Item | Value |
---|---|
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 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 843 | 187 | 64 | 42 | 49 | 12 | 19 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | ATGGC others(838): Show |
chr2 | 26965637 | 27032219 | ||
a0001c0002 | 1/0 | 843 | 70 | 22 | 8 | 37 | 2 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | ATGGC others(838): Show |
chr2 | 26965637 | 27032219 | ||
a0001c0003 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | ATGGC others(838): Show |
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 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0001t0002 | 0/0 | 1890 | 50 | 18 | 16 | 3 | 5 | 8 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0002t0001 | 0/0 | 1890 | 11 | 10 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0002t0002 | 1/0 | 1890 | 57 | 11 | 7 | 36 | 2 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0002t0003 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0002t0004 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
chr2 | 26965637 | 27032219 |
a0001c0003t0002 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | AGTGC others(1885): Show |
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 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0001g0157 | 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 |
a0001c0001t0002g0158 | 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 |
a0001c0001t0002g0161 | 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 | 0 | 0 | 0 | 1 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
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 |
a0001c0002t0002g0166 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
a0001c0002t0003g0213 | 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 | g0061 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0158 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | 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 | g0060 | 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 | g0062 | 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 | g0160 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0048 | 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 | g0162 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | 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 | g0166 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0165 | 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 | g0216 | 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 | g0159 | 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 | g0161 | AMR | PUR | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0129 | 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 | g0055 | 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 | g0059 | 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 | g0071 | 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 | g0164 | 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 | g0092 | AMR | CLM | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0093 | 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 | g0056 | AMR | PEL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0204 | 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 | g0212 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0207 | 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 | g0130 | 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 | g0066 | 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 | g0080 | 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 | g0163 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | 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 | g0131 | 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 | g0017 | 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 | g0072 | 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 | g0065 | 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 | g0052 | 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 | g0157 | 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 | g0045 | 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 | g0049 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0205 | 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 | g0050 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0211 | 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 | g0058 | 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 | g0217 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0208 | 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 | g0220 | 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 | g0069 | 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 | g0077 | 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 | g0218 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0221 | 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 | g0213 | 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 | g0209 | 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 | g0210 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0068 | 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 | g0215 | 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 | g0054 | 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 | g0047 | 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 | g0078 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0219 | 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 | g0206 | 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 | g0214 | EAS | JPT | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0075 | 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 | g0063 | 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 | g0070 | 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 | g0044 | 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 | g0064 | 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 | g0051 | EUR | TSI | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | g0128 | 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 | a0001 | c0001 | t0001 | g0082 | REF | REF | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0188 | REF | REF | MAPRE3_chr2_26965637_27032219 | MAPRE3 | chr2 | 26965637 | 27032219 |
view | 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 |
---|
view | 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 | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 |
view | 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 | a0001c0001t0001 a0001c0002t0001 |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): 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 |
view | 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 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0002g0235 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-8+2629G>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26973431 | |||||||
chr2:26973546 | GT | G | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): 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 | a0001c0002t0002g0142 a0001c0002t0002g0230 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0001g0227 a0001c0002t0001g0228 |
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 | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0002g0136 a0001c0001t0002g0143 |
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 | a0001c0001t0001g0203 a0001c0002t0002g0002 a0001c0002t0002g0003 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(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 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+5938T>G | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26976740 | |||||||
chr2:26976886 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): 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 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 others(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 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(97): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0095 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0133 |
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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): 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 | a0001c0002t0002g0179 a0001c0002t0002g0180 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0203 a0001c0001t0001g0236 others(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 | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): 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 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0002g0179 a0001c0002t0002g0180 |
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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0031 a0001c0002t0002g0152 a0001c0002t0002g0153 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): 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 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0002t0002g0155 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0157 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 74 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): 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 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | 97 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-8+23432T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 26994234 | |||||||
chr2:26994360 | G | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): 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 | a0001c0001t0001g0083 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): 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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0158 a0001c0001t0002g0160 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0077 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0034 others(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 |
23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0036 others(20): Show |
24 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(21): 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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0002t0002g0004 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0002g0242 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0088 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0074 a0001c0001t0002g0175 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0112 |
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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(125): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): 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 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0099 a0001c0001t0002g0186 |
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 | a0001c0001t0001g0203 a0001c0001t0001g0241 a0001c0001t0002g0184 others(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 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0001c0002t0001g0227 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 others(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 | a0001c0002t0001g0193 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0205 a0001c0002t0002g0206 others(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 | a0001c0002t0002g0152 a0001c0002t0002g0153 a0001c0002t0002g0179 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
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 | a0001c0002t0001g0193 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0002g0169 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0002g0148 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0203 a0001c0001t0002g0008 others(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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | a0001c0001t0001g0061 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0001g0060 | 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 | a0001c0002t0002g0210 a0001c0002t0002g0214 |
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 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): 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 | a0001c0001t0002g0165 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0002g0200 a0001c0002t0002g0204 a0001c0002t0002g0209 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0106 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): 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 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | 4 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0071 others(1): Show |
4 | HG01346.hp1 HG01928.hp1 HG01952.hp1 others(1): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0167 a0001c0001t0002g0169 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0203 a0001c0001t0001g0236 others(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 | a0001c0002t0002g0152 a0001c0002t0002g0153 a0001c0002t0002g0179 others(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 | a0001c0002t0002g0166 a0001c0002t0002g0172 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): 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 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
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 | a0001c0002t0003g0213 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | |||||||
chr2:27006783 | A | G | 1 | a0001c0002t0002g0205 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0002g0176 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 |
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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 |
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 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | a0001c0001t0002g0158 | 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 | a0001c0002t0002g0191 a0001c0002t0002g0192 |
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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0076 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-7-11613T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010599 | |||||||
chr2:27010921 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-7-11291T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010921 | |||||||
chr2:27010944 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-7-11268T>C | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27010944 | |||||||
chr2:27010991 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): 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 | a0001c0001t0002g0164 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0001c0001t0001g0240 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
125 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(122): 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 | a0001c0002t0002g0166 a0001c0002t0002g0172 a0001c0002t0002g0187 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0053 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0094 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-8146T>A | MAPRE3 | ENSG00000084764.12 | transcript | ENST00000233121.7 | protein_coding | 1/6 | chr2 | 27014066 | |||||||
chr2:27014242 | G | A | 2 | a0001c0001t0002g0235 a0001c0001t0002g0238 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 others(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 | a0001c0002t0001g0227 a0001c0002t0001g0228 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0086 |
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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0002g0204 a0001c0002t0002g0216 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0002g0183 |
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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): 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 | a0001c0002t0003g0213 | 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 | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 others(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 | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 others(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 | 90 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): 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 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0125 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0001g0117 |
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 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0203 a0001c0001t0001g0236 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0128 | 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 | ||||||
chr2:27019530 | 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 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0002g0178 |
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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0059 others(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 | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | a0001c0001t0001g0157 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0205 a0001c0002t0002g0206 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(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 | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0050 | 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 | a0001c0002t0002g0208 | 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 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0002t0002g0191 a0001c0002t0002g0192 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0002t0001g0139 others(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 |