288 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0346 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03654 | hp2 | a0001 | c0003 | t0004 | g0181 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03688 | hp1 | a0001 | c0001 | t0042 | g0139 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03704 | hp1 | a0002 | c0002 | t0015 | g0349 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03710 | hp1 | a0001 | c0001 | t0050 | g0220 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03710 | hp2 | a0002 | c0002 | t0095 | g0313 | SAS | PJL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03831 | hp1 | a0001 | c0001 | t0096 | g0143 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03831 | hp2 | a0001 | c0003 | t0004 | g0195 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0004 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03942 | hp1 | a0001 | c0001 | t0109 | g0225 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0097 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04115 | hp1 | a0001 | c0001 | t0042 | g0135 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04184 | hp1 | a0001 | c0001 | t0009 | g0283 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0140 | SAS | BEB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04199 | hp1 | a0002 | c0002 | t0082 | g0308 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0044 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG04204 | hp2 | a0001 | c0001 | t0114 | g0279 | SAS | STU | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18522 | hp1 | a0001 | c0003 | t0016 | g0134 | AFR | YRI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18522 | hp2 | a0001 | c0012 | t0045 | g0191 | AFR | YRI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18747 | hp1 | a0001 | c0001 | t0009 | g0254 | EAS | CHB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | CHB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18940 | hp1 | a0001 | c0001 | t0027 | g0079 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18940 | hp2 | a0001 | c0001 | t0118 | g0215 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18946 | hp1 | a0001 | c0001 | t0013 | g0041 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0360 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18949 | hp1 | a0001 | c0001 | t0033 | g0105 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18950 | hp1 | a0001 | c0001 | t0041 | g0052 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18951 | hp1 | a0001 | c0001 | t0011 | g0252 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18953 | hp1 | a0001 | c0001 | t0043 | g0029 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0359 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18956 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18956 | hp2 | a0001 | c0001 | t0009 | g0276 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18959 | hp1 | a0002 | c0002 | t0079 | g0344 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18960 | hp2 | a0001 | c0001 | t0014 | g0231 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18961 | hp1 | a0002 | c0002 | t0019 | g0335 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18963 | hp2 | a0001 | c0001 | t0072 | g0076 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18966 | hp1 | a0003 | c0006 | t0098 | g0345 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18966 | hp2 | a0001 | c0001 | t0101 | g0031 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18967 | hp1 | a0001 | c0001 | t0011 | g0281 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18967 | hp2 | a0001 | c0001 | t0084 | g0093 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18975 | hp2 | a0001 | c0001 | t0040 | g0104 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18978 | hp2 | a0003 | c0006 | t0089 | g0300 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18979 | hp2 | a0001 | c0019 | t0007 | g0168 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18980 | hp1 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18981 | hp1 | a0001 | c0001 | t0011 | g0249 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18982 | hp1 | a0001 | c0001 | t0047 | g0236 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18982 | hp2 | a0003 | c0006 | t0019 | g0364 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18983 | hp1 | a0001 | c0001 | t0110 | g0255 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18983 | hp2 | a0001 | c0001 | t0097 | g0024 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18984 | hp1 | a0002 | c0002 | t0021 | g0324 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18988 | hp2 | a0002 | c0011 | t0001 | g0333 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18990 | hp1 | a0001 | c0001 | t0080 | g0138 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18990 | hp2 | a0001 | c0001 | t0022 | g0066 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18994 | hp2 | a0002 | c0002 | t0021 | g0328 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18998 | hp1 | a0001 | c0001 | t0044 | g0136 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19003 | hp2 | a0007 | c0014 | t0047 | g0251 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19007 | hp1 | a0003 | c0006 | t0019 | g0352 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19009 | hp1 | a0001 | c0001 | t0024 | g0011 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19009 | hp2 | a0001 | c0001 | t0044 | g0144 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19043 | hp1 | a0001 | c0003 | t0004 | g0187 | AFR | LWK | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19043 | hp2 | a0001 | c0003 | t0069 | g0200 | AFR | LWK | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19060 | hp2 | a0001 | c0001 | t0040 | g0103 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19063 | hp1 | a0001 | c0001 | t0036 | g0074 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19063 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19065 | hp2 | a0001 | c0001 | t0014 | g0299 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19077 | hp2 | a0001 | c0001 | t0010 | g0114 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19083 | hp1 | a0001 | c0001 | t0043 | g0030 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19086 | hp1 | a0002 | c0002 | t0064 | g0329 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19087 | hp1 | a0001 | c0001 | t0014 | g0285 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19088 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19091 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19091 | hp2 | a0002 | c0002 | t0021 | g0354 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19240 | hp1 | a0001 | c0003 | t0090 | g0287 | AFR | YRI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA19240 | hp2 | a0001 | c0003 | t0007 | g0176 | AFR | YRI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0223 | AFR | ASW | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20129 | hp2 | a0001 | c0003 | t0035 | g0292 | AFR | ASW | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20752 | hp1 | a0001 | c0003 | t0106 | g0183 | EUR | TSI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20752 | hp2 | a0001 | c0001 | t0013 | g0028 | EUR | TSI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20805 | hp1 | a0001 | c0001 | t0029 | g0064 | EUR | TSI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20805 | hp2 | a0001 | c0003 | t0004 | g0197 | EUR | TSI | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0137 | SAS | GIH | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA20905 | hp2 | a0001 | c0001 | t0065 | g0083 | SAS | GIH | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02109 | hp2 | a0001 | c0008 | t0007 | g0129 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02486 | hp1 | a0001 | c0003 | t0016 | g0159 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0350 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02559 | hp1 | a0006 | c0010 | t0052 | g0012 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG02559 | hp2 | a0001 | c0003 | t0068 | g0153 | AFR | ACB | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03471 | hp1 | a0001 | c0001 | t0094 | g0141 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG03471 | hp2 | a0001 | c0003 | t0057 | g0163 | AFR | MSL | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG06807 | hp1 | a0001 | c0003 | t0103 | g0149 | AFR | USA | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0222 | AFR | USA | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA18955 | hp2 | a0001 | c0001 | t0070 | g0020 | EAS | JPT | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA21309 | hp1 | a0001 | c0005 | t0020 | g0118 | AFR | LWK | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
NA21309 | hp2 | a0001 | c0003 | t0028 | g0157 | AFR | LWK | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0062 | REF | REF | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0224 | REF | REF | KAT6A_chr8_41924479_42056987 | KAT6A | chr8 | 41924479 | 42056987 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41932519
|
C | T | 1 | a0009 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.5701G>A | p.Val1901Ile | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 6113/9153 | 5701/6015 | 1901/2004 | chr8 | 41932519 | ||
chr8:41932648
|
G | A | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.5572C>T | p.Arg1858Cys | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 5984/9153 | 5572/6015 | 1858/2004 | chr8 | 41932648 | ||
chr8:41933736
|
C | T | 1 | a0007 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.4484G>A | p.Arg1495His | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 4896/9153 | 4484/6015 | 1495/2004 | chr8 | 41933736 | ||
chr8:41934643
|
C | T | 1 | a0004 | 3 | HG02615.hp2 HG02896.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.3577G>A | p.Val1193Ile | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 3989/9153 | 3577/6015 | 1193/2004 | chr8 | 41934643 | ||
chr8:41934828
|
C | T | 1 | a0006 | 2 | HG02559.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.3392G>A | p.Arg1131His | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 3804/9153 | 3392/6015 | 1131/2004 | chr8 | 41934828 | ||
chr8:41937278
|
ATCT | A | 1 | a0003 | 4 | NA18966.hp1 NA18978.hp2 NA18982.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.3327_3329delAGA | p.Glu1109del | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/17 | 3741/9153 | 3327/6015 | 1109/2004 | chr8 | 41937278 | ||
chr8:41937406
|
C | T | 1 | a0010 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.3202G>A | p.Asp1068Asn | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/17 | 3614/9153 | 3202/6015 | 1068/2004 | chr8 | 41937406 | ||
chr8:41942856
|
T | G | 1 | a0005 | 2 | HG02148.hp2 HG02293.hp2 |
missense_variant | MODERATE | c.2373A>C | p.Glu791Asp | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/17 | 2785/9153 | 2373/6015 | 791/2004 | chr8 | 41942856 | ||
chr8:41977306
|
T | A | 1 | a0006 | 2 | HG02559.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.1065A>T | p.Lys355Asn | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/17 | 1477/9153 | 1065/6015 | 355/2004 | chr8 | 41977306 | ||
chr8:42048562
|
G | A | 1 | a0011 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.416C>T | p.Ala139Val | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/17 | 828/9153 | 416/6015 | 139/2004 | chr8 | 42048562 | ||
chr8:42048577
|
A | G | 2 | a0002a0003 | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
missense_variant | MODERATE | c.401T>C | p.Leu134Ser | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/17 | 813/9153 | 401/6015 | 134/2004 | chr8 | 42048577 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41932253
|
A | G | 1 | a0001c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.5967T>C | p.Ala1989Ala | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 6379/9153 | 5967/6015 | 1989/2004 | chr8 | 41932253 | ||
chr8:41932307
|
G | A | 1 | a0001c0017 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.5913C>T | p.Asn1971Asn | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 6325/9153 | 5913/6015 | 1971/2004 | chr8 | 41932307 | ||
chr8:41932841
|
C | T | 1 | a0001c0012 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.5379G>A | p.Gln1793Gln | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 5791/9153 | 5379/6015 | 1793/2004 | chr8 | 41932841 | ||
chr8:41933306
|
G | A | 2 | a0001c0004a0001c0008 | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
synonymous_variant | LOW | c.4914C>T | p.Cys1638Cys | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 5326/9153 | 4914/6015 | 1638/2004 | chr8 | 41933306 | ||
chr8:41933348
|
G | C | 3 | a0001c0004a0001c0008a0001c0019 | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
synonymous_variant | LOW | c.4872C>G | p.Val1624Val | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 5284/9153 | 4872/6015 | 1624/2004 | chr8 | 41933348 | ||
chr8:41933609
|
G | A | 1 | a0001c0020 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.4611C>T | p.Ser1537Ser | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 5023/9153 | 4611/6015 | 1537/2004 | chr8 | 41933609 | ||
chr8:41933765
|
G | A | 3 | a0002c0002a0002c0011a0003c0006 | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
synonymous_variant | LOW | c.4455C>T | p.Ser1485Ser | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 4867/9153 | 4455/6015 | 1485/2004 | chr8 | 41933765 | ||
chr8:41937416
|
C | T | 4 | a0001c0003a0001c0012a0002c0011others(1): Show | 57 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(54): Show |
synonymous_variant | LOW | c.3192G>A | p.Thr1064Thr | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/17 | 3604/9153 | 3192/6015 | 1064/2004 | chr8 | 41937416 | ||
chr8:41940899
|
C | T | 3 | a0002c0002a0002c0011a0003c0006 | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
synonymous_variant | LOW | c.2982G>A | p.Pro994Pro | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/17 | 3394/9153 | 2982/6015 | 994/2004 | chr8 | 41940899 | ||
chr8:41941187
|
T | C | 1 | a0001c0005 | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.2694A>G | p.Gln898Gln | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/17 | 3106/9153 | 2694/6015 | 898/2004 | chr8 | 41941187 | ||
chr8:41941394
|
T | C | 1 | a0001c0008 | 3 | HG01167.hp2 HG02109.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.2487A>G | p.Val829Val | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/17 | 2899/9153 | 2487/6015 | 829/2004 | chr8 | 41941394 | ||
chr8:41955367
|
G | A | 1 | a0001c0021 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.1527C>T | p.Pro509Pro | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/17 | 1939/9153 | 1527/6015 | 509/2004 | chr8 | 41955367 | ||
chr8:41980850
|
T | C | 1 | a0001c0022 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.903A>G | p.Pro301Pro | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/17 | 1315/9153 | 903/6015 | 301/2004 | chr8 | 41980850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41929610
|
C | T | 1 | a0001c0003t0107 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2595G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 2595 | chr8 | 41929610 | |||||
chr8:41929801
|
A | G | 1 | a0006c0010t0052 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2404T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 2404 | chr8 | 41929801 | |||||
chr8:41929805
|
A | C | 1 | a0009c0015t0099 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 2400 | chr8 | 41929805 | |||||
chr8:41929918
|
G | A | 1 | a0001c0003t0091 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2287C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 2287 | chr8 | 41929918 | |||||
chr8:41930187
|
CTCATT | C | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(47): Show | 174 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2013_*2017delAATG others(1): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 2013 | chr8 | 41930187 | |||||
chr8:41930410
|
G | A | 1 | a0002c0002t0078 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1795 | chr8 | 41930410 | |||||
chr8:41930440
|
GC | G | 2 | a0001c0001t0008a0001c0001t0072 | 7 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1764delG | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1764 | chr8 | 41930440 | |||||
chr8:41930580
|
A | G | 1 | a0001c0003t0087 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1625T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1625 | chr8 | 41930580 | |||||
chr8:41930616
|
T | C | 1 | a0002c0002t0079 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1589A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1589 | chr8 | 41930616 | |||||
chr8:41930682
|
A | ATG | 6 | a0001c0001t0047a0001c0003t0090a0001c0005t0020others(3): Show | 9 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1521_*1522dupCA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1522 | chr8 | 41930682 | |||||
chr8:41930682
|
A | ATGTG | 3 | a0001c0001t0044a0001c0003t0068a0001c0004t0063 | 4 | HG02257.hp1 HG02559.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1519_*1522dupCACA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1522 | chr8 | 41930682 | |||||
chr8:41930682
|
A | ATGTGTG | 6 | a0001c0001t0006a0001c0001t0042a0001c0001t0080others(3): Show | 15 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1517_*1522dupCACA others(2): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1522 | chr8 | 41930682 | |||||
chr8:41930682
|
A | G | 4 | a0001c0001t0114a0001c0003t0023a0001c0003t0103others(1): Show | 7 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1523T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1523 | chr8 | 41930682 | |||||
chr8:41930682
|
ATG | A | 6 | a0001c0001t0033a0001c0001t0038a0001c0001t0039others(3): Show | 10 | HG00544.hp1 HG01109.hp1 HG02027.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1521_*1522delCA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1521 | chr8 | 41930682 | |||||
chr8:41930682
|
ATGTG | A | 4 | a0001c0001t0059a0001c0001t0072a0001c0001t0118others(1): Show | 4 | HG02280.hp1 HG03098.hp2 NA18940.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1519_*1522delCACA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1519 | chr8 | 41930682 | |||||
chr8:41930682
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0004t0067 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1511_*1522delCACA others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1511 | chr8 | 41930682 | |||||
chr8:41930684
|
G | A | 3 | a0001c0001t0110a0001c0003t0075a0001c0004t0032 | 4 | HG02630.hp2 HG02818.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1521C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1521 | chr8 | 41930684 | |||||
chr8:41930686
|
G | A | 1 | a0001c0001t0110 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1519C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1519 | chr8 | 41930686 | |||||
chr8:41930704
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0061 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1491_*1500delTATA others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1491 | chr8 | 41930704 | |||||
chr8:41930706
|
G | A | 14 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(11): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1499C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1499 | chr8 | 41930706 | |||||
chr8:41930708
|
G | A | 24 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(21): Show | 86 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1497C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1497 | chr8 | 41930708 | |||||
chr8:41930708
|
G | GTA | 5 | a0001c0003t0004a0001c0003t0017a0001c0003t0028others(2): Show | 20 | HG00642.hp1 HG00741.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1496_*1497insTA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1496 | chr8 | 41930708 | |||||
chr8:41930710
|
G | A | 54 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(51): Show | 145 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1495C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1495 | chr8 | 41930710 | |||||
chr8:41930710
|
G | GTATA | 2 | a0001c0003t0016a0001c0003t0074 | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1491_*1494dupTATA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1494 | chr8 | 41930710 | |||||
chr8:41930710
|
G | GTGTGTAT others(3): Show |
1 | a0001c0003t0087 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494_*1495insTATA others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1494 | chr8 | 41930710 | |||||
chr8:41930710
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0025 | 2 | HG02257.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1494_*1495insTATA others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1494 | chr8 | 41930710 | |||||
chr8:41930710
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0054 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494_*1495insTATA others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1494 | chr8 | 41930710 | |||||
chr8:41930710
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0053 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494_*1495insTATA others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1494 | chr8 | 41930710 | |||||
chr8:41930712
|
A | G | 21 | a0001c0001t0014a0001c0001t0044a0001c0001t0048others(18): Show | 33 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1493T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1493 | chr8 | 41930712 | |||||
chr8:41930714
|
A | G | 6 | a0001c0001t0048a0001c0001t0077a0001c0001t0096others(3): Show | 6 | HG01943.hp2 HG02055.hp1 HG02148.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1491T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1491 | chr8 | 41930714 | |||||
chr8:41930726
|
ATAT | A | 3 | a0001c0001t0005a0001c0001t0008a0002c0002t0030 | 17 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1476_*1478delATA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1476 | chr8 | 41930726 | |||||
chr8:41930728
|
A | AT | 2 | a0001c0001t0009a0005c0009t0009 | 6 | HG02293.hp2 HG03834.hp1 HG04184.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1476dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1476 | chr8 | 41930728 | |||||
chr8:41930728
|
A | ATATATAT others(4): Show |
1 | a0001c0022t0058 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476_*1477insAAAT others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1476 | chr8 | 41930728 | |||||
chr8:41930728
|
A | ATATATAT others(5): Show |
1 | a0001c0003t0057 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1476_*1477insAAAA others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1476 | chr8 | 41930728 | |||||
chr8:41930728
|
AT | A | 17 | a0001c0001t0006a0001c0001t0036a0001c0001t0040others(14): Show | 28 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1476delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1476 | chr8 | 41930728 | |||||
chr8:41930728
|
ATTT | A | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(13): Show | 110 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1474_*1476delAAA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1474 | chr8 | 41930728 | |||||
chr8:41930729
|
T | TA | 16 | a0001c0001t0010a0001c0001t0050a0001c0001t0077others(13): Show | 23 | HG00639.hp2 HG01070.hp1 HG01099.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1475_*1476insT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930729 | |||||
chr8:41930729
|
T | TATA | 11 | a0001c0001t0048a0001c0001t0049a0001c0001t0096others(8): Show | 16 | HG01071.hp2 HG01255.hp1 HG01943.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1475_*1476insTAT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930729 | |||||
chr8:41930729
|
T | TATATA | 2 | a0001c0004t0032a0008c0018t0117 | 3 | HG01978.hp1 HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1475_*1476insTATA others(1): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930729 | |||||
chr8:41930729
|
T | TATATATA | 3 | a0001c0001t0085a0001c0003t0037a0001c0016t0102 | 4 | HG02055.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1475_*1476insTATA others(3): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930729 | |||||
chr8:41930729
|
T | TATATATA others(4): Show |
1 | a0006c0010t0052 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1475_*1476insTATA others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930729 | |||||
chr8:41930730
|
T | A | 36 | a0001c0001t0011a0001c0001t0025a0001c0001t0033others(33): Show | 67 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1475A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1475 | chr8 | 41930730 | |||||
chr8:41930731
|
T | A | 35 | a0001c0001t0006a0001c0001t0036a0001c0001t0040others(32): Show | 51 | HG00639.hp2 HG00673.hp2 HG01070.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1474A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1474 | chr8 | 41930731 | |||||
chr8:41930732
|
T | A | 23 | a0001c0001t0025a0001c0001t0038a0001c0001t0039others(20): Show | 36 | HG00544.hp1 HG01106.hp1 HG01109.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1473A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1473 | chr8 | 41930732 | |||||
chr8:41930733
|
T | A | 17 | a0001c0001t0006a0001c0001t0013a0001c0001t0022others(14): Show | 32 | HG00673.hp2 HG01168.hp1 HG01255.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1472A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1472 | chr8 | 41930733 | |||||
chr8:41930734
|
T | A | 8 | a0001c0001t0042a0001c0001t0043a0001c0001t0044others(5): Show | 13 | HG01106.hp1 HG02451.hp2 HG02717.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1471A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1471 | chr8 | 41930734 | |||||
chr8:41930735
|
T | A | 3 | a0001c0001t0100a0001c0001t0101a0001c0016t0102 | 3 | HG00673.hp2 HG02723.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1470A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1470 | chr8 | 41930735 | |||||
chr8:41930736
|
T | A | 3 | a0001c0001t0044a0001c0003t0103a0006c0010t0104 | 4 | HG03209.hp1 HG06807.hp1 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1469A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1469 | chr8 | 41930736 | |||||
chr8:41930738
|
T | A | 1 | a0001c0001t0044 | 2 | NA18998.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1467A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1467 | chr8 | 41930738 | |||||
chr8:41930763
|
C | A | 1 | a0001c0003t0108 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1442 | chr8 | 41930763 | |||||
chr8:41930772
|
G | C | 1 | a0001c0001t0120 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1433C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1433 | chr8 | 41930772 | |||||
chr8:41930779
|
G | T | 1 | a0001c0001t0109 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1426 | chr8 | 41930779 | |||||
chr8:41931050
|
C | T | 1 | a0001c0001t0056 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1155G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 1155 | chr8 | 41931050 | |||||
chr8:41931283
|
T | C | 1 | a0001c0001t0050 | 2 | HG00639.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*922A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 922 | chr8 | 41931283 | |||||
chr8:41931450
|
G | C | 1 | a0001c0001t0051 | 2 | HG00735.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*755C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 755 | chr8 | 41931450 | |||||
chr8:41932020
|
G | C | 8 | a0001c0003t0004a0001c0003t0045a0001c0003t0046others(5): Show | 21 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*185C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 17/17 | 185 | chr8 | 41932020 | |||||
chr8:42049169
|
C | G | 4 | a0001c0001t0025a0001c0001t0053a0001c0001t0054others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-192G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/17 | 192 | chr8 | 42049169 | |||||
chr8:42049176
|
A | T | 111 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(108): Show | 280 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(277): Show |
5_prime_UTR_variant | MODIFIER | c.-199T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/17 | 199 | chr8 | 42049176 | |||||
chr8:42051919
|
A | G | 1 | a0006c0010t0052 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-344T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/17 | 2942 | chr8 | 42051919 | |||||
chr8:42051949
|
G | T | 1 | a0001c0001t0024 | 2 | NA18956.hp1 NA19009.hp1 |
5_prime_UTR_variant | MODIFIER | c.-374C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/17 | 2972 | chr8 | 42051949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41934886
|
A | C | 1 | a0001c0001t0002g0290 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3353-19T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41934886 | ||||||
chr8:41935863
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3353-996A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41935863 | ||||||
chr8:41936032
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3353-1165G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936032 | ||||||
chr8:41936121
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(98): Show | 103 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3352+1135C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936121 | ||||||
chr8:41936153
|
T | C | 3 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0005g0038 | 3 | HG02080.hp1 NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3352+1103A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936153 | ||||||
chr8:41936246
|
G | C | 1 | a0001c0003t0045g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3352+1010C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936246 | ||||||
chr8:41936619
|
A | G | 1 | a0001c0001t0041g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3352+637T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936619 | ||||||
chr8:41936624
|
G | A | 1 | a0001c0001t0080g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3352+632C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936624 | ||||||
chr8:41936808
|
T | C | 2 | a0001c0016t0102g0170a0001c0022t0058g0115 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3352+448A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41936808 | ||||||
chr8:41937071
|
G | A | 1 | a0004c0007t0007g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3352+185C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41937071 | ||||||
chr8:41937189
|
T | G | 2 | a0001c0001t0002g0246a0001c0001t0120g0239 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3352+67A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 16/16 | chr8 | 41937189 | ||||||
chr8:41937629
|
C | A | 1 | a0005c0009t0009g0212 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3040-61G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41937629 | ||||||
chr8:41937629
|
C | T | 2 | a0001c0003t0069g0200a0002c0002t0018g0007 | 3 | HG01070.hp2 HG01071.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3040-61G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41937629 | ||||||
chr8:41937645
|
A | G | 3 | a0001c0001t0002g0235a0001c0001t0002g0267a0001c0001t0002g0268 | 3 | NA18971.hp1 NA18979.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.3040-77T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41937645 | ||||||
chr8:41937651
|
T | C | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3040-83A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41937651 | ||||||
chr8:41937928
|
A | T | 1 | a0001c0001t0025g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3040-360T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41937928 | ||||||
chr8:41938086
|
G | C | 2 | a0001c0003t0068g0153a0001c0003t0074g0152 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3040-518C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938086 | ||||||
chr8:41938282
|
T | C | 1 | a0002c0002t0082g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3040-714A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938282 | ||||||
chr8:41938674
|
C | T | 1 | a0001c0016t0102g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3040-1106G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938674 | ||||||
chr8:41938680
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3040-1112G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938680 | ||||||
chr8:41938910
|
T | C | 4 | a0002c0002t0015g0348a0002c0002t0015g0349a0002c0002t0015g0357others(1): Show | 4 | HG00735.hp1 HG01975.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.3040-1342A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938910 | ||||||
chr8:41938946
|
T | A | 56 | a0001c0001t0038g0154a0001c0003t0004g0180a0001c0003t0004g0181others(53): Show | 56 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.3040-1378A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938946 | ||||||
chr8:41938954
|
G | GA | 28 | a0001c0001t0002g0247a0001c0001t0002g0260a0001c0001t0002g0267others(25): Show | 28 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.3040-1387dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938954 | ||||||
chr8:41938954
|
GA | G | 78 | a0001c0001t0006g0023a0001c0003t0031g0160a0001c0004t0012g0122others(75): Show | 83 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.3040-1387delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41938954 | ||||||
chr8:41939003
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.3040-1435T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939003 | ||||||
chr8:41939088
|
T | C | 1 | a0001c0001t0109g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3040-1520A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939088 | ||||||
chr8:41939459
|
G | A | 4 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3039+1383C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939459 | ||||||
chr8:41939565
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3039+1277G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939565 | ||||||
chr8:41939706
|
G | A | 2 | a0001c0001t0083g0171a0001c0001t0085g0172 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3039+1136C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939706 | ||||||
chr8:41939803
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(90): Show | 95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.3039+1039G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939803 | ||||||
chr8:41939941
|
G | A | 1 | a0010c0013t0119g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3039+901C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41939941 | ||||||
chr8:41940136
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3039+706C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940136 | ||||||
chr8:41940176
|
T | G | 48 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(45): Show | 48 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3039+666A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940176 | ||||||
chr8:41940261
|
T | C | 18 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(15): Show | 18 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.3039+581A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940261 | ||||||
chr8:41940378
|
C | T | 2 | a0001c0003t0004g0181a0001c0003t0004g0185 | 2 | HG02004.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3039+464G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940378 | ||||||
chr8:41940384
|
T | G | 164 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(161): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.3039+458A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940384 | ||||||
chr8:41940397
|
C | T | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3039+445G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940397 | ||||||
chr8:41940587
|
T | A | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3039+255A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940587 | ||||||
chr8:41940684
|
G | T | 105 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(102): Show | 107 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.3039+158C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940684 | ||||||
chr8:41940812
|
G | A | 2 | a0001c0001t0010g0284a0011c0023t0010g0298 | 2 | HG01099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3039+30C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 15/16 | chr8 | 41940812 | ||||||
chr8:41941711
|
T | C | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2437-267A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41941711 | ||||||
chr8:41941762
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.2437-318T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41941762 | ||||||
chr8:41941937
|
C | T | 1 | a0001c0001t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2437-493G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41941937 | ||||||
chr8:41941994
|
A | T | 2 | a0001c0001t0048g0258a0005c0009t0048g0262 | 2 | HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2437-550T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41941994 | ||||||
chr8:41942126
|
A | G | 1 | a0001c0003t0004g0194 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2436+667T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41942126 | ||||||
chr8:41942339
|
G | T | 1 | a0001c0001t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2436+454C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41942339 | ||||||
chr8:41942375
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.2436+418T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41942375 | ||||||
chr8:41942714
|
A | G | 2 | a0002c0002t0001g0306a0002c0002t0001g0330 | 2 | NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2436+79T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41942714 | ||||||
chr8:41942757
|
T | C | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2436+36A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 14/16 | chr8 | 41942757 | ||||||
chr8:41943069
|
G | A | 1 | a0001c0001t0081g0090 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2229-69C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 13/16 | chr8 | 41943069 | ||||||
chr8:41943153
|
A | G | 1 | a0001c0001t0034g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2229-153T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 13/16 | chr8 | 41943153 | ||||||
chr8:41943209
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2229-209C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 13/16 | chr8 | 41943209 | ||||||
chr8:41943438
|
T | C | 2 | a0002c0002t0001g0006a0002c0011t0001g0333 | 3 | NA18988.hp2 NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2228+310A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 13/16 | chr8 | 41943438 | ||||||
chr8:41944269
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1997-290G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944269 | ||||||
chr8:41944349
|
G | A | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1997-370C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944349 | ||||||
chr8:41944434
|
C | T | 3 | a0002c0002t0001g0008a0002c0002t0001g0350a0002c0002t0001g0351 | 4 | HG01257.hp1 HG01258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-455G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944434 | ||||||
chr8:41944670
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(88): Show | 93 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1997-691C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944670 | ||||||
chr8:41944736
|
A | G | 2 | a0001c0003t0090g0287a0001c0003t0091g0288 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1997-757T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944736 | ||||||
chr8:41944791
|
A | T | 4 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-812T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944791 | ||||||
chr8:41944837
|
G | T | 2 | a0001c0003t0037g0145a0001c0003t0037g0146 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1997-858C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41944837 | ||||||
chr8:41945065
|
T | G | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1997-1086A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945065 | ||||||
chr8:41945357
|
A | G | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1996+1234T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945357 | ||||||
chr8:41945413
|
G | A | 1 | a0001c0003t0023g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1996+1178C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945413 | ||||||
chr8:41945447
|
T | C | 1 | a0002c0002t0001g0339 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1996+1144A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945447 | ||||||
chr8:41945566
|
G | A | 1 | a0001c0003t0105g0193 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1996+1025C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945566 | ||||||
chr8:41945573
|
A | C | 1 | a0001c0001t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1996+1018T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945573 | ||||||
chr8:41945636
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1996+955A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945636 | ||||||
chr8:41945738
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(104): Show | 109 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1996+853G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945738 | ||||||
chr8:41945747
|
G | A | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1996+844C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945747 | ||||||
chr8:41945856
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(104): Show | 109 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1996+735C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945856 | ||||||
chr8:41945886
|
G | A | 3 | a0004c0007t0007g0166a0004c0007t0007g0177a0004c0007t0007g0178 | 3 | HG02615.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1996+705C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41945886 | ||||||
chr8:41946031
|
C | CA | 6 | a0001c0001t0003g0108a0001c0001t0006g0025a0001c0001t0116g0265others(3): Show | 6 | HG01516.hp2 HG01934.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1996+559dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946031 | ||||||
chr8:41946031
|
CA | C | 74 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(71): Show | 79 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1996+559delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946031 | ||||||
chr8:41946146
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1996+445C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946146 | ||||||
chr8:41946313
|
A | C | 3 | a0002c0002t0001g0347a0002c0002t0001g0356a0002c0002t0001g0358 | 3 | HG00438.hp1 HG00621.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1996+278T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946313 | ||||||
chr8:41946481
|
AAT | A | 8 | a0001c0001t0002g0272a0001c0001t0003g0037a0001c0001t0029g0064others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1996+108_1996+109d others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946481 | ||||||
chr8:41946489
|
TATATACA others(1): Show |
T | 4 | a0001c0003t0007g0176a0001c0003t0027g0175a0004c0007t0007g0177others(1): Show | 4 | HG02615.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1996+94_1996+101de others(9): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946489 | ||||||
chr8:41946489
|
TATATACA others(5): Show |
T | 2 | a0001c0003t0023g0150a0001c0003t0037g0145 | 2 | HG01106.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1996+90_1996+101de others(13): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946489 | ||||||
chr8:41946491
|
T | C | 7 | a0001c0001t0003g0032a0001c0001t0003g0043a0001c0001t0005g0038others(4): Show | 7 | HG01175.hp2 HG01496.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1996+100A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATAC | T | 5 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0280others(2): Show | 5 | HG00735.hp2 HG02004.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1996+96_1996+99del others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATACAC | T | 4 | a0001c0003t0004g0181a0001c0003t0004g0185a0001c0003t0004g0187others(1): Show | 4 | HG02004.hp2 HG03654.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1996+94_1996+99del others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATACACA others(3): Show |
T | 12 | a0001c0003t0004g0180a0001c0003t0004g0194a0001c0003t0004g0195others(9): Show | 12 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1996+90_1996+99del others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATACACA others(5): Show |
T | 23 | a0001c0003t0004g0188a0001c0003t0004g0190a0001c0003t0016g0134others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1996+88_1996+99del others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATACACA others(7): Show |
T | 1 | a0001c0003t0016g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1996+86_1996+99del others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946491
|
TATACACA others(19): Show |
T | 2 | a0001c0003t0068g0153a0001c0003t0074g0152 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1996+74_1996+99del others(26): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946491 | ||||||
chr8:41946493
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(87): Show | 92 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1996+98A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
T | TAC | 6 | a0001c0001t0002g0237a0001c0001t0002g0241a0001c0001t0002g0264others(3): Show | 6 | HG00741.hp1 HG01099.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996+96_1996+97dup others(2): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
T | TACAC | 3 | a0001c0001t0002g0277a0001c0001t0002g0286a0001c0001t0049g0270 | 3 | HG01975.hp2 NA18975.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1996+94_1996+97dup others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
TAC | T | 10 | a0001c0001t0002g0226a0001c0001t0002g0243a0001c0001t0002g0260others(7): Show | 10 | HG00738.hp2 HG01109.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996+96_1996+97del others(2): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
TACACACA others(3): Show |
T | 1 | a0001c0003t0004g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1996+88_1996+97del others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0206 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1996+84_1996+97del others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
TACACACA others(11): Show |
T | 2 | a0001c0003t0087g0174a0002c0002t0079g0344 | 2 | HG01891.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1996+80_1996+97del others(18): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946493
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0010g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1996+76_1996+97del others(22): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946493 | ||||||
chr8:41946495
|
C | T | 2 | a0001c0001t0002g0232a0001c0001t0014g0231 | 2 | HG02083.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1996+96G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946495 | ||||||
chr8:41946529
|
C | CACACACA others(7): Show |
1 | a0001c0001t0006g0022 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1996+61_1996+62ins others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CACACACA others(5): Show |
12 | a0001c0001t0006g0025a0001c0001t0008g0042a0001c0001t0025g0016others(9): Show | 12 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CACACACA others(3): Show |
14 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0137others(11): Show | 14 | HG02074.hp1 HG02132.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CACACACA others(1): Show |
15 | a0001c0001t0005g0068a0001c0001t0005g0095a0001c0001t0008g0003others(12): Show | 16 | HG00609.hp1 HG00673.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CACACAT | 8 | a0001c0001t0003g0101a0001c0001t0006g0023a0001c0001t0006g0026others(5): Show | 8 | HG02723.hp1 NA18956.hp1 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CACAT | 26 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0050others(23): Show | 27 | HG01099.hp2 HG01975.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | CAT | 105 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(102): Show | 108 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1996+61_1996+62ins others(2): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946529
|
C | T | 33 | a0001c0001t0003g0037a0001c0001t0003g0082a0001c0001t0029g0064others(30): Show | 35 | HG00438.hp1 HG00621.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1996+62G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946529 | ||||||
chr8:41946543
|
G | C | 1 | a0001c0001t0002g0229 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1996+48C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 12/16 | chr8 | 41946543 | ||||||
chr8:41946748
|
T | TAAGAAAC others(310): Show |
6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-65_1903-64ins others(317): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41946748 | ||||||
chr8:41946863
|
A | AT | 6 | a0001c0001t0002g0204a0001c0001t0002g0209a0001c0001t0002g0216others(3): Show | 6 | HG00609.hp2 NA19000.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-180dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41946863 | ||||||
chr8:41946890
|
G | A | 5 | a0001c0003t0017g0295a0001c0003t0017g0296a0001c0003t0028g0294others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1903-206C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41946890 | ||||||
chr8:41947137
|
C | T | 1 | a0002c0002t0018g0007 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1903-453G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947137 | ||||||
chr8:41947368
|
C | T | 4 | a0001c0001t0022g0061a0001c0001t0022g0066a0001c0001t0022g0088others(1): Show | 4 | HG02040.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902+383G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947368 | ||||||
chr8:41947441
|
G | C | 1 | a0001c0001t0061g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1902+310C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947441 | ||||||
chr8:41947483
|
C | G | 9 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(6): Show | 9 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1902+268G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947483 | ||||||
chr8:41947655
|
A | C | 49 | a0001c0001t0003g0035a0001c0001t0003g0046a0001c0001t0003g0049others(46): Show | 50 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1902+96T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947655 | ||||||
chr8:41947731
|
C | T | 36 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(33): Show | 36 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1902+20G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 11/16 | chr8 | 41947731 | ||||||
chr8:41948094
|
T | G | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1741-182A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948094 | ||||||
chr8:41948245
|
G | A | 1 | a0002c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1741-333C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948245 | ||||||
chr8:41948563
|
G | A | 4 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741-651C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948563 | ||||||
chr8:41948794
|
TA | T | 272 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(269): Show | 279 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.1740+427delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948794 | ||||||
chr8:41948900
|
C | CGCATCA | 3 | a0002c0002t0001g0323a0002c0002t0001g0325a0002c0002t0021g0324 | 3 | NA18984.hp1 NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1740+321_1740+322i others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948900 | ||||||
chr8:41948901
|
A | ACAT | 61 | a0001c0001t0002g0272a0001c0003t0004g0180a0001c0003t0004g0181others(58): Show | 61 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.1740+318_1740+320d others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948901 | ||||||
chr8:41948901
|
A | ACATCAT | 41 | a0001c0003t0016g0179a0002c0002t0001g0005a0002c0002t0001g0006others(38): Show | 43 | HG00621.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1740+315_1740+320d others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948901 | ||||||
chr8:41948901
|
A | ACATCATC others(2): Show |
24 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0013others(21): Show | 27 | HG00438.hp1 HG00735.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1740+312_1740+320d others(11): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948901 | ||||||
chr8:41948901
|
A | T | 3 | a0002c0002t0001g0323a0002c0002t0001g0325a0002c0002t0021g0324 | 3 | NA18984.hp1 NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1740+321T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948901 | ||||||
chr8:41948901
|
ACAT | A | 11 | a0001c0001t0002g0269a0001c0001t0007g0155a0001c0001t0007g0202others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1740+318_1740+320d others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 10/16 | chr8 | 41948901 | ||||||
chr8:41949371
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1599-8G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949371 | ||||||
chr8:41949372
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1599-9C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949372 | ||||||
chr8:41949811
|
T | G | 1 | a0001c0001t0002g0207 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1599-448A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949811 | ||||||
chr8:41949830
|
G | A | 1 | a0001c0003t0069g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1599-467C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949830 | ||||||
chr8:41949857
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(238): Show | 248 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1599-494G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949857 | ||||||
chr8:41949869
|
A | C | 1 | a0001c0001t0042g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1599-506T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41949869 | ||||||
chr8:41950035
|
T | A | 1 | a0001c0001t0003g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1599-672A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950035 | ||||||
chr8:41950118
|
T | C | 1 | a0003c0006t0098g0345 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1599-755A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950118 | ||||||
chr8:41950232
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1599-869T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950232 | ||||||
chr8:41950578
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(236): Show | 246 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.1599-1215T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950578 | ||||||
chr8:41950647
|
A | C | 1 | a0001c0001t0003g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1599-1284T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950647 | ||||||
chr8:41950909
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1599-1546C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950909 | ||||||
chr8:41950931
|
GA | G | 6 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0075others(3): Show | 7 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599-1569delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41950931 | ||||||
chr8:41951183
|
A | C | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599-1820T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951183 | ||||||
chr8:41951184
|
C | A | 3 | a0001c0001t0002g0241a0001c0001t0002g0264a0002c0002t0001g0350 | 3 | HG00741.hp1 HG01496.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1599-1821G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951184 | ||||||
chr8:41951316
|
G | C | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599-1953C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951316 | ||||||
chr8:41951506
|
T | C | 1 | a0002c0002t0018g0310 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1599-2143A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951506 | ||||||
chr8:41951536
|
C | T | 1 | a0001c0003t0023g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1599-2173G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951536 | ||||||
chr8:41951777
|
T | C | 1 | a0001c0003t0016g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1599-2414A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951777 | ||||||
chr8:41951867
|
C | T | 4 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1599-2504G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951867 | ||||||
chr8:41951913
|
G | A | 4 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1599-2550C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41951913 | ||||||
chr8:41952261
|
A | G | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599-2898T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41952261 | ||||||
chr8:41952403
|
T | C | 1 | a0002c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1598+2893A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41952403 | ||||||
chr8:41952751
|
T | C | 1 | a0001c0003t0068g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1598+2545A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41952751 | ||||||
chr8:41952771
|
G | T | 2 | a0001c0001t0002g0232a0001c0001t0014g0231 | 2 | HG02083.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1598+2525C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41952771 | ||||||
chr8:41952832
|
A | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1598+2464T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41952832 | ||||||
chr8:41953224
|
ACAAAAGT others(20): Show |
A | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1598+2045_1598+207 others(31): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953224 | ||||||
chr8:41953255
|
T | G | 3 | a0001c0001t0002g0289a0001c0001t0010g0284a0011c0023t0010g0298 | 3 | HG01099.hp1 HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1598+2041A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953255 | ||||||
chr8:41953330
|
C | T | 56 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(53): Show | 56 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1598+1966G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953330 | ||||||
chr8:41953520
|
C | T | 1 | a0002c0002t0001g0312 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1598+1776G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953520 | ||||||
chr8:41953537
|
G | A | 1 | a0001c0001t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1598+1759C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953537 | ||||||
chr8:41953631
|
G | A | 4 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0033g0105others(1): Show | 4 | HG02293.hp1 NA18949.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1598+1665C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953631 | ||||||
chr8:41953760
|
T | C | 18 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(15): Show | 18 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.1598+1536A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953760 | ||||||
chr8:41953830
|
C | T | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1598+1466G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953830 | ||||||
chr8:41953943
|
A | C | 1 | a0001c0001t0112g0221 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1598+1353T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41953943 | ||||||
chr8:41954003
|
A | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1598+1293T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954003 | ||||||
chr8:41954158
|
C | A | 1 | a0001c0003t0004g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1598+1138G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954158 | ||||||
chr8:41954216
|
A | T | 1 | a0001c0001t0034g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1598+1080T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954216 | ||||||
chr8:41954290
|
C | T | 1 | a0001c0001t0039g0047 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1598+1006G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954290 | ||||||
chr8:41954316
|
T | C | 1 | a0002c0002t0001g0360 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1598+980A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954316 | ||||||
chr8:41954434
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1598+862A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954434 | ||||||
chr8:41954550
|
CTTTTAA | C | 34 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(31): Show | 34 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1598+740_1598+745d others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954550 | ||||||
chr8:41954704
|
T | C | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1598+592A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954704 | ||||||
chr8:41954912
|
T | C | 1 | a0001c0001t0041g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1598+384A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41954912 | ||||||
chr8:41955023
|
T | TA | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1598+272dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41955023 | ||||||
chr8:41955221
|
C | T | 1 | a0002c0002t0001g0362 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1598+75G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 9/16 | chr8 | 41955221 | ||||||
chr8:41955600
|
T | A | 1 | a0001c0001t0027g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1483-189A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955600 | ||||||
chr8:41955601
|
A | T | 1 | a0001c0001t0027g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1483-190T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955601 | ||||||
chr8:41955648
|
C | T | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1483-237G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955648 | ||||||
chr8:41955653
|
C | A | 1 | a0002c0002t0001g0302 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1483-242G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955653 | ||||||
chr8:41955741
|
T | C | 1 | a0002c0002t0001g0356 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1483-330A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955741 | ||||||
chr8:41955774
|
G | A | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1483-363C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955774 | ||||||
chr8:41955841
|
T | C | 36 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(33): Show | 36 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1483-430A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41955841 | ||||||
chr8:41956157
|
C | T | 4 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-746G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41956157 | ||||||
chr8:41956526
|
G | T | 2 | a0001c0001t0006g0137a0001c0001t0042g0139 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1483-1115C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41956526 | ||||||
chr8:41956542
|
G | A | 4 | a0001c0001t0003g0077a0001c0001t0005g0096a0001c0001t0005g0097others(1): Show | 4 | HG00639.hp1 HG01255.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-1131C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41956542 | ||||||
chr8:41956639
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1483-1228A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41956639 | ||||||
chr8:41956945
|
T | C | 1 | a0001c0001t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1483-1534A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41956945 | ||||||
chr8:41957056
|
G | A | 28 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(25): Show | 28 | HG00673.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1483-1645C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957056 | ||||||
chr8:41957251
|
G | A | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1483-1840C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957251 | ||||||
chr8:41957315
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483-1904G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957315 | ||||||
chr8:41957382
|
T | C | 9 | a0001c0001t0077g0094a0001c0001t0081g0090a0001c0005t0020g0118others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1483-1971A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957382 | ||||||
chr8:41957457
|
C | T | 1 | a0001c0001t0009g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1483-2046G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957457 | ||||||
chr8:41957632
|
C | T | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483-2221G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41957632 | ||||||
chr8:41958177
|
G | A | 1 | a0001c0003t0068g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1483-2766C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958177 | ||||||
chr8:41958211
|
C | G | 1 | a0001c0001t0120g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1483-2800G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958211 | ||||||
chr8:41958281
|
C | G | 1 | a0001c0003t0028g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1483-2870G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958281 | ||||||
chr8:41958372
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(88): Show | 93 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1483-2961G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958372 | ||||||
chr8:41958407
|
G | A | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-2996C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958407 | ||||||
chr8:41958438
|
G | A | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-3027C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958438 | ||||||
chr8:41958842
|
G | A | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-3431C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958842 | ||||||
chr8:41958942
|
G | A | 8 | a0002c0002t0001g0005a0002c0002t0001g0309a0002c0002t0001g0314others(5): Show | 9 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1483-3531C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41958942 | ||||||
chr8:41959080
|
G | A | 3 | a0001c0001t0043g0029a0001c0001t0043g0030a0001c0001t0101g0031 | 3 | NA18953.hp1 NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1483-3669C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959080 | ||||||
chr8:41959094
|
G | C | 1 | a0003c0006t0019g0364 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1483-3683C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959094 | ||||||
chr8:41959151
|
A | ACT | 274 | a0001c0001t0001g0002a0001c0001t0002g0259a0001c0001t0003g0032others(271): Show | 281 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(278): Show |
intron_variant | MODIFIER | c.1483-3742_1483-374 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959151 | ||||||
chr8:41959155
|
T | C | 72 | a0001c0001t0002g0259a0002c0002t0001g0005a0002c0002t0001g0006others(69): Show | 77 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1483-3744A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959155 | ||||||
chr8:41959159
|
GA | G | 229 | a0001c0001t0001g0002a0001c0001t0002g0229a0001c0001t0002g0261others(226): Show | 233 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.1483-3749delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959159 | ||||||
chr8:41959161
|
A | G | 2 | a0001c0003t0090g0287a0001c0003t0091g0288 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1483-3750T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959161 | ||||||
chr8:41959180
|
A | T | 72 | a0001c0001t0002g0259a0002c0002t0001g0005a0002c0002t0001g0006others(69): Show | 77 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1483-3769T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959180 | ||||||
chr8:41959674
|
A | G | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1483-4263T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959674 | ||||||
chr8:41959683
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1483-4272G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959683 | ||||||
chr8:41959723
|
C | T | 4 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-4312G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959723 | ||||||
chr8:41959798
|
A | G | 2 | a0001c0003t0016g0134a0001c0003t0028g0157 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1483-4387T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959798 | ||||||
chr8:41959818
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1483-4407C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959818 | ||||||
chr8:41959900
|
G | A | 1 | a0005c0009t0009g0212 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1483-4489C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959900 | ||||||
chr8:41959960
|
G | GA | 9 | a0001c0001t0003g0108a0001c0001t0083g0171a0001c0001t0085g0172others(6): Show | 9 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1483-4550dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41959960 | ||||||
chr8:41960186
|
G | C | 1 | a0001c0003t0004g0185 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1483-4775C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960186 | ||||||
chr8:41960204
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(239): Show | 249 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.1483-4793T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960204 | ||||||
chr8:41960272
|
T | C | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1483-4861A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960272 | ||||||
chr8:41960442
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1483-5031C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960442 | ||||||
chr8:41960486
|
G | A | 2 | a0001c0001t0003g0046a0001c0001t0039g0047 | 2 | HG00621.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1483-5075C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960486 | ||||||
chr8:41960506
|
C | CA | 152 | a0001c0001t0001g0002a0001c0001t0002g0268a0001c0001t0003g0032others(149): Show | 158 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1483-5096dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960506 | ||||||
chr8:41960506
|
C | CAA | 29 | a0001c0001t0003g0050a0001c0001t0003g0071a0001c0001t0003g0072others(26): Show | 30 | HG00609.hp1 HG02109.hp2 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.1483-5097_1483-509 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960506 | ||||||
chr8:41960506
|
CA | C | 8 | a0001c0001t0111g0278a0001c0003t0004g0187a0001c0003t0023g0150others(5): Show | 8 | HG00099.hp1 HG01106.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1483-5096delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960506 | ||||||
chr8:41960527
|
G | T | 1 | a0003c0006t0019g0352 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1483-5116C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960527 | ||||||
chr8:41960644
|
T | C | 1 | a0002c0002t0001g0319 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1483-5233A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960644 | ||||||
chr8:41960714
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1483-5303A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960714 | ||||||
chr8:41960966
|
T | C | 1 | a0001c0001t0038g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1483-5555A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41960966 | ||||||
chr8:41961005
|
T | C | 1 | a0002c0002t0019g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1483-5594A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961005 | ||||||
chr8:41961175
|
C | A | 2 | a0001c0003t0037g0145a0001c0003t0037g0146 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1483-5764G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961175 | ||||||
chr8:41961263
|
T | C | 2 | a0001c0001t0083g0171a0001c0001t0085g0172 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1483-5852A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961263 | ||||||
chr8:41961312
|
G | A | 1 | a0002c0002t0018g0310 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1483-5901C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961312 | ||||||
chr8:41961386
|
C | T | 1 | a0001c0001t0009g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1483-5975G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961386 | ||||||
chr8:41961426
|
A | G | 1 | a0001c0005t0020g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1483-6015T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961426 | ||||||
chr8:41961682
|
C | T | 1 | a0001c0001t0011g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1483-6271G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961682 | ||||||
chr8:41961751
|
C | CA | 11 | a0001c0001t0003g0073a0001c0001t0005g0111a0001c0001t0007g0155others(8): Show | 11 | HG00544.hp1 HG01978.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483-6341dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961751 | ||||||
chr8:41961751
|
CA | C | 17 | a0001c0001t0002g0245a0001c0001t0002g0257a0001c0001t0003g0045others(14): Show | 17 | HG01192.hp2 HG01255.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1483-6341delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961751 | ||||||
chr8:41961820
|
G | A | 1 | a0001c0003t0068g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1483-6409C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41961820 | ||||||
chr8:41962318
|
C | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1483-6907G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962318 | ||||||
chr8:41962361
|
C | G | 1 | a0001c0001t0110g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1483-6950G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962361 | ||||||
chr8:41962796
|
A | C | 1 | a0001c0001t0054g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1483-7385T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962796 | ||||||
chr8:41962806
|
C | T | 2 | a0003c0006t0019g0352a0003c0006t0098g0345 | 2 | NA18966.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1483-7395G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962806 | ||||||
chr8:41962881
|
T | C | 2 | a0001c0003t0087g0174a0001c0019t0007g0168 | 2 | HG01891.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1483-7470A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962881 | ||||||
chr8:41962910
|
G | T | 1 | a0001c0001t0096g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1483-7499C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41962910 | ||||||
chr8:41963563
|
T | G | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1483-8152A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41963563 | ||||||
chr8:41963740
|
C | CTAAA | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483-8330_1483-832 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41963740 | ||||||
chr8:41963763
|
T | A | 1 | a0001c0001t0080g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1483-8352A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41963763 | ||||||
chr8:41963906
|
C | T | 1 | a0001c0001t0111g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1483-8495G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41963906 | ||||||
chr8:41963987
|
A | C | 1 | a0001c0001t0002g0204 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1483-8576T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41963987 | ||||||
chr8:41964149
|
G | A | 4 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-8738C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964149 | ||||||
chr8:41964201
|
G | C | 2 | a0001c0003t0076g0173a0001c0003t0087g0174 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1483-8790C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964201 | ||||||
chr8:41964384
|
C | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1483-8973G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964384 | ||||||
chr8:41964429
|
T | C | 1 | a0001c0001t0077g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1483-9018A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964429 | ||||||
chr8:41964448
|
G | A | 1 | a0001c0001t0065g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1483-9037C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964448 | ||||||
chr8:41964556
|
G | A | 1 | a0001c0001t0096g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1483-9145C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964556 | ||||||
chr8:41964591
|
G | A | 12 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1483-9180C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964591 | ||||||
chr8:41964627
|
GA | G | 6 | a0001c0001t0002g0245a0001c0001t0002g0257a0001c0001t0002g0290others(3): Show | 6 | HG02027.hp1 HG02055.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483-9217delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964627 | ||||||
chr8:41964627
|
GAA | G | 116 | a0001c0001t0003g0080a0001c0001t0005g0097a0001c0001t0025g0016others(113): Show | 120 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.1483-9218_1483-921 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964627 | ||||||
chr8:41964627
|
GAAA | G | 121 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(118): Show | 124 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1483-9219_1483-921 others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964627 | ||||||
chr8:41964627
|
GAAAA | G | 27 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(24): Show | 27 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1483-9220_1483-921 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964627 | ||||||
chr8:41964889
|
T | G | 1 | a0001c0001t0014g0299 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1483-9478A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964889 | ||||||
chr8:41964920
|
A | G | 1 | a0002c0002t0001g0347 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1483-9509T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41964920 | ||||||
chr8:41965256
|
C | T | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1482+9448G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965256 | ||||||
chr8:41965259
|
A | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0274 | 2 | HG02080.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1482+9445T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965259 | ||||||
chr8:41965290
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1482+9414A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965290 | ||||||
chr8:41965805
|
C | T | 1 | a0001c0001t0011g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1482+8899G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965805 | ||||||
chr8:41965829
|
C | G | 1 | a0001c0001t0077g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1482+8875G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965829 | ||||||
chr8:41965862
|
G | A | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+8842C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41965862 | ||||||
chr8:41966020
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(162): Show | 167 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1482+8684A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966020 | ||||||
chr8:41966048
|
A | G | 1 | a0001c0001t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1482+8656T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966048 | ||||||
chr8:41966223
|
C | T | 2 | a0001c0003t0004g0188a0001c0003t0004g0190 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1482+8481G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966223 | ||||||
chr8:41966286
|
G | A | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1482+8418C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966286 | ||||||
chr8:41966409
|
A | G | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1482+8295T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966409 | ||||||
chr8:41966471
|
G | C | 1 | a0001c0001t0109g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1482+8233C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966471 | ||||||
chr8:41966473
|
G | C | 1 | a0001c0001t0003g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1482+8231C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966473 | ||||||
chr8:41966475
|
G | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1482+8229C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966475 | ||||||
chr8:41966516
|
T | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1482+8188A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966516 | ||||||
chr8:41966517
|
T | C | 19 | a0002c0002t0001g0009a0002c0002t0001g0013a0002c0002t0001g0346others(16): Show | 21 | HG00438.hp1 HG00621.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482+8187A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41966517 | ||||||
chr8:41967264
|
T | A | 1 | a0001c0001t0014g0231 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1482+7440A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967264 | ||||||
chr8:41967265
|
A | T | 171 | a0001c0001t0001g0002a0001c0001t0002g0204a0001c0001t0002g0209others(168): Show | 173 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1482+7439T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967265 | ||||||
chr8:41967274
|
A | AAATTT | 8 | a0001c0001t0003g0080a0001c0001t0003g0092a0001c0003t0007g0176others(5): Show | 8 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+7429_1482+743 others(9): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AAATTTAT others(2): Show |
12 | a0001c0001t0008g0075a0001c0001t0013g0051a0001c0001t0081g0090others(9): Show | 12 | HG01106.hp1 HG01255.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482+7429_1482+743 others(13): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AAATTTAT others(6): Show |
113 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(110): Show | 115 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1482+7429_1482+743 others(17): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AAATTTAT others(10): Show |
26 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0003g0063others(23): Show | 26 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1482+7429_1482+743 others(21): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AAATTTAT others(14): Show |
1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1482+7429_1482+743 others(25): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AATTT | 69 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(66): Show | 74 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.1482+7426_1482+742 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AATTTATT others(1): Show |
24 | a0001c0001t0002g0290a0001c0001t0006g0019a0001c0001t0006g0021others(21): Show | 24 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1482+7422_1482+742 others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AATTTATT others(5): Show |
13 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0042g0139others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1482+7418_1482+742 others(16): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AATTTATT others(9): Show |
2 | a0001c0001t0055g0015a0001c0001t0085g0172 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1482+7414_1482+742 others(20): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967274
|
A | AATTTTAT others(6): Show |
1 | a0001c0001t0003g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1482+7429_1482+743 others(17): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967274 | ||||||
chr8:41967524
|
C | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG00738.hp2 HG01257.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1482+7180G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967524 | ||||||
chr8:41967815
|
C | T | 13 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(10): Show | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1482+6889G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967815 | ||||||
chr8:41967817
|
T | C | 13 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(10): Show | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1482+6887A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41967817 | ||||||
chr8:41968068
|
G | T | 1 | a0001c0001t0009g0276 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1482+6636C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968068 | ||||||
chr8:41968097
|
C | T | 2 | a0001c0001t0044g0136a0001c0001t0044g0144 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1482+6607G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968097 | ||||||
chr8:41968191
|
C | T | 1 | a0001c0001t0097g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1482+6513G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968191 | ||||||
chr8:41968195
|
A | G | 1 | a0001c0001t0097g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1482+6509T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968195 | ||||||
chr8:41968219
|
T | G | 1 | a0001c0020t0073g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1482+6485A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968219 | ||||||
chr8:41968234
|
G | T | 1 | a0001c0001t0014g0231 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1482+6470C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968234 | ||||||
chr8:41968247
|
G | C | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1482+6457C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968247 | ||||||
chr8:41968259
|
A | C | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1482+6445T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968259 | ||||||
chr8:41968364
|
A | T | 1 | a0001c0001t0109g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1482+6340T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968364 | ||||||
chr8:41968912
|
A | T | 48 | a0001c0001t0002g0269a0001c0001t0002g0289a0001c0003t0004g0180others(45): Show | 48 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1482+5792T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41968912 | ||||||
chr8:41969086
|
G | A | 4 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+5618C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969086 | ||||||
chr8:41969201
|
A | G | 3 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0280 | 3 | HG02132.hp1 NA18955.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1482+5503T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969201 | ||||||
chr8:41969299
|
A | G | 57 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(54): Show | 57 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.1482+5405T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969299 | ||||||
chr8:41969570
|
C | T | 245 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(242): Show | 252 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.1482+5134G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969570 | ||||||
chr8:41969667
|
A | T | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1482+5037T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969667 | ||||||
chr8:41969768
|
T | TTCACCTT others(4): Show |
5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+4925_1482+493 others(15): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969768 | ||||||
chr8:41969992
|
A | T | 1 | a0003c0006t0098g0345 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1482+4712T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41969992 | ||||||
chr8:41970101
|
ATCTG | A | 86 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(83): Show | 88 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1482+4599_1482+460 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970101 | ||||||
chr8:41970154
|
T | C | 1 | a0001c0001t0014g0285 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1482+4550A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970154 | ||||||
chr8:41970353
|
G | C | 1 | a0001c0001t0041g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1482+4351C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970353 | ||||||
chr8:41970481
|
T | C | 1 | a0001c0016t0102g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1482+4223A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970481 | ||||||
chr8:41970519
|
C | G | 3 | a0002c0002t0001g0323a0002c0002t0001g0325a0002c0002t0021g0324 | 3 | NA18984.hp1 NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1482+4185G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970519 | ||||||
chr8:41970545
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(86): Show | 91 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1482+4159G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41970545 | ||||||
chr8:41971069
|
G | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0034g0109 | 3 | HG00438.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1482+3635C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971069 | ||||||
chr8:41971174
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(265): Show | 275 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.1482+3530G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971174 | ||||||
chr8:41971226
|
TA | T | 148 | a0001c0001t0003g0043a0001c0001t0003g0056a0001c0001t0003g0062others(145): Show | 153 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(150): Show |
intron_variant | MODIFIER | c.1482+3477delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971226 | ||||||
chr8:41971226
|
TAA | T | 7 | a0001c0001t0006g0025a0001c0003t0023g0151a0001c0003t0023g0164others(4): Show | 7 | HG01081.hp2 HG01168.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+3476_1482+347 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971226 | ||||||
chr8:41971227
|
A | T | 1 | a0002c0002t0001g0355 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1482+3477T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971227 | ||||||
chr8:41971361
|
G | A | 1 | a0001c0003t0004g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1482+3343C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971361 | ||||||
chr8:41971508
|
G | T | 5 | a0001c0001t0003g0035a0001c0001t0003g0049a0001c0001t0003g0087others(2): Show | 5 | HG00673.hp1 NA18961.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482+3196C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971508 | ||||||
chr8:41971516
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+3188C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971516 | ||||||
chr8:41971520
|
G | A | 1 | a0001c0003t0087g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1482+3184C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971520 | ||||||
chr8:41971610
|
CT | C | 267 | a0001c0001t0001g0002a0001c0001t0002g0241a0001c0001t0002g0264others(264): Show | 274 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.1482+3093delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971610 | ||||||
chr8:41971897
|
G | GA | 69 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(66): Show | 74 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.1482+2806dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971897 | ||||||
chr8:41971925
|
T | C | 12 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1482+2779A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41971925 | ||||||
chr8:41972194
|
C | CAAAT | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1482+2506_1482+250 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972194 | ||||||
chr8:41972334
|
T | G | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+2370A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972334 | ||||||
chr8:41972467
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1482+2237G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972467 | ||||||
chr8:41972571
|
A | G | 1 | a0001c0001t0042g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1482+2133T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972571 | ||||||
chr8:41972602
|
A | G | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1482+2102T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972602 | ||||||
chr8:41972686
|
G | A | 2 | a0001c0001t0002g0241a0001c0001t0002g0264 | 2 | HG00741.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1482+2018C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41972686 | ||||||
chr8:41973175
|
T | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+1529A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973175 | ||||||
chr8:41973217
|
T | A | 1 | a0001c0001t0097g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1482+1487A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973217 | ||||||
chr8:41973294
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(91): Show | 96 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1482+1410G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973294 | ||||||
chr8:41973308
|
C | T | 1 | a0001c0001t0050g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1482+1396G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973308 | ||||||
chr8:41973420
|
A | G | 1 | a0001c0001t0042g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1482+1284T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973420 | ||||||
chr8:41973481
|
A | G | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1482+1223T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973481 | ||||||
chr8:41973655
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1482+1049T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973655 | ||||||
chr8:41973682
|
C | T | 2 | a0001c0003t0090g0287a0001c0003t0091g0288 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1482+1022G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973682 | ||||||
chr8:41973803
|
T | C | 1 | a0001c0001t0011g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1482+901A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973803 | ||||||
chr8:41973818
|
T | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1482+886A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973818 | ||||||
chr8:41973950
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1482+754T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41973950 | ||||||
chr8:41974050
|
C | T | 39 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(36): Show | 39 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1482+654G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41974050 | ||||||
chr8:41974080
|
A | AT | 9 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(6): Show | 9 | HG01981.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1482+623dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41974080 | ||||||
chr8:41974516
|
A | G | 3 | a0001c0001t0077g0094a0001c0001t0081g0090a0009c0015t0099g0142 | 3 | HG02055.hp1 HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1482+188T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41974516 | ||||||
chr8:41974545
|
A | G | 1 | a0001c0001t0081g0090 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1482+159T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 8/16 | chr8 | 41974545 | ||||||
chr8:41975037
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1364-215T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975037 | ||||||
chr8:41975359
|
T | C | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1364-537A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975359 | ||||||
chr8:41975444
|
C | A | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1364-622G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975444 | ||||||
chr8:41975718
|
A | T | 1 | a0001c0001t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1364-896T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975718 | ||||||
chr8:41975770
|
A | G | 2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | NA18939.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1364-948T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975770 | ||||||
chr8:41975981
|
T | C | 1 | a0001c0001t0011g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1363+1027A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41975981 | ||||||
chr8:41976047
|
G | T | 2 | a0004c0007t0007g0166a0004c0007t0007g0177 | 2 | HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1363+961C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41976047 | ||||||
chr8:41976170
|
A | G | 2 | a0006c0010t0052g0012a0006c0010t0104g0169 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1363+838T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41976170 | ||||||
chr8:41976260
|
A | G | 2 | a0002c0002t0001g0307a0002c0002t0095g0313 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1363+748T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41976260 | ||||||
chr8:41976588
|
CTTTT | C | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1363+416_1363+419d others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41976588 | ||||||
chr8:41976596
|
T | C | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1363+412A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 7/16 | chr8 | 41976596 | ||||||
chr8:41977384
|
T | C | 7 | a0001c0001t0003g0032a0001c0001t0003g0043a0001c0001t0003g0045others(4): Show | 7 | HG01175.hp2 HG01261.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044-57A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41977384 | ||||||
chr8:41977607
|
G | A | 4 | a0002c0002t0015g0348a0002c0002t0015g0349a0002c0002t0015g0357others(1): Show | 4 | HG00735.hp1 HG01975.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-280C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41977607 | ||||||
chr8:41977881
|
C | T | 1 | a0002c0002t0095g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1044-554G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41977881 | ||||||
chr8:41977920
|
C | T | 1 | a0001c0001t0038g0053 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1044-593G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41977920 | ||||||
chr8:41978295
|
A | C | 1 | a0001c0001t0011g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1043+347T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41978295 | ||||||
chr8:41978409
|
G | A | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1043+233C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41978409 | ||||||
chr8:41978498
|
G | A | 1 | a0002c0002t0001g0351 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1043+144C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 6/16 | chr8 | 41978498 | ||||||
chr8:41978979
|
C | A | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908-202G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41978979 | ||||||
chr8:41979132
|
G | A | 34 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(31): Show | 34 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.908-355C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979132 | ||||||
chr8:41979166
|
G | C | 4 | a0001c0001t0002g0228a0001c0001t0002g0250a0001c0001t0009g0004others(1): Show | 5 | HG02135.hp2 HG02155.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.908-389C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979166 | ||||||
chr8:41979221
|
T | C | 1 | a0001c0004t0012g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.908-444A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979221 | ||||||
chr8:41979246
|
C | T | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.908-469G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979246 | ||||||
chr8:41979265
|
C | T | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.908-488G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979265 | ||||||
chr8:41979349
|
T | G | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.908-572A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979349 | ||||||
chr8:41979551
|
C | T | 1 | a0001c0001t0008g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.908-774G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979551 | ||||||
chr8:41979728
|
C | T | 6 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.908-951G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979728 | ||||||
chr8:41979771
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(88): Show | 93 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.908-994G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979771 | ||||||
chr8:41979933
|
A | G | 3 | a0002c0002t0026g0341a0002c0002t0026g0343a0002c0002t0093g0342 | 3 | HG03130.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.907+913T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979933 | ||||||
chr8:41979963
|
AGAGT | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.907+879_907+882del others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979963 | ||||||
chr8:41979966
|
G | A | 5 | a0001c0003t0017g0295a0001c0003t0017g0296a0001c0003t0028g0294others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+880C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979966 | ||||||
chr8:41979987
|
G | T | 2 | a0001c0001t0002g0246a0001c0001t0120g0239 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.907+859C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41979987 | ||||||
chr8:41980087
|
T | A | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.907+759A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980087 | ||||||
chr8:41980206
|
C | A | 1 | a0001c0001t0013g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.907+640G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980206 | ||||||
chr8:41980210
|
T | C | 8 | a0002c0002t0001g0009a0002c0002t0001g0346a0002c0002t0001g0353others(5): Show | 9 | HG02040.hp1 HG03654.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.907+636A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980210 | ||||||
chr8:41980223
|
A | G | 2 | a0002c0002t0001g0318a0002c0002t0018g0304 | 2 | HG02027.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.907+623T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980223 | ||||||
chr8:41980289
|
A | C | 13 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(10): Show | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.907+557T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980289 | ||||||
chr8:41980543
|
T | C | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.907+303A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980543 | ||||||
chr8:41980651
|
G | A | 1 | a0001c0001t0011g0252 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.907+195C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980651 | ||||||
chr8:41980739
|
C | CAAAAAGA others(338): Show |
1 | a0001c0001t0003g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.907+106_907+107ins others(345): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 5/16 | chr8 | 41980739 | ||||||
chr8:41980985
|
G | A | 53 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.826-58C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41980985 | ||||||
chr8:41981045
|
C | A | 4 | a0001c0003t0004g0180a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-118G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981045 | ||||||
chr8:41981158
|
AAATAC | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.826-236_826-232del others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981158 | ||||||
chr8:41981174
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.826-247G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981174 | ||||||
chr8:41981211
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0034g0109 | 3 | HG00438.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.826-284T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981211 | ||||||
chr8:41981296
|
C | T | 1 | a0001c0001t0096g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.826-369G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981296 | ||||||
chr8:41981322
|
A | T | 164 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(161): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.826-395T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981322 | ||||||
chr8:41981344
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.826-417C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981344 | ||||||
chr8:41981393
|
T | C | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.825+446A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981393 | ||||||
chr8:41981618
|
C | T | 1 | a0002c0002t0001g0360 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.825+221G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981618 | ||||||
chr8:41981786
|
C | G | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.825+53G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 4/16 | chr8 | 41981786 | ||||||
chr8:41982120
|
G | C | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.710-166C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41982120 | ||||||
chr8:41982169
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.710-215G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41982169 | ||||||
chr8:41982270
|
T | G | 1 | a0002c0002t0001g0311 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.710-316A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41982270 | ||||||
chr8:41982335
|
G | A | 2 | a0006c0010t0052g0012a0006c0010t0104g0169 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.710-381C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41982335 | ||||||
chr8:41982595
|
G | C | 1 | a0006c0010t0104g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.710-641C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41982595 | ||||||
chr8:41983439
|
G | A | 1 | a0001c0004t0012g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.710-1485C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41983439 | ||||||
chr8:41983567
|
C | T | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-1613G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41983567 | ||||||
chr8:41983741
|
T | G | 1 | a0001c0001t0002g0273 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.710-1787A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41983741 | ||||||
chr8:41983961
|
T | C | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.710-2007A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41983961 | ||||||
chr8:41983996
|
C | T | 1 | a0001c0001t0013g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.710-2042G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41983996 | ||||||
chr8:41984027
|
A | G | 1 | a0002c0002t0015g0357 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.710-2073T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984027 | ||||||
chr8:41984096
|
A | G | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.710-2142T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984096 | ||||||
chr8:41984195
|
T | C | 83 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(80): Show | 88 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.710-2241A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984195 | ||||||
chr8:41984457
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.710-2503T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984457 | ||||||
chr8:41984459
|
C | T | 15 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0302others(12): Show | 17 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.710-2505G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984459 | ||||||
chr8:41984809
|
C | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+2646G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984809 | ||||||
chr8:41984824
|
A | T | 1 | a0002c0002t0001g0307 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.709+2631T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984824 | ||||||
chr8:41984876
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.709+2579G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984876 | ||||||
chr8:41984980
|
C | CA | 6 | a0001c0001t0005g0095a0001c0003t0016g0159a0001c0003t0016g0162others(3): Show | 6 | HG02486.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+2474dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41984980 | ||||||
chr8:41985013
|
A | G | 1 | a0001c0001t0097g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.709+2442T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985013 | ||||||
chr8:41985052
|
G | A | 3 | a0002c0002t0001g0323a0002c0002t0001g0325a0002c0002t0021g0324 | 3 | NA18984.hp1 NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.709+2403C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985052 | ||||||
chr8:41985294
|
G | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+2161C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985294 | ||||||
chr8:41985303
|
C | T | 1 | a0001c0001t0070g0020 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.709+2152G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985303 | ||||||
chr8:41985400
|
G | A | 2 | a0001c0001t0005g0068a0001c0001t0005g0095 | 2 | NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.709+2055C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985400 | ||||||
chr8:41985412
|
T | C | 1 | a0001c0004t0012g0125 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.709+2043A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985412 | ||||||
chr8:41985704
|
A | G | 1 | a0001c0001t0041g0052 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.709+1751T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985704 | ||||||
chr8:41985846
|
T | C | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.709+1609A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985846 | ||||||
chr8:41985934
|
T | G | 80 | a0001c0001t0003g0037a0001c0001t0038g0154a0001c0001t0083g0171others(77): Show | 85 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.709+1521A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41985934 | ||||||
chr8:41986066
|
G | C | 2 | a0001c0003t0023g0151a0001c0003t0023g0164 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.709+1389C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986066 | ||||||
chr8:41986097
|
C | T | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.709+1358G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986097 | ||||||
chr8:41986099
|
C | T | 2 | a0001c0001t0038g0154a0001c0020t0073g0167 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+1356G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986099 | ||||||
chr8:41986161
|
G | A | 4 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286others(1): Show | 4 | NA18956.hp2 NA18975.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+1294C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986161 | ||||||
chr8:41986171
|
C | G | 1 | a0001c0001t0051g0282 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.709+1284G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986171 | ||||||
chr8:41986340
|
C | T | 1 | a0002c0002t0095g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.709+1115G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986340 | ||||||
chr8:41986855
|
T | C | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.709+600A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986855 | ||||||
chr8:41986893
|
C | A | 1 | a0001c0001t0003g0039 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.709+562G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41986893 | ||||||
chr8:41987080
|
C | A | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.709+375G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41987080 | ||||||
chr8:41987125
|
T | G | 41 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0301others(38): Show | 43 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.709+330A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41987125 | ||||||
chr8:41987175
|
T | C | 1 | a0001c0001t0096g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.709+280A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 3/16 | chr8 | 41987175 | ||||||
chr8:41987745
|
T | C | 1 | a0002c0002t0001g0339 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.601-182A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41987745 | ||||||
chr8:41987746
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-183C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41987746 | ||||||
chr8:41988021
|
C | A | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-458G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988021 | ||||||
chr8:41988147
|
T | C | 1 | a0001c0001t0042g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.601-584A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988147 | ||||||
chr8:41988316
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-753T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988316 | ||||||
chr8:41988420
|
T | C | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-857A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988420 | ||||||
chr8:41988500
|
C | T | 1 | a0001c0003t0076g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.601-937G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988500 | ||||||
chr8:41988811
|
T | C | 1 | a0001c0003t0031g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.601-1248A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988811 | ||||||
chr8:41988914
|
T | C | 1 | a0001c0001t0115g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.601-1351A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988914 | ||||||
chr8:41988970
|
T | A | 1 | a0002c0002t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.601-1407A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41988970 | ||||||
chr8:41989023
|
A | G | 71 | a0001c0001t0002g0244a0001c0001t0002g0274a0002c0002t0001g0005others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-1460T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989023 | ||||||
chr8:41989101
|
G | C | 1 | a0001c0001t0013g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601-1538C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989101 | ||||||
chr8:41989169
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(103): Show | 108 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.601-1606C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989169 | ||||||
chr8:41989224
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-1661A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989224 | ||||||
chr8:41989322
|
A | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-1759T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989322 | ||||||
chr8:41989370
|
G | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1807C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989370 | ||||||
chr8:41989424
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.601-1861C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989424 | ||||||
chr8:41989458
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1895C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989458 | ||||||
chr8:41989470
|
T | C | 1 | a0010c0013t0119g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.601-1907A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989470 | ||||||
chr8:41989493
|
G | C | 20 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(17): Show | 20 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.601-1930C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989493 | ||||||
chr8:41989528
|
A | AACGTG | 124 | a0001c0001t0001g0002a0001c0001t0002g0245a0001c0001t0002g0274others(121): Show | 126 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.601-1970_601-1966d others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989528 | ||||||
chr8:41989528
|
A | AACGTGAC others(8): Show |
1 | a0001c0001t0003g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.601-1966_601-1965i others(17): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989528 | ||||||
chr8:41989528
|
A | AACGTGAC others(3): Show |
11 | a0001c0001t0003g0049a0001c0001t0003g0087a0001c0001t0003g0099others(8): Show | 11 | HG00673.hp1 HG02155.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-1975_601-1966d others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989528 | ||||||
chr8:41989528
|
A | AACGTGAC others(8): Show |
3 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173 | 3 | HG02818.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.601-1980_601-1966d others(17): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989528 | ||||||
chr8:41989546
|
G | A | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1983C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989546 | ||||||
chr8:41989550
|
C | CGTGACGT others(3): Show |
2 | a0006c0010t0052g0012a0006c0010t0104g0169 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.601-1988_601-1987i others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989550 | ||||||
chr8:41989681
|
A | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-2118T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989681 | ||||||
chr8:41989689
|
A | G | 1 | a0001c0001t0005g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.601-2126T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989689 | ||||||
chr8:41989762
|
G | T | 13 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(10): Show | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-2199C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41989762 | ||||||
chr8:41990052
|
A | G | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-2489T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990052 | ||||||
chr8:41990124
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601-2561T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990124 | ||||||
chr8:41990610
|
A | G | 1 | a0001c0001t0036g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.601-3047T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990610 | ||||||
chr8:41990634
|
C | T | 361 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0204others(358): Show | 371 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.601-3071G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990634 | ||||||
chr8:41990877
|
C | A | 1 | a0001c0001t0003g0037 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.601-3314G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990877 | ||||||
chr8:41990932
|
T | C | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.601-3369A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990932 | ||||||
chr8:41990980
|
G | T | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-3417C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990980 | ||||||
chr8:41990989
|
C | T | 1 | a0001c0001t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-3426G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990989 | ||||||
chr8:41990994
|
C | CA | 15 | a0001c0001t0002g0208a0001c0001t0002g0229a0001c0001t0002g0233others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-3432dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990994 | ||||||
chr8:41990994
|
CAAA | C | 10 | a0001c0001t0003g0084a0001c0001t0003g0101a0001c0001t0006g0025others(7): Show | 10 | HG01167.hp1 HG01361.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-3434_601-3432d others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990994 | ||||||
chr8:41990994
|
CAAAA | C | 256 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(253): Show | 263 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.601-3435_601-3432d others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990994 | ||||||
chr8:41990994
|
CAAAAA | C | 6 | a0001c0001t0003g0040a0001c0001t0006g0023a0001c0001t0043g0029others(3): Show | 6 | HG01168.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-3436_601-3432d others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41990994 | ||||||
chr8:41991142
|
T | C | 1 | a0001c0001t0113g0219 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.601-3579A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41991142 | ||||||
chr8:41991632
|
C | A | 70 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(67): Show | 75 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.601-4069G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41991632 | ||||||
chr8:41991816
|
G | C | 1 | a0001c0004t0012g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601-4253C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41991816 | ||||||
chr8:41991995
|
G | A | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-4432C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41991995 | ||||||
chr8:41992269
|
G | A | 1 | a0001c0001t0014g0231 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.601-4706C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992269 | ||||||
chr8:41992388
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0011g0240 | 2 | HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.601-4825G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992388 | ||||||
chr8:41992531
|
T | A | 2 | a0001c0001t0040g0103a0001c0001t0040g0104 | 2 | NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.601-4968A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992531 | ||||||
chr8:41992534
|
T | C | 1 | a0001c0001t0014g0299 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.601-4971A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992534 | ||||||
chr8:41992557
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-4994A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992557 | ||||||
chr8:41992704
|
C | G | 108 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(105): Show | 110 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.601-5141G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992704 | ||||||
chr8:41992797
|
T | A | 10 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(7): Show | 10 | HG02074.hp1 HG02132.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-5234A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992797 | ||||||
chr8:41992829
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-5266T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41992829 | ||||||
chr8:41993004
|
C | CA | 89 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(86): Show | 91 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.601-5442dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993004 | ||||||
chr8:41993476
|
C | G | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-5913G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993476 | ||||||
chr8:41993502
|
C | A | 2 | a0006c0010t0052g0012a0006c0010t0104g0169 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.601-5939G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993502 | ||||||
chr8:41993567
|
A | G | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.601-6004T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993567 | ||||||
chr8:41993586
|
A | C | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.601-6023T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993586 | ||||||
chr8:41993811
|
A | C | 1 | a0001c0004t0032g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601-6248T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993811 | ||||||
chr8:41993998
|
T | TCTACAAG others(314): Show |
3 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0067g0124 | 3 | HG02572.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.601-6436_601-6435i others(323): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41993998 | ||||||
chr8:41994056
|
G | GA | 26 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(23): Show | 26 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.601-6494dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994056 | ||||||
chr8:41994057
|
A | C | 35 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(32): Show | 35 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-6494T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994057 | ||||||
chr8:41994187
|
A | C | 10 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-6624T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994187 | ||||||
chr8:41994299
|
T | G | 1 | a0001c0001t0011g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.601-6736A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994299 | ||||||
chr8:41994318
|
C | T | 4 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286others(1): Show | 4 | NA18956.hp2 NA18975.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-6755G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994318 | ||||||
chr8:41994504
|
C | T | 2 | a0001c0001t0003g0054a0001c0001t0003g0082 | 2 | NA18948.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601-6941G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994504 | ||||||
chr8:41994562
|
T | G | 5 | a0001c0003t0017g0295a0001c0003t0017g0296a0001c0003t0028g0294others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-6999A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41994562 | ||||||
chr8:41995017
|
C | CT | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-7455dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995017 | ||||||
chr8:41995021
|
A | G | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.601-7458T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995021 | ||||||
chr8:41995060
|
A | C | 2 | a0002c0002t0001g0311a0002c0002t0001g0312 | 2 | NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.601-7497T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995060 | ||||||
chr8:41995061
|
A | AAAAAAT | 45 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(42): Show | 45 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-7504_601-7499d others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995061 | ||||||
chr8:41995091
|
C | G | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7528G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995091 | ||||||
chr8:41995368
|
T | C | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-7805A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995368 | ||||||
chr8:41995387
|
G | A | 1 | a0001c0001t0034g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.601-7824C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995387 | ||||||
chr8:41995389
|
T | C | 1 | a0001c0003t0045g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.601-7826A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995389 | ||||||
chr8:41995674
|
CT | C | 245 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0037others(242): Show | 252 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.601-8112delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995674 | ||||||
chr8:41995746
|
A | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-8183T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995746 | ||||||
chr8:41995971
|
C | T | 1 | a0001c0016t0102g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.601-8408G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41995971 | ||||||
chr8:41996085
|
C | T | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601-8522G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41996085 | ||||||
chr8:41996416
|
A | G | 3 | a0001c0001t0013g0041a0001c0001t0029g0064a0001c0001t0118g0215 | 3 | NA18940.hp2 NA18946.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.601-8853T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41996416 | ||||||
chr8:41996583
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.601-9020T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41996583 | ||||||
chr8:41996929
|
ATATTATA others(3): Show |
A | 1 | a0001c0001t0003g0069 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601-9376_601-9367d others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41996929 | ||||||
chr8:41996938
|
A | G | 7 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-9375T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41996938 | ||||||
chr8:41997401
|
G | A | 1 | a0001c0001t0006g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-9838C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41997401 | ||||||
chr8:41997554
|
A | T | 1 | a0001c0001t0033g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.601-9991T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41997554 | ||||||
chr8:41997683
|
T | C | 47 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(44): Show | 47 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.601-10120A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41997683 | ||||||
chr8:41998075
|
A | G | 3 | a0001c0003t0069g0200a0001c0003t0090g0287a0001c0003t0091g0288 | 3 | HG03579.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.601-10512T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998075 | ||||||
chr8:41998172
|
G | T | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.601-10609C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998172 | ||||||
chr8:41998208
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601-10645A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998208 | ||||||
chr8:41998266
|
C | T | 55 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(52): Show | 55 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.601-10703G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998266 | ||||||
chr8:41998397
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-10834C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998397 | ||||||
chr8:41998617
|
G | A | 1 | a0001c0003t0087g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.601-11054C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998617 | ||||||
chr8:41998698
|
A | G | 1 | a0001c0001t0006g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-11135T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998698 | ||||||
chr8:41998770
|
G | T | 1 | a0002c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.601-11207C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41998770 | ||||||
chr8:41999078
|
T | C | 1 | a0001c0003t0007g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.601-11515A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999078 | ||||||
chr8:41999271
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-11708C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999271 | ||||||
chr8:41999362
|
A | G | 1 | a0001c0003t0004g0195 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.601-11799T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999362 | ||||||
chr8:41999525
|
A | T | 1 | a0001c0001t0003g0101 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.601-11962T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999525 | ||||||
chr8:41999526
|
T | A | 1 | a0001c0001t0003g0101 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.601-11963A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999526 | ||||||
chr8:41999822
|
T | G | 1 | a0002c0002t0001g0346 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.601-12259A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 41999822 | ||||||
chr8:42000163
|
G | T | 1 | a0001c0001t0034g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.601-12600C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000163 | ||||||
chr8:42000275
|
G | A | 1 | a0001c0001t0009g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.601-12712C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000275 | ||||||
chr8:42000379
|
C | T | 1 | a0001c0003t0046g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.601-12816G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000379 | ||||||
chr8:42000406
|
C | T | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-12843G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000406 | ||||||
chr8:42000564
|
A | G | 6 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(3): Show | 6 | HG01106.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-13001T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000564 | ||||||
chr8:42000588
|
G | T | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-13025C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000588 | ||||||
chr8:42000780
|
T | C | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-13217A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000780 | ||||||
chr8:42000825
|
C | T | 2 | a0001c0001t0002g0266a0001c0001t0009g0254 | 2 | NA18747.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.601-13262G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000825 | ||||||
chr8:42000989
|
A | C | 3 | a0001c0001t0001g0002a0001c0001t0036g0036a0001c0001t0061g0058 | 4 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-13426T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000989 | ||||||
chr8:42000995
|
C | A | 3 | a0001c0003t0004g0180a0001c0003t0004g0186a0001c0003t0004g0187 | 3 | HG01361.hp2 HG01516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.601-13432G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42000995 | ||||||
chr8:42001023
|
G | A | 2 | a0001c0001t0044g0136a0001c0001t0044g0144 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.601-13460C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001023 | ||||||
chr8:42001024
|
A | T | 3 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286 | 3 | NA18975.hp1 NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.601-13461T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001024 | ||||||
chr8:42001033
|
G | A | 2 | a0001c0001t0040g0103a0001c0001t0040g0104 | 2 | NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.601-13470C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001033 | ||||||
chr8:42001221
|
C | T | 1 | a0001c0001t0008g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.601-13658G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001221 | ||||||
chr8:42001320
|
A | G | 1 | a0001c0004t0063g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.601-13757T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001320 | ||||||
chr8:42001329
|
G | C | 10 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-13766C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001329 | ||||||
chr8:42001489
|
T | C | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-13926A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001489 | ||||||
chr8:42001576
|
T | C | 1 | a0011c0023t0010g0298 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.601-14013A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001576 | ||||||
chr8:42001755
|
T | G | 4 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0063g0132others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-14192A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001755 | ||||||
chr8:42001902
|
C | T | 1 | a0001c0001t0056g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.601-14339G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42001902 | ||||||
chr8:42002015
|
CTA | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-14454_601-1445 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002015 | ||||||
chr8:42002023
|
C | T | 1 | a0002c0002t0001g0356 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.601-14460G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002023 | ||||||
chr8:42002334
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.601-14771A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002334 | ||||||
chr8:42002474
|
T | A | 1 | a0002c0002t0001g0360 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.601-14911A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002474 | ||||||
chr8:42002488
|
G | T | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601-14925C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002488 | ||||||
chr8:42002584
|
G | A | 4 | a0003c0006t0019g0352a0003c0006t0019g0364a0003c0006t0089g0300others(1): Show | 4 | NA18966.hp1 NA18978.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-15021C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002584 | ||||||
chr8:42002727
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.601-15164A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42002727 | ||||||
chr8:42003207
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-15644C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003207 | ||||||
chr8:42003217
|
G | A | 1 | a0001c0001t0002g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.601-15654C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003217 | ||||||
chr8:42003306
|
C | A | 66 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(63): Show | 70 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.601-15743G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003306 | ||||||
chr8:42003445
|
CT | C | 38 | a0001c0001t0003g0099a0001c0001t0047g0236a0001c0003t0004g0180others(35): Show | 38 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.601-15883delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003445 | ||||||
chr8:42003453
|
T | G | 3 | a0001c0001t0005g0068a0001c0001t0005g0111a0001c0001t0005g0112 | 3 | NA18947.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.601-15890A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003453 | ||||||
chr8:42003457
|
T | G | 18 | a0001c0001t0003g0050a0001c0001t0003g0070a0001c0001t0003g0101others(15): Show | 19 | HG00544.hp1 HG00609.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.601-15894A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003457 | ||||||
chr8:42003460
|
T | C | 1 | a0001c0001t0002g0204 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.601-15897A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003460 | ||||||
chr8:42003588
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-16025G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003588 | ||||||
chr8:42003823
|
A | G | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.601-16260T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003823 | ||||||
chr8:42003887
|
G | A | 1 | a0001c0001t0059g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.601-16324C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003887 | ||||||
chr8:42003922
|
T | C | 1 | a0001c0001t0100g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.601-16359A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003922 | ||||||
chr8:42003992
|
G | A | 1 | a0001c0001t0059g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.601-16429C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42003992 | ||||||
chr8:42004000
|
G | T | 1 | a0001c0001t0033g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.601-16437C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004000 | ||||||
chr8:42004024
|
T | C | 1 | a0002c0002t0019g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.601-16461A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004024 | ||||||
chr8:42004033
|
A | G | 1 | a0001c0001t0110g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.601-16470T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004033 | ||||||
chr8:42004111
|
G | T | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.601-16548C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004111 | ||||||
chr8:42004342
|
T | G | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.601-16779A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004342 | ||||||
chr8:42004696
|
C | T | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-17133G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004696 | ||||||
chr8:42004852
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.601-17289A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004852 | ||||||
chr8:42004877
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-17314C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004877 | ||||||
chr8:42004907
|
G | A | 1 | a0002c0002t0001g0330 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.601-17344C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42004907 | ||||||
chr8:42005276
|
C | A | 1 | a0001c0001t0002g0273 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.601-17713G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005276 | ||||||
chr8:42005485
|
G | C | 2 | a0001c0003t0007g0176a0001c0003t0027g0175 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601-17922C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005485 | ||||||
chr8:42005763
|
T | TAC | 21 | a0001c0001t0002g0257a0001c0001t0006g0019a0001c0001t0006g0021others(18): Show | 21 | HG00673.hp2 HG01934.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.601-18202_601-1820 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005763
|
T | TACAC | 4 | a0001c0001t0010g0284a0001c0005t0020g0119a0001c0005t0020g0120others(1): Show | 4 | HG01099.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-18204_601-1820 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005763
|
TAC | T | 27 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0209others(24): Show | 27 | HG00544.hp2 HG00609.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.601-18202_601-1820 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005763
|
TACAC | T | 5 | a0001c0001t0002g0234a0001c0001t0002g0237a0001c0001t0002g0261others(2): Show | 5 | HG00741.hp1 HG01257.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-18204_601-1820 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005763
|
TACACAC | T | 3 | a0002c0002t0001g0008a0002c0002t0001g0346a0002c0002t0001g0351 | 4 | HG01257.hp1 HG01258.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-18206_601-1820 others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005763
|
TACACACA others(1): Show |
T | 70 | a0001c0001t0038g0053a0001c0003t0007g0176a0002c0002t0001g0005others(67): Show | 74 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.601-18208_601-1820 others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005763 | ||||||
chr8:42005796
|
A | ACACACAC others(9): Show |
1 | a0001c0003t0060g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.601-18234_601-1823 others(20): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACACACAC others(5): Show |
9 | a0001c0001t0003g0037a0001c0003t0017g0295a0001c0003t0057g0163others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-18234_601-1823 others(16): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACACACAC others(3): Show |
7 | a0001c0001t0003g0039a0001c0001t0003g0054a0001c0001t0003g0082others(4): Show | 7 | HG01167.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-18234_601-1823 others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACACACAC others(1): Show |
31 | a0001c0001t0003g0100a0001c0001t0005g0038a0001c0001t0007g0155others(28): Show | 31 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.601-18234_601-1823 others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACACACT | 27 | a0001c0001t0003g0040a0001c0001t0003g0071a0001c0001t0003g0073others(24): Show | 27 | HG01978.hp2 HG02040.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.601-18234_601-1823 others(10): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACACT | 74 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(71): Show | 76 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-18237_601-1823 others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | ACT | 14 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0086others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-18234_601-1823 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005796
|
A | T | 84 | a0001c0001t0003g0063a0001c0001t0038g0053a0001c0003t0007g0176others(81): Show | 89 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.601-18233T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005796 | ||||||
chr8:42005859
|
G | A | 2 | a0001c0003t0090g0287a0001c0003t0091g0288 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.601-18296C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42005859 | ||||||
chr8:42006099
|
A | G | 2 | a0002c0002t0030g0337a0002c0002t0030g0338 | 2 | HG00642.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.601-18536T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006099 | ||||||
chr8:42006159
|
A | G | 4 | a0002c0002t0001g0301a0002c0002t0001g0303a0002c0002t0001g0326others(1): Show | 4 | NA18972.hp1 NA18986.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-18596T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006159 | ||||||
chr8:42006770
|
C | T | 1 | a0001c0001t0049g0270 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.601-19207G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006770 | ||||||
chr8:42006790
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601-19227C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006790 | ||||||
chr8:42006854
|
G | A | 1 | a0001c0001t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-19291C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006854 | ||||||
chr8:42006886
|
C | T | 1 | a0001c0003t0046g0148 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.601-19323G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006886 | ||||||
chr8:42006894
|
G | A | 41 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0301others(38): Show | 43 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.601-19331C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006894 | ||||||
chr8:42006957
|
C | A | 2 | a0001c0003t0068g0153a0001c0003t0074g0152 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.601-19394G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006957 | ||||||
chr8:42006988
|
T | C | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-19425A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006988 | ||||||
chr8:42006995
|
C | CA | 130 | a0001c0001t0002g0226a0001c0001t0002g0260a0001c0001t0002g0273others(127): Show | 131 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.601-19433dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006995 | ||||||
chr8:42006995
|
C | CAA | 41 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0043others(38): Show | 42 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.601-19434_601-1943 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006995 | ||||||
chr8:42006995
|
C | CAAA | 11 | a0001c0001t0003g0037a0001c0001t0003g0039a0001c0001t0003g0040others(8): Show | 11 | HG01106.hp1 HG02080.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-19435_601-1943 others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42006995 | ||||||
chr8:42007178
|
GAC | G | 110 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(107): Show | 112 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.601-19617_601-1961 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007178 | ||||||
chr8:42007471
|
T | C | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-19908A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007471 | ||||||
chr8:42007633
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-20070C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007633 | ||||||
chr8:42007878
|
C | T | 4 | a0001c0001t0014g0213a0001c0001t0014g0263a0001c0001t0014g0285others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-20315G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007878 | ||||||
chr8:42007879
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.601-20316C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007879 | ||||||
chr8:42007916
|
CGTGCCAC others(3771): Show |
C | 1 | a0001c0001t0002g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.601-24131_601-2035 others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007916 | ||||||
chr8:42007941
|
G | C | 1 | a0002c0002t0015g0363 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.601-20378C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007941 | ||||||
chr8:42007960
|
T | TC | 4 | a0001c0001t0022g0061a0001c0001t0022g0066a0001c0001t0022g0088others(1): Show | 4 | HG02135.hp1 HG02165.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-20398dupG | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007960 | ||||||
chr8:42007961
|
C | CA | 72 | a0001c0001t0002g0001a0001c0001t0002g0211a0001c0001t0002g0234others(69): Show | 74 | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.601-20399dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007961 | ||||||
chr8:42007961
|
C | CAA | 22 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0054g0014others(19): Show | 22 | HG01106.hp1 HG01891.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.601-20400_601-2039 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007961 | ||||||
chr8:42007961
|
C | CAAAAAAA others(3): Show |
1 | a0004c0007t0007g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.601-20408_601-2039 others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007961 | ||||||
chr8:42007961
|
CA | C | 8 | a0001c0001t0002g0207a0001c0001t0002g0245a0001c0001t0003g0045others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-20399delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007961 | ||||||
chr8:42007961
|
CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0006g0019a0001c0001t0006g0022a0001c0001t0006g0023others(12): Show | 15 | HG00673.hp2 HG02074.hp1 HG03471.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-20406_601-2039 others(12): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007961 | ||||||
chr8:42007962
|
A | C | 1 | a0001c0021t0013g0067 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-20399T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007962 | ||||||
chr8:42007986
|
AAT | A | 59 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(56): Show | 64 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.601-20425_601-2042 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007986 | ||||||
chr8:42007987
|
AT | A | 12 | a0002c0002t0001g0309a0002c0002t0001g0312a0002c0002t0001g0316others(9): Show | 12 | HG00735.hp1 HG01981.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-20425delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007987 | ||||||
chr8:42007988
|
T | A | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-20425A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42007988 | ||||||
chr8:42008038
|
GTCAGTAT others(9): Show |
G | 1 | a0003c0006t0019g0352 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.601-20491_601-2047 others(20): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008038 | ||||||
chr8:42008257
|
C | T | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-20694G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008257 | ||||||
chr8:42008276
|
C | T | 1 | a0001c0020t0073g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.601-20713G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008276 | ||||||
chr8:42008291
|
T | G | 3 | a0002c0002t0015g0348a0002c0002t0015g0349a0002c0002t0015g0363 | 3 | HG01975.hp1 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.601-20728A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008291 | ||||||
chr8:42008494
|
C | T | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.601-20931G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008494 | ||||||
chr8:42008559
|
G | A | 7 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-20996C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008559 | ||||||
chr8:42008823
|
A | T | 1 | a0001c0001t0002g0290 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.601-21260T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008823 | ||||||
chr8:42008894
|
A | G | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-21331T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008894 | ||||||
chr8:42008903
|
T | C | 1 | a0001c0001t0077g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.601-21340A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008903 | ||||||
chr8:42008940
|
G | C | 1 | a0001c0001t0003g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601-21377C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42008940 | ||||||
chr8:42009166
|
G | C | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-21603C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009166 | ||||||
chr8:42009248
|
G | A | 2 | a0002c0002t0001g0356a0002c0002t0001g0358 | 2 | HG00621.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.601-21685C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009248 | ||||||
chr8:42009517
|
C | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0092 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.601-21954G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009517 | ||||||
chr8:42009529
|
G | A | 2 | a0001c0001t0002g0232a0001c0001t0014g0231 | 2 | HG02083.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.601-21966C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009529 | ||||||
chr8:42009676
|
G | C | 1 | a0001c0001t0005g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.601-22113C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009676 | ||||||
chr8:42009701
|
C | T | 1 | a0001c0001t0022g0066 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.601-22138G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009701 | ||||||
chr8:42009894
|
C | CA | 45 | a0001c0001t0001g0002a0001c0001t0002g0217a0001c0001t0002g0229others(42): Show | 46 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-22332dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009894 | ||||||
chr8:42009894
|
CA | C | 14 | a0001c0003t0057g0163a0001c0005t0020g0118a0001c0005t0020g0119others(11): Show | 14 | HG00621.hp2 HG00735.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-22332delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009894 | ||||||
chr8:42009894
|
CAA | C | 67 | a0001c0001t0055g0015a0002c0002t0001g0005a0002c0002t0001g0006others(64): Show | 72 | HG00438.hp1 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.601-22333_601-2233 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009894 | ||||||
chr8:42009908
|
A | C | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.601-22345T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009908 | ||||||
chr8:42009909
|
A | C | 1 | a0001c0003t0069g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.601-22346T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009909 | ||||||
chr8:42009911
|
A | C | 1 | a0001c0003t0031g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.601-22348T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009911 | ||||||
chr8:42009913
|
A | AC | 4 | a0001c0001t0022g0061a0001c0001t0022g0066a0001c0001t0022g0088others(1): Show | 4 | HG02040.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-22351_601-2235 others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009913 | ||||||
chr8:42009913
|
AAC | A | 14 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0027others(11): Show | 14 | HG00673.hp2 HG03471.hp1 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-22352_601-2235 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009913 | ||||||
chr8:42009914
|
AC | A | 5 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0025others(2): Show | 5 | HG02074.hp1 HG02132.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-22352delG | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009914 | ||||||
chr8:42009915
|
C | A | 18 | a0001c0001t0002g0227a0001c0001t0002g0250a0001c0001t0009g0283others(15): Show | 18 | HG00099.hp1 HG00544.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.601-22352G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009915 | ||||||
chr8:42009915
|
C | CA | 27 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(24): Show | 27 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.601-22353dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009915 | ||||||
chr8:42009918
|
A | AC | 5 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(2): Show | 5 | HG01192.hp2 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-22356_601-2235 others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009918 | ||||||
chr8:42009925
|
C | A | 45 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(42): Show | 45 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-22362G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42009925 | ||||||
chr8:42010133
|
T | C | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-22570A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010133 | ||||||
chr8:42010157
|
T | A | 2 | a0001c0001t0083g0171a0001c0001t0085g0172 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.601-22594A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010157 | ||||||
chr8:42010245
|
C | A | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601-22682G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010245 | ||||||
chr8:42010284
|
G | A | 1 | a0002c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.601-22721C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010284 | ||||||
chr8:42010402
|
T | C | 21 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(18): Show | 21 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.601-22839A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010402 | ||||||
chr8:42010804
|
T | G | 5 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0098others(2): Show | 5 | HG02071.hp1 HG02293.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-23241A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010804 | ||||||
chr8:42010825
|
T | C | 4 | a0001c0003t0016g0159a0001c0003t0016g0162a0001c0003t0031g0156others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-23262A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42010825 | ||||||
chr8:42011085
|
C | G | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601-23522G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011085 | ||||||
chr8:42011288
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(161): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.601-23725G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011288 | ||||||
chr8:42011403
|
G | T | 164 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(161): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.601-23840C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011403 | ||||||
chr8:42011433
|
C | G | 1 | a0002c0002t0001g0312 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.601-23870G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011433 | ||||||
chr8:42011526
|
T | G | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-23963A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011526 | ||||||
chr8:42011601
|
G | A | 70 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(67): Show | 75 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.601-24038C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011601 | ||||||
chr8:42011665
|
A | G | 4 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286others(1): Show | 4 | NA18956.hp2 NA18975.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-24102T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011665 | ||||||
chr8:42011918
|
A | G | 1 | a0001c0003t0091g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.601-24355T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011918 | ||||||
chr8:42011935
|
C | T | 1 | a0001c0004t0012g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601-24372G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011935 | ||||||
chr8:42011964
|
G | A | 12 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-24401C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42011964 | ||||||
chr8:42012053
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-24490G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012053 | ||||||
chr8:42012250
|
G | A | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-24687C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012250 | ||||||
chr8:42012388
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-24825A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012388 | ||||||
chr8:42012396
|
G | A | 1 | a0001c0022t0058g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-24833C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012396 | ||||||
chr8:42012645
|
C | T | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-25082G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012645 | ||||||
chr8:42012732
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.601-25169A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012732 | ||||||
chr8:42012909
|
T | C | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.601-25346A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42012909 | ||||||
chr8:42013121
|
G | A | 1 | a0001c0001t0022g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.601-25558C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013121 | ||||||
chr8:42013250
|
T | C | 1 | a0001c0001t0003g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.601-25687A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013250 | ||||||
chr8:42013260
|
CT | C | 243 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(240): Show | 250 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.601-25698delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013260 | ||||||
chr8:42013379
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.601-25816C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013379 | ||||||
chr8:42013520
|
A | G | 1 | a0001c0003t0074g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-25957T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013520 | ||||||
chr8:42013682
|
G | A | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-26119C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013682 | ||||||
chr8:42013708
|
C | G | 3 | a0001c0003t0069g0200a0001c0003t0090g0287a0001c0003t0091g0288 | 3 | HG03579.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.601-26145G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013708 | ||||||
chr8:42013764
|
G | A | 1 | a0001c0003t0087g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.601-26201C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013764 | ||||||
chr8:42013950
|
C | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-26387G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013950 | ||||||
chr8:42013965
|
C | CG | 3 | a0001c0001t0006g0025a0001c0003t0004g0181a0001c0003t0037g0146 | 3 | HG03486.hp2 HG03654.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.601-26403dupC | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42013965 | ||||||
chr8:42014076
|
T | G | 1 | a0001c0001t0011g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.601-26513A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014076 | ||||||
chr8:42014120
|
T | TA | 7 | a0001c0001t0002g0245a0001c0001t0002g0266a0001c0001t0003g0098others(4): Show | 7 | HG00639.hp1 HG02055.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-26558dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014120 | ||||||
chr8:42014121
|
A | T | 1 | a0001c0001t0006g0019 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.601-26558T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014121 | ||||||
chr8:42014490
|
T | C | 4 | a0002c0002t0015g0348a0002c0002t0015g0349a0002c0002t0015g0357others(1): Show | 4 | HG00735.hp1 HG01975.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-26927A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014490 | ||||||
chr8:42014606
|
C | G | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-27043G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014606 | ||||||
chr8:42014962
|
C | T | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601-27399G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42014962 | ||||||
chr8:42015022
|
C | T | 1 | a0001c0003t0004g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.601-27459G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015022 | ||||||
chr8:42015129
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0075others(4): Show | 8 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-27566A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015129 | ||||||
chr8:42015200
|
T | C | 1 | a0001c0001t0039g0047 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601-27637A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015200 | ||||||
chr8:42015231
|
C | G | 3 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0067g0124 | 3 | HG02572.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.601-27668G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015231 | ||||||
chr8:42015271
|
A | T | 1 | a0001c0001t0080g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601-27708T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015271 | ||||||
chr8:42015272
|
G | T | 1 | a0001c0001t0080g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601-27709C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015272 | ||||||
chr8:42015273
|
C | T | 1 | a0001c0001t0080g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601-27710G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015273 | ||||||
chr8:42015741
|
G | C | 1 | a0001c0001t0003g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.601-28178C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015741 | ||||||
chr8:42015903
|
G | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0297a0001c0001t0013g0028others(2): Show | 5 | HG01106.hp2 HG01175.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-28340C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015903 | ||||||
chr8:42015968
|
T | C | 5 | a0001c0001t0003g0035a0001c0001t0003g0049a0001c0001t0003g0087others(2): Show | 5 | HG00673.hp1 NA18961.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-28405A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42015968 | ||||||
chr8:42016630
|
G | A | 1 | a0001c0004t0032g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601-29067C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016630 | ||||||
chr8:42016702
|
C | T | 1 | a0001c0020t0073g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.601-29139G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016702 | ||||||
chr8:42016722
|
T | C | 1 | a0004c0007t0007g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.601-29159A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016722 | ||||||
chr8:42016723
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601-29160T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016723 | ||||||
chr8:42016733
|
T | C | 2 | a0001c0001t0009g0283a0001c0001t0111g0278 | 2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.601-29170A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016733 | ||||||
chr8:42016852
|
T | C | 26 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(23): Show | 26 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.601-29289A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016852 | ||||||
chr8:42016863
|
T | C | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-29300A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016863 | ||||||
chr8:42016952
|
C | T | 1 | a0001c0016t0102g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.601-29389G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016952 | ||||||
chr8:42016963
|
C | T | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.601-29400G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42016963 | ||||||
chr8:42017073
|
A | T | 165 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(162): Show | 167 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.601-29510T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42017073 | ||||||
chr8:42017655
|
G | A | 1 | a0002c0002t0019g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.601-30092C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42017655 | ||||||
chr8:42017706
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.601-30143C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42017706 | ||||||
chr8:42017902
|
G | A | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-30339C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42017902 | ||||||
chr8:42017906
|
T | C | 2 | a0001c0001t0003g0054a0001c0001t0003g0082 | 2 | NA18948.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601-30343A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42017906 | ||||||
chr8:42018295
|
G | A | 1 | a0001c0003t0016g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.600+30083C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42018295 | ||||||
chr8:42018660
|
T | C | 1 | a0001c0001t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.600+29718A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42018660 | ||||||
chr8:42018856
|
G | A | 1 | a0001c0001t0038g0053 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.600+29522C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42018856 | ||||||
chr8:42018885
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.600+29493G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42018885 | ||||||
chr8:42018976
|
G | A | 2 | a0001c0001t0006g0137a0001c0001t0042g0139 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.600+29402C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42018976 | ||||||
chr8:42019134
|
G | T | 1 | a0001c0001t0111g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.600+29244C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019134 | ||||||
chr8:42019416
|
C | T | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+28962G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019416 | ||||||
chr8:42019420
|
A | T | 351 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0204others(348): Show | 361 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(358): Show |
intron_variant | MODIFIER | c.600+28958T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019420 | ||||||
chr8:42019600
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.600+28778G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019600 | ||||||
chr8:42019656
|
C | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+28722G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019656 | ||||||
chr8:42019799
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(270): Show | 280 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.600+28579C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019799 | ||||||
chr8:42019867
|
C | T | 2 | a0001c0001t0010g0284a0011c0023t0010g0298 | 2 | HG01099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.600+28511G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42019867 | ||||||
chr8:42020028
|
T | C | 3 | a0001c0001t0007g0155a0001c0001t0007g0202a0001c0001t0059g0203 | 3 | HG02109.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600+28350A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020028 | ||||||
chr8:42020046
|
G | A | 7 | a0001c0001t0003g0078a0001c0001t0003g0084a0001c0001t0003g0085others(4): Show | 7 | HG02071.hp1 HG02293.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+28332C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020046 | ||||||
chr8:42020089
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+28289A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020089 | ||||||
chr8:42020418
|
GTCAAAAA others(7): Show |
G | 1 | a0001c0001t0006g0022 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.600+27946_600+2795 others(18): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020418 | ||||||
chr8:42020573
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(270): Show | 280 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.600+27805A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020573 | ||||||
chr8:42020608
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.600+27770A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020608 | ||||||
chr8:42020909
|
T | G | 165 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(162): Show | 167 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.600+27469A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42020909 | ||||||
chr8:42021012
|
T | G | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.600+27366A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021012 | ||||||
chr8:42021188
|
G | A | 3 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0280 | 3 | HG02132.hp1 NA18955.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.600+27190C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021188 | ||||||
chr8:42021546
|
A | G | 23 | a0001c0001t0002g0001a0001c0001t0002g0206a0001c0001t0002g0208others(20): Show | 25 | HG01109.hp2 HG02129.hp2 HG02148.hp2 others(22): Show |
intron_variant | MODIFIER | c.600+26832T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021546 | ||||||
chr8:42021685
|
C | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+26693G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021685 | ||||||
chr8:42021738
|
C | T | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+26640G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021738 | ||||||
chr8:42021775
|
A | G | 26 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(23): Show | 26 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.600+26603T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021775 | ||||||
chr8:42021829
|
G | C | 2 | a0001c0003t0057g0163a0001c0003t0060g0165 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.600+26549C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021829 | ||||||
chr8:42021920
|
G | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+26458C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021920 | ||||||
chr8:42021925
|
AAAAAC | A | 72 | a0001c0001t0003g0077a0002c0002t0001g0005a0002c0002t0001g0006others(69): Show | 77 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.600+26448_600+2645 others(9): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42021925 | ||||||
chr8:42022010
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+26368T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022010 | ||||||
chr8:42022130
|
T | G | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+26248A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022130 | ||||||
chr8:42022173
|
G | C | 3 | a0001c0003t0069g0200a0001c0003t0090g0287a0001c0003t0091g0288 | 3 | HG03579.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.600+26205C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022173 | ||||||
chr8:42022307
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+26071A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022307 | ||||||
chr8:42022380
|
TA | T | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+25997delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022380 | ||||||
chr8:42022419
|
T | C | 1 | a0001c0001t0049g0230 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.600+25959A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022419 | ||||||
chr8:42022443
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(161): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.600+25935G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022443 | ||||||
chr8:42022444
|
A | G | 1 | a0002c0002t0001g0356 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.600+25934T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022444 | ||||||
chr8:42022461
|
A | T | 1 | a0001c0001t0006g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.600+25917T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022461 | ||||||
chr8:42022672
|
A | G | 3 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0100 | 3 | HG01192.hp1 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.600+25706T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022672 | ||||||
chr8:42022773
|
C | CA | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+25604dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022773 | ||||||
chr8:42022831
|
T | C | 7 | a0001c0001t0003g0078a0001c0001t0003g0084a0001c0001t0003g0085others(4): Show | 7 | HG02071.hp1 HG02293.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+25547A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022831 | ||||||
chr8:42022917
|
T | C | 1 | a0008c0018t0117g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.600+25461A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022917 | ||||||
chr8:42022957
|
T | A | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.600+25421A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42022957 | ||||||
chr8:42023098
|
T | C | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+25280A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023098 | ||||||
chr8:42023239
|
A | G | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.600+25139T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023239 | ||||||
chr8:42023275
|
G | A | 2 | a0001c0004t0012g0127a0001c0004t0012g0128 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.600+25103C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023275 | ||||||
chr8:42023386
|
T | C | 7 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+24992A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023386 | ||||||
chr8:42023495
|
C | CT | 201 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(198): Show | 203 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.600+24882dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023495 | ||||||
chr8:42023495
|
C | CTT | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+24881_600+2488 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023495 | ||||||
chr8:42023569
|
CCTCAACC others(7): Show |
C | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0034g0109 | 3 | HG00438.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.600+24795_600+2480 others(18): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023569 | ||||||
chr8:42023590
|
T | C | 1 | a0002c0002t0015g0363 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.600+24788A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023590 | ||||||
chr8:42023628
|
T | C | 1 | a0001c0016t0102g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.600+24750A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023628 | ||||||
chr8:42023637
|
G | A | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+24741C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023637 | ||||||
chr8:42023660
|
G | C | 6 | a0002c0002t0001g0346a0002c0002t0001g0353a0002c0002t0001g0355others(3): Show | 6 | HG03654.hp1 NA18939.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+24718C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023660 | ||||||
chr8:42023757
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(90): Show | 95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.600+24621C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023757 | ||||||
chr8:42023827
|
CA | C | 81 | a0001c0001t0003g0082a0001c0001t0006g0025a0001c0001t0022g0061others(78): Show | 86 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.600+24550delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023827 | ||||||
chr8:42023844
|
A | T | 1 | a0005c0009t0048g0262 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.600+24534T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023844 | ||||||
chr8:42023869
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.600+24509A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023869 | ||||||
chr8:42023931
|
G | A | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.600+24447C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42023931 | ||||||
chr8:42024303
|
C | T | 1 | a0002c0002t0001g0311 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.600+24075G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42024303 | ||||||
chr8:42024389
|
A | G | 1 | a0001c0017t0003g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.600+23989T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42024389 | ||||||
chr8:42024587
|
AC | A | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+23790delG | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42024587 | ||||||
chr8:42024676
|
C | T | 1 | a0001c0003t0076g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+23702G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42024676 | ||||||
chr8:42024914
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0034g0109 | 3 | HG00438.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.600+23464T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42024914 | ||||||
chr8:42025038
|
G | A | 1 | a0001c0001t0111g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.600+23340C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025038 | ||||||
chr8:42025063
|
C | A | 1 | a0001c0001t0002g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.600+23315G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025063 | ||||||
chr8:42025142
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.600+23236C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025142 | ||||||
chr8:42025203
|
G | GT | 74 | a0001c0003t0057g0163a0001c0003t0060g0165a0001c0022t0058g0115others(71): Show | 79 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.600+23174dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025203 | ||||||
chr8:42025281
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.600+23097C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025281 | ||||||
chr8:42025365
|
C | T | 26 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(23): Show | 26 | HG00673.hp2 HG01891.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.600+23013G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025365 | ||||||
chr8:42025365
|
CCAT | C | 53 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.600+23010_600+2301 others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025365 | ||||||
chr8:42025401
|
C | T | 1 | a0002c0002t0001g0306 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.600+22977G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025401 | ||||||
chr8:42025440
|
TA | T | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+22937delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025440 | ||||||
chr8:42025442
|
C | G | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+22936G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025442 | ||||||
chr8:42025810
|
C | T | 3 | a0001c0001t0043g0029a0001c0001t0043g0030a0001c0001t0101g0031 | 3 | NA18953.hp1 NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.600+22568G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025810 | ||||||
chr8:42025893
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+22485A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42025893 | ||||||
chr8:42026077
|
T | C | 2 | a0001c0001t0003g0080a0001c0001t0003g0092 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.600+22301A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42026077 | ||||||
chr8:42026255
|
G | T | 2 | a0001c0001t0044g0136a0001c0001t0044g0144 | 2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.600+22123C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42026255 | ||||||
chr8:42026438
|
A | G | 1 | a0002c0002t0001g0353 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.600+21940T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42026438 | ||||||
chr8:42026520
|
T | C | 3 | a0001c0001t0043g0029a0001c0001t0043g0030a0001c0001t0101g0031 | 3 | NA18953.hp1 NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.600+21858A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42026520 | ||||||
chr8:42026697
|
A | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0234a0007c0014t0047g0251 | 3 | NA18954.hp2 NA18985.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.600+21681T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42026697 | ||||||
chr8:42027060
|
C | T | 2 | a0001c0001t0002g0232a0001c0001t0014g0231 | 2 | HG02083.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.600+21318G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027060 | ||||||
chr8:42027244
|
G | T | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+21134C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027244 | ||||||
chr8:42027528
|
T | C | 1 | a0001c0003t0016g0162 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.600+20850A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027528 | ||||||
chr8:42027602
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.600+20776A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027602 | ||||||
chr8:42027793
|
A | AT | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+20584dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027793 | ||||||
chr8:42027796
|
A | C | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+20582T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027796 | ||||||
chr8:42027813
|
A | G | 1 | a0001c0001t0033g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.600+20565T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027813 | ||||||
chr8:42027849
|
T | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+20529A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42027849 | ||||||
chr8:42028108
|
A | C | 3 | a0001c0001t0043g0029a0001c0001t0043g0030a0001c0001t0101g0031 | 3 | NA18953.hp1 NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.600+20270T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42028108 | ||||||
chr8:42028380
|
C | G | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+19998G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42028380 | ||||||
chr8:42028424
|
G | A | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+19954C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42028424 | ||||||
chr8:42028458
|
G | A | 2 | a0001c0003t0068g0153a0001c0003t0074g0152 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.600+19920C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42028458 | ||||||
chr8:42028749
|
C | T | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+19629G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42028749 | ||||||
chr8:42029569
|
G | GT | 14 | a0001c0001t0002g0257a0001c0001t0002g0273a0001c0001t0003g0099others(11): Show | 15 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.600+18808dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42029569 | ||||||
chr8:42029570
|
T | G | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.600+18808A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42029570 | ||||||
chr8:42029658
|
A | T | 3 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286 | 3 | NA18975.hp1 NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.600+18720T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42029658 | ||||||
chr8:42029887
|
C | A | 1 | a0001c0001t0039g0047 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.600+18491G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42029887 | ||||||
chr8:42029956
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(270): Show | 280 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.600+18422G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42029956 | ||||||
chr8:42030165
|
C | G | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+18213G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030165 | ||||||
chr8:42030252
|
G | A | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+18126C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030252 | ||||||
chr8:42030393
|
T | C | 3 | a0001c0001t0006g0023a0001c0001t0006g0027a0001c0001t0097g0024 | 3 | NA18977.hp1 NA18983.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.600+17985A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030393 | ||||||
chr8:42030487
|
T | C | 1 | a0001c0003t0074g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+17891A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030487 | ||||||
chr8:42030602
|
T | C | 1 | a0001c0001t0011g0248 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.600+17776A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030602 | ||||||
chr8:42030675
|
G | A | 4 | a0001c0001t0002g0228a0001c0001t0002g0250a0001c0001t0009g0004others(1): Show | 5 | HG02135.hp2 HG02155.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+17703C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030675 | ||||||
chr8:42030684
|
C | A | 1 | a0002c0002t0018g0310 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.600+17694G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030684 | ||||||
chr8:42030738
|
G | T | 1 | a0001c0019t0007g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.600+17640C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030738 | ||||||
chr8:42030875
|
G | A | 6 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+17503C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030875 | ||||||
chr8:42030960
|
T | C | 1 | a0001c0003t0027g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.600+17418A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030960 | ||||||
chr8:42030962
|
T | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+17416A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42030962 | ||||||
chr8:42031026
|
C | CA | 28 | a0001c0001t0003g0082a0001c0003t0007g0176a0001c0003t0016g0134others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.600+17351dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031026 | ||||||
chr8:42031037
|
A | AG | 3 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0103g0149 | 3 | HG01106.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.600+17340_600+1734 others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031037 | ||||||
chr8:42031038
|
A | AAG | 104 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0043others(101): Show | 107 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.600+17339_600+1734 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031038 | ||||||
chr8:42031038
|
A | AAGG | 21 | a0001c0001t0003g0037a0001c0001t0003g0039a0001c0001t0003g0040others(18): Show | 21 | HG00099.hp2 HG01070.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.600+17339_600+1734 others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031038 | ||||||
chr8:42031038
|
A | AG | 84 | a0001c0001t0002g0229a0001c0001t0002g0273a0001c0001t0006g0019others(81): Show | 88 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.600+17339dupC | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031038 | ||||||
chr8:42031038
|
A | G | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+17340T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031038 | ||||||
chr8:42031040
|
G | T | 2 | a0001c0001t0003g0056a0001c0001t0003g0100 | 2 | HG01192.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.600+17338C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031040 | ||||||
chr8:42031062
|
A | C | 1 | a0002c0002t0001g0314 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.600+17316T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031062 | ||||||
chr8:42031602
|
T | C | 1 | a0001c0001t0005g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.600+16776A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031602 | ||||||
chr8:42031608
|
G | C | 1 | a0002c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.600+16770C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031608 | ||||||
chr8:42031617
|
C | CT | 13 | a0001c0003t0004g0180a0001c0003t0004g0185a0001c0003t0004g0186others(10): Show | 13 | HG00642.hp1 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+16760dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CT | C | 187 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0002g0204others(184): Show | 191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.600+16760delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CTT | C | 39 | a0001c0001t0002g0266a0001c0001t0003g0045a0001c0001t0005g0044others(36): Show | 42 | HG00621.hp2 HG00642.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.600+16759_600+1676 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CTTTTTTT | C | 21 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0302others(18): Show | 23 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.600+16754_600+1676 others(11): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0003g0080a0001c0001t0003g0092 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.600+16751_600+1676 others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0045g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.600+16750_600+1676 others(15): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031617
|
CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0009g0283a0001c0001t0111g0278 | 2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.600+16744_600+1676 others(21): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031617 | ||||||
chr8:42031819
|
T | G | 13 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(10): Show | 13 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+16559A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031819 | ||||||
chr8:42031888
|
C | T | 1 | a0002c0002t0082g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.600+16490G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031888 | ||||||
chr8:42031952
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+16426G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42031952 | ||||||
chr8:42032023
|
G | A | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+16355C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032023 | ||||||
chr8:42032054
|
C | G | 2 | a0001c0001t0051g0271a0001c0001t0051g0282 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.600+16324G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032054 | ||||||
chr8:42032055
|
G | A | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+16323C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032055 | ||||||
chr8:42032101
|
C | T | 1 | a0002c0002t0001g0362 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.600+16277G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032101 | ||||||
chr8:42032141
|
G | T | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+16237C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032141 | ||||||
chr8:42032202
|
T | C | 7 | a0001c0001t0003g0035a0001c0001t0003g0046a0001c0001t0003g0049others(4): Show | 7 | HG00621.hp1 HG00673.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+16176A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032202 | ||||||
chr8:42032259
|
T | G | 1 | a0001c0003t0087g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+16119A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032259 | ||||||
chr8:42032452
|
T | A | 3 | a0002c0002t0001g0323a0002c0002t0001g0325a0002c0002t0021g0324 | 3 | NA18984.hp1 NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.600+15926A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032452 | ||||||
chr8:42032539
|
T | C | 1 | a0001c0003t0074g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+15839A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032539 | ||||||
chr8:42032701
|
C | T | 1 | a0001c0003t0004g0195 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.600+15677G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032701 | ||||||
chr8:42032867
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(88): Show | 93 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.600+15511A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032867 | ||||||
chr8:42032871
|
C | CT | 48 | a0001c0001t0002g0209a0001c0001t0002g0211a0001c0001t0002g0269others(45): Show | 48 | HG00621.hp2 HG00735.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.600+15506dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032871 | ||||||
chr8:42032871
|
C | CTT | 13 | a0001c0001t0011g0281a0001c0004t0012g0122a0001c0004t0012g0125others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+15505_600+1550 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032871 | ||||||
chr8:42032871
|
CT | C | 34 | a0001c0001t0002g0266a0001c0001t0003g0081a0001c0001t0003g0082others(31): Show | 34 | HG00673.hp2 HG01106.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.600+15506delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032871 | ||||||
chr8:42032956
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(270): Show | 280 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.600+15422C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42032956 | ||||||
chr8:42033000
|
C | A | 1 | a0002c0002t0019g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.600+15378G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033000 | ||||||
chr8:42033153
|
G | A | 1 | a0001c0001t0033g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.600+15225C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033153 | ||||||
chr8:42033275
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0091 | 4 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+15103A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033275 | ||||||
chr8:42033371
|
A | G | 1 | a0004c0007t0007g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.600+15007T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033371 | ||||||
chr8:42033447
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(95): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.600+14931C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033447 | ||||||
chr8:42033817
|
T | C | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.600+14561A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42033817 | ||||||
chr8:42034085
|
T | C | 8 | a0002c0002t0001g0009a0002c0002t0001g0346a0002c0002t0001g0353others(5): Show | 9 | HG02040.hp1 HG03654.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.600+14293A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034085 | ||||||
chr8:42034585
|
T | C | 1 | a0001c0003t0068g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.600+13793A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034585 | ||||||
chr8:42034743
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+13635A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034743 | ||||||
chr8:42034771
|
T | C | 2 | a0001c0003t0068g0153a0001c0003t0074g0152 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.600+13607A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034771 | ||||||
chr8:42034936
|
T | G | 2 | a0001c0003t0017g0161a0001c0003t0028g0157 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.600+13442A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034936 | ||||||
chr8:42034970
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.600+13408G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42034970 | ||||||
chr8:42035016
|
T | A | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+13362A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42035016 | ||||||
chr8:42035156
|
G | A | 4 | a0001c0003t0023g0150a0001c0003t0023g0151a0001c0003t0023g0164others(1): Show | 4 | HG01106.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+13222C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42035156 | ||||||
chr8:42035322
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.600+13056C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42035322 | ||||||
chr8:42035561
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(243): Show | 253 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.600+12817G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42035561 | ||||||
chr8:42036169
|
A | G | 1 | a0001c0001t0013g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.600+12209T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036169 | ||||||
chr8:42036229
|
C | T | 1 | a0001c0001t0116g0265 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.600+12149G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036229 | ||||||
chr8:42036231
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600+12147A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036231 | ||||||
chr8:42036440
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+11938C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036440 | ||||||
chr8:42036566
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+11812A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036566 | ||||||
chr8:42036567
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.600+11811G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036567 | ||||||
chr8:42036683
|
A | G | 73 | a0001c0003t0090g0287a0001c0003t0091g0288a0002c0002t0001g0005others(70): Show | 78 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.600+11695T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036683 | ||||||
chr8:42036919
|
G | A | 1 | a0001c0001t0077g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.600+11459C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42036919 | ||||||
chr8:42037142
|
C | G | 1 | a0003c0006t0019g0364 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.600+11236G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037142 | ||||||
chr8:42037199
|
A | T | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+11179T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037199 | ||||||
chr8:42037407
|
T | C | 3 | a0001c0001t0006g0023a0001c0001t0006g0027a0001c0001t0097g0024 | 3 | NA18977.hp1 NA18983.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.600+10971A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037407 | ||||||
chr8:42037445
|
A | C | 2 | a0001c0001t0009g0283a0001c0001t0111g0278 | 2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.600+10933T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037445 | ||||||
chr8:42037623
|
G | A | 5 | a0001c0001t0003g0035a0001c0001t0003g0049a0001c0001t0003g0087others(2): Show | 5 | HG00673.hp1 NA18961.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+10755C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037623 | ||||||
chr8:42037636
|
C | G | 1 | a0001c0001t0010g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.600+10742G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037636 | ||||||
chr8:42037691
|
C | CT | 256 | a0001c0001t0001g0002a0001c0001t0002g0208a0001c0001t0002g0269others(253): Show | 263 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.600+10686dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037691 | ||||||
chr8:42037691
|
C | CTT | 16 | a0001c0001t0003g0050a0001c0001t0005g0038a0001c0001t0033g0105others(13): Show | 16 | HG00642.hp2 HG01192.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+10685_600+1068 others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037691 | ||||||
chr8:42037795
|
T | A | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+10583A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42037795 | ||||||
chr8:42038044
|
T | C | 1 | a0001c0001t0065g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.600+10334A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038044 | ||||||
chr8:42038398
|
CA | C | 7 | a0001c0001t0003g0035a0001c0001t0003g0046a0001c0001t0003g0049others(4): Show | 7 | HG00621.hp1 HG00673.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+9979delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038398 | ||||||
chr8:42038463
|
T | C | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.600+9915A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038463 | ||||||
chr8:42038526
|
C | CA | 96 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.600+9851dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038526 | ||||||
chr8:42038795
|
C | T | 1 | a0001c0003t0017g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.600+9583G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038795 | ||||||
chr8:42038931
|
T | C | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.600+9447A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038931 | ||||||
chr8:42038963
|
T | C | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+9415A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038963 | ||||||
chr8:42038989
|
C | T | 1 | a0001c0001t0051g0282 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.600+9389G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42038989 | ||||||
chr8:42039584
|
A | T | 1 | a0001c0003t0045g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.600+8794T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039584 | ||||||
chr8:42039604
|
A | G | 7 | a0001c0001t0003g0032a0001c0001t0003g0043a0001c0001t0003g0045others(4): Show | 7 | HG01175.hp2 HG01261.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+8774T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039604 | ||||||
chr8:42039794
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(106): Show | 111 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.600+8584G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039794 | ||||||
chr8:42039835
|
G | A | 1 | a0001c0003t0076g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+8543C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039835 | ||||||
chr8:42039883
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+8495T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039883 | ||||||
chr8:42039902
|
A | AT | 148 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(145): Show | 153 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(150): Show |
intron_variant | MODIFIER | c.600+8475dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039902 | ||||||
chr8:42039918
|
T | C | 5 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0098others(2): Show | 5 | HG02071.hp1 HG02293.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+8460A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039918 | ||||||
chr8:42039990
|
G | A | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+8388C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42039990 | ||||||
chr8:42040087
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600+8291A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040087 | ||||||
chr8:42040140
|
A | G | 1 | a0001c0003t0106g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.600+8238T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040140 | ||||||
chr8:42040165
|
TAA | T | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+8211_600+8212d others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040165 | ||||||
chr8:42040166
|
A | T | 1 | a0001c0003t0028g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.600+8212T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040166 | ||||||
chr8:42040274
|
A | G | 2 | a0002c0002t0001g0306a0002c0002t0001g0330 | 2 | NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.600+8104T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040274 | ||||||
chr8:42040338
|
G | T | 1 | a0002c0002t0001g0305 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.600+8040C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040338 | ||||||
chr8:42040381
|
G | A | 1 | a0001c0001t0096g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.600+7997C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040381 | ||||||
chr8:42040667
|
G | A | 1 | a0001c0001t0110g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.600+7711C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040667 | ||||||
chr8:42040735
|
C | CA | 51 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0266others(48): Show | 51 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.600+7642dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
C | CAA | 16 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0005g0038others(13): Show | 16 | HG01192.hp2 HG01255.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+7641_600+7642d others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
C | CAAA | 81 | a0001c0001t0001g0002a0001c0001t0003g0035a0001c0001t0003g0043others(78): Show | 83 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.600+7640_600+7642d others(5): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
C | CAAAA | 22 | a0001c0001t0003g0087a0001c0001t0003g0092a0001c0001t0003g0101others(19): Show | 22 | HG00323.hp1 HG00609.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.600+7639_600+7642d others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
C | CAAAAA | 8 | a0001c0001t0003g0032a0001c0001t0077g0094a0001c0008t0007g0129others(5): Show | 8 | HG01167.hp2 HG01175.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+7638_600+7642d others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
C | CAAAAAA | 6 | a0001c0001t0007g0155a0001c0001t0059g0203a0001c0001t0083g0171others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+7637_600+7642d others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
CAAAAAA | C | 44 | a0001c0003t0090g0287a0002c0002t0001g0005a0002c0002t0001g0006others(41): Show | 46 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+7637_600+7642d others(8): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42040735
|
CAAAAAAA | C | 27 | a0001c0001t0094g0141a0002c0002t0001g0008a0002c0002t0001g0009others(24): Show | 30 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.600+7636_600+7642d others(9): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42040735 | ||||||
chr8:42041032
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.600+7346A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041032 | ||||||
chr8:42041122
|
G | A | 1 | a0002c0002t0078g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.600+7256C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041122 | ||||||
chr8:42041138
|
T | G | 34 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(31): Show | 34 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.600+7240A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041138 | ||||||
chr8:42041192
|
C | CA | 10 | a0001c0001t0002g0264a0001c0001t0002g0266a0001c0001t0002g0269others(7): Show | 10 | HG00741.hp1 HG01934.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+7185dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041192 | ||||||
chr8:42041192
|
CA | C | 251 | a0001c0001t0001g0002a0001c0001t0002g0206a0001c0001t0002g0207others(248): Show | 258 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.600+7185delT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041192 | ||||||
chr8:42041216
|
G | C | 2 | a0001c0001t0005g0096a0001c0001t0005g0097 | 2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.600+7162C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041216 | ||||||
chr8:42041262
|
C | CT | 3 | a0002c0002t0026g0341a0002c0002t0026g0343a0002c0002t0093g0342 | 3 | HG03130.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.600+7115dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041262 | ||||||
chr8:42041553
|
C | T | 1 | a0001c0003t0057g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.600+6825G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041553 | ||||||
chr8:42041554
|
A | G | 19 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(16): Show | 19 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.600+6824T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041554 | ||||||
chr8:42041826
|
G | GATAAT | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+6547_600+6551d others(7): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041826 | ||||||
chr8:42041878
|
C | G | 1 | a0001c0001t0055g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.600+6500G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041878 | ||||||
chr8:42041981
|
C | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | NA18979.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.600+6397G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42041981 | ||||||
chr8:42042069
|
C | G | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+6309G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042069 | ||||||
chr8:42042181
|
G | A | 1 | a0001c0001t0094g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600+6197C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042181 | ||||||
chr8:42042234
|
G | A | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+6144C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042234 | ||||||
chr8:42042254
|
C | T | 1 | a0001c0020t0073g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.600+6124G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042254 | ||||||
chr8:42042322
|
T | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+6056A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042322 | ||||||
chr8:42042394
|
G | A | 4 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+5984C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042394 | ||||||
chr8:42042443
|
C | CA | 8 | a0001c0001t0002g0269a0001c0001t0003g0098a0001c0001t0011g0281others(5): Show | 8 | HG02071.hp1 HG03486.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+5934dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042443 | ||||||
chr8:42042635
|
G | C | 3 | a0002c0002t0026g0341a0002c0002t0026g0343a0002c0002t0093g0342 | 3 | HG03130.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.600+5743C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042635 | ||||||
chr8:42042722
|
C | T | 1 | a0002c0002t0001g0346 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.600+5656G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42042722 | ||||||
chr8:42043409
|
T | C | 1 | a0001c0001t0002g0290 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.600+4969A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043409 | ||||||
chr8:42043549
|
T | G | 1 | a0001c0001t0049g0270 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.600+4829A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043549 | ||||||
chr8:42043655
|
T | C | 1 | a0002c0002t0001g0301 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.600+4723A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043655 | ||||||
chr8:42043679
|
A | G | 12 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.600+4699T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043679 | ||||||
chr8:42043911
|
T | G | 1 | a0001c0003t0004g0198 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.600+4467A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043911 | ||||||
chr8:42043922
|
ATAAC | A | 5 | a0001c0003t0004g0196a0001c0003t0004g0197a0001c0003t0004g0198others(2): Show | 5 | HG00642.hp1 HG00741.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+4452_600+4455d others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043922 | ||||||
chr8:42043959
|
G | T | 1 | a0001c0005t0088g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.600+4419C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42043959 | ||||||
chr8:42044098
|
C | CT | 13 | a0001c0001t0003g0032a0001c0001t0003g0035a0001c0001t0003g0100others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+4279dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044098 | ||||||
chr8:42044098
|
CT | C | 76 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0003g0099others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+4279delA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044098 | ||||||
chr8:42044348
|
C | A | 1 | a0001c0001t0002g0277 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.600+4030G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044348 | ||||||
chr8:42044348
|
C | G | 2 | a0001c0001t0002g0274a0001c0017t0003g0033 | 2 | HG01516.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.600+4030G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044348 | ||||||
chr8:42044348
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.600+4030G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044348 | ||||||
chr8:42044349
|
C | A | 72 | a0001c0019t0007g0168a0002c0002t0001g0005a0002c0002t0001g0006others(69): Show | 77 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.600+4029G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044349 | ||||||
chr8:42044350
|
C | T | 1 | a0001c0001t0011g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.600+4028G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044350 | ||||||
chr8:42044535
|
T | C | 1 | a0001c0001t0002g0274 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.600+3843A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044535 | ||||||
chr8:42044554
|
G | A | 5 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0286others(2): Show | 5 | HG02040.hp1 NA18956.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+3824C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044554 | ||||||
chr8:42044594
|
C | CA | 5 | a0001c0001t0044g0144a0001c0003t0023g0164a0001c0003t0057g0163others(2): Show | 5 | HG02809.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+3783dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044594 | ||||||
chr8:42044688
|
T | A | 1 | a0001c0003t0076g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+3690A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044688 | ||||||
chr8:42044690
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+3688G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044690 | ||||||
chr8:42044979
|
T | G | 7 | a0001c0001t0083g0171a0001c0001t0085g0172a0001c0003t0076g0173others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+3399A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044979 | ||||||
chr8:42044983
|
T | C | 1 | a0009c0015t0099g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+3395A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42044983 | ||||||
chr8:42045168
|
T | C | 6 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+3210A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045168 | ||||||
chr8:42045251
|
T | C | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+3127A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045251 | ||||||
chr8:42045349
|
T | A | 1 | a0001c0003t0087g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+3029A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045349 | ||||||
chr8:42045454
|
T | C | 1 | a0002c0002t0001g0362 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.600+2924A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045454 | ||||||
chr8:42045478
|
C | A | 1 | a0002c0002t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.600+2900G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045478 | ||||||
chr8:42045562
|
C | CA | 102 | a0001c0001t0002g0280a0001c0001t0003g0100a0001c0001t0003g0101others(99): Show | 106 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.600+2815dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045562 | ||||||
chr8:42045562
|
C | CAA | 13 | a0001c0001t0009g0283a0001c0004t0063g0132a0001c0004t0086g0133others(10): Show | 14 | HG02071.hp2 HG02148.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.600+2814_600+2815d others(4): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045562 | ||||||
chr8:42045573
|
A | C | 3 | a0001c0001t0043g0029a0001c0001t0043g0030a0001c0001t0101g0031 | 3 | NA18953.hp1 NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.600+2805T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045573 | ||||||
chr8:42045574
|
A | C | 1 | a0001c0001t0002g0204 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.600+2804T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045574 | ||||||
chr8:42045579
|
C | A | 8 | a0001c0003t0007g0176a0001c0003t0016g0179a0001c0003t0027g0175others(5): Show | 8 | HG02615.hp2 HG02723.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+2799G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045579 | ||||||
chr8:42045603
|
T | C | 21 | a0001c0003t0004g0180a0001c0003t0004g0181a0001c0003t0004g0185others(18): Show | 21 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.600+2775A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045603 | ||||||
chr8:42045691
|
G | T | 1 | a0001c0003t0046g0148 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.600+2687C>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045691 | ||||||
chr8:42045750
|
G | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0034g0109 | 3 | HG00438.hp2 NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.600+2628C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045750 | ||||||
chr8:42045793
|
G | A | 3 | a0001c0001t0002g0289a0001c0001t0010g0284a0011c0023t0010g0298 | 3 | HG01099.hp1 HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.600+2585C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045793 | ||||||
chr8:42045817
|
C | CA | 73 | a0001c0001t0002g0286a0001c0001t0008g0110a0001c0001t0014g0285others(70): Show | 78 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.600+2560dupT | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045817 | ||||||
chr8:42045837
|
T | A | 26 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0013others(23): Show | 29 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.600+2541A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045837 | ||||||
chr8:42045884
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+2494A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42045884 | ||||||
chr8:42046200
|
A | T | 1 | a0001c0001t0013g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.600+2178T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046200 | ||||||
chr8:42046263
|
C | T | 3 | a0001c0003t0037g0145a0001c0003t0037g0146a0001c0003t0075g0147 | 3 | HG02055.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+2115G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046263 | ||||||
chr8:42046509
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(244): Show | 254 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.600+1869A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046509 | ||||||
chr8:42046535
|
A | C | 1 | a0001c0003t0016g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+1843T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046535 | ||||||
chr8:42046599
|
C | A | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.600+1779G>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046599 | ||||||
chr8:42046771
|
C | CT | 12 | a0001c0004t0012g0122a0001c0004t0012g0125a0001c0004t0012g0127others(9): Show | 12 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.600+1606dupA | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046771 | ||||||
chr8:42046810
|
T | C | 1 | a0002c0002t0019g0335 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.600+1568A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046810 | ||||||
chr8:42046823
|
T | A | 1 | a0001c0001t0100g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.600+1555A>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046823 | ||||||
chr8:42046856
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.600+1522A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046856 | ||||||
chr8:42046931
|
T | C | 1 | a0002c0002t0019g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.600+1447A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42046931 | ||||||
chr8:42047226
|
T | C | 2 | a0001c0001t0007g0202a0001c0001t0059g0203 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600+1152A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42047226 | ||||||
chr8:42047327
|
T | G | 2 | a0002c0002t0030g0337a0002c0002t0030g0338 | 2 | HG00642.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.600+1051A>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42047327 | ||||||
chr8:42047527
|
G | A | 1 | a0001c0001t0041g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.600+851C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42047527 | ||||||
chr8:42048095
|
A | T | 6 | a0001c0005t0020g0118a0001c0005t0020g0119a0001c0005t0020g0120others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+283T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 2/16 | chr8 | 42048095 | ||||||
chr8:42049431
|
T | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-325-129A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42049431 | ||||||
chr8:42049518
|
G | C | 1 | a0002c0002t0001g0339 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-325-216C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42049518 | ||||||
chr8:42049787
|
G | A | 2 | a0001c0003t0090g0287a0001c0003t0091g0288 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-325-485C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42049787 | ||||||
chr8:42049886
|
A | G | 1 | a0001c0022t0058g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-325-584T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42049886 | ||||||
chr8:42049923
|
A | G | 41 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0301others(38): Show | 43 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.-325-621T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42049923 | ||||||
chr8:42050019
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-325-717A>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050019 | ||||||
chr8:42050049
|
A | C | 1 | a0001c0001t0010g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-325-747T>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050049 | ||||||
chr8:42050055
|
G | C | 1 | a0001c0001t0002g0290 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-325-753C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050055 | ||||||
chr8:42050056
|
TGTAA | T | 91 | a0001c0001t0001g0002a0001c0001t0003g0032a0001c0001t0003g0035others(88): Show | 93 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-325-758_-325-755d others(6): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050056 | ||||||
chr8:42050146
|
GAAAAAGA others(16): Show |
G | 1 | a0001c0001t0002g0291 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-325-867_-325-845d others(25): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050146 | ||||||
chr8:42050630
|
A | G | 76 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(73): Show | 81 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-326+1271T>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050630 | ||||||
chr8:42050633
|
A | T | 9 | a0001c0001t0006g0019a0001c0001t0006g0021a0001c0001t0006g0022others(6): Show | 9 | HG02074.hp1 HG02132.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.-326+1268T>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050633 | ||||||
chr8:42050659
|
G | A | 5 | a0001c0003t0017g0295a0001c0003t0017g0296a0001c0003t0028g0294others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-326+1242C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050659 | ||||||
chr8:42050802
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-326+1099C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050802 | ||||||
chr8:42050824
|
C | T | 5 | a0001c0001t0025g0016a0001c0001t0025g0017a0001c0001t0053g0018others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-326+1077G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42050824 | ||||||
chr8:42051190
|
G | C | 1 | a0011c0023t0010g0298 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-326+711C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051190 | ||||||
chr8:42051256
|
C | G | 1 | a0003c0006t0089g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-326+645G>C | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051256 | ||||||
chr8:42051379
|
GGCCGGAG others(5): Show |
G | 1 | a0001c0001t0054g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-326+510_-326+521d others(14): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051379 | ||||||
chr8:42051615
|
G | GGCGCGGG others(8): Show |
1 | a0001c0001t0014g0299 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-326+271_-326+285d others(17): Show |
KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051615 | ||||||
chr8:42051629
|
G | C | 71 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0008others(68): Show | 76 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-326+272C>G | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051629 | ||||||
chr8:42051863
|
G | A | 1 | a0003c0006t0019g0364 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-326+38C>T | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051863 | ||||||
chr8:42051876
|
C | T | 1 | a0002c0002t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-326+25G>A | KAT6A | ENSG00000083168.11 | transcript | ENST00000265713.8 | protein_coding | 1/16 | chr8 | 42051876 |