geneid | 3032 |
---|---|
ensemblid | ENSG00000138029.14 |
hgncid | 4803 |
symbol | HADHB |
name | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta |
refseq_nuc | NM_000183.3 |
refseq_prot | NP_000174.1 |
ensembl_nuc | ENST00000317799.10 |
ensembl_prot | ENSP00000325136.5 |
mane_status | MANE Select |
chr | chr2 |
start | 26244939 |
end | 26290465 |
strand | + |
ver | v1.2 |
region | chr2:26244939-26290465 |
region5000 | chr2:26239939-26295465 |
regionname0 | HADHB_chr2_26244939_26290465 |
regionname5000 | HADHB_chr2_26239939_26295465 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 475 | 188 | 60 | 48 | 42 | 14 | 23 | 34 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0002 | 1/0 | 474 | 95 | 14 | 20 | 54 | 0 | 6 | 38 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0003 | 0/0 | 475 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0004 | 0/0 | 474 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0005 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1428 | 127 | 49 | 41 | 14 | 8 | 14 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0002 | 1/0 | 1425 | 95 | 14 | 20 | 54 | 0 | 6 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0003 | 0/0 | 1428 | 53 | 3 | 7 | 28 | 6 | 9 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0004 | 0/0 | 1428 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0005 | 0/0 | 1428 | 5 | 3 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0006 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
c0007 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 573 | 175 | 50 | 46 | 41 | 14 | 23 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
t0002 | 1/0 | 573 | 94 | 13 | 19 | 54 | 0 | 7 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
t0003 | 0/0 | 573 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
t0004 | 0/0 | 573 | 6 | 4 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
t0005 | 0/0 | 573 | 6 | 3 | 3 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
t0006 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 4 | 12 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1428 | 127 | 49 | 41 | 14 | 8 | 14 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0003 | 0/0 | 1428 | 53 | 3 | 7 | 28 | 6 | 9 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0004 | 0/0 | 1428 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0002c0002 | 1/0 | 1425 | 95 | 14 | 20 | 54 | 0 | 6 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0003c0005 | 0/0 | 1428 | 5 | 3 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0004c0007 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0005c0006 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2000 | 120 | 45 | 38 | 14 | 8 | 14 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0001t0004 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0001t0005 | 0/0 | 2000 | 6 | 3 | 3 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0003t0001 | 0/0 | 2000 | 52 | 3 | 7 | 27 | 6 | 9 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0003t0006 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0001c0004t0003 | 0/0 | 2000 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0002c0002t0001 | 0/0 | 1997 | 2 | 1 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0002c0002t0002 | 1/0 | 1997 | 93 | 13 | 19 | 54 | 0 | 6 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0003c0005t0004 | 0/0 | 2000 | 5 | 3 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0004c0007t0002 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
a0005c0006t0001 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | copy fasta | chr2 | 26239939 | 26295465 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0005g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0003t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0001c0004t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0001 | 0/0 | 16 | 0 | 4 | 12 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0003c0005t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0003c0005t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0003c0005t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0003c0005t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0004c0007t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
a0005c0006t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0035 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0052 | EUR | FIN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0045 | EUR | FIN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | CHS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CHS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0239 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0230 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01167 | hp2 | a0003 | c0005 | t0004 | g0017 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01169 | hp2 | a0003 | c0005 | t0004 | g0017 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0196 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0226 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0201 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0238 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0055 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0206 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | CDX | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | CDX | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0192 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02572 | hp2 | a0001 | c0004 | t0003 | g0219 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0212 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0165 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0185 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02717 | hp1 | a0005 | c0006 | t0001 | g0243 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0166 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0036 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03017 | hp2 | a0004 | c0007 | t0002 | g0088 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0237 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03195 | hp2 | a0001 | c0004 | t0003 | g0218 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03225 | hp1 | a0001 | c0004 | t0003 | g0217 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03225 | hp2 | a0003 | c0005 | t0004 | g0081 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03486 | hp2 | a0003 | c0005 | t0004 | g0089 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03516 | hp2 | a0001 | c0004 | t0003 | g0193 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03540 | hp2 | a0001 | c0004 | t0003 | g0187 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0010 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0044 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0210 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0222 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0179 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | CHB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18988 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18991 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19070 | hp2 | a0001 | c0003 | t0006 | g0061 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0026 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0010 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0054 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
HG06807 | hp2 | a0003 | c0005 | t0004 | g0245 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0188 | REF | REF | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26254257
|
G | GACT | 3 | a0001a0003a0005 | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
disruptive_inframe_insertion | MODERATE | c.5_7dupCTA | p.Thr2dup | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 2/16 | 68/1997 | 8/1425 | 3/474 | INFO_REALIGN_3_PRIME | chr2 | 26254257 | |
chr2:26280012
|
A | G | 1 | a0003 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
missense_variant | MODERATE | c.830A>G | p.Lys277Arg | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 890/1997 | 830/1425 | 277/474 | chr2 | 26280012 | ||
chr2:26285512
|
A | G | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1330A>G | p.Arg444Gly | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/16 | 1390/1997 | 1330/1425 | 444/474 | chr2 | 26285512 | ||
chr2:26285566
|
G | A | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1384G>A | p.Gly462Arg | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/16 | 1444/1997 | 1384/1425 | 462/474 | chr2 | 26285566 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26279284
|
C | T | 1 | a0003c0005 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.780C>T | p.Leu260Leu | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/16 | 840/1997 | 780/1425 | 260/474 | chr2 | 26279284 | ||
chr2:26280007
|
T | C | 1 | a0001c0003 | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
synonymous_variant | LOW | c.825T>C | p.Val275Val | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 885/1997 | 825/1425 | 275/474 | chr2 | 26280007 | ||
chr2:26280073
|
C | T | 1 | a0003c0005 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.891C>T | p.Ile297Ile | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 951/1997 | 891/1425 | 297/474 | chr2 | 26280073 | ||
chr2:26282877
|
G | A | 1 | a0001c0004 | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
synonymous_variant | LOW | c.966G>A | p.Ala322Ala | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 11/16 | 1026/1997 | 966/1425 | 322/474 | chr2 | 26282877 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26290005
|
A | G | 1 | a0001c0003t0006 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 52 | chr2 | 26290005 | |||||
chr2:26290089
|
G | C | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(6): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 136 | chr2 | 26290089 | |||||
chr2:26290149
|
A | G | 2 | a0001c0001t0005a0001c0004t0003 | 14 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 196 | chr2 | 26290149 | |||||
chr2:26290304
|
C | G | 1 | a0001c0004t0003 | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*351C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 351 | chr2 | 26290304 | |||||
chr2:26290439
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0004t0003others(1): Show | 20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*486G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 486 | chr2 | 26290439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26245135
|
A | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+145A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245135 | ||||||
chr2:26245263
|
G | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+273G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245263 | ||||||
chr2:26245263
|
GGTGT | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+287_-9+290delTG others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245263 | |||||
chr2:26245265
|
T | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 7 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+275T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245265 | ||||||
chr2:26245265
|
TGTGTGTG others(21): Show |
T | 1 | a0002c0002t0002g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+283_-9+310delTG others(26): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245265 | |||||
chr2:26245281
|
G | T | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+291G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245281 | ||||||
chr2:26245283
|
TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | NA18980.hp1 NA18989.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-9+306_-9+315delGT others(8): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245283 | |||||
chr2:26245285
|
T | G | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+295T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245285 | ||||||
chr2:26245475
|
G | C | 1 | a0002c0002t0002g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9+485G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245475 | ||||||
chr2:26245497
|
G | C | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+507G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245497 | ||||||
chr2:26245556
|
A | G | 1 | a0002c0002t0002g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+566A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245556 | ||||||
chr2:26245563
|
C | T | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+573C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245563 | ||||||
chr2:26245825
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+835C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245825 | ||||||
chr2:26245850
|
G | A | 3 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0073 | 3 | HG02809.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+860G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245850 | ||||||
chr2:26245910
|
C | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+920C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245910 | ||||||
chr2:26245923
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-9+933C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245923 | ||||||
chr2:26246210
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG01346.hp2 HG01358.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1220G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246210 | ||||||
chr2:26246285
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+1295G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246285 | ||||||
chr2:26246347
|
C | CTT | 45 | a0001c0001t0004g0236a0001c0003t0001g0005a0001c0003t0001g0008others(42): Show | 50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-9+1370_-9+1371dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | |||||
chr2:26246347
|
C | CTTT | 6 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+1369_-9+1371dup others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | |||||
chr2:26246347
|
CT | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+1371delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | |||||
chr2:26246366
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9+1376C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246366 | ||||||
chr2:26246475
|
G | A | 1 | a0004c0007t0002g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-9+1485G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246475 | ||||||
chr2:26246575
|
A | C | 1 | a0002c0002t0002g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+1585A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246575 | ||||||
chr2:26246589
|
C | G | 52 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(49): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-9+1599C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246589 | ||||||
chr2:26246792
|
TATA | T | 5 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(2): Show | 8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1805_-9+1807del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246792 | |||||
chr2:26246920
|
G | A | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+1930G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246920 | ||||||
chr2:26246974
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+1984G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246974 | ||||||
chr2:26247161
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-9+2171C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247161 | ||||||
chr2:26247182
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2192G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247182 | ||||||
chr2:26247276
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2286T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247276 | ||||||
chr2:26247349
|
A | T | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+2359A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247349 | ||||||
chr2:26247414
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2424T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247414 | ||||||
chr2:26247616
|
T | A | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+2626T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247616 | ||||||
chr2:26247700
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2710G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247700 | ||||||
chr2:26247701
|
A | G | 1 | a0002c0002t0002g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+2711A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247701 | ||||||
chr2:26247719
|
T | G | 1 | a0002c0002t0002g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+2729T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247719 | ||||||
chr2:26247888
|
T | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2898T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247888 | ||||||
chr2:26248025
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9+3035G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248025 | ||||||
chr2:26248281
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9+3291G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248281 | ||||||
chr2:26248305
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3315G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248305 | ||||||
chr2:26248385
|
C | CTT | 4 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0003t0001g0237others(1): Show | 7 | HG00733.hp2 HG01167.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3407_-9+3408dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248385 | |||||
chr2:26248402
|
A | G | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+3412A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248402 | ||||||
chr2:26248473
|
T | TTTC | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3485_-9+3486ins others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248473 | |||||
chr2:26248486
|
A | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3496A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248486 | ||||||
chr2:26248490
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+3500A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248490 | ||||||
chr2:26248496
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-9+3506G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248496 | ||||||
chr2:26248598
|
T | C | 1 | a0002c0002t0002g0093 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-9+3608T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248598 | ||||||
chr2:26248650
|
C | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(95): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.-9+3660C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248650 | ||||||
chr2:26248751
|
A | AAAC | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3779_-9+3781dup others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248751 | |||||
chr2:26248755
|
A | C | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+3765A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248755 | ||||||
chr2:26248783
|
G | A | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+3793G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248783 | ||||||
chr2:26248918
|
G | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3928G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248918 | ||||||
chr2:26248972
|
G | A | 1 | a0002c0002t0002g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+3982G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248972 | ||||||
chr2:26249011
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-9+4021C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249011 | ||||||
chr2:26249028
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4038A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249028 | ||||||
chr2:26249081
|
T | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4091T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249081 | ||||||
chr2:26249309
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9+4319G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249309 | ||||||
chr2:26249328
|
C | T | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+4338C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249328 | ||||||
chr2:26249344
|
C | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4354C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249344 | ||||||
chr2:26249454
|
T | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4464T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249454 | ||||||
chr2:26249466
|
G | A | 1 | a0002c0002t0002g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-9+4476G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249466 | ||||||
chr2:26249565
|
A | G | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+4575A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249565 | ||||||
chr2:26249629
|
T | C | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-4618T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249629 | ||||||
chr2:26249675
|
T | G | 2 | a0001c0004t0003g0165a0001c0004t0003g0166 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8-4572T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249675 | ||||||
chr2:26249800
|
GT | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4446delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249800 | ||||||
chr2:26249850
|
T | C | 43 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(40): Show | 48 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8-4397T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249850 | ||||||
chr2:26249985
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8-4262T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249985 | ||||||
chr2:26250024
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-8-4223G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250024 | ||||||
chr2:26250033
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-4214G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250033 | ||||||
chr2:26250153
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4094T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250153 | ||||||
chr2:26250157
|
A | G | 1 | a0002c0002t0002g0231 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-8-4090A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250157 | ||||||
chr2:26250230
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-8-4017C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250230 | ||||||
chr2:26250342
|
A | G | 1 | a0001c0003t0001g0010 | 2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-8-3905A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250342 | ||||||
chr2:26250377
|
A | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-3870A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250377 | ||||||
chr2:26250789
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3458A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250789 | ||||||
chr2:26250866
|
ATGT | A | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-3379_-8-3377del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26250866 | |||||
chr2:26251036
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3211C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251036 | ||||||
chr2:26251066
|
A | ACACTAAA others(323): Show |
1 | a0001c0003t0001g0025 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(330): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251066
|
A | ACACTAAA others(324): Show |
25 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(22): Show | 30 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(331): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251066
|
A | ACACTAAA others(324): Show |
1 | a0001c0003t0001g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(331): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251066
|
A | ACACTAAA others(325): Show |
17 | a0001c0003t0001g0024a0001c0003t0001g0043a0001c0003t0001g0044others(14): Show | 17 | HG00280.hp1 HG00280.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(332): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251066
|
A | ACACTAAA others(325): Show |
1 | a0001c0003t0001g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(332): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251066
|
A | ACACTAAA others(326): Show |
1 | a0001c0003t0001g0059 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(333): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | |||||
chr2:26251132
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-8-3115G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251132 | ||||||
chr2:26251190
|
T | C | 1 | a0002c0002t0002g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-8-3057T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251190 | ||||||
chr2:26251517
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2730G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251517 | ||||||
chr2:26251580
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2667C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251580 | ||||||
chr2:26251661
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-8-2586G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251661 | ||||||
chr2:26251763
|
T | A | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-2484T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251763 | ||||||
chr2:26251951
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-8-2296G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251951 | ||||||
chr2:26252035
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-2212C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252035 | ||||||
chr2:26252178
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2069G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252178 | ||||||
chr2:26252400
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-8-1847T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252400 | ||||||
chr2:26252452
|
CT | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1794delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252452 | ||||||
chr2:26252554
|
A | G | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-1693A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252554 | ||||||
chr2:26252608
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1639A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252608 | ||||||
chr2:26252634
|
A | G | 1 | a0002c0002t0002g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-1613A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252634 | ||||||
chr2:26252792
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1455T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252792 | ||||||
chr2:26253057
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-1190A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253057 | ||||||
chr2:26253072
|
C | T | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-8-1175C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253072 | ||||||
chr2:26253296
|
G | GA | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-8-946dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253296 | |||||
chr2:26253361
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8-886G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253361 | ||||||
chr2:26253366
|
T | C | 2 | a0001c0003t0001g0060a0001c0003t0006g0061 | 2 | HG01069.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-8-881T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253366 | ||||||
chr2:26253478
|
T | C | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-769T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253478 | ||||||
chr2:26253580
|
C | T | 1 | a0002c0002t0002g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8-667C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253580 | ||||||
chr2:26253583
|
T | C | 1 | a0002c0002t0002g0169 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-8-664T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253583 | ||||||
chr2:26253683
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-564G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253683 | ||||||
chr2:26253698
|
A | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-549A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253698 | ||||||
chr2:26253795
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-452G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253795 | ||||||
chr2:26253857
|
A | AAAAT | 77 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0018others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-8-346_-8-343dupTA others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | |||||
chr2:26253857
|
A | AAAATAAA others(1): Show |
29 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0067others(26): Show | 31 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-350_-8-343dupTA others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | |||||
chr2:26253857
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0002t0002g0229 | 3 | HG03704.hp1 NA18944.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-8-354_-8-343dupTA others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | |||||
chr2:26253857
|
AAAAT | A | 54 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(51): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-346_-8-343delTA others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | |||||
chr2:26253857
|
AAAATAAA others(1): Show |
A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-350_-8-343delTA others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | |||||
chr2:26253861
|
T | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0003t0001g0040 | 6 | HG00733.hp2 HG01167.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-386T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253861 | ||||||
chr2:26253865
|
T | A | 40 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(37): Show | 45 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-382T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253865 | ||||||
chr2:26253869
|
T | A | 12 | a0001c0003t0001g0008a0001c0003t0001g0026a0001c0003t0001g0027others(9): Show | 13 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-378T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253869 | ||||||
chr2:26253912
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-335G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253912 | ||||||
chr2:26254109
|
A | G | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(167): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-8-138A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26254109 | ||||||
chr2:26254376
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-54C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 2/15 | chr2 | 26254376 | ||||||
chr2:26254682
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+208A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254682 | ||||||
chr2:26254747
|
T | G | 1 | a0002c0002t0002g0181 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.109+273T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254747 | ||||||
chr2:26254782
|
G | A | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.109+308G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254782 | ||||||
chr2:26254845
|
A | G | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.109+371A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254845 | ||||||
chr2:26254923
|
T | G | 1 | a0002c0002t0002g0182 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.109+449T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254923 | ||||||
chr2:26255185
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+711C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255185 | ||||||
chr2:26255193
|
A | G | 1 | a0002c0002t0002g0216 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.109+719A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255193 | ||||||
chr2:26255227
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+753C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255227 | ||||||
chr2:26255228
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+754G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255228 | ||||||
chr2:26255321
|
G | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+847G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255321 | ||||||
chr2:26255485
|
C | T | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+1011C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255485 | ||||||
chr2:26255498
|
CA | C | 54 | a0001c0001t0001g0022a0001c0001t0001g0097a0001c0003t0001g0030others(51): Show | 76 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+1040delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26255498 | |||||
chr2:26255511
|
A | G | 1 | a0002c0002t0002g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+1037A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255511 | ||||||
chr2:26255523
|
G | GA | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.109+1055dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26255523 | |||||
chr2:26255577
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.109+1103G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255577 | ||||||
chr2:26255603
|
C | A | 2 | a0002c0002t0002g0183a0002c0002t0002g0184 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.109+1129C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255603 | ||||||
chr2:26255655
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1181G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255655 | ||||||
chr2:26255818
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.109+1344G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255818 | ||||||
chr2:26255930
|
G | T | 1 | a0002c0002t0002g0014 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.109+1456G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255930 | ||||||
chr2:26256115
|
T | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+1641T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256115 | ||||||
chr2:26256201
|
G | A | 1 | a0001c0004t0003g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+1727G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256201 | ||||||
chr2:26256285
|
AT | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1821delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256285 | |||||
chr2:26256527
|
GTA | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(162): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.109+2072_109+2073d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256527 | |||||
chr2:26256527
|
GTATA | G | 49 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(46): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.109+2070_109+2073d others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256527 | |||||
chr2:26256529
|
A | G | 2 | a0003c0005t0004g0081a0003c0005t0004g0089 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+2055A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256529 | ||||||
chr2:26256531
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0167a0003c0005t0004g0017others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2057A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256531 | ||||||
chr2:26256583
|
C | G | 5 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(2): Show | 8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+2109C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256583 | ||||||
chr2:26256867
|
C | A | 3 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0003t0001g0049 | 3 | HG03688.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.109+2393C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256867 | ||||||
chr2:26257043
|
A | G | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+2569A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257043 | ||||||
chr2:26257078
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.109+2604A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257078 | ||||||
chr2:26257084
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2610C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257084 | ||||||
chr2:26257160
|
G | A | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.109+2686G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257160 | ||||||
chr2:26257269
|
C | T | 1 | a0001c0004t0003g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+2795C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257269 | ||||||
chr2:26257375
|
C | T | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.109+2901C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257375 | ||||||
chr2:26257560
|
C | T | 43 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(40): Show | 64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.109+3086C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257560 | ||||||
chr2:26257752
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109+3278G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257752 | ||||||
chr2:26257774
|
C | G | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.109+3300C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257774 | ||||||
chr2:26257836
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3362A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257836 | ||||||
chr2:26257892
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3418G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257892 | ||||||
chr2:26257906
|
C | G | 2 | a0003c0005t0004g0081a0003c0005t0004g0089 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+3432C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257906 | ||||||
chr2:26257930
|
C | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3456C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257930 | ||||||
chr2:26257989
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3515A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257989 | ||||||
chr2:26258116
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.109+3642G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258116 | ||||||
chr2:26258173
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109+3699A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258173 | ||||||
chr2:26258176
|
C | G | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+3702C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258176 | ||||||
chr2:26258190
|
T | C | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+3716T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258190 | ||||||
chr2:26258419
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3945C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258419 | ||||||
chr2:26258433
|
A | G | 1 | a0001c0003t0001g0056 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.109+3959A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258433 | ||||||
chr2:26258578
|
A | G | 232 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(229): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.109+4104A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258578 | ||||||
chr2:26258591
|
G | A | 45 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0066others(42): Show | 48 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.109+4117G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258591 | ||||||
chr2:26258917
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+4443C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258917 | ||||||
chr2:26258938
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-4442T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258938 | ||||||
chr2:26259091
|
C | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-4289C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259091 | ||||||
chr2:26259117
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-4263T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259117 | ||||||
chr2:26259261
|
A | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-4119A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259261 | ||||||
chr2:26259492
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.110-3888C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259492 | ||||||
chr2:26259493
|
C | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-3887C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259493 | ||||||
chr2:26259544
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3836A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259544 | ||||||
chr2:26259558
|
A | G | 6 | a0002c0002t0002g0014a0002c0002t0002g0069a0002c0002t0002g0183others(3): Show | 7 | HG02257.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-3822A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259558 | ||||||
chr2:26259826
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-3554C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259826 | ||||||
chr2:26259946
|
C | T | 1 | a0001c0003t0001g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.110-3434C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259946 | ||||||
chr2:26259964
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | NA18980.hp1 NA18989.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.110-3416G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259964 | ||||||
chr2:26260013
|
T | C | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.110-3367T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260013 | ||||||
chr2:26260081
|
G | GGTT | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.110-3299_110-3298i others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260081 | ||||||
chr2:26260081
|
G | GT | 51 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0123others(48): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.110-3281dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | |||||
chr2:26260081
|
G | GTT | 10 | a0001c0001t0004g0236a0001c0003t0001g0010a0001c0003t0001g0028others(7): Show | 11 | HG00738.hp1 HG01981.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-3282_110-3281d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | |||||
chr2:26260081
|
G | GTTT | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-3283_110-3281d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | |||||
chr2:26260176
|
T | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-3204T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260176 | ||||||
chr2:26260203
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3177T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260203 | ||||||
chr2:26260222
|
T | C | 5 | a0002c0002t0002g0069a0002c0002t0002g0183a0002c0002t0002g0184others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-3158T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260222 | ||||||
chr2:26260240
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0248others(1): Show | 4 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-3140C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260240 | ||||||
chr2:26260359
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-3021G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260359 | ||||||
chr2:26260491
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.110-2889G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260491 | ||||||
chr2:26260510
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-2870T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260510 | ||||||
chr2:26260594
|
C | G | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-2786C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260594 | ||||||
chr2:26260596
|
C | T | 1 | a0002c0002t0002g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110-2784C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260596 | ||||||
chr2:26260602
|
A | C | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-2778A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260602 | ||||||
chr2:26260696
|
C | G | 1 | a0002c0002t0002g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.110-2684C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260696 | ||||||
chr2:26260832
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.110-2548C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260832 | ||||||
chr2:26260833
|
A | G | 2 | a0002c0002t0002g0209a0002c0002t0002g0212 | 2 | HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.110-2547A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260833 | ||||||
chr2:26261190
|
AAAC | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-2179_110-2177d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261190 | |||||
chr2:26261212
|
A | AC | 18 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0075others(15): Show | 19 | HG00735.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.110-2158dupC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | |||||
chr2:26261212
|
A | ACC | 66 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0018others(63): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.110-2159_110-2158d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | |||||
chr2:26261212
|
A | ACCC | 16 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0120others(13): Show | 16 | HG00741.hp2 HG01175.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-2160_110-2158d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | |||||
chr2:26261212
|
AC | A | 14 | a0001c0003t0001g0237a0001c0003t0001g0238a0001c0004t0003g0165others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-2158delC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | |||||
chr2:26261257
|
A | G | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-2123A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261257 | ||||||
chr2:26261321
|
A | T | 2 | a0003c0005t0004g0081a0003c0005t0004g0089 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-2059A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261321 | ||||||
chr2:26261481
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.110-1899G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261481 | ||||||
chr2:26261500
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1880C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261500 | ||||||
chr2:26261512
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1868T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261512 | ||||||
chr2:26261535
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.110-1845G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261535 | ||||||
chr2:26261642
|
T | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1738T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261642 | ||||||
chr2:26261770
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1610A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261770 | ||||||
chr2:26261990
|
A | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1390A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261990 | ||||||
chr2:26262167
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-1213C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262167 | ||||||
chr2:26262337
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1043G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262337 | ||||||
chr2:26262455
|
A | T | 1 | a0002c0002t0001g0221 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-925A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262455 | ||||||
chr2:26262471
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-909C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262471 | ||||||
chr2:26262718
|
A | G | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-662A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262718 | ||||||
chr2:26262722
|
C | T | 2 | a0001c0003t0001g0026a0001c0003t0001g0046 | 2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.110-658C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262722 | ||||||
chr2:26262892
|
A | C | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-488A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262892 | ||||||
chr2:26263144
|
C | G | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.110-236C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26263144 | ||||||
chr2:26263298
|
TA | T | 14 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(11): Show | 14 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-65delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26263298 | |||||
chr2:26263538
|
T | C | 1 | a0001c0001t0005g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.209+59T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26263538 | ||||||
chr2:26263687
|
C | T | 1 | a0001c0003t0001g0037 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.209+208C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26263687 | ||||||
chr2:26264035
|
G | A | 1 | a0002c0002t0002g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.209+556G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264035 | ||||||
chr2:26264457
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209+978G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264457 | ||||||
chr2:26264498
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.209+1019C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264498 | ||||||
chr2:26264546
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1067T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264546 | ||||||
chr2:26264553
|
C | CA | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(92): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.209+1094dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | |||||
chr2:26264553
|
C | CAA | 10 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0001t0001g0096others(7): Show | 10 | HG00738.hp2 HG01952.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.209+1093_209+1094d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | |||||
chr2:26264553
|
CA | C | 10 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(7): Show | 13 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.209+1094delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | |||||
chr2:26264573
|
A | G | 42 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(39): Show | 63 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.209+1094A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264573 | ||||||
chr2:26264625
|
A | ATG | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 52 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264625 | |||||
chr2:26264625
|
A | G | 1 | a0001c0003t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.209+1146A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264625 | ||||||
chr2:26264625
|
ATG | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264625 | |||||
chr2:26264749
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1270C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264749 | ||||||
chr2:26264838
|
A | T | 1 | a0002c0002t0002g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.209+1359A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264838 | ||||||
chr2:26264864
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1385C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264864 | ||||||
chr2:26265002
|
AAAG | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+1533_209+1535d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265002 | |||||
chr2:26265041
|
G | A | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.209+1562G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265041 | ||||||
chr2:26265338
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209+1859G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265338 | ||||||
chr2:26265347
|
A | G | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.209+1868A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265347 | ||||||
chr2:26265352
|
T | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0241others(2): Show | 5 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+1873T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265352 | ||||||
chr2:26265358
|
G | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+1879G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265358 | ||||||
chr2:26265497
|
G | C | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.209+2018G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265497 | ||||||
chr2:26265585
|
A | G | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209+2106A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265585 | ||||||
chr2:26265595
|
C | G | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209+2116C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265595 | ||||||
chr2:26265597
|
A | AAAC | 9 | a0001c0001t0001g0108a0001c0001t0001g0154a0001c0001t0001g0242others(6): Show | 12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.209+2142_209+2144d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | |||||
chr2:26265597
|
A | AAACAACA others(2): Show |
43 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(40): Show | 48 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.209+2136_209+2144d others(11): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | |||||
chr2:26265597
|
A | AAACAACA others(8): Show |
2 | a0001c0003t0001g0045a0001c0003t0001g0052 | 2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.209+2130_209+2144d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | |||||
chr2:26265597
|
AAAC | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+2142_209+2144d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | |||||
chr2:26265953
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.209+2474C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265953 | ||||||
chr2:26266172
|
G | A | 10 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(7): Show | 14 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.209+2693G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266172 | ||||||
chr2:26266220
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.209+2741C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266220 | ||||||
chr2:26266570
|
T | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+3091T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266570 | ||||||
chr2:26266655
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.209+3176G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266655 | ||||||
chr2:26266708
|
T | C | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209+3229T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266708 | ||||||
chr2:26266709
|
A | G | 1 | a0002c0002t0002g0182 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.209+3230A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266709 | ||||||
chr2:26266748
|
C | T | 1 | a0001c0003t0001g0039 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.210-3205C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266748 | ||||||
chr2:26266752
|
C | T | 1 | a0001c0003t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210-3201C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266752 | ||||||
chr2:26266753
|
A | G | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.210-3200A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266753 | ||||||
chr2:26266862
|
A | T | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.210-3091A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266862 | ||||||
chr2:26266871
|
C | CA | 11 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(8): Show | 14 | HG00733.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.210-3059dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(47): Show | 54 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.210-3068_210-3059d others(12): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0066a0001c0001t0001g0095a0001c0001t0001g0098others(15): Show | 18 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.210-3069_210-3059d others(13): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(5): Show |
10 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0110others(7): Show | 10 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-3070_210-3059d others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210-3071_210-3059d others(15): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0086a0001c0001t0001g0125a0001c0001t0001g0154others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-3072_210-3059d others(16): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-3073_210-3059d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0083 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.210-3074_210-3059d others(18): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.210-3078_210-3059d others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.210-3079_210-3059d others(23): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0128 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.210-3059_210-3058i others(32): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0246 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.210-3059_210-3058i others(33): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210-3059_210-3058i others(34): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266871
|
CA | C | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-3059delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | |||||
chr2:26266930
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.210-3023T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266930 | ||||||
chr2:26266998
|
A | G | 1 | a0002c0002t0002g0206 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.210-2955A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266998 | ||||||
chr2:26267029
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2924C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267029 | ||||||
chr2:26267063
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2890T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267063 | ||||||
chr2:26267119
|
A | C | 5 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(2): Show | 8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-2834A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267119 | ||||||
chr2:26267142
|
TTAAAAA | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-2806_210-2801d others(8): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26267142 | |||||
chr2:26267189
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2764T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267189 | ||||||
chr2:26267229
|
G | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2724G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267229 | ||||||
chr2:26267527
|
A | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2426A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267527 | ||||||
chr2:26267608
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.210-2345C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267608 | ||||||
chr2:26267631
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2322A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267631 | ||||||
chr2:26267743
|
G | T | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.210-2210G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267743 | ||||||
chr2:26267771
|
C | CA | 52 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0097others(49): Show | 73 | HG00408.hp1 HG01081.hp1 HG01123.hp1 others(70): Show |
intron_variant | MODIFIER | c.210-2164dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26267771 | |||||
chr2:26267850
|
T | C | 1 | a0001c0003t0001g0025 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.210-2103T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267850 | ||||||
chr2:26268003
|
G | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-1950G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268003 | ||||||
chr2:26268052
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1901A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268052 | ||||||
chr2:26268067
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1886A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268067 | ||||||
chr2:26268154
|
T | TAAATA | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1796_210-1792d others(7): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26268154 | |||||
chr2:26268254
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1699A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268254 | ||||||
chr2:26268297
|
T | C | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.210-1656T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268297 | ||||||
chr2:26268312
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210-1641A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268312 | ||||||
chr2:26268481
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.210-1472C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268481 | ||||||
chr2:26268493
|
T | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1460T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268493 | ||||||
chr2:26268524
|
A | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(84): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.210-1429A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268524 | ||||||
chr2:26268630
|
A | G | 5 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0217others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-1323A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268630 | ||||||
chr2:26268763
|
A | C | 1 | a0003c0005t0004g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.210-1190A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268763 | ||||||
chr2:26269042
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0140 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.210-911G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269042 | ||||||
chr2:26269201
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-752C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269201 | ||||||
chr2:26269249
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-704T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269249 | ||||||
chr2:26269352
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.210-601G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269352 | ||||||
chr2:26269443
|
A | G | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-510A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269443 | ||||||
chr2:26269496
|
T | C | 222 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(219): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.210-457T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269496 | ||||||
chr2:26269499
|
C | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.210-454C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269499 | ||||||
chr2:26269813
|
TGATGGAC others(7): Show |
T | 2 | a0001c0001t0001g0078a0001c0001t0001g0246 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.210-136_210-123del others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26269813 | |||||
chr2:26270235
|
A | T | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.254+238A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270235 | ||||||
chr2:26270308
|
G | A | 3 | a0002c0002t0002g0194a0002c0002t0002g0222a0002c0002t0002g0223 | 3 | HG00642.hp2 HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.254+311G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270308 | ||||||
chr2:26270579
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.254+582A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270579 | ||||||
chr2:26270640
|
C | T | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.254+643C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270640 | ||||||
chr2:26270729
|
C | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(160): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.254+732C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270729 | ||||||
chr2:26270749
|
A | G | 1 | a0001c0003t0001g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.254+752A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270749 | ||||||
chr2:26270878
|
C | CT | 10 | a0001c0001t0001g0085a0001c0001t0001g0124a0001c0001t0001g0129others(7): Show | 10 | HG00642.hp2 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.254+899dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26270878 | |||||
chr2:26270878
|
CT | C | 49 | a0001c0001t0001g0078a0001c0001t0001g0246a0001c0003t0001g0005others(46): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.254+899delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26270878 | |||||
chr2:26270885
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+888T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270885 | ||||||
chr2:26270910
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.254+913G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270910 | ||||||
chr2:26270934
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.254+937A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270934 | ||||||
chr2:26271004
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+1007G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271004 | ||||||
chr2:26271056
|
C | CT | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.254+1071dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26271056 | |||||
chr2:26271067
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.254+1070T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271067 | ||||||
chr2:26271451
|
G | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.254+1454G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271451 | ||||||
chr2:26271483
|
G | A | 4 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(1): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+1486G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271483 | ||||||
chr2:26271502
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.254+1505C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271502 | ||||||
chr2:26271560
|
T | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.254+1563T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271560 | ||||||
chr2:26271761
|
A | G | 1 | a0002c0002t0002g0190 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.254+1764A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271761 | ||||||
chr2:26271827
|
G | C | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.255-1824G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271827 | ||||||
chr2:26271887
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.255-1764A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271887 | ||||||
chr2:26271909
|
A | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-1742A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271909 | ||||||
chr2:26271918
|
A | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0067others(19): Show | 24 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.255-1733A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271918 | ||||||
chr2:26272227
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-1424G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272227 | ||||||
chr2:26272241
|
T | C | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.255-1410T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272241 | ||||||
chr2:26272346
|
C | CT | 7 | a0001c0001t0001g0147a0001c0001t0004g0236a0001c0001t0005g0004others(4): Show | 10 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.255-1289dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26272346 | |||||
chr2:26272346
|
CT | C | 45 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(42): Show | 67 | HG00408.hp1 HG01081.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.255-1289delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26272346 | |||||
chr2:26272424
|
C | T | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-1227C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272424 | ||||||
chr2:26272674
|
G | A | 1 | a0002c0002t0002g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.255-977G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272674 | ||||||
chr2:26272695
|
A | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-956A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272695 | ||||||
chr2:26272808
|
G | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-843G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272808 | ||||||
chr2:26272810
|
A | G | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-841A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272810 | ||||||
chr2:26272901
|
T | C | 5 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(2): Show | 8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-750T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272901 | ||||||
chr2:26272956
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-695G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272956 | ||||||
chr2:26273084
|
T | C | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.255-567T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273084 | ||||||
chr2:26273244
|
C | CAAACTAA others(15): Show |
2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-406_255-405ins others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26273244 | |||||
chr2:26273246
|
G | A | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-405G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273246 | ||||||
chr2:26273247
|
G | A | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-404G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273247 | ||||||
chr2:26273261
|
T | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(89): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.255-390T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273261 | ||||||
chr2:26273263
|
A | AT | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-380dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26273263 | |||||
chr2:26273318
|
G | C | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.255-333G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273318 | ||||||
chr2:26273431
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.255-220A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273431 | ||||||
chr2:26273441
|
C | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-210C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273441 | ||||||
chr2:26273556
|
C | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG00639.hp1 HG00642.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-95C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273556 | ||||||
chr2:26273850
|
G | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+100G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26273850 | ||||||
chr2:26274075
|
T | C | 1 | a0002c0002t0002g0197 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.354+325T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274075 | ||||||
chr2:26274157
|
C | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+407C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274157 | ||||||
chr2:26274158
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.354+408T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274158 | ||||||
chr2:26274313
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.354+563G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274313 | ||||||
chr2:26274360
|
C | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+610C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274360 | ||||||
chr2:26274406
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0111 | 2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.354+656T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274406 | ||||||
chr2:26274414
|
G | C | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.354+664G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274414 | ||||||
chr2:26274445
|
A | G | 1 | a0002c0002t0002g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.354+695A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274445 | ||||||
chr2:26274584
|
A | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+834A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274584 | ||||||
chr2:26274585
|
C | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+835C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274585 | ||||||
chr2:26274659
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+909G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274659 | ||||||
chr2:26274673
|
C | T | 46 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(43): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.354+923C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274673 | ||||||
chr2:26274785
|
C | G | 2 | a0001c0003t0001g0036a0001c0003t0001g0063 | 2 | HG02040.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.354+1035C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274785 | ||||||
chr2:26275005
|
C | T | 2 | a0003c0005t0004g0081a0003c0005t0004g0089 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.354+1255C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275005 | ||||||
chr2:26275190
|
ATTTCTTA others(77): Show |
A | 3 | a0002c0002t0002g0015a0002c0002t0002g0189a0002c0002t0002g0190 | 4 | HG00408.hp2 HG02056.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+1488_354+1571d others(86): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 26275190 | |||||
chr2:26275263
|
T | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+1513T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275263 | ||||||
chr2:26275354
|
G | A | 43 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(40): Show | 64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.354+1604G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275354 | ||||||
chr2:26275591
|
G | GC | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1479dupC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 26275591 | |||||
chr2:26275946
|
A | C | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1127A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275946 | ||||||
chr2:26276357
|
G | A | 2 | a0001c0003t0001g0024a0001c0003t0001g0055 | 2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.355-716G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26276357 | ||||||
chr2:26276485
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-588C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26276485 | ||||||
chr2:26277004
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.355-69T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26277004 | ||||||
chr2:26277047
|
C | A | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355-26C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26277047 | ||||||
chr2:26277182
|
C | T | 1 | a0002c0002t0002g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442+22C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277182 | ||||||
chr2:26277233
|
C | CT | 17 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 19 | HG00639.hp1 HG00642.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.442+95dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | |||||
chr2:26277233
|
CT | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(33): Show | 40 | HG00639.hp2 HG00733.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.442+95delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | |||||
chr2:26277233
|
CTT | C | 41 | a0001c0001t0001g0164a0001c0003t0001g0005a0001c0003t0001g0008others(38): Show | 45 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.442+94_442+95delTT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | |||||
chr2:26277284
|
C | G | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.442+124C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277284 | ||||||
chr2:26277683
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.442+523C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277683 | ||||||
chr2:26277763
|
G | A | 1 | a0003c0005t0004g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442+603G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277763 | ||||||
chr2:26277935
|
T | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-679T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277935 | ||||||
chr2:26277936
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-678C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277936 | ||||||
chr2:26277937
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-677A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277937 | ||||||
chr2:26278131
|
G | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-483G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278131 | ||||||
chr2:26278135
|
G | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-479G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278135 | ||||||
chr2:26278219
|
T | TA | 6 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0124others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-394dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26278219 | |||||
chr2:26278222
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.443-392G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278222 | ||||||
chr2:26278231
|
G | A | 6 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(3): Show | 9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-383G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278231 | ||||||
chr2:26278376
|
T | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.443-238T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278376 | ||||||
chr2:26278521
|
C | T | 7 | a0001c0003t0001g0008a0001c0003t0001g0026a0001c0003t0001g0029others(4): Show | 8 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-93C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278521 | ||||||
chr2:26279085
|
C | A | 56 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(53): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.631-50C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 8/15 | chr2 | 26279085 | ||||||
chr2:26279878
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.812-116T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279878 | ||||||
chr2:26279900
|
C | T | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.812-94C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279900 | ||||||
chr2:26279989
|
A | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.812-5A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279989 | ||||||
chr2:26280278
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+163C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280278 | ||||||
chr2:26280291
|
C | G | 3 | a0001c0003t0001g0062a0001c0003t0001g0237a0001c0003t0001g0238 | 3 | HG02055.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.933+176C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280291 | ||||||
chr2:26280570
|
A | G | 180 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(177): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.933+455A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280570 | ||||||
chr2:26280571
|
G | A | 43 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(40): Show | 64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+456G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280571 | ||||||
chr2:26280578
|
T | C | 16 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(13): Show | 20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.933+463T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280578 | ||||||
chr2:26280606
|
A | G | 43 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(40): Show | 64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+491A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280606 | ||||||
chr2:26280648
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.933+533T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280648 | ||||||
chr2:26280682
|
G | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 27 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.933+567G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280682 | ||||||
chr2:26280695
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.933+580A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280695 | ||||||
chr2:26280775
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02109.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.933+660C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280775 | ||||||
chr2:26280786
|
T | C | 64 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(61): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.933+671T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280786 | ||||||
chr2:26280853
|
C | CA | 6 | a0001c0001t0001g0021a0001c0001t0001g0095a0001c0001t0001g0102others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+766dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | |||||
chr2:26280853
|
CA | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0066others(82): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.933+766delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | |||||
chr2:26280853
|
CAA | C | 68 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0082others(65): Show | 85 | HG00408.hp1 HG00639.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.933+765_933+766del others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | |||||
chr2:26280853
|
CAAA | C | 45 | a0001c0001t0005g0004a0001c0001t0005g0240a0001c0003t0001g0005others(42): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.933+764_933+766del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | |||||
chr2:26280853
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0003t0001g0030a0001c0003t0001g0062 | 2 | NA19058.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.933+757_933+766del others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | |||||
chr2:26280926
|
A | G | 2 | a0001c0003t0001g0024a0001c0003t0001g0055 | 2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.933+811A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280926 | ||||||
chr2:26281151
|
T | TGTA | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.933+1038_933+1040d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26281151 | |||||
chr2:26281301
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0167 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.933+1186A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281301 | ||||||
chr2:26281314
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.933+1199A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281314 | ||||||
chr2:26281542
|
A | G | 2 | a0001c0003t0001g0009a0001c0003t0001g0051 | 3 | HG02074.hp1 NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.934-1303A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281542 | ||||||
chr2:26281568
|
G | A | 1 | a0001c0003t0001g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.934-1277G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281568 | ||||||
chr2:26281611
|
C | T | 1 | a0001c0003t0001g0039 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.934-1234C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281611 | ||||||
chr2:26281663
|
G | T | 1 | a0002c0002t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.934-1182G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281663 | ||||||
chr2:26281787
|
GC | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1057delC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281787 | ||||||
chr2:26282248
|
T | G | 1 | a0001c0003t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934-597T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282248 | ||||||
chr2:26282251
|
C | CTT | 11 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.934-574_934-573dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26282251 | |||||
chr2:26282251
|
CT | C | 55 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0117others(52): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.934-573delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26282251 | |||||
chr2:26282255
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.934-590T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282255 | ||||||
chr2:26282461
|
C | T | 1 | a0001c0003t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.934-384C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282461 | ||||||
chr2:26282469
|
C | T | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-376C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282469 | ||||||
chr2:26282505
|
C | T | 3 | a0002c0002t0002g0194a0002c0002t0002g0222a0002c0002t0002g0223 | 3 | HG00642.hp2 HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.934-340C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282505 | ||||||
chr2:26282576
|
T | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-269T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282576 | ||||||
chr2:26282578
|
T | C | 2 | a0003c0005t0004g0017a0003c0005t0004g0245 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.934-267T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282578 | ||||||
chr2:26282620
|
G | T | 1 | a0002c0002t0002g0231 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.934-225G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282620 | ||||||
chr2:26282990
|
A | G | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014-14A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 11/15 | chr2 | 26282990 | ||||||
chr2:26283231
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1061+180T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283231 | ||||||
chr2:26283449
|
G | A | 12 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(9): Show | 15 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1061+398G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283449 | ||||||
chr2:26283531
|
T | A | 4 | a0002c0002t0002g0199a0002c0002t0002g0213a0002c0002t0002g0214others(1): Show | 4 | HG00408.hp1 NA18612.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+480T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283531 | ||||||
chr2:26284208
|
A | T | 46 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(43): Show | 67 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.1149+4A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284208 | ||||||
chr2:26284238
|
A | G | 2 | a0001c0001t0001g0242a0005c0006t0001g0243 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149+34A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284238 | ||||||
chr2:26284322
|
A | G | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+118A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284322 | ||||||
chr2:26284350
|
A | T | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+146A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284350 | ||||||
chr2:26284548
|
C | T | 9 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0124others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-335C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284548 | ||||||
chr2:26284556
|
A | T | 1 | a0001c0003t0001g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1150-327A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284556 | ||||||
chr2:26284619
|
A | G | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-264A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284619 | ||||||
chr2:26284856
|
T | C | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1150-27T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284856 | ||||||
chr2:26285013
|
T | A | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224+56T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285013 | ||||||
chr2:26285048
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0137 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1224+91G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285048 | ||||||
chr2:26285208
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1225-199C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285208 | ||||||
chr2:26285319
|
A | G | 49 | a0001c0001t0001g0232a0001c0003t0001g0005a0001c0003t0001g0008others(46): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1225-88A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285319 | ||||||
chr2:26285333
|
G | A | 1 | a0002c0002t0002g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1225-74G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285333 | ||||||
chr2:26285345
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1225-62G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285345 | ||||||
chr2:26285628
|
G | A | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+57G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285628 | ||||||
chr2:26285739
|
G | GT | 6 | a0001c0001t0001g0160a0002c0002t0002g0168a0002c0002t0002g0184others(3): Show | 6 | HG02056.hp1 HG02074.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+186dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(1): Show |
33 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(30): Show | 38 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1389+179_1389+186d others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(2): Show |
12 | a0001c0003t0001g0034a0001c0003t0001g0036a0001c0003t0001g0040others(9): Show | 12 | HG00280.hp2 HG01175.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+178_1389+186d others(11): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(3): Show |
7 | a0001c0001t0001g0154a0001c0001t0005g0004a0001c0001t0005g0239others(4): Show | 10 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+177_1389+186d others(12): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0083a0001c0001t0004g0236 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1389+176_1389+186d others(13): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(5): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0084others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+175_1389+186d others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0082a0001c0001t0001g0164a0001c0001t0001g0167others(2): Show | 5 | HG01106.hp2 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+174_1389+186d others(15): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0115 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1389+182_1389+183i others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1389+172_1389+186d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0095 | 2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1389+170_1389+186d others(19): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(11): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(27): Show | 33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1389+169_1389+186d others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(12): Show |
32 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0079others(29): Show | 32 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(21): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(13): Show |
19 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 20 | HG00735.hp1 HG01261.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(14): Show |
10 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0097others(7): Show | 10 | HG01255.hp2 HG01981.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(23): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(15): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0129a0001c0001t0001g0161 | 3 | HG02280.hp1 HG03130.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1389+186_1389+187i others(24): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(16): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0134 | 3 | HG01346.hp2 HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1389+186_1389+187i others(25): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0110 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1389+186_1389+187i others(26): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285739
|
G | GTTTTTTT others(20): Show |
1 | a0001c0001t0001g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1389+186_1389+187i others(29): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | |||||
chr2:26285847
|
C | T | 4 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(1): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+276C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285847 | ||||||
chr2:26285913
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1389+342T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285913 | ||||||
chr2:26285984
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+413C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285984 | ||||||
chr2:26286273
|
A | G | 1 | a0001c0004t0003g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1389+702A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286273 | ||||||
chr2:26286594
|
G | C | 16 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(13): Show | 20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1389+1023G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286594 | ||||||
chr2:26286612
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+1041C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286612 | ||||||
chr2:26286726
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1389+1155G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286726 | ||||||
chr2:26286749
|
G | A | 48 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1389+1178G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286749 | ||||||
chr2:26286782
|
A | G | 43 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0012others(40): Show | 64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.1389+1211A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286782 | ||||||
chr2:26286811
|
TTG | T | 12 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(9): Show | 13 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1389+1242_1389+124 others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286811 | |||||
chr2:26286812
|
TG | T | 2 | a0001c0001t0005g0004a0001c0001t0005g0240 | 5 | HG01074.hp1 HG01167.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+1242delG | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286812 | ||||||
chr2:26286813
|
G | GT | 16 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0070others(13): Show | 16 | HG01261.hp2 HG01517.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1389+1260dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286813 | |||||
chr2:26286813
|
G | T | 10 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(7): Show | 10 | HG00639.hp2 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389+1242G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286813 | ||||||
chr2:26286813
|
GT | G | 46 | a0001c0001t0001g0118a0002c0002t0002g0001a0002c0002t0002g0003others(43): Show | 67 | HG00408.hp1 HG01070.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1389+1260delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286813 | |||||
chr2:26286819
|
T | G | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+1248T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286819 | ||||||
chr2:26286823
|
T | G | 1 | a0002c0002t0001g0221 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1389+1252T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286823 | ||||||
chr2:26286850
|
T | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+1279T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286850 | ||||||
chr2:26287161
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1389+1590G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287161 | ||||||
chr2:26287227
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1389+1656C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287227 | ||||||
chr2:26287281
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1389+1710A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287281 | ||||||
chr2:26287414
|
G | A | 8 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(5): Show | 12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+1843G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287414 | ||||||
chr2:26287787
|
T | G | 25 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(22): Show | 29 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1390-2131T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287787 | ||||||
chr2:26287995
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1390-1923G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287995 | ||||||
chr2:26288015
|
G | C | 4 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(1): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-1903G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288015 | ||||||
chr2:26288065
|
G | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240 | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-1853G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288065 | ||||||
chr2:26288070
|
T | C | 16 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(13): Show | 20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1390-1848T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288070 | ||||||
chr2:26288104
|
C | T | 8 | a0001c0001t0004g0236a0001c0001t0005g0004a0001c0001t0005g0239others(5): Show | 12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-1814C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288104 | ||||||
chr2:26288190
|
G | A | 8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1728G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288190 | ||||||
chr2:26288339
|
A | G | 1 | a0001c0003t0001g0050 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1390-1579A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288339 | ||||||
chr2:26288633
|
C | T | 4 | a0003c0005t0004g0017a0003c0005t0004g0081a0003c0005t0004g0089others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-1285C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288633 | ||||||
chr2:26288708
|
C | CA | 13 | a0001c0001t0005g0004a0001c0001t0005g0239a0001c0001t0005g0240others(10): Show | 16 | HG00733.hp2 HG01074.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1390-1202dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26288708 | |||||
chr2:26288708
|
C | CAA | 5 | a0001c0001t0004g0236a0003c0005t0004g0017a0003c0005t0004g0081others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1390-1203_1390-120 others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26288708 | |||||
chr2:26288973
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1390-945C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288973 | ||||||
chr2:26289016
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0118 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1390-902C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289016 | ||||||
chr2:26289017
|
G | A | 2 | a0001c0001t0001g0019a0002c0002t0002g0213 | 2 | NA19065.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1390-901G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289017 | ||||||
chr2:26289066
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1390-852C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289066 | ||||||
chr2:26289106
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1390-812C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289106 | ||||||
chr2:26289125
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1390-793C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289125 | ||||||
chr2:26289241
|
C | T | 1 | a0002c0002t0002g0201 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390-677C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289241 | ||||||
chr2:26289242
|
G | A | 2 | a0002c0002t0001g0220a0002c0002t0001g0221 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-676G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289242 | ||||||
chr2:26289432
|
T | TCACTTAA others(11): Show |
8 | a0001c0004t0003g0165a0001c0004t0003g0166a0001c0004t0003g0185others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-484_1390-467d others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26289432 | |||||
chr2:26289671
|
A | T | 1 | a0001c0003t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1390-247A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289671 | ||||||
chr2:26289733
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1390-185G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289733 | ||||||
chr2:26289733
|
G | C | 1 | a0002c0002t0002g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-185G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289733 | ||||||
chr2:26289865
|
T | G | 50 | a0001c0003t0001g0005a0001c0003t0001g0008a0001c0003t0001g0009others(47): Show | 55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1390-53T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289865 |