geneid | 8520 |
---|---|
ensemblid | ENSG00000128708.13 |
hgncid | 4821 |
symbol | HAT1 |
name | histone acetyltransferase 1 |
refseq_nuc | NM_003642.4 |
refseq_prot | NP_003633.2 |
ensembl_nuc | ENST00000264108.5 |
ensembl_prot | ENSP00000264108.4 |
mane_status | MANE Select |
chr | chr2 |
start | 171922461 |
end | 171983686 |
strand | + |
ver | v1.2 |
region | chr2:171922461-171983686 |
region5000 | chr2:171917461-171988686 |
regionname0 | HAT1_chr2_171922461_171983686 |
regionname5000 | HAT1_chr2_171917461_171988686 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 419 | 317 | 68 | 58 | 140 | 8 | 42 | 110 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
a0002 | 1/0 | 419 | 9 | 8 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 375 | 326 | 76 | 58 | 140 | 8 | 42 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1260 | 317 | 68 | 58 | 140 | 8 | 42 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
a0002c0002 | 1/0 | 1260 | 9 | 8 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1634 | 317 | 68 | 58 | 140 | 8 | 42 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
a0002c0002t0001 | 1/0 | 1634 | 9 | 8 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | copy fasta | chr2 | 171917461 | 171988686 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | ASW | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | ASW | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | GIH | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0236 | REF | REF | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0244 | REF | REF | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171976274
|
T | C | 1 | a0001 | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
missense_variant | MODERATE | c.941T>C | p.Val314Ala | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/11 | 981/1634 | 941/1260 | 314/419 | chr2 | 171976274 |
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 |
---|
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 |
---|
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171922612
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.7+105C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171922612 | ||||||
chr2:171922681
|
C | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02040.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.7+174C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171922681 | ||||||
chr2:171923159
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(52): Show | 56 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+652G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923159 | ||||||
chr2:171923182
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.7+675A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923182 | ||||||
chr2:171923187
|
G | A | 6 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+680G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923187 | ||||||
chr2:171923367
|
C | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.7+860C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923367 | ||||||
chr2:171923576
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.7+1069T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923576 | ||||||
chr2:171923622
|
T | C | 73 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(70): Show | 73 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.7+1115T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923622 | ||||||
chr2:171923880
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.7+1373T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923880 | ||||||
chr2:171924048
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | NA18946.hp1 NA18986.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-1489G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924048 | ||||||
chr2:171924210
|
A | AT | 9 | a0001c0001t0001g0144a0001c0001t0001g0257a0001c0001t0001g0258others(6): Show | 9 | HG01123.hp2 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-1313dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171924210 | |||||
chr2:171924235
|
T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-1302T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924235 | ||||||
chr2:171924239
|
G | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.8-1298G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924239 | ||||||
chr2:171924350
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-1187C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924350 | ||||||
chr2:171924362
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.8-1175A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924362 | ||||||
chr2:171924944
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8-593C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924944 | ||||||
chr2:171924970
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.8-567C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924970 | ||||||
chr2:171924992
|
C | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | HG01175.hp2 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-545C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924992 | ||||||
chr2:171925069
|
CT | C | 266 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(263): Show | 266 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.8-447delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171925069 | |||||
chr2:171925069
|
CTT | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0077others(10): Show | 13 | HG00099.hp2 HG01256.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.8-448_8-447delTT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171925069 | |||||
chr2:171925180
|
C | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.8-357C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925180 | ||||||
chr2:171925233
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-304C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925233 | ||||||
chr2:171925291
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0141 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.8-246C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925291 | ||||||
chr2:171925360
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8-177G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925360 | ||||||
chr2:171925971
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+330G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171925971 | ||||||
chr2:171926008
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.112+367G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926008 | ||||||
chr2:171926120
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+479T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926120 | ||||||
chr2:171926688
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG01109.hp2 HG01168.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+1047C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926688 | ||||||
chr2:171926726
|
T | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.112+1085T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926726 | ||||||
chr2:171926838
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.112+1197A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926838 | ||||||
chr2:171927131
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112+1490C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927131 | ||||||
chr2:171927132
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02647.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.112+1491G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927132 | ||||||
chr2:171927242
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.112+1601T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927242 | ||||||
chr2:171927340
|
T | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+1699T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927340 | ||||||
chr2:171927424
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.112+1783G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927424 | ||||||
chr2:171927794
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+2153T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927794 | ||||||
chr2:171927950
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.112+2309G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927950 | ||||||
chr2:171928034
|
C | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.112+2393C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928034 | ||||||
chr2:171928066
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.112+2425T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928066 | ||||||
chr2:171928182
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.112+2541G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928182 | ||||||
chr2:171928495
|
T | A | 77 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(74): Show | 77 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.112+2854T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928495 | ||||||
chr2:171928497
|
C | T | 77 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(74): Show | 77 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.112+2856C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928497 | ||||||
chr2:171928653
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.112+3012C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928653 | ||||||
chr2:171928697
|
G | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+3056G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928697 | ||||||
chr2:171929078
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112+3437A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929078 | ||||||
chr2:171929080
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01070.hp1 HG01071.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.112+3439A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929080 | ||||||
chr2:171929204
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+3563T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929204 | ||||||
chr2:171929466
|
T | C | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+3825T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929466 | ||||||
chr2:171929555
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.112+3914A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929555 | ||||||
chr2:171930033
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+4392T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930033 | ||||||
chr2:171930051
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.112+4410A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930051 | ||||||
chr2:171930185
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.112+4544G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930185 | ||||||
chr2:171930399
|
G | T | 73 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(70): Show | 73 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.112+4758G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930399 | ||||||
chr2:171930641
|
G | T | 1 | a0001c0001t0001g0311 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.112+5000G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930641 | ||||||
chr2:171930835
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.112+5194G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930835 | ||||||
chr2:171931179
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.112+5538C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931179 | ||||||
chr2:171931229
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+5588A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931229 | ||||||
chr2:171931417
|
T | C | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.112+5776T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931417 | ||||||
chr2:171931428
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.112+5787G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931428 | ||||||
chr2:171931441
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02083.hp1 NA18998.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+5800G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931441 | ||||||
chr2:171931595
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.112+5954G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931595 | ||||||
chr2:171931645
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.112+6004G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931645 | ||||||
chr2:171931702
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+6061T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931702 | ||||||
chr2:171932116
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112+6475T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932116 | ||||||
chr2:171932400
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112+6759G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932400 | ||||||
chr2:171932849
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.112+7208A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932849 | ||||||
chr2:171933006
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.112+7365T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933006 | ||||||
chr2:171933401
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.112+7760T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933401 | ||||||
chr2:171933475
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.112+7834C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933475 | ||||||
chr2:171933842
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.112+8201T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933842 | ||||||
chr2:171933909
|
A | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+8268A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933909 | ||||||
chr2:171933982
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0258 | 2 | HG00597.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.112+8341C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933982 | ||||||
chr2:171934005
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | NA18986.hp2 NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.112+8364A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934005 | ||||||
chr2:171934048
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.112+8407G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934048 | ||||||
chr2:171934754
|
G | GT | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.112+9131dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | |||||
chr2:171934754
|
G | GTT | 75 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(72): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.112+9130_112+9131d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | |||||
chr2:171934754
|
G | GTTT | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(5): Show | 8 | HG02027.hp2 NA18966.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+9129_112+9131d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | |||||
chr2:171934754
|
GT | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0210others(27): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.112+9131delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | |||||
chr2:171934899
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.112+9258G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934899 | ||||||
chr2:171935014
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.112+9373C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935014 | ||||||
chr2:171935019
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+9378G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935019 | ||||||
chr2:171935076
|
G | A | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+9435G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935076 | ||||||
chr2:171935312
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+9671C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935312 | ||||||
chr2:171935515
|
C | CA | 23 | a0001c0001t0001g0084a0001c0001t0001g0145a0001c0001t0001g0152others(20): Show | 23 | HG00438.hp1 HG00438.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.112+9897dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | |||||
chr2:171935515
|
C | CAA | 53 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(50): Show | 54 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+9896_112+9897d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | |||||
chr2:171935515
|
CA | C | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(63): Show | 66 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.112+9897delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | |||||
chr2:171935536
|
A | AG | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+9895_112+9896i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935536 | ||||||
chr2:171935536
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01069.hp1 HG01168.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+9895A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935536 | ||||||
chr2:171935552
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.112+9911T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935552 | ||||||
chr2:171935647
|
C | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0270others(29): Show | 33 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.112+10006C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935647 | ||||||
chr2:171935805
|
G | T | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+10164G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935805 | ||||||
chr2:171935833
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.112+10192T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935833 | ||||||
chr2:171936046
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.112+10405G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936046 | ||||||
chr2:171936087
|
G | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+10446G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936087 | ||||||
chr2:171936106
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.112+10465T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936106 | ||||||
chr2:171936204
|
G | T | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10504G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936204 | ||||||
chr2:171936227
|
A | G | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10481A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936227 | ||||||
chr2:171936257
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-10451G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936257 | ||||||
chr2:171936929
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.113-9779A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936929 | ||||||
chr2:171937026
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-9682C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937026 | ||||||
chr2:171937077
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.113-9631C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937077 | ||||||
chr2:171937112
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-9596G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937112 | ||||||
chr2:171937135
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-9573T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937135 | ||||||
chr2:171937170
|
G | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320 | 3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-9538G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937170 | ||||||
chr2:171937541
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-9167C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937541 | ||||||
chr2:171937660
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.113-9048T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937660 | ||||||
chr2:171937717
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.113-8991A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937717 | ||||||
chr2:171938024
|
T | TTC | 27 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0071others(24): Show | 27 | HG00323.hp2 HG01099.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.113-8634_113-8633d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTC | 27 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0078others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.113-8636_113-8633d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTC | 30 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0087others(27): Show | 30 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.113-8638_113-8633d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(1): Show |
25 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0106others(22): Show | 25 | HG00558.hp1 HG01361.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.113-8640_113-8633d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(3): Show |
17 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0001t0001g0104others(14): Show | 17 | HG00438.hp1 HG01071.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.113-8642_113-8633d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(5): Show |
15 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0137others(12): Show | 15 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-8644_113-8633d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(7): Show |
9 | a0001c0001t0001g0072a0001c0001t0001g0098a0001c0001t0001g0099others(6): Show | 9 | HG00140.hp1 HG01496.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-8646_113-8633d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(9): Show |
5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0158others(2): Show | 5 | HG00597.hp1 HG02300.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-8648_113-8633d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(13): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0095 | 2 | HG01975.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.113-8652_113-8633d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
T | TTCTCTCT others(15): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18985.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.113-8654_113-8633d others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTC | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0066others(11): Show | 14 | HG01168.hp1 HG02165.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-8634_113-8633d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTC | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0076others(8): Show | 11 | HG01175.hp2 HG02027.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-8636_113-8633d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTC | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | HG00733.hp1 HG01074.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.113-8638_113-8633d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(1): Show |
T | 8 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0241others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-8640_113-8633d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0001g0034a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8642_113-8633d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(5): Show |
T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0063others(1): Show | 4 | HG01123.hp1 HG01517.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8644_113-8633d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(7): Show |
T | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(38): Show | 41 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.113-8646_113-8633d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(9): Show |
T | 2 | a0001c0001t0001g0248a0001c0001t0001g0319 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.113-8648_113-8633d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-8650_113-8633d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938024
|
TTCTCTCT others(13): Show |
T | 7 | a0001c0001t0001g0001a0001c0001t0001g0216a0001c0001t0001g0237others(4): Show | 8 | HG00099.hp1 HG01109.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-8652_113-8633d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | |||||
chr2:171938039
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-8658_113-8657i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938039 | |||||
chr2:171938060
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-8646_113-8631d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938060 | |||||
chr2:171938064
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.113-8642_113-8631d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938064 | |||||
chr2:171938075
|
T | TC | 3 | a0001c0001t0001g0020a0001c0001t0001g0184a0001c0001t0001g0276 | 3 | HG02083.hp2 HG03130.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTC | 3 | a0001c0001t0001g0084a0001c0001t0001g0119a0001c0001t0001g0136 | 3 | HG00438.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTC | 7 | a0001c0001t0001g0081a0001c0001t0001g0112a0001c0001t0001g0134others(4): Show | 7 | HG00621.hp2 HG00735.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-8633_113-8632i others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTCTC | 3 | a0001c0001t0001g0167a0001c0001t0001g0270a0001c0001t0001g0297 | 3 | HG01934.hp1 HG03490.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTCTC others(2): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0258 | 3 | NA18747.hp1 NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTCTC others(4): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0160 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTCTC others(8): Show |
1 | a0001c0001t0001g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113-8633_113-8632i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938075
|
T | TCTCTCTC others(20): Show |
1 | a0001c0001t0001g0130 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.113-8633_113-8632i others(29): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | ||||||
chr2:171938076
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-8632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938076 | ||||||
chr2:171938249
|
A | G | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.113-8459A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938249 | ||||||
chr2:171938382
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-8326G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938382 | ||||||
chr2:171938647
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | NA18963.hp2 NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.113-8061G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938647 | ||||||
chr2:171938777
|
A | G | 2 | a0001c0001t0001g0209a0002c0002t0001g0247 | 2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.113-7931A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938777 | ||||||
chr2:171938977
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.113-7731G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938977 | ||||||
chr2:171938989
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.113-7719C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938989 | ||||||
chr2:171939037
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01123.hp2 HG04199.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-7671G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939037 | ||||||
chr2:171939040
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-7668T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939040 | ||||||
chr2:171939044
|
A | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-7664A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939044 | ||||||
chr2:171939048
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.113-7660C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939048 | ||||||
chr2:171939141
|
C | T | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7567C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939141 | ||||||
chr2:171939249
|
A | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0191 | 3 | HG01934.hp2 HG01943.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.113-7459A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939249 | ||||||
chr2:171939426
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-7282G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939426 | ||||||
chr2:171939523
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-7185A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939523 | ||||||
chr2:171939796
|
CT | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0081others(4): Show | 7 | HG01070.hp2 HG01256.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-6898delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171939796 | |||||
chr2:171939981
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.113-6727G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939981 | ||||||
chr2:171940061
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-6647C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940061 | ||||||
chr2:171940254
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0212others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.113-6454A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940254 | ||||||
chr2:171940270
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113-6438A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940270 | ||||||
chr2:171940584
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-6124C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940584 | ||||||
chr2:171940761
|
C | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.113-5947C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940761 | ||||||
chr2:171941003
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.113-5705A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941003 | ||||||
chr2:171941277
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113-5431A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941277 | ||||||
chr2:171941369
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0160others(3): Show | 6 | HG00438.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-5339C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941369 | ||||||
chr2:171941742
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.113-4966C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941742 | ||||||
chr2:171942048
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0113 | 2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.113-4660G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942048 | ||||||
chr2:171942135
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.113-4573C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942135 | ||||||
chr2:171942211
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-4497T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942211 | ||||||
chr2:171942255
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4453G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942255 | ||||||
chr2:171942259
|
A | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(60): Show | 64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.113-4449A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942259 | ||||||
chr2:171942284
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4424C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942284 | ||||||
chr2:171942445
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0136 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.113-4263C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942445 | ||||||
chr2:171942454
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.113-4254C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942454 | ||||||
chr2:171942681
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.113-4027A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942681 | ||||||
chr2:171942715
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG01070.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.113-3993A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942715 | ||||||
chr2:171942743
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.113-3965C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942743 | ||||||
chr2:171942754
|
A | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0140 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-3954A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942754 | ||||||
chr2:171942824
|
CAG | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0144 | 3 | HG00735.hp2 HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.113-3883_113-3882d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942824 | ||||||
chr2:171942953
|
AT | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0168a0001c0001t0001g0185 | 3 | NA18941.hp2 NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.113-3754delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942953 | ||||||
chr2:171943055
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0142 | 2 | HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.113-3653G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943055 | ||||||
chr2:171943072
|
AG | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.113-3635delG | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943072 | ||||||
chr2:171943072
|
AGT | A | 34 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(31): Show | 34 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-3635_113-3634d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943072 | ||||||
chr2:171943074
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.113-3634T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943074 | ||||||
chr2:171943075
|
T | C | 34 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(31): Show | 34 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-3633T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943075 | ||||||
chr2:171943076
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.113-3632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943076 | ||||||
chr2:171943262
|
C | T | 1 | a0002c0002t0001g0246 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113-3446C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943262 | ||||||
chr2:171943275
|
G | A | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.113-3433G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943275 | ||||||
chr2:171943410
|
C | CA | 10 | a0001c0001t0001g0149a0001c0001t0001g0248a0001c0001t0001g0252others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-3273dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943410
|
C | CAA | 168 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0077others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.113-3274_113-3273d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943410
|
C | CAAA | 68 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0071others(65): Show | 68 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.113-3275_113-3273d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943410
|
C | CAAAA | 7 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0075others(4): Show | 7 | HG01099.hp2 HG01943.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-3276_113-3273d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943410
|
CAAA | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG00735.hp1 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-3275_113-3273d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943410
|
CAAAA | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.113-3276_113-3273d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | |||||
chr2:171943456
|
G | T | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.113-3252G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943456 | ||||||
chr2:171943726
|
C | CAT | 34 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(31): Show | 34 | HG01257.hp1 HG02165.hp2 HG02451.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-2959_113-2958d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943726
|
C | CATAT | 52 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.113-2961_113-2958d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943726
|
C | CATATAT | 13 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0091others(10): Show | 13 | HG00140.hp1 HG00621.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-2963_113-2958d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943726
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0104 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.113-2969_113-2958d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943726
|
CAT | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.113-2959_113-2958d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943726
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.113-2969_113-2958d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | |||||
chr2:171943808
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.113-2900C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943808 | ||||||
chr2:171943857
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.113-2851A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943857 | ||||||
chr2:171944143
|
CA | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.113-2550delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171944143 | |||||
chr2:171944159
|
T | A | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.113-2549T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944159 | ||||||
chr2:171944441
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.113-2267G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944441 | ||||||
chr2:171944489
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.113-2219C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944489 | ||||||
chr2:171944908
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.113-1800A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944908 | ||||||
chr2:171944924
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.113-1784C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944924 | ||||||
chr2:171945161
|
G | A | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.113-1547G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945161 | ||||||
chr2:171945492
|
T | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02083.hp1 NA18963.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-1216T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945492 | ||||||
chr2:171945498
|
A | AT | 64 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0071others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.113-1191dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171945498 | |||||
chr2:171945498
|
AT | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.113-1191delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171945498 | |||||
chr2:171945602
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113-1106T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945602 | ||||||
chr2:171945607
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.113-1101C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945607 | ||||||
chr2:171945754
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | NA18964.hp2 NA18995.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-954C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945754 | ||||||
chr2:171945755
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-953G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945755 | ||||||
chr2:171945830
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-878C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945830 | ||||||
chr2:171945831
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.113-877G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945831 | ||||||
chr2:171946203
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.113-505A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946203 | ||||||
chr2:171946254
|
G | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320 | 3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-454G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946254 | ||||||
chr2:171946563
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0225 | 3 | HG02004.hp1 HG06807.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.113-145A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946563 | ||||||
chr2:171946807
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.188+24G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171946807 | ||||||
chr2:171946879
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+96T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171946879 | ||||||
chr2:171947304
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.188+521G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947304 | ||||||
chr2:171947349
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+566G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947349 | ||||||
chr2:171947358
|
A | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02258.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.188+575A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947358 | ||||||
chr2:171947430
|
A | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0099 | 2 | HG00140.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.188+647A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947430 | ||||||
chr2:171947452
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0027 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.188+669C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947452 | ||||||
chr2:171947575
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.188+792G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947575 | ||||||
chr2:171948430
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.188+1647G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948430 | ||||||
chr2:171948845
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.188+2062A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948845 | ||||||
chr2:171948862
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.188+2079G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948862 | ||||||
chr2:171949001
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.188+2218G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949001 | ||||||
chr2:171949192
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+2409A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949192 | ||||||
chr2:171949358
|
G | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.188+2575G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949358 | ||||||
chr2:171949673
|
C | CA | 8 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0039others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+2906dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171949673 | |||||
chr2:171949673
|
CA | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0071others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.188+2906delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171949673 | |||||
chr2:171949689
|
A | T | 5 | a0001c0001t0001g0252a0002c0002t0001g0253a0002c0002t0001g0254others(2): Show | 5 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+2906A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949689 | ||||||
chr2:171949817
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0182 | 2 | HG02602.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.188+3034A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949817 | ||||||
chr2:171949859
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.189-3022G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949859 | ||||||
chr2:171950023
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-2858C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950023 | ||||||
chr2:171950396
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189-2485G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950396 | ||||||
chr2:171950438
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.189-2443C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950438 | ||||||
chr2:171950460
|
C | T | 65 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(62): Show | 65 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.189-2421C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950460 | ||||||
chr2:171950711
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.189-2170C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950711 | ||||||
chr2:171950939
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.189-1942C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950939 | ||||||
chr2:171951071
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0069others(64): Show | 68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.189-1810G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951071 | ||||||
chr2:171951101
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.189-1780G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951101 | ||||||
chr2:171951112
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.189-1769T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951112 | ||||||
chr2:171951230
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.189-1651T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951230 | ||||||
chr2:171951363
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-1518C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951363 | ||||||
chr2:171951442
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.189-1439C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951442 | ||||||
chr2:171951585
|
A | AT | 45 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0042others(42): Show | 45 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-1277dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | |||||
chr2:171951585
|
A | ATT | 7 | a0001c0001t0001g0104a0001c0001t0001g0160a0001c0001t0001g0218others(4): Show | 7 | HG01168.hp2 HG01433.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-1278_189-1277d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | |||||
chr2:171951585
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189-1296A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951585 | ||||||
chr2:171951585
|
AT | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0101others(4): Show | 7 | HG02895.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1277delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | |||||
chr2:171951604
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(60): Show | 64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-1277T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951604 | ||||||
chr2:171951672
|
TC | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.189-1201delC | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951672 | |||||
chr2:171951680
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.189-1201C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951680 | ||||||
chr2:171951723
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.189-1158C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951723 | ||||||
chr2:171951724
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.189-1157G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951724 | ||||||
chr2:171951773
|
C | G | 1 | a0001c0001t0001g0020 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.189-1108C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951773 | ||||||
chr2:171951773
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189-1108C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951773 | ||||||
chr2:171951813
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-1068C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951813 | ||||||
chr2:171951859
|
G | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG02723.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.189-1022G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951859 | ||||||
chr2:171952068
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.189-813A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952068 | ||||||
chr2:171952211
|
C | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0126 | 2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.189-670C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952211 | ||||||
chr2:171952262
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0168a0001c0001t0001g0185 | 3 | NA18941.hp2 NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.189-619T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952262 | ||||||
chr2:171952535
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.189-346T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952535 | ||||||
chr2:171952844
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-37A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952844 | ||||||
chr2:171953188
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309+187C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953188 | ||||||
chr2:171953207
|
G | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0096a0001c0001t0001g0100others(2): Show | 5 | HG01975.hp2 NA18959.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+206G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953207 | ||||||
chr2:171953446
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.309+445T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953446 | ||||||
chr2:171953597
|
C | G | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309+596C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953597 | ||||||
chr2:171953626
|
T | TAAAA | 41 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00558.hp2 HG00609.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.309+651_309+654dup others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAA | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(17): Show | 20 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.309+650_309+654dup others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0154others(5): Show | 8 | HG02818.hp2 NA18941.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+647_309+654dup others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(2): Show |
31 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0147others(28): Show | 32 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+646_309+654dup others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(3): Show |
48 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0150others(45): Show | 48 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.309+645_309+654dup others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(4): Show |
18 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0165others(15): Show | 18 | HG00323.hp2 HG00621.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.309+644_309+654dup others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0279others(2): Show | 5 | HG01943.hp1 HG02300.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+643_309+654dup others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(6): Show |
2 | a0001c0001t0001g0242a0001c0001t0001g0286 | 2 | HG02027.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.309+642_309+654dup others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(7): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0317 | 3 | HG02451.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.309+641_309+654dup others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0163a0001c0001t0001g0201a0001c0001t0001g0267others(4): Show | 7 | HG01261.hp2 HG02647.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+640_309+654dup others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0275a0001c0001t0001g0282a0001c0001t0001g0284others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+639_309+654dup others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0283 | 3 | HG06807.hp1 NA18962.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.309+638_309+654dup others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0176 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.309+636_309+654dup others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+635_309+654dup others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0266 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309+633_309+654dup others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(19): Show |
1 | a0001c0001t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.309+629_309+654dup others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(20): Show |
1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.309+628_309+654dup others(27): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+626_309+654dup others(29): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
TAAAAAAA | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0120others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+648_309+654del others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
TAAAAAAA others(1): Show |
T | 62 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(59): Show | 62 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.309+647_309+654del others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0075a0001c0001t0001g0085a0001c0001t0001g0116others(3): Show | 6 | HG01070.hp1 HG01975.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+646_309+654del others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
TAAAAAAA others(3): Show |
T | 30 | a0001c0001t0001g0156a0001c0001t0001g0212a0001c0001t0001g0214others(27): Show | 30 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.309+645_309+654del others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953626
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0213a0001c0001t0001g0263 | 2 | HG01256.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.309+644_309+654del others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | |||||
chr2:171953666
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.309+665A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953666 | ||||||
chr2:171953686
|
C | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.309+685C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953686 | ||||||
chr2:171953839
|
A | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+838A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953839 | ||||||
chr2:171954507
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.309+1506A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954507 | ||||||
chr2:171954515
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG02615.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.309+1514G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954515 | ||||||
chr2:171954529
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0130 | 2 | HG00609.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.309+1528T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954529 | ||||||
chr2:171954627
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0230others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+1626A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954627 | ||||||
chr2:171954642
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0230others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+1641C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954642 | ||||||
chr2:171954704
|
G | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0140 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.309+1703G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954704 | ||||||
chr2:171954808
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.309+1807G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954808 | ||||||
chr2:171954829
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.309+1828G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954829 | ||||||
chr2:171954861
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.309+1860A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954861 | ||||||
chr2:171955088
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0297a0001c0001t0001g0300 | 3 | HG01361.hp1 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.309+2087C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955088 | ||||||
chr2:171955089
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.309+2088G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955089 | ||||||
chr2:171955180
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.309+2179G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955180 | ||||||
chr2:171955518
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.309+2517G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955518 | ||||||
chr2:171955758
|
A | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+2757A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955758 | ||||||
chr2:171955765
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.309+2764C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955765 | ||||||
chr2:171955772
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.309+2771C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955772 | ||||||
chr2:171955813
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+2812A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955813 | ||||||
chr2:171955818
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.309+2817A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955818 | ||||||
chr2:171955937
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.309+2936C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955937 | ||||||
chr2:171955962
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.309+2961C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955962 | ||||||
chr2:171955994
|
G | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+2993G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955994 | ||||||
chr2:171956000
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.309+2999G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956000 | ||||||
chr2:171956001
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+3000C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956001 | ||||||
chr2:171956023
|
C | A | 30 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(27): Show | 30 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.309+3022C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956023 | ||||||
chr2:171956066
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.309+3065C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956066 | ||||||
chr2:171956178
|
T | TA | 84 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0040others(81): Show | 85 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.309+3200dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956178 | |||||
chr2:171956178
|
TA | T | 8 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0110others(5): Show | 8 | HG01070.hp2 HG01256.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+3200delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956178 | |||||
chr2:171956284
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309+3283G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956284 | ||||||
chr2:171956311
|
CA | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0230others(30): Show | 34 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+3311delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956311 | ||||||
chr2:171956515
|
A | AAAAC | 66 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0230others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+3530_309+3533d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956515 | |||||
chr2:171956520
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0089others(3): Show | 6 | HG00408.hp1 HG00438.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+3519A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956520 | ||||||
chr2:171956539
|
C | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.309+3538C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956539 | ||||||
chr2:171956552
|
G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320 | 3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309+3551G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956552 | ||||||
chr2:171956692
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.309+3691G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956692 | ||||||
chr2:171956693
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.309+3692G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956693 | ||||||
chr2:171956715
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.309+3714C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956715 | ||||||
chr2:171956719
|
G | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(67): Show | 71 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.309+3718G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956719 | ||||||
chr2:171957380
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.309+4379C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957380 | ||||||
chr2:171957583
|
G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320 | 3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309+4582G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957583 | ||||||
chr2:171957729
|
T | C | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.309+4728T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957729 | ||||||
chr2:171957792
|
A | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+4791A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957792 | ||||||
chr2:171957922
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.309+4921A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957922 | ||||||
chr2:171957941
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0230others(60): Show | 64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.309+4940C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957941 | ||||||
chr2:171957946
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.309+4945C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957946 | ||||||
chr2:171958023
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5022C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958023 | ||||||
chr2:171958171
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+5170A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958171 | ||||||
chr2:171958476
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.309+5475C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958476 | ||||||
chr2:171958514
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+5513C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958514 | ||||||
chr2:171958680
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0031 | 3 | HG02056.hp1 HG03927.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.309+5679A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958680 | ||||||
chr2:171958860
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.309+5859G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958860 | ||||||
chr2:171958881
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.309+5880A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958881 | ||||||
chr2:171958984
|
G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(68): Show | 72 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+5983G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958984 | ||||||
chr2:171959486
|
T | A | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.310-5852T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959486 | ||||||
chr2:171959703
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.310-5635A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959703 | ||||||
chr2:171959727
|
A | C | 69 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.310-5611A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959727 | ||||||
chr2:171960338
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.310-5000T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960338 | ||||||
chr2:171960348
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.310-4990G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960348 | ||||||
chr2:171960375
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.310-4963A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960375 | ||||||
chr2:171960390
|
C | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.310-4948C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960390 | ||||||
chr2:171960401
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.310-4937T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960401 | ||||||
chr2:171960482
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.310-4856T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960482 | ||||||
chr2:171960534
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-4804T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960534 | ||||||
chr2:171960535
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.310-4803C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960535 | ||||||
chr2:171960711
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.310-4627G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960711 | ||||||
chr2:171960761
|
C | T | 70 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.310-4577C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960761 | ||||||
chr2:171960913
|
G | GGACAGGT others(11): Show |
1 | a0001c0001t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.310-4424_310-4407d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171960913 | |||||
chr2:171961132
|
ACT | A | 6 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0120others(3): Show | 6 | HG00621.hp2 HG02132.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-4203_310-4202d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961132 | |||||
chr2:171961268
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.310-4070A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961268 | ||||||
chr2:171961409
|
GA | G | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0293others(2): Show | 5 | NA18959.hp1 NA18964.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-3925delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961409 | |||||
chr2:171961576
|
ATACT | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-3760_310-3757d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961576 | |||||
chr2:171961731
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.310-3607C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961731 | ||||||
chr2:171961825
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.310-3513A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961825 | ||||||
chr2:171961891
|
G | GT | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.310-3433dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | |||||
chr2:171961891
|
G | GTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG01978.hp2 HG02083.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-3434_310-3433d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | |||||
chr2:171961891
|
GT | G | 39 | a0001c0001t0001g0173a0001c0001t0001g0181a0001c0001t0001g0183others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.310-3433delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | |||||
chr2:171961945
|
T | G | 26 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.310-3393T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961945 | ||||||
chr2:171962004
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.310-3334T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962004 | ||||||
chr2:171962145
|
G | A | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255others(1): Show | 4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-3193G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962145 | ||||||
chr2:171962487
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.310-2851C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962487 | ||||||
chr2:171962639
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.310-2699G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962639 | ||||||
chr2:171963176
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.310-2162G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963176 | ||||||
chr2:171963192
|
C | CATATTTA others(23): Show |
1 | a0001c0001t0001g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310-2134_310-2105d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171963192 | |||||
chr2:171963605
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.310-1733T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963605 | ||||||
chr2:171963728
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(54): Show | 58 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.310-1610C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963728 | ||||||
chr2:171963738
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.310-1600G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963738 | ||||||
chr2:171963793
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.310-1545T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963793 | ||||||
chr2:171964701
|
G | A | 24 | a0001c0001t0001g0212a0001c0001t0001g0216a0001c0001t0001g0217others(21): Show | 24 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.310-637G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171964701 | ||||||
chr2:171964706
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310-632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171964706 | ||||||
chr2:171964836
|
AT | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-497delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171964836 | |||||
chr2:171965218
|
T | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-120T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171965218 | ||||||
chr2:171966124
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+216G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966124 | ||||||
chr2:171966171
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612-238C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966171 | ||||||
chr2:171966208
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.612-201A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966208 | ||||||
chr2:171966663
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.716+150T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 7/10 | chr2 | 171966663 | ||||||
chr2:171966963
|
G | GA | 8 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG00609.hp1 NA18941.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+15dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171966963 | |||||
chr2:171966967
|
T | G | 8 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG00609.hp1 NA18941.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+18T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171966967 | ||||||
chr2:171967073
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.823+124C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967073 | ||||||
chr2:171967535
|
C | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+586C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967535 | ||||||
chr2:171967884
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.823+935C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967884 | ||||||
chr2:171968797
|
T | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0218a0001c0001t0001g0222others(3): Show | 6 | HG01256.hp2 HG02004.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1848T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171968797 | ||||||
chr2:171968822
|
G | A | 70 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(67): Show | 70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.823+1873G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171968822 | ||||||
chr2:171969206
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 5 | HG00609.hp2 NA18949.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2257A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969206 | ||||||
chr2:171969645
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.823+2696A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969645 | ||||||
chr2:171969679
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0134others(4): Show | 7 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+2730G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969679 | ||||||
chr2:171970095
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.823+3146G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970095 | ||||||
chr2:171970147
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.823+3198G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970147 | ||||||
chr2:171970337
|
C | G | 1 | a0001c0001t0001g0202 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.823+3388C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970337 | ||||||
chr2:171970434
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0001g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.823+3493_823+3504d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970434 | |||||
chr2:171970496
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0313 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.823+3574_823+3588d others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
C | CTTTTTTT others(12): Show |
2 | a0002c0002t0001g0245a0002c0002t0001g0247 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+3570_823+3588d others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CT | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0079others(13): Show | 16 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+3588delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTT | C | 20 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0086others(17): Show | 20 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.823+3587_823+3588d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTT | C | 13 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0078others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+3586_823+3588d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0278a0001c0001t0001g0287a0001c0001t0001g0290others(8): Show | 11 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+3579_823+3588d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(4): Show |
C | 42 | a0001c0001t0001g0071a0001c0001t0001g0261a0001c0001t0001g0262others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.823+3578_823+3588d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0001a0001c0001t0001g0132a0001c0001t0001g0265others(5): Show | 9 | HG02809.hp1 HG02976.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+3577_823+3588d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(6): Show |
C | 10 | a0001c0001t0001g0105a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG00408.hp2 HG02027.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+3576_823+3588d others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(7): Show |
C | 57 | a0001c0001t0001g0069a0001c0001t0001g0148a0001c0001t0001g0149others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.823+3575_823+3588d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0070a0001c0001t0001g0106a0001c0001t0001g0158others(3): Show | 6 | HG01123.hp2 HG01943.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+3574_823+3588d others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.823+3573_823+3588d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(12): Show |
C | 7 | a0001c0001t0001g0081a0001c0001t0001g0141a0001c0001t0001g0143others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+3570_823+3588d others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(13): Show |
C | 35 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0126others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.823+3569_823+3588d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0001g0136a0001c0001t0001g0219 | 2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.823+3568_823+3588d others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(15): Show |
C | 6 | a0001c0001t0001g0030a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG01109.hp2 HG01168.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+3567_823+3588d others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(16): Show |
C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.823+3566_823+3588d others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970496
|
CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0008a0001c0001t0001g0021 | 2 | HG03491.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.823+3565_823+3588d others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | |||||
chr2:171970580
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(64): Show | 68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.823+3631T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970580 | ||||||
chr2:171970612
|
C | T | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320others(1): Show | 4 | HG01074.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+3663C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970612 | ||||||
chr2:171970662
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.823+3713G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970662 | ||||||
chr2:171970784
|
C | T | 68 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(65): Show | 68 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.823+3835C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970784 | ||||||
chr2:171970800
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.823+3851G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970800 | ||||||
chr2:171970869
|
A | G | 1 | a0002c0002t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.823+3920A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970869 | ||||||
chr2:171970939
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0053 | 3 | HG01261.hp1 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.823+3990G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970939 | ||||||
chr2:171970966
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.823+4017C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970966 | ||||||
chr2:171971199
|
C | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.823+4250C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971199 | ||||||
chr2:171971286
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0132 | 2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.823+4337G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971286 | ||||||
chr2:171971461
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823+4512T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971461 | ||||||
chr2:171971546
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.823+4597C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971546 | ||||||
chr2:171971624
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-4533G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971624 | ||||||
chr2:171971821
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.824-4336T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971821 | ||||||
chr2:171972007
|
T | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0287 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.824-4150T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972007 | ||||||
chr2:171972214
|
GT | G | 205 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(202): Show | 205 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.824-3931delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171972214 | |||||
chr2:171972223
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0263 | 2 | HG02572.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.824-3934T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972223 | ||||||
chr2:171972253
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.824-3904T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972253 | ||||||
chr2:171972289
|
A | G | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-3868A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972289 | ||||||
chr2:171972632
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-3525A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972632 | ||||||
chr2:171972756
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-3401G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972756 | ||||||
chr2:171972764
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.824-3393A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972764 | ||||||
chr2:171972970
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0242 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.824-3187G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972970 | ||||||
chr2:171973127
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.824-3030C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973127 | ||||||
chr2:171973172
|
C | A | 24 | a0001c0001t0001g0212a0001c0001t0001g0216a0001c0001t0001g0217others(21): Show | 24 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-2985C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973172 | ||||||
chr2:171973400
|
C | CA | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.824-2740dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171973400 | |||||
chr2:171973400
|
C | CAA | 81 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0048others(78): Show | 82 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.824-2741_824-2740d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171973400 | |||||
chr2:171973453
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.824-2704T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973453 | ||||||
chr2:171973653
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-2504A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973653 | ||||||
chr2:171973720
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.824-2437C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973720 | ||||||
chr2:171973787
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.824-2370C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973787 | ||||||
chr2:171973914
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.824-2243T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973914 | ||||||
chr2:171973946
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(64): Show | 68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.824-2211A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973946 | ||||||
chr2:171973980
|
G | A | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0287 | 3 | HG01261.hp2 HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.824-2177G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973980 | ||||||
chr2:171974055
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.824-2102C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974055 | ||||||
chr2:171974125
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-2032G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974125 | ||||||
chr2:171974173
|
C | CA | 35 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0086others(32): Show | 35 | HG00408.hp1 HG00621.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.824-1965dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | |||||
chr2:171974173
|
C | CAA | 58 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0145others(55): Show | 58 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.824-1966_824-1965d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | |||||
chr2:171974173
|
C | CAAA | 14 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0150others(11): Show | 14 | HG00408.hp2 HG00597.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-1967_824-1965d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | |||||
chr2:171974189
|
AAAAGAAA others(25): Show |
A | 2 | a0001c0001t0001g0009a0001c0001t0001g0059 | 2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.824-1964_824-1933d others(34): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974189 | |||||
chr2:171974190
|
AAAGAAAA others(24): Show |
A | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.824-1964_824-1934d others(33): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974190 | |||||
chr2:171974191
|
AAGAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0299a0001c0001t0001g0307 | 2 | HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.824-1964_824-1955d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974191 | |||||
chr2:171974191
|
AAGAAAAA others(23): Show |
A | 7 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0041others(4): Show | 7 | HG01175.hp1 HG01517.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-1964_824-1935d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974191 | |||||
chr2:171974192
|
AG | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0290others(11): Show | 15 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-1964delG | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974192 | ||||||
chr2:171974192
|
AGAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0037 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.824-1964_824-1932d others(35): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974192 | ||||||
chr2:171974193
|
G | A | 231 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(228): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.824-1964G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974193 | ||||||
chr2:171974199
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-1958A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974199 | ||||||
chr2:171974201
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(66): Show | 70 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.824-1956G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974201 | ||||||
chr2:171974203
|
A | G | 7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0259others(4): Show | 7 | HG01123.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-1954A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974203 | ||||||
chr2:171974204
|
A | AG | 24 | a0001c0001t0001g0263a0001c0001t0001g0267a0001c0001t0001g0271others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-1953_824-1952i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974204 | ||||||
chr2:171974204
|
A | G | 22 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0264others(19): Show | 22 | HG01261.hp2 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-1953A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974204 | ||||||
chr2:171974207
|
G | A | 53 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0259others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.824-1950G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974207 | ||||||
chr2:171974209
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0259others(1): Show | 4 | HG01123.hp2 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1948A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974209 | ||||||
chr2:171974210
|
A | AAAG | 15 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0270others(12): Show | 16 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-1945_824-1944i others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974210 | |||||
chr2:171974210
|
A | G | 46 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.824-1947A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974210 | ||||||
chr2:171974225
|
T | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0046others(3): Show | 6 | HG00609.hp2 HG03710.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1932T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974225 | ||||||
chr2:171974280
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0125others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1877T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974280 | ||||||
chr2:171974442
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.824-1715T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974442 | ||||||
chr2:171974578
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0027 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.824-1579G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974578 | ||||||
chr2:171974736
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.824-1421A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974736 | ||||||
chr2:171974808
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.824-1349G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974808 | ||||||
chr2:171975102
|
C | CT | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0057others(13): Show | 16 | HG01074.hp1 HG01934.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.824-1039dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171975102 | |||||
chr2:171975512
|
G | T | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-645G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171975512 | ||||||
chr2:171976018
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.824-139A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171976018 | ||||||
chr2:171976041
|
G | A | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320others(1): Show | 4 | HG01074.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-116G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171976041 | ||||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0258 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0264 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0292a0001c0001t0001g0300a0001c0001t0001g0303 | 3 | HG01361.hp1 HG02818.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0266 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
2 | a0001c0001t0001g0305a0001c0001t0001g0307 | 2 | HG00323.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0272 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
13 | a0001c0001t0001g0071a0001c0001t0001g0271a0001c0001t0001g0288others(10): Show | 13 | HG00140.hp2 HG00733.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
17 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0267others(14): Show | 17 | HG01261.hp2 HG01884.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0273a0001c0001t0001g0296others(4): Show | 8 | HG02040.hp2 NA18960.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0281 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0302 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0067 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8413): Show |
1 | a0001c0001t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8418): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0316 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0315a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG03139.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8457): Show |
1 | a0001c0001t0001g0251 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8462): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8454): Show |
1 | a0001c0001t0001g0179 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8459): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8448): Show |
1 | a0001c0001t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8453): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8446): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8451): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8446): Show |
1 | a0001c0001t0001g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8451): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0167 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8443): Show |
1 | a0001c0001t0001g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8448): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0175 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8442): Show |
1 | a0001c0001t0001g0183 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8447): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8441): Show |
1 | a0001c0001t0001g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8446): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8441): Show |
1 | a0001c0001t0001g0154 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8446): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8440): Show |
1 | a0001c0001t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8445): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8439): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0168 | 2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8444): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8436): Show |
1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8441): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8437): Show |
2 | a0001c0001t0001g0162a0001c0001t0001g0164 | 2 | HG01258.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8442): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8435): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0161 | 3 | HG00621.hp1 HG02523.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8434): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0192a0001c0001t0001g0195 | 3 | NA18942.hp1 NA18964.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8434): Show |
1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8432): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0149a0001c0001t0001g0197 | 3 | NA18962.hp2 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8437): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8434): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0153 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0150a0001c0001t0001g0200 | 3 | HG04228.hp1 NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0140others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0123 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0104 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0202 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
4 | a0001c0001t0001g0170a0001c0001t0001g0188a0001c0001t0001g0199others(1): Show | 4 | HG00558.hp1 HG02132.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0185 | 2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0136 | 3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
6 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG00621.hp2 HG01975.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0097 | 2 | NA18941.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0092 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0106 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
9 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG00408.hp1 HG00735.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0130 | 2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0120 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0116a0001c0001t0001g0159others(1): Show | 4 | NA18943.hp1 NA18943.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0114 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0109 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0094 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
9 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0107others(6): Show | 9 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0111 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0088 | 2 | HG00438.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0122 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0201 | 3 | NA19009.hp1 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
3 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0184 | 3 | HG02083.hp2 NA18946.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0132 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0257 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0145 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8417): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | NA18953.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8422): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0187 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0198 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0158 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8416): Show |
1 | a0002c0002t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
1 | a0002c0002t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8414): Show |
2 | a0002c0002t0001g0254a0002c0002t0001g0256 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8406): Show |
1 | a0001c0001t0001g0169 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8411): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0081 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8450): Show |
1 | a0001c0001t0001g0238 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8455): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8440): Show |
2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8445): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8439): Show |
1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8444): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8436): Show |
1 | a0001c0001t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8441): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8435): Show |
6 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG02698.hp2 HG03491.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8435): Show |
2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8434): Show |
1 | a0001c0001t0001g0219 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8434): Show |
5 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0234others(2): Show | 5 | HG00733.hp1 HG01496.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8433): Show |
1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8438): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0212 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8433): Show |
1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8438): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0068 | 3 | HG01167.hp2 HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0022 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0027 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0052 | 2 | HG02027.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(12): Show | 15 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0021 | 2 | NA18968.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0065 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0036others(1): Show | 4 | HG01070.hp2 HG02735.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0058 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
24 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(21): Show | 24 | HG00099.hp2 HG00558.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0044 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0063 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8423): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0006 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8417): Show |
1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8422): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0218 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8415): Show |
2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976066
|
C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0239 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | |||||
chr2:171976322
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.975+14G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976322 | ||||||
chr2:171976496
|
G | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0218a0001c0001t0001g0222others(3): Show | 6 | HG01256.hp2 HG02004.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+188G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976496 | ||||||
chr2:171976529
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.975+221C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976529 | ||||||
chr2:171976678
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.975+370C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976678 | ||||||
chr2:171976692
|
T | C | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.975+384T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976692 | ||||||
chr2:171976991
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(54): Show | 58 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.975+683T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976991 | ||||||
chr2:171977065
|
G | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0282others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+757G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977065 | ||||||
chr2:171977160
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.975+852G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977160 | ||||||
chr2:171977401
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(61): Show | 65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.975+1093G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977401 | ||||||
chr2:171977439
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.975+1131G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977439 | ||||||
chr2:171977461
|
T | TA | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.975+1167dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977461 | |||||
chr2:171977467
|
A | G | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0282others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+1159A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977467 | ||||||
chr2:171977524
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.975+1217_975+1218i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0226 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.975+1217_975+1218i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AAAATATA others(23): Show |
1 | a0001c0001t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.975+1217_975+1218i others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AAT | 8 | a0001c0001t0001g0074a0001c0001t0001g0112a0001c0001t0001g0114others(5): Show | 8 | HG00621.hp2 HG02132.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.975+1249_975+1250d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATAT | 3 | a0001c0001t0001g0086a0001c0001t0001g0120a0001c0001t0001g0229 | 3 | HG04199.hp2 NA18949.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.975+1247_975+1250d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATAT | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0218others(2): Show | 5 | HG02004.hp1 HG02922.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1245_975+1250d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0234 | 2 | HG01099.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.975+1241_975+1250d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0216 | 2 | HG00099.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.975+1239_975+1250d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0239a0001c0001t0001g0250 | 3 | HG01981.hp2 HG02738.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1237_975+1250d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.975+1235_975+1250d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977524
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.975+1233_975+1250d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | |||||
chr2:171977525
|
ATATATAT others(35): Show |
A | 1 | a0001c0001t0001g0231 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.975+1219_975+1260d others(44): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977525 | |||||
chr2:171977526
|
T | A | 1 | a0001c0001t0001g0249 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.975+1218T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977526 | ||||||
chr2:171977535
|
ATATATAT others(29): Show |
A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.975+1229_975+1264d others(38): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977535 | |||||
chr2:171977539
|
ATATATAT others(23): Show |
A | 14 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.975+1233_975+1262d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977539 | |||||
chr2:171977539
|
ATATATAT others(24): Show |
A | 2 | a0001c0001t0001g0284a0001c0001t0001g0319 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.975+1233_975+1263d others(33): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977539 | |||||
chr2:171977541
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.975+1235_975+1258d others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977541 | |||||
chr2:171977541
|
ATATATAT others(23): Show |
A | 48 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0261others(45): Show | 49 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.975+1235_975+1264d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977541 | |||||
chr2:171977542
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18964.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.975+1235_975+1245d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977542 | ||||||
chr2:171977544
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.975+1237_975+1247d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977544 | ||||||
chr2:171977551
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.975+1245_975+1256d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977551 | |||||
chr2:171977553
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.975+1246_975+1247i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977553 | |||||
chr2:171977553
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.975+1245A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977553 | ||||||
chr2:171977553
|
ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0217a0001c0001t0001g0221 | 2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.975+1247_975+1256d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977553 | |||||
chr2:171977555
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.975+1248_975+1249i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977555 | |||||
chr2:171977555
|
A | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(7): Show | 10 | HG01192.hp1 HG02056.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.975+1247A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977555 | ||||||
chr2:171977555
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.975+1249_975+1260d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977555 | |||||
chr2:171977557
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(31): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(15): Show |
3 | a0001c0001t0001g0132a0001c0001t0001g0174a0001c0001t0001g0203 | 3 | NA18963.hp1 NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(30): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0238 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0198 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(28): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0163 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0162 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0155 | 2 | HG02056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0313 | 2 | HG02083.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0001t0001g0181 | 3 | HG00323.hp1 HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0182 | 2 | NA18943.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0167a0001c0001t0001g0196a0001c0001t0001g0242 | 3 | HG00408.hp2 HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0197 | 2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0186 | 2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0171 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0158 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0154 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0185 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0200 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG00597.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0176 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0111 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG03209.hp2 NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0179 | 3 | NA18968.hp1 NA18983.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0202 | 2 | NA18966.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0201 | 2 | NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0251 | 2 | NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0255a0002c0002t0001g0256 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0312others(1): Show | 4 | HG01109.hp2 HG01517.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0192 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATTT others(2): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01975.hp1 HG02735.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0052 | 3 | HG02027.hp1 HG03942.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATTT others(4): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0057others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATTT others(5): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 2 | HG01168.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0153 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATTTTT others(3): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0050 | 3 | HG00609.hp2 NA18952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0060 | 2 | HG01074.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATATTTTT others(5): Show |
1 | a0001c0001t0001g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0034others(5): Show | 8 | HG00738.hp2 HG01070.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+1264_975+1271d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0048others(1): Show | 4 | HG00735.hp1 NA18949.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+1262_975+1271d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
A | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 26 | HG01192.hp1 HG01978.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.975+1249A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977557 | ||||||
chr2:171977557
|
AT | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0088a0001c0001t0001g0096others(11): Show | 14 | HG00140.hp1 HG00609.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.975+1271delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977557
|
ATTT | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0117others(3): Show | 6 | HG01361.hp2 HG02300.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+1269_975+1271d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | |||||
chr2:171977558
|
T | TA | 14 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0089others(11): Show | 14 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977558
|
T | TATATATA | 3 | a0001c0001t0001g0093a0001c0001t0001g0104a0001c0001t0001g0131 | 3 | HG01168.hp2 NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977558
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977558
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977558
|
T | TATATATA others(12): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0249 | 2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977558
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0212 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | ||||||
chr2:171977559
|
T | A | 34 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0086others(31): Show | 34 | HG00099.hp1 HG00621.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.975+1251T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977559 | ||||||
chr2:171977560
|
T | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0094others(23): Show | 26 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.975+1252T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977560 | ||||||
chr2:171977561
|
T | A | 25 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0102others(22): Show | 25 | HG00099.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.975+1253T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977561 | ||||||
chr2:171977562
|
T | A | 19 | a0001c0001t0001g0075a0001c0001t0001g0095a0001c0001t0001g0097others(16): Show | 19 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.975+1254T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977562 | ||||||
chr2:171977563
|
T | A | 17 | a0001c0001t0001g0086a0001c0001t0001g0147a0001c0001t0001g0210others(14): Show | 17 | HG00099.hp1 HG01099.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+1255T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977563 | ||||||
chr2:171977564
|
T | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0001g0209others(2): Show | 5 | HG00738.hp1 HG02300.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1256T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977564 | ||||||
chr2:171977565
|
T | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0213a0001c0001t0001g0222others(4): Show | 7 | HG01256.hp2 HG02622.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.975+1257T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977565 | ||||||
chr2:171977566
|
T | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0209a0001c0001t0001g0223others(1): Show | 4 | HG01943.hp2 HG03017.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1258T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977566 | ||||||
chr2:171977567
|
T | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0240 | 3 | HG02622.hp1 HG03453.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1259T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977567 | ||||||
chr2:171977568
|
T | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0209a0001c0001t0001g0223others(1): Show | 4 | HG01943.hp2 HG03017.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1260T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977568 | ||||||
chr2:171977569
|
T | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0240 | 2 | HG02622.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1261T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977569 | ||||||
chr2:171977572
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.975+1264T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977572 | ||||||
chr2:171977670
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.975+1362C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977670 | ||||||
chr2:171977710
|
C | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.975+1402C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977710 | ||||||
chr2:171977894
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | NA18963.hp1 NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.976-1353T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977894 | ||||||
chr2:171977957
|
T | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG02615.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.976-1290T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977957 | ||||||
chr2:171978059
|
C | CT | 69 | a0001c0001t0001g0050a0001c0001t0001g0072a0001c0001t0001g0073others(66): Show | 69 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.976-1173dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978059 | |||||
chr2:171978128
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.976-1119G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978128 | ||||||
chr2:171978172
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0205 | 2 | NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.976-1075C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978172 | ||||||
chr2:171978213
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(68): Show | 71 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.976-1034C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978213 | ||||||
chr2:171978369
|
T | G | 32 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(29): Show | 32 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.976-878T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978369 | ||||||
chr2:171978438
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.976-809C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978438 | ||||||
chr2:171978562
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.976-685C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978562 | ||||||
chr2:171978579
|
C | CTGAG | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.976-667_976-666ins others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978579 | |||||
chr2:171978671
|
G | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG02723.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.976-576G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978671 | ||||||
chr2:171978695
|
T | G | 13 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0167others(10): Show | 13 | HG02056.hp2 NA18941.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.976-552T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978695 | ||||||
chr2:171978922
|
C | CA | 34 | a0001c0001t0001g0043a0001c0001t0001g0117a0001c0001t0001g0118others(31): Show | 34 | HG00558.hp1 HG00733.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.976-304dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978922 | |||||
chr2:171979046
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0270others(28): Show | 32 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.976-201G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979046 | ||||||
chr2:171979090
|
C | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.976-157C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979090 | ||||||
chr2:171979240
|
A | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0058 | 2 | HG01069.hp1 HG01071.hp1 |
splice_region_variant&intron_variant | LOW | c.976-7A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979240 | ||||||
chr2:171979450
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1092+87T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979450 | ||||||
chr2:171979516
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1092+153T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979516 | ||||||
chr2:171979559
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1092+196G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979559 | ||||||
chr2:171979678
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 5 | HG00609.hp2 NA18949.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+315G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979678 | ||||||
chr2:171979754
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1092+391C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979754 | ||||||
chr2:171979806
|
T | TGAAAA | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0159 | 3 | HG02809.hp2 HG02970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1092+464_1092+468d others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 171979806 | |||||
chr2:171979999
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0065 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1092+636C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979999 | ||||||
chr2:171980111
|
T | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1092+748T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980111 | ||||||
chr2:171980419
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1092+1056A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980419 | ||||||
chr2:171980622
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0320 | 3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1092+1259G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980622 | ||||||
chr2:171980681
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1092+1318C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980681 | ||||||
chr2:171980855
|
C | CA | 6 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0001g0204others(3): Show | 6 | HG02056.hp2 HG02074.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+1508dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 171980855 | |||||
chr2:171980871
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1092+1508A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980871 | ||||||
chr2:171980873
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1092+1510T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980873 | ||||||
chr2:171980873
|
T | TA | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 60 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1092+1510_1092+151 others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980873 | ||||||
chr2:171980874
|
T | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1092+1511T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980874 | ||||||
chr2:171980875
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0238 | 3 | HG03942.hp2 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1092+1512A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980875 | ||||||
chr2:171980941
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1092+1578G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980941 | ||||||
chr2:171980976
|
C | T | 68 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0146others(65): Show | 68 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1092+1613C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980976 | ||||||
chr2:171981112
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1092+1749G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981112 | ||||||
chr2:171981332
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1093-1853T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981332 | ||||||
chr2:171981343
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1093-1842G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981343 | ||||||
chr2:171982039
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1093-1146G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982039 | ||||||
chr2:171982203
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1093-982A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982203 | ||||||
chr2:171982589
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0225 | 3 | HG02004.hp1 HG06807.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1093-596C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982589 | ||||||
chr2:171982912
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-273T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982912 | ||||||
chr2:171982914
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-271G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982914 | ||||||
chr2:171982915
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-270A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982915 | ||||||
chr2:171983049
|
C | A | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1093-136C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171983049 | ||||||
chr2:171983081
|
G | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0270others(29): Show | 33 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1093-104G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171983081 |