geneid | 22924 |
---|---|
ensemblid | ENSG00000084764.12 |
hgncid | 6892 |
symbol | MAPRE3 |
name | microtubule associated protein RP/EB family member 3 |
refseq_nuc | NM_012326.4 |
refseq_prot | NP_036458.2 |
ensembl_nuc | ENST00000233121.7 |
ensembl_prot | ENSP00000233121.2 |
mane_status | MANE Select |
chr | chr2 |
start | 26970637 |
end | 27027219 |
strand | + |
ver | v1.2 |
region | chr2:26970637-27027219 |
region5000 | chr2:26965637-27032219 |
regionname0 | MAPRE3_chr2_26970637_27027219 |
regionname5000 | MAPRE3_chr2_26965637_27032219 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 281 | 258 | 86 | 50 | 86 | 14 | 20 | 66 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 846 | 187 | 64 | 42 | 49 | 12 | 19 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
c0002 | 1/0 | 846 | 70 | 22 | 8 | 37 | 2 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
c0003 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1045 | 148 | 56 | 27 | 46 | 7 | 11 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
t0002 | 1/0 | 1045 | 108 | 29 | 23 | 39 | 7 | 9 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
t0003 | 0/0 | 1045 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
t0004 | 0/0 | 1045 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 846 | 187 | 64 | 42 | 49 | 12 | 19 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0002 | 1/0 | 846 | 70 | 22 | 8 | 37 | 2 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0003 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1890 | 137 | 46 | 26 | 46 | 7 | 11 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0001t0002 | 0/0 | 1890 | 50 | 18 | 16 | 3 | 5 | 8 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0002t0001 | 0/0 | 1890 | 11 | 10 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0002t0002 | 1/0 | 1890 | 57 | 11 | 7 | 36 | 2 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0002t0003 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0002t0004 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
a0001c0003t0002 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | copy fasta | chr2 | 26965637 | 27032219 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | FIN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | IBS | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | CDX | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02976 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0168 | SAS | STU | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | ASW | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0171 | EUR | TSI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0172 | EUR | TSI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | USA | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | USA | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | USA | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0188 | REF | REF | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27022293
|
C | T | 1 | a0001c0003 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.75C>T | p.Asn25Asn | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/7 | 248/1890 | 75/846 | 25/281 | chr2 | 27022293 | ||
chr2:27023417
|
C | T | 1 | a0001c0001 | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
synonymous_variant | LOW | c.207C>T | p.His69His | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 3/7 | 380/1890 | 207/846 | 69/281 | chr2 | 27023417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27026377
|
A | G | 2 | a0001c0001t0001a0001c0002t0001 | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*29A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 7/7 | 29 | chr2 | 27026377 | |||||
chr2:27026488
|
G | A | 1 | a0001c0002t0003 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 7/7 | 140 | chr2 | 27026488 | |||||
chr2:27026782
|
C | T | 1 | a0001c0002t0004 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 7/7 | 434 | chr2 | 27026782 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26970893
|
C | T | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+91C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26970893 | ||||||
chr2:26970993
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+191C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26970993 | ||||||
chr2:26971129
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-8+327A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971129 | ||||||
chr2:26971145
|
T | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-8+343T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971145 | ||||||
chr2:26971275
|
C | A | 1 | a0001c0001t0002g0118 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-8+473C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971275 | ||||||
chr2:26971540
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-8+738G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971540 | ||||||
chr2:26971545
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8+743C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971545 | ||||||
chr2:26971581
|
G | C | 1 | a0001c0002t0002g0120 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8+779G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971581 | ||||||
chr2:26971602
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+800C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971602 | ||||||
chr2:26971605
|
A | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+803A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971605 | ||||||
chr2:26971895
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8+1093G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26971895 | ||||||
chr2:26972017
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-8+1215T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972017 | ||||||
chr2:26972043
|
AG | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0002g0235others(1): Show | 4 | HG01109.hp2 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+1242delG | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972043 | ||||||
chr2:26972195
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-8+1393C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972195 | ||||||
chr2:26972283
|
T | C | 1 | a0001c0002t0002g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-8+1481T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972283 | ||||||
chr2:26972499
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8+1697C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972499 | ||||||
chr2:26972545
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+1743G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972545 | ||||||
chr2:26972695
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8+1893C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972695 | ||||||
chr2:26972758
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-8+1956G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972758 | ||||||
chr2:26972987
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+2185A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26972987 | ||||||
chr2:26973360
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8+2558T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973360 | ||||||
chr2:26973431
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-8+2629G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973431 | ||||||
chr2:26973546
|
GT | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-8+2763delT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26973546 | |||||
chr2:26973552
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8+2750T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973552 | ||||||
chr2:26973755
|
C | T | 1 | a0001c0002t0002g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-8+2953C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973755 | ||||||
chr2:26973847
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8+3045G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973847 | ||||||
chr2:26974237
|
T | A | 1 | a0001c0001t0002g0141 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8+3435T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26974237 | ||||||
chr2:26974479
|
G | A | 2 | a0001c0002t0002g0142a0001c0002t0002g0230 | 2 | HG02523.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-8+3677G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26974479 | ||||||
chr2:26974561
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+3759C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26974561 | ||||||
chr2:26975038
|
C | T | 2 | a0001c0002t0001g0227a0001c0002t0001g0228 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-8+4236C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975038 | ||||||
chr2:26975280
|
C | T | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-8+4478C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975280 | ||||||
chr2:26975396
|
G | A | 1 | a0001c0002t0001g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8+4594G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975396 | ||||||
chr2:26975581
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+4779G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975581 | ||||||
chr2:26975632
|
A | AAAGGGGA others(220): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+4834_-8+5060dup others(227): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26975632 | |||||
chr2:26975752
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(1): Show | 6 | HG00738.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+4950T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975752 | ||||||
chr2:26975769
|
GCTGC | G | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+4970_-8+4973del others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26975769 | |||||
chr2:26975798
|
G | A | 2 | a0001c0001t0002g0136a0001c0001t0002g0143 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-8+4996G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26975798 | ||||||
chr2:26976553
|
A | C | 34 | a0001c0001t0001g0203a0001c0002t0002g0002a0001c0002t0002g0003others(31): Show | 41 | HG00438.hp1 HG00544.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8+5751A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976553 | ||||||
chr2:26976662
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0104others(1): Show | 4 | HG00408.hp2 HG00438.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+5860G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976662 | ||||||
chr2:26976699
|
C | G | 7 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+5897C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976699 | ||||||
chr2:26976740
|
T | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+5938T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976740 | ||||||
chr2:26976886
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+6084A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976886 | ||||||
chr2:26977219
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-8+6417G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26977219 | ||||||
chr2:26977338
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8+6536C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26977338 | ||||||
chr2:26977397
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-8+6595G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26977397 | ||||||
chr2:26977780
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-8+6978C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26977780 | ||||||
chr2:26977942
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8+7140A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26977942 | ||||||
chr2:26978199
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8+7397A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978199 | ||||||
chr2:26978294
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017 | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+7492G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978294 | ||||||
chr2:26978333
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8+7531C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978333 | ||||||
chr2:26978437
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8+7635A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978437 | ||||||
chr2:26978841
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-8+8039G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978841 | ||||||
chr2:26978841
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-8+8039G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978841 | ||||||
chr2:26978989
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(96): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-8+8187T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26978989 | ||||||
chr2:26979252
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-8+8450A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26979252 | ||||||
chr2:26979510
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-8+8708C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26979510 | ||||||
chr2:26979968
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-8+9166A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26979968 | ||||||
chr2:26980046
|
G | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+9244G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26980046 | ||||||
chr2:26981023
|
C | T | 6 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+10221C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981023 | ||||||
chr2:26981177
|
T | C | 5 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(2): Show | 5 | HG01074.hp2 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+10375T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981177 | ||||||
chr2:26981370
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+10568T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981370 | ||||||
chr2:26981408
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8+10606A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981408 | ||||||
chr2:26981554
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+10752C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981554 | ||||||
chr2:26981669
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8+10867T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981669 | ||||||
chr2:26981766
|
T | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-8+10964T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981766 | ||||||
chr2:26981782
|
C | T | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-8+10980C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26981782 | ||||||
chr2:26982011
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-8+11209G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982011 | ||||||
chr2:26982096
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+11294T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982096 | ||||||
chr2:26982259
|
T | G | 1 | a0001c0001t0002g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8+11457T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982259 | ||||||
chr2:26982330
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8+11528G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982330 | ||||||
chr2:26982434
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8+11632T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982434 | ||||||
chr2:26982451
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+11649T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982451 | ||||||
chr2:26982609
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-8+11807A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982609 | ||||||
chr2:26982660
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8+11858A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26982660 | ||||||
chr2:26983363
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8+12561C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26983363 | ||||||
chr2:26983606
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8+12804T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26983606 | ||||||
chr2:26983648
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-8+12846T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26983648 | ||||||
chr2:26983873
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+13071A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26983873 | ||||||
chr2:26984300
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8+13498C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26984300 | ||||||
chr2:26984405
|
A | T | 1 | a0001c0002t0001g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8+13603A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26984405 | ||||||
chr2:26984515
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8+13713G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26984515 | ||||||
chr2:26984528
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8+13726G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26984528 | ||||||
chr2:26984841
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8+14039G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26984841 | ||||||
chr2:26985289
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+14487A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985289 | ||||||
chr2:26985407
|
T | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+14605T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985407 | ||||||
chr2:26985545
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-8+14743C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985545 | ||||||
chr2:26985703
|
A | G | 10 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+14901A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985703 | ||||||
chr2:26985753
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0113others(1): Show | 4 | NA18959.hp2 NA18985.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14951C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985753 | ||||||
chr2:26985916
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8+15114A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985916 | ||||||
chr2:26985999
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(96): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-8+15197T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26985999 | ||||||
chr2:26986017
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01517.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.-8+15215T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986017 | ||||||
chr2:26986082
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+15280A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986082 | ||||||
chr2:26986621
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8+15819C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986621 | ||||||
chr2:26986728
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8+15926C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986728 | ||||||
chr2:26986738
|
T | A | 10 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+15936T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986738 | ||||||
chr2:26986780
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG00140.hp2 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+15978A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986780 | ||||||
chr2:26986943
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+16141C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26986943 | ||||||
chr2:26987193
|
T | C | 1 | a0001c0002t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8+16391T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987193 | ||||||
chr2:26987281
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0133 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-8+16479G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987281 | ||||||
chr2:26987337
|
G | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-8+16535G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987337 | ||||||
chr2:26987337
|
G | T | 1 | a0001c0001t0002g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8+16535G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987337 | ||||||
chr2:26987362
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+16560C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987362 | ||||||
chr2:26987434
|
C | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-8+16632C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987434 | ||||||
chr2:26987531
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+16729G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987531 | ||||||
chr2:26987593
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-8+16791G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26987593 | ||||||
chr2:26988344
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-8+17542A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26988344 | ||||||
chr2:26988376
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+17574A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26988376 | ||||||
chr2:26988394
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+17592A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26988394 | ||||||
chr2:26988543
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+17741G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26988543 | ||||||
chr2:26988957
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00408.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+18155C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26988957 | ||||||
chr2:26989041
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+18239G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989041 | ||||||
chr2:26989359
|
T | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+18557T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989359 | ||||||
chr2:26989492
|
G | A | 1 | a0001c0002t0002g0200 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-8+18690G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989492 | ||||||
chr2:26989658
|
A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+18856A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989658 | ||||||
chr2:26989711
|
C | G | 2 | a0001c0002t0002g0179a0001c0002t0002g0180 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-8+18909C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989711 | ||||||
chr2:26989728
|
G | A | 96 | a0001c0001t0001g0158a0001c0001t0001g0203a0001c0001t0001g0236others(93): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-8+18926G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989728 | ||||||
chr2:26989775
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-8+18973G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26989775 | ||||||
chr2:26990063
|
C | T | 7 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+19261C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990063 | ||||||
chr2:26990214
|
AAGTTTGA others(9): Show |
A | 1 | a0001c0001t0002g0118 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-8+19413_-8+19428d others(18): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990214 | ||||||
chr2:26990279
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-8+19477C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990279 | ||||||
chr2:26990293
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+19491C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990293 | ||||||
chr2:26990469
|
A | G | 2 | a0001c0002t0002g0179a0001c0002t0002g0180 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-8+19667A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990469 | ||||||
chr2:26990907
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+20105C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26990907 | ||||||
chr2:26991069
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-8+20267T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991069 | ||||||
chr2:26991081
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(5): Show | 10 | HG00738.hp1 HG01074.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+20279G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991081 | ||||||
chr2:26991099
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-8+20297A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991099 | ||||||
chr2:26991107
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-8+20305A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991107 | ||||||
chr2:26991122
|
T | C | 5 | a0001c0001t0001g0031a0001c0002t0002g0152a0001c0002t0002g0153others(2): Show | 5 | HG00741.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+20320T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991122 | ||||||
chr2:26991193
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8+20391G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991193 | ||||||
chr2:26991330
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8+20528G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991330 | ||||||
chr2:26991516
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-8+20714C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991516 | ||||||
chr2:26991545
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-8+20743T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26991545 | ||||||
chr2:26992166
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-8+21364C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992166 | ||||||
chr2:26992226
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8+21424A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992226 | ||||||
chr2:26992229
|
A | AT | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+21441dupT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26992229 | |||||
chr2:26992384
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8+21582G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992384 | ||||||
chr2:26992401
|
A | AT | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-8+21602dupT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26992401 | |||||
chr2:26992458
|
C | A | 3 | a0001c0001t0002g0154a0001c0001t0002g0156a0001c0002t0002g0155 | 3 | HG02886.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-8+21656C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992458 | ||||||
chr2:26992520
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-8+21718C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992520 | ||||||
chr2:26992531
|
AT | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0158a0001c0001t0001g0240others(2): Show | 5 | HG00140.hp1 HG01167.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+21746delT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26992531 | |||||
chr2:26992548
|
T | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-8+21746T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992548 | ||||||
chr2:26992548
|
T | TA | 75 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-8+21748dupA | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26992548 | |||||
chr2:26992682
|
C | A | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8+21880C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992682 | ||||||
chr2:26992959
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8+22157T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26992959 | ||||||
chr2:26993094
|
G | T | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-8+22292G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993094 | ||||||
chr2:26993105
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG00140.hp2 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+22303C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993105 | ||||||
chr2:26993215
|
A | G | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+22413A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993215 | ||||||
chr2:26993280
|
G | A | 1 | a0001c0002t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8+22478G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993280 | ||||||
chr2:26993934
|
C | G | 1 | a0001c0001t0001g0006 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+23132C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993934 | ||||||
chr2:26993935
|
C | A | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+23133C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26993935 | ||||||
chr2:26994234
|
T | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-8+23432T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994234 | ||||||
chr2:26994360
|
G | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-8+23558G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994360 | ||||||
chr2:26994719
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0112 | 2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-8+23917A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994719 | ||||||
chr2:26994806
|
TTTC | T | 24 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(21): Show | 24 | HG01069.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8+24022_-8+24024d others(5): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26994806 | |||||
chr2:26994822
|
TTC | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8+24022_-8+24023d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26994822 | |||||
chr2:26994824
|
CT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(87): Show | 102 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-8+24042delT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26994824 | |||||
chr2:26994824
|
CTT | C | 9 | a0001c0001t0002g0119a0001c0001t0002g0157a0001c0001t0002g0159others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+24041_-8+24042d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26994824 | |||||
chr2:26994828
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8+24026T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994828 | ||||||
chr2:26994912
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8+24110C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994912 | ||||||
chr2:26994962
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-8+24160G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994962 | ||||||
chr2:26995250
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-8+24448C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26995250 | ||||||
chr2:26995638
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+24836A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26995638 | ||||||
chr2:26995780
|
G | GGT | 11 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG00733.hp1 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+25027_-8+25028d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGT | 19 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0087others(16): Show | 19 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8+25025_-8+25028d others(6): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGT | 23 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0034others(20): Show | 24 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8+25023_-8+25028d others(8): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(1): Show |
24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0036others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8+25021_-8+25028d others(10): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(3): Show |
27 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(24): Show | 30 | HG00741.hp2 HG01106.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8+25019_-8+25028d others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(5): Show |
27 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0040others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8+25017_-8+25028d others(14): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0041a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 18 | HG01074.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8+25015_-8+25028d others(16): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(9): Show |
27 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0042others(24): Show | 29 | HG00438.hp1 HG01243.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8+25013_-8+25028d others(18): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(11): Show |
10 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0081others(7): Show | 10 | HG01255.hp2 HG01517.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+25011_-8+25028d others(20): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(13): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0079a0001c0002t0002g0004others(1): Show | 6 | HG02523.hp1 HG03017.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+25009_-8+25028d others(22): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(15): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0108 | 2 | NA18951.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-8+25007_-8+25028d others(24): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
G | GGTGTGTG others(19): Show |
1 | a0001c0002t0002g0142 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-8+25003_-8+25028d others(28): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
GGT | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+25027_-8+25028d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
GGTGT | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0002g0242others(1): Show | 6 | HG02818.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+25025_-8+25028d others(6): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
GGTGTGT | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0044others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+25023_-8+25028d others(8): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995780
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0002g0201 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-8+25019_-8+25028d others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995780 | |||||
chr2:26995825
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8+25028_-8+25029i others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995825
|
G | GTGTGTGT others(5): Show |
5 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0104others(2): Show | 5 | HG00438.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+25028_-8+25029i others(14): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995825
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8+25028_-8+25029i others(16): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995825
|
G | GTGTGTGT others(9): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0095others(1): Show | 4 | HG00408.hp1 NA19002.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+25028_-8+25029i others(18): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995825
|
G | GTGTGTGT others(11): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0110others(1): Show | 4 | HG00408.hp2 HG00544.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+25028_-8+25029i others(20): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995825
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8+25028_-8+25029i others(24): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995825 | |||||
chr2:26995829
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-8+25028_-8+25029i others(20): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26995829 | |||||
chr2:26995831
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0002g0175 | 2 | HG02738.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-8+25029A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26995831 | ||||||
chr2:26995968
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0112 | 2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-8+25166A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26995968 | ||||||
chr2:26995991
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8+25189C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26995991 | ||||||
chr2:26996115
|
A | AATTTT | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(126): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-8+25358_-8+25362d others(7): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
A | AATTTTAT others(3): Show |
20 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0016others(17): Show | 21 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8+25353_-8+25362d others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
A | AATTTTAT others(8): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0002g0186 | 4 | HG01884.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+25348_-8+25362d others(17): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
A | AATTTTAT others(13): Show |
1 | a0001c0001t0001g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-8+25343_-8+25362d others(22): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
A | AATTTTAT others(18): Show |
1 | a0001c0001t0001g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8+25338_-8+25362d others(27): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
AATTTT | A | 9 | a0001c0001t0001g0203a0001c0001t0001g0241a0001c0001t0002g0184others(6): Show | 10 | HG01891.hp1 HG02040.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+25358_-8+25362d others(7): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
AATTTTAT others(3): Show |
A | 4 | a0001c0002t0001g0139a0001c0002t0001g0140a0001c0002t0001g0227others(1): Show | 4 | HG02451.hp1 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+25353_-8+25362d others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996115
|
AATTTTAT others(8): Show |
A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0106others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+25348_-8+25362d others(17): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26996115 | |||||
chr2:26996233
|
G | C | 5 | a0001c0002t0001g0193a0001c0002t0001g0196a0001c0002t0001g0197others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+25431G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26996233 | ||||||
chr2:26996374
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+25572C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26996374 | ||||||
chr2:26996525
|
G | T | 1 | a0001c0001t0002g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-7-25687G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26996525 | ||||||
chr2:26996599
|
G | A | 7 | a0001c0002t0002g0002a0001c0002t0002g0208a0001c0002t0002g0209others(4): Show | 9 | HG02083.hp2 HG02155.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-25613G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26996599 | ||||||
chr2:26997496
|
G | A | 4 | a0001c0002t0002g0152a0001c0002t0002g0153a0001c0002t0002g0179others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-24716G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26997496 | ||||||
chr2:26997567
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-24645G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26997567 | ||||||
chr2:26997944
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-24268C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26997944 | ||||||
chr2:26997963
|
G | A | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7-24249G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26997963 | ||||||
chr2:26998175
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-7-24037A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26998175 | ||||||
chr2:26998243
|
T | C | 5 | a0001c0002t0001g0193a0001c0002t0001g0196a0001c0002t0001g0197others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-23969T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26998243 | ||||||
chr2:26998683
|
G | T | 1 | a0001c0001t0002g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7-23529G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26998683 | ||||||
chr2:26998845
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-23367A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26998845 | ||||||
chr2:26998900
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-23312G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26998900 | ||||||
chr2:26999047
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-23165G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26999047 | ||||||
chr2:26999051
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7-23161A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26999051 | ||||||
chr2:26999488
|
C | CT | 12 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0169others(9): Show | 12 | HG02258.hp1 HG02622.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-22697dupT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26999488 | |||||
chr2:26999488
|
C | CTT | 76 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(73): Show | 85 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-7-22698_-7-22697d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26999488 | |||||
chr2:26999488
|
C | CTTT | 33 | a0001c0001t0001g0023a0001c0001t0001g0116a0001c0001t0001g0117others(30): Show | 33 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-7-22699_-7-22697d others(5): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26999488 | |||||
chr2:26999488
|
C | CTTTT | 5 | a0001c0001t0001g0022a0001c0001t0001g0106a0001c0001t0002g0148others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-22700_-7-22697d others(6): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26999488 | |||||
chr2:26999488
|
CTTTTTTT others(1): Show |
C | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-7-22704_-7-22697d others(10): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 26999488 | |||||
chr2:26999517
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.-7-22695G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26999517 | ||||||
chr2:27000785
|
G | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-21427G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27000785 | ||||||
chr2:27000916
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-7-21296A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27000916 | ||||||
chr2:27001033
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-7-21179C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001033 | ||||||
chr2:27001131
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-21081A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001131 | ||||||
chr2:27001155
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-21057C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001155 | ||||||
chr2:27001210
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-21002C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001210 | ||||||
chr2:27001341
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-7-20871T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001341 | ||||||
chr2:27001779
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-20433C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27001779 | ||||||
chr2:27002126
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-7-20086A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27002126 | ||||||
chr2:27002135
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7-20077A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27002135 | ||||||
chr2:27002276
|
C | A | 85 | a0001c0001t0001g0158a0001c0001t0001g0203a0001c0001t0002g0008others(82): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7-19936C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27002276 | ||||||
chr2:27002412
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-7-19800T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27002412 | ||||||
chr2:27002419
|
C | CT | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-7-19780dupT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27002419 | |||||
chr2:27003055
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-7-19157G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003055 | ||||||
chr2:27003214
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.-7-18998T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003214 | ||||||
chr2:27003478
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-7-18734C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003478 | ||||||
chr2:27003525
|
T | C | 2 | a0001c0002t0002g0212a0001c0002t0002g0216 | 2 | NA18993.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-7-18687T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003525 | ||||||
chr2:27003933
|
T | C | 1 | a0001c0002t0004g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7-18279T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003933 | ||||||
chr2:27003961
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-7-18251C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003961 | ||||||
chr2:27003962
|
G | A | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7-18250G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27003962 | ||||||
chr2:27004055
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-18157A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004055 | ||||||
chr2:27004086
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-7-18126A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004086 | ||||||
chr2:27004102
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-7-18110C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004102 | ||||||
chr2:27004140
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-18072G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004140 | ||||||
chr2:27004450
|
G | A | 5 | a0001c0002t0002g0200a0001c0002t0002g0207a0001c0002t0002g0211others(2): Show | 5 | HG01106.hp2 HG01928.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-17762G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004450 | ||||||
chr2:27004635
|
G | T | 1 | a0001c0002t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-17577G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004635 | ||||||
chr2:27004728
|
T | TA | 8 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0106others(5): Show | 8 | HG01433.hp1 HG01981.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-17466dupA | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27004728 | |||||
chr2:27004839
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-7-17373A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004839 | ||||||
chr2:27004841
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0041others(4): Show | 9 | HG01106.hp1 HG01346.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-17371G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27004841 | ||||||
chr2:27005904
|
C | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0073others(2): Show | 5 | HG01346.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-16308C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27005904 | ||||||
chr2:27005910
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-16302C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27005910 | ||||||
chr2:27005964
|
C | T | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-16248C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27005964 | ||||||
chr2:27006055
|
G | A | 1 | a0001c0001t0002g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-7-16157G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006055 | ||||||
chr2:27006177
|
G | A | 4 | a0001c0001t0002g0151a0001c0001t0002g0167a0001c0001t0002g0169others(1): Show | 4 | HG01496.hp1 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-16035G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006177 | ||||||
chr2:27006205
|
C | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-16007C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006205 | ||||||
chr2:27006211
|
A | C | 93 | a0001c0001t0001g0158a0001c0001t0001g0203a0001c0001t0001g0236others(90): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-7-16001A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006211 | ||||||
chr2:27006213
|
A | C | 4 | a0001c0002t0002g0152a0001c0002t0002g0153a0001c0002t0002g0179others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15999A>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006213 | ||||||
chr2:27006338
|
G | A | 2 | a0001c0002t0002g0161a0001c0002t0002g0172 | 2 | HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-7-15874G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006338 | ||||||
chr2:27006350
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-15862T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006350 | ||||||
chr2:27006504
|
C | G | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-7-15708C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006504 | ||||||
chr2:27006587
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7-15625C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006587 | ||||||
chr2:27006588
|
G | A | 1 | a0001c0002t0003g0215 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-15624G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006588 | ||||||
chr2:27006605
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | HG02083.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-15607A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006605 | ||||||
chr2:27006665
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-7-15547C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006665 | ||||||
chr2:27006680
|
C | T | 1 | a0001c0001t0001g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-7-15532C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006680 | ||||||
chr2:27006783
|
A | G | 1 | a0001c0002t0002g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7-15429A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006783 | ||||||
chr2:27006952
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-7-15260G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006952 | ||||||
chr2:27006962
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-15250A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27006962 | ||||||
chr2:27007023
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(96): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7-15189T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007023 | ||||||
chr2:27007024
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(96): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7-15188C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007024 | ||||||
chr2:27007078
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-15134T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007078 | ||||||
chr2:27007376
|
C | T | 4 | a0001c0001t0002g0170a0001c0001t0002g0173a0001c0001t0002g0176others(1): Show | 4 | HG02572.hp2 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-14836C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007376 | ||||||
chr2:27007416
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145 | 5 | HG01106.hp1 HG01346.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-14796T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007416 | ||||||
chr2:27007485
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-7-14727C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007485 | ||||||
chr2:27007703
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7-14509G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27007703 | ||||||
chr2:27008277
|
G | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-7-13935G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008277 | ||||||
chr2:27008298
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0106 | 3 | HG02257.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-13914G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008298 | ||||||
chr2:27008324
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-7-13888G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008324 | ||||||
chr2:27008690
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-7-13522G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008690 | ||||||
chr2:27008891
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG03130.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-13321C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008891 | ||||||
chr2:27008920
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-13292C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008920 | ||||||
chr2:27008982
|
C | T | 1 | a0001c0002t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-13230C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27008982 | ||||||
chr2:27009023
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-7-13189T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009023 | ||||||
chr2:27009048
|
G | T | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-13164G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009048 | ||||||
chr2:27009083
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-7-13129A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009083 | ||||||
chr2:27009115
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-7-13097T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009115 | ||||||
chr2:27009399
|
G | A | 2 | a0001c0002t0002g0191a0001c0002t0002g0192 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-7-12813G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009399 | ||||||
chr2:27009702
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-7-12510G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009702 | ||||||
chr2:27009916
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0104others(1): Show | 4 | HG00408.hp2 HG00438.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-12296G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27009916 | ||||||
chr2:27010320
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-11892G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010320 | ||||||
chr2:27010358
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-7-11854T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010358 | ||||||
chr2:27010439
|
C | CT | 20 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(17): Show | 20 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7-11754dupT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27010439 | |||||
chr2:27010439
|
C | CTT | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-7-11755_-7-11754d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27010439 | |||||
chr2:27010599
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7-11613T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010599 | ||||||
chr2:27010921
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7-11291T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010921 | ||||||
chr2:27010944
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(235): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-7-11268T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010944 | ||||||
chr2:27010991
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7-11221T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010991 | ||||||
chr2:27011274
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-7-10938C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27011274 | ||||||
chr2:27011429
|
A | G | 1 | a0001c0003t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7-10783A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27011429 | ||||||
chr2:27011664
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7-10548G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27011664 | ||||||
chr2:27011845
|
C | CA | 34 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0240others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-7-10348dupA | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27011845 | |||||
chr2:27011845
|
C | CAA | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 126 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-7-10349_-7-10348d others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27011845 | |||||
chr2:27011881
|
G | A | 3 | a0001c0002t0002g0161a0001c0002t0002g0172a0001c0002t0002g0187 | 3 | HG00642.hp2 HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-7-10331G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27011881 | ||||||
chr2:27012143
|
T | C | 1 | a0001c0002t0002g0190 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-10069T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27012143 | ||||||
chr2:27012176
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-10036A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27012176 | ||||||
chr2:27012217
|
A | AAAAG | 9 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0059others(6): Show | 9 | HG00639.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-9993_-7-9992ins others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27012217 | |||||
chr2:27012217
|
A | AAAG | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-7-9980_-7-9978dup others(3): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27012217 | |||||
chr2:27012461
|
A | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-9751A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27012461 | ||||||
chr2:27012967
|
G | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-9245G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27012967 | ||||||
chr2:27013106
|
A | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0070 | 2 | NA18945.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-7-9106A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27013106 | ||||||
chr2:27013254
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-7-8958G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27013254 | ||||||
chr2:27013560
|
C | CCATT | 5 | a0001c0001t0001g0030a0001c0001t0001g0094a0001c0001t0001g0101others(2): Show | 5 | HG02622.hp2 HG03453.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8633_-7-8630dup others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27013560 | |||||
chr2:27013816
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-8396T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27013816 | ||||||
chr2:27013826
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7-8386C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27013826 | ||||||
chr2:27013843
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7-8369G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27013843 | ||||||
chr2:27014066
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-8146T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014066 | ||||||
chr2:27014241
|
C | T | 1 | a0001c0001t0001g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-7-7971C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014241 | ||||||
chr2:27014242
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0238 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-7970G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014242 | ||||||
chr2:27014491
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0108 | 2 | NA18951.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-7-7721C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014491 | ||||||
chr2:27014499
|
A | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0106others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-7713A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014499 | ||||||
chr2:27014527
|
G | T | 2 | a0001c0002t0001g0227a0001c0002t0001g0228 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-7-7685G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014527 | ||||||
chr2:27014549
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0073 | 2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-7-7663C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014549 | ||||||
chr2:27014564
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-7-7648A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014564 | ||||||
chr2:27014746
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-7-7466A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014746 | ||||||
chr2:27015092
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-7120A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27015092 | ||||||
chr2:27015181
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-7031T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27015181 | ||||||
chr2:27015530
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0218 | 2 | HG01106.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-7-6682C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27015530 | ||||||
chr2:27016060
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7-6152T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27016060 | ||||||
chr2:27016381
|
CT | C | 11 | a0001c0001t0001g0084a0001c0001t0001g0100a0001c0001t0001g0104others(8): Show | 11 | HG00735.hp2 HG01069.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-5810delT | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27016381 | |||||
chr2:27016509
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0183 | 3 | HG02622.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-5703T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27016509 | ||||||
chr2:27017081
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-7-5131G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017081 | ||||||
chr2:27017151
|
G | T | 1 | a0001c0002t0003g0215 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-5061G>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017151 | ||||||
chr2:27017248
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-7-4964T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017248 | ||||||
chr2:27017536
|
C | T | 4 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG02451.hp2 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-4676C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017536 | ||||||
chr2:27017630
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-4582C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017630 | ||||||
chr2:27017803
|
ATG | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-7-4393_-7-4392del others(2): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27017803 | |||||
chr2:27017980
|
T | C | 1 | a0001c0002t0002g0222 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-7-4232T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27017980 | ||||||
chr2:27018357
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-7-3855G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018357 | ||||||
chr2:27018788
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0106others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-3424T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018788 | ||||||
chr2:27018895
|
T | TTTTA | 91 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-7-3285_-7-3282dup others(4): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTATTT others(1): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0037others(10): Show | 15 | HG01106.hp1 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-3289_-7-3282dup others(8): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTATTT others(5): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(3): Show | 8 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-3293_-7-3282dup others(12): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTATTT others(9): Show |
9 | a0001c0001t0001g0098a0001c0001t0001g0125a0001c0001t0001g0129others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-3297_-7-3282dup others(16): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTATTT others(13): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG02109.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-3301_-7-3282dup others(20): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTTTTT others(9): Show |
1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-7-3314_-7-3313ins others(16): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTTTTT others(13): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02486.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-3314_-7-3313ins others(20): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018895
|
T | TTTTTTTT others(17): Show |
1 | a0001c0001t0001g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-3314_-7-3313ins others(24): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27018895 | |||||
chr2:27018899
|
A | T | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-3313A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018899 | ||||||
chr2:27018919
|
A | T | 1 | a0001c0002t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7-3293A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018919 | ||||||
chr2:27018923
|
A | T | 17 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-3289A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018923 | ||||||
chr2:27018927
|
A | T | 105 | a0001c0001t0001g0158a0001c0001t0001g0203a0001c0001t0001g0236others(102): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-7-3285A>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27018927 | ||||||
chr2:27019371
|
T | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-7-2841T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019371 | ||||||
chr2:27019377
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-7-2835A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019377 | ||||||
chr2:27019385
|
G | GGCAGGGG others(4): Show |
1 | a0001c0001t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-7-2826_-7-2816dup others(11): Show |
MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 27019385 | |||||
chr2:27019442
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-7-2770T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019442 | ||||||
chr2:27019530
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-7-2682C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019530 | ||||||
chr2:27019607
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0173a0001c0001t0002g0178 | 3 | HG02572.hp2 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-7-2605G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019607 | ||||||
chr2:27019758
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-7-2454G>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019758 | ||||||
chr2:27019893
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0066others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-2319C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27019893 | ||||||
chr2:27020067
|
C | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.-7-2145C>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020067 | ||||||
chr2:27020133
|
C | T | 50 | a0001c0001t0001g0158a0001c0001t0001g0236a0001c0001t0001g0237others(47): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-7-2079C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020133 | ||||||
chr2:27020279
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7-1933G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020279 | ||||||
chr2:27020496
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-7-1716A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020496 | ||||||
chr2:27020788
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017 | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-1424G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020788 | ||||||
chr2:27020998
|
T | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-1214T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27020998 | ||||||
chr2:27021030
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7-1182T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021030 | ||||||
chr2:27021138
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7-1074G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021138 | ||||||
chr2:27021232
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-980T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021232 | ||||||
chr2:27021250
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7-962G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021250 | ||||||
chr2:27021364
|
C | A | 7 | a0001c0002t0002g0002a0001c0002t0002g0208a0001c0002t0002g0209others(4): Show | 9 | HG02083.hp2 HG02155.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-848C>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021364 | ||||||
chr2:27021584
|
C | T | 10 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-628C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021584 | ||||||
chr2:27021844
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-7-368C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021844 | ||||||
chr2:27021876
|
C | T | 4 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG02451.hp2 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-336C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021876 | ||||||
chr2:27021931
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-281T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27021931 | ||||||
chr2:27022567
|
C | T | 1 | a0001c0002t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.121+228C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/6 | chr2 | 27022567 | ||||||
chr2:27022607
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(95): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.121+268T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/6 | chr2 | 27022607 | ||||||
chr2:27022761
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.121+422T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/6 | chr2 | 27022761 | ||||||
chr2:27023139
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01517.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.122-193C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/6 | chr2 | 27023139 | ||||||
chr2:27023154
|
T | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-178T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 2/6 | chr2 | 27023154 | ||||||
chr2:27023489
|
C | T | 1 | a0001c0002t0002g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.267+12C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 3/6 | chr2 | 27023489 | ||||||
chr2:27023802
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.268-294T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 3/6 | chr2 | 27023802 | ||||||
chr2:27023811
|
G | A | 1 | a0001c0002t0002g0204 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.268-285G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 3/6 | chr2 | 27023811 | ||||||
chr2:27023820
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-276A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 3/6 | chr2 | 27023820 | ||||||
chr2:27024351
|
T | G | 7 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+54T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | chr2 | 27024351 | ||||||
chr2:27024377
|
CG | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+82delG | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 27024377 | |||||
chr2:27024851
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0070others(3): Show | 6 | HG02074.hp2 NA18747.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+554G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | chr2 | 27024851 | ||||||
chr2:27024964
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.470-619T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | chr2 | 27024964 | ||||||
chr2:27025168
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.470-415A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | chr2 | 27025168 | ||||||
chr2:27025376
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0059others(3): Show | 6 | NA18949.hp1 NA18982.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-207C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 4/6 | chr2 | 27025376 | ||||||
chr2:27025756
|
G | A | 2 | a0001c0002t0002g0191a0001c0002t0002g0192 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.624+19G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 5/6 | chr2 | 27025756 | ||||||
chr2:27025832
|
A | G | 13 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0002t0001g0139others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-48A>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 5/6 | chr2 | 27025832 | ||||||
chr2:27026212
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.778-68T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 6/6 | chr2 | 27026212 | ||||||
chr2:27026270
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.778-10C>T | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 6/6 | chr2 | 27026270 |