Item | Value |
---|---|
geneid | 55840 |
ensemblid | ENSG00000145088.9 |
hgncid | 23115 |
symbol | EAF2 |
name | ELL associated factor 2 |
refseq_nuc | NM_018456.6 |
refseq_prot | NP_060926.2 |
ensembl_nuc | ENST00000273668.7 |
ensembl_prot | ENSP00000273668.2 |
mane_status | MANE Select |
chr | chr3 |
start | 121835209 |
end | 121886526 |
strand | + |
ver | v1.2 |
region | chr3:121835209-121886526 |
region5000 | chr3:121830209-121891526 |
regionname0 | EAF2_chr3_121835209_121886526 |
regionname5000 | EAF2_chr3_121830209_121891526 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 260 | 311 | 82 | 72 | 103 | 14 | 38 | 73 | EAF2_chr3_121830209_121891526 | EAF2 | MNSAA others(255): Show |
chr3 | 121830209 | 121891526 |
a0002 | 0/0 | 260 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | MNSAA others(255): Show |
chr3 | 121830209 | 121891526 |
a0003 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | MNSAA others(255): Show |
chr3 | 121830209 | 121891526 |
a0004 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | MNSAA others(255): Show |
chr3 | 121830209 | 121891526 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 780 | 223 | 65 | 57 | 55 | 14 | 30 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0001c0002 | 0/0 | 780 | 84 | 14 | 15 | 48 | 0 | 7 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0001c0004 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0001c0007 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0001c0008 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0002c0003 | 0/0 | 780 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0003c0005 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 | ||
a0004c0006 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | ATGAA others(775): Show |
chr3 | 121830209 | 121891526 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 998 | 221 | 65 | 57 | 55 | 13 | 29 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0001t0002 | 0/0 | 998 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0001t0003 | 0/0 | 998 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | TAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0002t0001 | 0/0 | 998 | 84 | 14 | 15 | 48 | 0 | 7 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0004t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0007t0001 | 0/0 | 998 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0001c0008t0001 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0002c0003t0001 | 0/0 | 998 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0003c0005t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
a0004c0006t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | AAGTG others(993): Show |
chr3 | 121830209 | 121891526 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0001 | 0/0 | 12 | 0 | 0 | 9 | 0 | 3 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0003c0005t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0004c0006t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0199 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02257 | hp1 | a0003 | c0005 | t0001 | g0034 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02965 | hp2 | a0004 | c0006 | t0001 | g0035 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03041 | hp2 | a0001 | c0008 | t0001 | g0176 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03139 | hp2 | a0004 | c0006 | t0001 | g0035 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04199 | hp2 | a0001 | c0007 | t0001 | g0193 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | CHB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18997 | hp1 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | GIH | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02486 | hp1 | a0003 | c0005 | t0001 | g0034 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0160 | REF | REF | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835362 | A | G | 1 | a0004 | 2 | HG02965.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.77A>G | p.Gln26Arg | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 154/998 | 77/783 | 26/260 | chr3 | 121835362 | |||
chr3:121872672 | C | T | 1 | a0002 | 3 | HG02027.hp2 HG02074.hp1 NA18997.hp1 |
missense_variant | MODERATE | c.620C>T | p.Ser207Phe | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 697/998 | 620/783 | 207/260 | chr3 | 121872672 | |||
chr3:121872760 | C | G | 1 | a0003 | 2 | HG02257.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.708C>G | p.Asp236Glu | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 785/998 | 708/783 | 236/260 | chr3 | 121872760 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835300 | G | A | 1 | a0001c0007 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.15G>A | p.Ala5Ala | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 92/998 | 15/783 | 5/260 | chr3 | 121835300 | |||
chr3:121844508 | T | C | 1 | a0001c0002 | 84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
synonymous_variant | LOW | c.162T>C | p.Gly54Gly | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/6 | 239/998 | 162/783 | 54/260 | chr3 | 121844508 | |||
chr3:121854815 | A | G | 1 | a0001c0008 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.330A>G | p.Lys110Lys | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/6 | 407/998 | 330/783 | 110/260 | chr3 | 121854815 | |||
chr3:121872769 | C | A | 1 | a0001c0004 | 2 | HG02145.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.717C>A | p.Gly239Gly | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 794/998 | 717/783 | 239/260 | chr3 | 121872769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835209 | A | T | 1 | a0001c0001t0003 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 77 | chr3 | 121835209 | ||||||
chr3:121835255 | G | A | 1 | a0001c0001t0002 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 31 | chr3 | 121835255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835482 | C | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.106+91C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121835482 | |||||||
chr3:121835752 | G | T | 1 | a0001c0001t0003g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.106+361G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121835752 | |||||||
chr3:121836133 | T | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+742T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836133 | |||||||
chr3:121836336 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.106+945T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836336 | |||||||
chr3:121836536 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.106+1145G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836536 | |||||||
chr3:121836599 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.106+1208C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836599 | |||||||
chr3:121836934 | A | G | 1 | a0001c0002t0001g0240 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+1543A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836934 | |||||||
chr3:121837026 | T | C | 6 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(3): Show |
6 | HG01952.hp1 NA18947.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1635T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837026 | |||||||
chr3:121837049 | TAAAC | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.106+1662_106+1665d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121837049 | ||||||
chr3:121837160 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.106+1769C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837160 | |||||||
chr3:121837372 | C | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.106+1981C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837372 | |||||||
chr3:121837426 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(1): Show |
6 | HG02258.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+2035G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837426 | |||||||
chr3:121837496 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.106+2105A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837496 | |||||||
chr3:121837623 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.106+2232A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837623 | |||||||
chr3:121837882 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.106+2491A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837882 | |||||||
chr3:121837904 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(26): Show |
35 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+2513G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837904 | |||||||
chr3:121838052 | G | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.106+2661G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838052 | |||||||
chr3:121838381 | C | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.106+2990C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838381 | |||||||
chr3:121838404 | A | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.106+3013A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838404 | |||||||
chr3:121838686 | G | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.106+3295G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838686 | |||||||
chr3:121838859 | A | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0237 others(1): Show |
6 | HG01981.hp1 NA18957.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+3468A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838859 | |||||||
chr3:121838877 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+3486G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838877 | |||||||
chr3:121839101 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+3710A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839101 | |||||||
chr3:121839268 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.106+3877A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839268 | |||||||
chr3:121839290 | G | T | 1 | a0001c0002t0001g0179 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.106+3899G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839290 | |||||||
chr3:121839499 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0110 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.106+4108G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839499 | |||||||
chr3:121839925 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.107-4528G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839925 | |||||||
chr3:121840047 | G | GC | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.107-4405dupC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840047 | ||||||
chr3:121840064 | A | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.107-4389A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840064 | |||||||
chr3:121840189 | G | GA | 16 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0072 others(13): Show |
17 | HG00597.hp1 HG00642.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.107-4242dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | ||||||
chr3:121840189 | GA | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(48): Show |
67 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.107-4242delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | ||||||
chr3:121840189 | GAA | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
97 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-4243_107-4242d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | ||||||
chr3:121840319 | C | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4134C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840319 | |||||||
chr3:121840320 | G | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4133G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840320 | |||||||
chr3:121840413 | C | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.107-4040C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840413 | |||||||
chr3:121840428 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107-4025T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840428 | |||||||
chr3:121840488 | T | TA | 12 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0111 others(9): Show |
16 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.107-3945dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | ||||||
chr3:121840488 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0186 |
3 | HG01074.hp1 HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.107-3954_107-3945d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | ||||||
chr3:121840488 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107-3955_107-3945d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | ||||||
chr3:121840488 | TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0001g0175 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.107-3955_107-3945d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | ||||||
chr3:121840494 | AAAAAAAA others(8): Show |
A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
42 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.107-3946_107-3932d others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840494 | ||||||
chr3:121840495 | AAAAAAAA others(7): Show |
A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0090 others(2): Show |
5 | HG00280.hp1 HG01261.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-3945_107-3932d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840495 | ||||||
chr3:121840498 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0233 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107-3944_107-3934d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840498 | ||||||
chr3:121840504 | AAAAAG | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0052 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3944_107-3940d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840504 | ||||||
chr3:121840505 | A | G | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.107-3948A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840505 | |||||||
chr3:121840505 | AAAAG | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0042 others(8): Show |
14 | HG01256.hp1 HG02145.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-3944_107-3941d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840505 | ||||||
chr3:121840506 | AAAG | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(6): Show |
12 | HG00423.hp1 HG01109.hp1 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.107-3944_107-3942d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840506 | ||||||
chr3:121840507 | A | G | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-3946A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840507 | |||||||
chr3:121840508 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-3945A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840508 | |||||||
chr3:121840509 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
100 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.107-3944G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840509 | |||||||
chr3:121840515 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.107-3932_107-3931i others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.107-3932_107-3931i others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(5): Show |
9 | a0001c0001t0001g0036 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
11 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(4): Show |
17 | a0001c0001t0001g0037 a0001c0001t0001g0194 a0001c0001t0001g0195 others(14): Show |
18 | HG00597.hp2 HG00673.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(3): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(16): Show |
40 | HG00609.hp2 HG00642.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(2): Show |
12 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0220 others(9): Show |
14 | HG00323.hp1 HG01433.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(11): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.107-3932_107-3931i others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | ||||||
chr3:121840515 | A | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0237 |
3 | HG02040.hp1 HG03471.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.107-3938A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840515 | |||||||
chr3:121840664 | G | A | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-3789G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840664 | |||||||
chr3:121840666 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0230 |
2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.107-3787G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840666 | |||||||
chr3:121840772 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-3681C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840772 | |||||||
chr3:121840805 | C | CA | 91 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(88): Show |
126 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.107-3628dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | ||||||
chr3:121840805 | C | CAA | 13 | a0001c0001t0001g0043 a0001c0001t0001g0080 a0001c0001t0001g0084 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-3629_107-3628d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | ||||||
chr3:121840805 | C | CAAA | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
83 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.107-3630_107-3628d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | ||||||
chr3:121840805 | C | CAAAA | 36 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(33): Show |
47 | HG00423.hp1 HG01109.hp1 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-3631_107-3628d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | ||||||
chr3:121840922 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0102 |
3 | HG01169.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.107-3531C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840922 | |||||||
chr3:121841048 | C | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-3405C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841048 | |||||||
chr3:121841275 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-3178G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841275 | |||||||
chr3:121841376 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-3077A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841376 | |||||||
chr3:121841496 | C | A | 1 | a0001c0002t0001g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.107-2957C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841496 | |||||||
chr3:121841504 | C | CAA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0155 others(3): Show |
9 | HG00140.hp2 HG00323.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-2911_107-2910d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | C | CAAAAAAA others(1): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0113 others(1): Show |
6 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-2917_107-2910d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-2919_107-2910d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0154 a0001c0002t0001g0132 a0001c0002t0001g0239 |
3 | HG01261.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.107-2921_107-2910d others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.107-2923_107-2910d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAA | C | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0115 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-2913_107-2910d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0140 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-2922_107-2910d others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(7): Show |
C | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2923_107-2910d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.107-2924_107-2910d others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(9): Show |
C | 2 | a0001c0002t0001g0141 a0001c0002t0001g0179 |
2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.107-2925_107-2910d others(18): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(10): Show |
C | 6 | a0001c0002t0001g0027 a0001c0002t0001g0073 a0001c0002t0001g0074 others(3): Show |
7 | HG01952.hp1 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-2926_107-2910d others(19): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(11): Show |
C | 25 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0011 others(22): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.107-2927_107-2910d others(20): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(12): Show |
C | 3 | a0001c0002t0001g0078 a0001c0002t0001g0152 a0001c0002t0001g0153 |
3 | NA18946.hp1 NA18959.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.107-2928_107-2910d others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841504 | CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.107-2929_107-2910d others(22): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | ||||||
chr3:121841517 | AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01070.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.107-2932_107-2906d others(29): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841517 | ||||||
chr3:121841518 | AAAAAAAA others(19): Show |
A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
93 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.107-2931_107-2906d others(28): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841518 | ||||||
chr3:121841519 | AAAAAAAA others(18): Show |
A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0019 others(32): Show |
40 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.107-2930_107-2906d others(27): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841519 | ||||||
chr3:121841520 | AAAAAAAA others(17): Show |
A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0092 others(5): Show |
10 | HG01255.hp1 HG01261.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-2929_107-2906d others(26): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841520 | ||||||
chr3:121841524 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107-2925_107-2906d others(22): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841524 | ||||||
chr3:121841525 | AAAAAAAA others(12): Show |
A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2924_107-2906d others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841525 | ||||||
chr3:121841531 | AAAAAAAA others(6): Show |
A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
26 | HG00423.hp1 HG01256.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.107-2918_107-2906d others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841531 | ||||||
chr3:121841532 | AAAAAAAA others(5): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0056 others(3): Show |
9 | HG01109.hp1 HG02280.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-2917_107-2906d others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841532 | ||||||
chr3:121841567 | G | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-2886G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841567 | |||||||
chr3:121841621 | C | A | 1 | a0001c0002t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.107-2832C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841621 | |||||||
chr3:121841643 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.107-2810C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841643 | |||||||
chr3:121841794 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.107-2659G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841794 | |||||||
chr3:121841863 | G | A | 1 | a0001c0007t0001g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-2590G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841863 | |||||||
chr3:121841874 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-2579T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841874 | |||||||
chr3:121841875 | G | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-2578G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841875 | |||||||
chr3:121841881 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107-2572C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841881 | |||||||
chr3:121842016 | A | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
23 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.107-2437A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842016 | |||||||
chr3:121842024 | A | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-2429A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842024 | |||||||
chr3:121842032 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.107-2421A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842032 | |||||||
chr3:121842051 | T | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.107-2402T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842051 | |||||||
chr3:121842147 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-2306G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842147 | |||||||
chr3:121842148 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
36 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-2305C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842148 | |||||||
chr3:121842200 | T | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.107-2253T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842200 | |||||||
chr3:121842250 | G | A | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2203G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842250 | |||||||
chr3:121842256 | C | T | 2 | a0001c0002t0001g0123 a0001c0002t0001g0124 |
2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.107-2197C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842256 | |||||||
chr3:121842287 | T | C | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2166T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842287 | |||||||
chr3:121842552 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.107-1901G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842552 | |||||||
chr3:121842653 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.107-1800T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842653 | |||||||
chr3:121842772 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.107-1681G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842772 | |||||||
chr3:121842786 | C | G | 1 | a0001c0001t0001g0007 | 3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.107-1667C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842786 | |||||||
chr3:121842798 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
185 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.107-1655A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842798 | |||||||
chr3:121842888 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107-1565C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842888 | |||||||
chr3:121842918 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-1535C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842918 | |||||||
chr3:121843026 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-1427C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843026 | |||||||
chr3:121843026 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-1427C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843026 | |||||||
chr3:121843068 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.107-1385T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843068 | |||||||
chr3:121843103 | C | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-1350C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843103 | |||||||
chr3:121843243 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107-1210C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843243 | |||||||
chr3:121843453 | G | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-1000G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843453 | |||||||
chr3:121843457 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-996C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843457 | |||||||
chr3:121843587 | A | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-866A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843587 | |||||||
chr3:121843633 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-820G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843633 | |||||||
chr3:121844073 | T | A | 2 | a0001c0002t0001g0132 a0001c0002t0001g0239 |
2 | HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.107-380T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844073 | |||||||
chr3:121844080 | G | C | 1 | a0001c0002t0001g0127 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.107-373G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844080 | |||||||
chr3:121844106 | T | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-347T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844106 | |||||||
chr3:121844193 | T | TG | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-259dupG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121844193 | ||||||
chr3:121844326 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.107-127G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844326 | |||||||
chr3:121844365 | A | C | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-88A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844365 | |||||||
chr3:121844424 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-29C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844424 | |||||||
chr3:121844438 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-15T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844438 | |||||||
chr3:121844647 | G | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+100G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844647 | |||||||
chr3:121844705 | A | AT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+158_201+159ins others(1): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844705 | |||||||
chr3:121844881 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201+334C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844881 | |||||||
chr3:121845043 | G | C | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.201+496G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845043 | |||||||
chr3:121845061 | CA | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+517delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845061 | ||||||
chr3:121845158 | G | A | 9 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0111 others(6): Show |
13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.201+611G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845158 | |||||||
chr3:121845221 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.201+674C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845221 | |||||||
chr3:121845268 | A | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+721A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845268 | |||||||
chr3:121845440 | C | CA | 53 | a0001c0001t0001g0113 a0001c0001t0001g0159 a0001c0002t0001g0001 others(50): Show |
79 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.201+915dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845440 | ||||||
chr3:121845459 | A | AAAAAAAG | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG01256.hp2 HG02738.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | ||||||
chr3:121845459 | A | AAAAAAG | 32 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(29): Show |
40 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | ||||||
chr3:121845459 | A | AAAAAAGA others(3): Show |
1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.201+915_201+916ins others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | ||||||
chr3:121845459 | A | AAAAAG | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
130 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | ||||||
chr3:121845459 | A | AGAAAG | 3 | a0001c0001t0001g0185 a0001c0001t0001g0230 a0001c0001t0001g0232 |
3 | HG02055.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.201+912_201+913ins others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845459 | |||||||
chr3:121845459 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.201+912A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845459 | |||||||
chr3:121845789 | AG | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+1246delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845789 | ||||||
chr3:121845997 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.201+1450C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845997 | |||||||
chr3:121846039 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.201+1492G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846039 | |||||||
chr3:121846142 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+1595G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846142 | |||||||
chr3:121846717 | G | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+2170G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846717 | |||||||
chr3:121846719 | A | AT | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.201+2183dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121846719 | ||||||
chr3:121847214 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.201+2667C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847214 | |||||||
chr3:121847349 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+2802T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847349 | |||||||
chr3:121847435 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.201+2888T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847435 | |||||||
chr3:121847522 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+2975C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847522 | |||||||
chr3:121847613 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+3066A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847613 | |||||||
chr3:121847634 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+3087G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847634 | |||||||
chr3:121847646 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3099G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847646 | |||||||
chr3:121847648 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG01496.hp2 HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.201+3101G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847648 | |||||||
chr3:121847651 | G | T | 29 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0029 others(26): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.201+3104G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847651 | |||||||
chr3:121847882 | C | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
36 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.201+3335C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847882 | |||||||
chr3:121847997 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0196 a0001c0001t0001g0208 others(3): Show |
8 | HG01255.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+3450C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847997 | |||||||
chr3:121848012 | G | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.201+3465G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848012 | |||||||
chr3:121848229 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3682G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848229 | |||||||
chr3:121848352 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201+3805C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848352 | |||||||
chr3:121848380 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+3833T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848380 | |||||||
chr3:121848383 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.201+3836T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848383 | |||||||
chr3:121848439 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3892T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848439 | |||||||
chr3:121848584 | C | CT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(69): Show |
88 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.201+4046dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121848584 | ||||||
chr3:121848613 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201+4066G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848613 | |||||||
chr3:121848837 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+4290G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848837 | |||||||
chr3:121848850 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4303C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848850 | |||||||
chr3:121848851 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4304T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848851 | |||||||
chr3:121848852 | T | A | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4305T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848852 | |||||||
chr3:121848853 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4306T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848853 | |||||||
chr3:121848856 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4309A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848856 | |||||||
chr3:121848858 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4311A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848858 | |||||||
chr3:121848859 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4312A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848859 | |||||||
chr3:121848860 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4313A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848860 | |||||||
chr3:121848861 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4314T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848861 | |||||||
chr3:121848862 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4315A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848862 | |||||||
chr3:121848863 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4316A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848863 | |||||||
chr3:121848865 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4318G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848865 | |||||||
chr3:121848866 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4319G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848866 | |||||||
chr3:121848878 | GC | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+4340delC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121848878 | ||||||
chr3:121848886 | C | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+4339C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848886 | |||||||
chr3:121848931 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+4384G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848931 | |||||||
chr3:121848942 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.201+4395A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848942 | |||||||
chr3:121849016 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+4469T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849016 | |||||||
chr3:121849190 | G | C | 58 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0008 others(55): Show |
84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.201+4643G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849190 | |||||||
chr3:121849308 | G | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.201+4761G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849308 | |||||||
chr3:121849330 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
2 | HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.201+4783T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849330 | |||||||
chr3:121849364 | A | C | 1 | a0001c0001t0001g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.201+4817A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849364 | |||||||
chr3:121849481 | A | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+4934A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849481 | |||||||
chr3:121849667 | G | A | 58 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0008 others(55): Show |
84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202-5020G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849667 | |||||||
chr3:121849748 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.202-4939C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849748 | |||||||
chr3:121849849 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-4838A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849849 | |||||||
chr3:121849864 | A | G | 39 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.202-4823A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849864 | |||||||
chr3:121849921 | GAT | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0226 |
5 | HG01433.hp2 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-4753_202-4752d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849921 | ||||||
chr3:121849937 | T | C | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.202-4750T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849937 | |||||||
chr3:121849957 | A | AACCTTTT others(312): Show |
16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(13): Show |
23 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-4715_202-4714i others(321): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849957 | ||||||
chr3:121849957 | A | AACCTTTT others(313): Show |
11 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-4715_202-4714i others(322): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849957 | ||||||
chr3:121850232 | T | TTTTA | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.202-4453_202-4450d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121850232 | ||||||
chr3:121850358 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.202-4329A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850358 | |||||||
chr3:121850607 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.202-4080A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850607 | |||||||
chr3:121850619 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.202-4068A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850619 | |||||||
chr3:121850641 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0113 others(3): Show |
8 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-4046C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850641 | |||||||
chr3:121850704 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-3983T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850704 | |||||||
chr3:121850714 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.202-3973T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850714 | |||||||
chr3:121850773 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-3914T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850773 | |||||||
chr3:121850891 | G | C | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-3796G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850891 | |||||||
chr3:121851052 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-3635T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851052 | |||||||
chr3:121851304 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.202-3383A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851304 | |||||||
chr3:121851351 | G | GT | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(49): Show |
65 | HG00558.hp2 HG00642.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.202-3326dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851351 | ||||||
chr3:121851351 | G | GTT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0040 others(9): Show |
23 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-3327_202-3326d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851351 | ||||||
chr3:121851360 | T | G | 4 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0002t0001g0132 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3327T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851360 | |||||||
chr3:121851457 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.202-3230A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851457 | |||||||
chr3:121851715 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-2972A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851715 | |||||||
chr3:121851738 | TG | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-2945delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851738 | ||||||
chr3:121851848 | T | C | 9 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0111 others(6): Show |
13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-2839T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851848 | |||||||
chr3:121852049 | A | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0235 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.202-2638A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852049 | |||||||
chr3:121852714 | A | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0130 |
2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.202-1973A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852714 | |||||||
chr3:121852975 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-1712T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852975 | |||||||
chr3:121852984 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-1703A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852984 | |||||||
chr3:121853061 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-1626T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853061 | |||||||
chr3:121853169 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1518T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853169 | |||||||
chr3:121853247 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-1440C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853247 | |||||||
chr3:121853286 | G | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-1401G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853286 | |||||||
chr3:121853405 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-1282T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853405 | |||||||
chr3:121853413 | C | T | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-1274C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853413 | |||||||
chr3:121853475 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-1212G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853475 | |||||||
chr3:121853525 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1162C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853525 | |||||||
chr3:121853852 | T | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.202-835T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853852 | |||||||
chr3:121854015 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.202-672A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854015 | |||||||
chr3:121854176 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-511C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854176 | |||||||
chr3:121854180 | G | A | 3 | a0002c0003t0001g0183 a0002c0003t0001g0190 a0002c0003t0001g0199 |
3 | HG02027.hp2 HG02074.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.202-507G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854180 | |||||||
chr3:121854315 | C | CA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
141 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.202-353dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121854315 | ||||||
chr3:121854315 | C | CAA | 81 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(78): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.202-354_202-353dup others(2): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121854315 | ||||||
chr3:121854576 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.202-111G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854576 | |||||||
chr3:121854588 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202-99A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854588 | |||||||
chr3:121854608 | C | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-79C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854608 | |||||||
chr3:121854882 | T | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.338+59T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121854882 | |||||||
chr3:121855003 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.338+180T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855003 | |||||||
chr3:121855084 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.338+261C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855084 | |||||||
chr3:121855321 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+498T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855321 | |||||||
chr3:121855325 | C | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.338+502C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855325 | |||||||
chr3:121855368 | T | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.338+545T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855368 | |||||||
chr3:121855372 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(35): Show |
46 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.338+549C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855372 | |||||||
chr3:121855384 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0086 |
2 | HG01361.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.338+561T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855384 | |||||||
chr3:121855386 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.338+563G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855386 | |||||||
chr3:121855411 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.338+588G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855411 | |||||||
chr3:121855622 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+799C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855622 | |||||||
chr3:121856242 | G | A | 1 | a0001c0002t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.339-769G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856242 | |||||||
chr3:121856319 | C | CT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0044 others(14): Show |
19 | HG00280.hp1 HG01074.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.339-678dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 121856319 | ||||||
chr3:121856319 | C | CTTT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
37 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.339-680_339-678dup others(3): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 121856319 | ||||||
chr3:121856365 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.339-646T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856365 | |||||||
chr3:121856395 | T | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-616T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856395 | |||||||
chr3:121856696 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.339-315G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856696 | |||||||
chr3:121856929 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.339-82G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856929 | |||||||
chr3:121857181 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.484+25C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857181 | |||||||
chr3:121857268 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.484+112C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857268 | |||||||
chr3:121857574 | G | A | 2 | a0001c0002t0001g0123 a0001c0002t0001g0124 |
2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.484+418G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857574 | |||||||
chr3:121857591 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484+435A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857591 | |||||||
chr3:121857649 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484+493A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857649 | |||||||
chr3:121857655 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+499A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857655 | |||||||
chr3:121857673 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+517T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857673 | |||||||
chr3:121857705 | G | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.484+549G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857705 | |||||||
chr3:121857856 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0090 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+700T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857856 | |||||||
chr3:121857894 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0230 a0001c0001t0001g0232 |
3 | HG02055.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484+738C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857894 | |||||||
chr3:121858018 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.484+862C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858018 | |||||||
chr3:121858131 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(44): Show |
57 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.484+975C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858131 | |||||||
chr3:121858255 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.484+1099G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858255 | |||||||
chr3:121858786 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+1630C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858786 | |||||||
chr3:121858917 | T | G | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.484+1761T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858917 | |||||||
chr3:121858921 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+1765C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858921 | |||||||
chr3:121859054 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.484+1898G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859054 | |||||||
chr3:121859113 | G | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(25): Show |
36 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.484+1957G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859113 | |||||||
chr3:121859121 | T | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.484+1965T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859121 | |||||||
chr3:121859220 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.484+2064G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859220 | |||||||
chr3:121859362 | T | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2206T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859362 | |||||||
chr3:121859474 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2318T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859474 | |||||||
chr3:121859569 | G | T | 1 | a0001c0002t0001g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.484+2413G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859569 | |||||||
chr3:121859693 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2537G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859693 | |||||||
chr3:121859840 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.484+2684C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859840 | |||||||
chr3:121859900 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.484+2744G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859900 | |||||||
chr3:121859930 | T | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
59 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.484+2774T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859930 | |||||||
chr3:121859991 | T | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+2835T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859991 | |||||||
chr3:121860000 | C | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0184 a0001c0001t0001g0202 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.484+2844C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860000 | |||||||
chr3:121860104 | G | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+2948G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860104 | |||||||
chr3:121860219 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG01884.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.484+3063C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860219 | |||||||
chr3:121860301 | G | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+3145G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860301 | |||||||
chr3:121860367 | G | C | 2 | a0001c0002t0001g0131 a0001c0002t0001g0144 |
2 | NA18941.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.484+3211G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860367 | |||||||
chr3:121860389 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+3233T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860389 | |||||||
chr3:121860435 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+3279C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860435 | |||||||
chr3:121860679 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484+3523C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860679 | |||||||
chr3:121860752 | C | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+3596C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860752 | |||||||
chr3:121860824 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484+3668C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860824 | |||||||
chr3:121860916 | A | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+3760A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860916 | |||||||
chr3:121860947 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+3791G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860947 | |||||||
chr3:121861018 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.484+3862C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861018 | |||||||
chr3:121861119 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484+3963T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861119 | |||||||
chr3:121861131 | A | G | 1 | a0001c0001t0001g0007 | 3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.484+3975A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861131 | |||||||
chr3:121861269 | G | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+4113G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861269 | |||||||
chr3:121861365 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+4209G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861365 | |||||||
chr3:121861486 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+4330T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861486 | |||||||
chr3:121861596 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+4440T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861596 | |||||||
chr3:121862277 | T | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+5121T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862277 | |||||||
chr3:121862344 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+5188G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862344 | |||||||
chr3:121862409 | T | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+5253T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862409 | |||||||
chr3:121862436 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+5280A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862436 | |||||||
chr3:121862498 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484+5342C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862498 | |||||||
chr3:121862576 | C | CT | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+5426dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121862576 | ||||||
chr3:121862688 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.484+5532C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862688 | |||||||
chr3:121863171 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.484+6015C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863171 | |||||||
chr3:121863293 | G | T | 35 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(32): Show |
43 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.484+6137G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863293 | |||||||
chr3:121863405 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.484+6249G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863405 | |||||||
chr3:121863459 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484+6303A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863459 | |||||||
chr3:121863477 | G | A | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.484+6321G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863477 | |||||||
chr3:121863501 | G | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0129 |
7 | HG02015.hp2 HG02027.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.484+6345G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863501 | |||||||
chr3:121863505 | C | T | 7 | a0001c0001t0001g0114 a0001c0001t0001g0138 a0001c0001t0001g0168 others(4): Show |
9 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+6349C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863505 | |||||||
chr3:121863789 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+6633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863789 | |||||||
chr3:121864367 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.484+7211C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864367 | |||||||
chr3:121864545 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+7389G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864545 | |||||||
chr3:121864568 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.484+7412T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864568 | |||||||
chr3:121864637 | A | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+7481A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864637 | |||||||
chr3:121864652 | CAA | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(83): Show |
118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.484+7502_484+7503d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121864652 | ||||||
chr3:121864659 | A | T | 86 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(83): Show |
118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.484+7503A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864659 | |||||||
chr3:121864711 | G | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+7555G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864711 | |||||||
chr3:121864738 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484+7582C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864738 | |||||||
chr3:121864744 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+7588G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864744 | |||||||
chr3:121864848 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-7689G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864848 | |||||||
chr3:121865218 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-7319G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865218 | |||||||
chr3:121865291 | G | GGTTAA | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-7245_485-7241d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121865291 | ||||||
chr3:121865622 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.485-6915G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865622 | |||||||
chr3:121865672 | AT | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-6864delT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865672 | |||||||
chr3:121865673 | TA | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-6863delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865673 | |||||||
chr3:121865675 | T | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 |
3 | HG01074.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.485-6862T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865675 | |||||||
chr3:121865731 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.485-6806A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865731 | |||||||
chr3:121865959 | A | T | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485-6578A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865959 | |||||||
chr3:121865998 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-6539G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865998 | |||||||
chr3:121866152 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
52 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.485-6385C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866152 | |||||||
chr3:121866299 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.485-6238T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866299 | |||||||
chr3:121866304 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-6233C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866304 | |||||||
chr3:121866609 | C | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-5928C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866609 | |||||||
chr3:121866732 | T | TA | 9 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0111 others(6): Show |
13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.485-5797dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121866732 | ||||||
chr3:121866748 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.485-5789T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866748 | |||||||
chr3:121866754 | G | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-5783G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866754 | |||||||
chr3:121866784 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.485-5753G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866784 | |||||||
chr3:121867539 | T | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-4998T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867539 | |||||||
chr3:121867639 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.485-4898G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867639 | |||||||
chr3:121867820 | C | T | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-4717C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867820 | |||||||
chr3:121867830 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.485-4707A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867830 | |||||||
chr3:121867934 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 |
5 | NA18992.hp2 NA19005.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-4603G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867934 | |||||||
chr3:121868017 | A | T | 9 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0111 others(6): Show |
13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.485-4520A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868017 | |||||||
chr3:121868233 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485-4304T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868233 | |||||||
chr3:121868235 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.485-4302T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868235 | |||||||
chr3:121868279 | A | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-4258A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868279 | |||||||
chr3:121868320 | C | T | 1 | a0001c0002t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.485-4217C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868320 | |||||||
chr3:121868365 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-4172G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868365 | |||||||
chr3:121868425 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-4112C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868425 | |||||||
chr3:121868437 | A | G | 9 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0053 others(6): Show |
9 | HG00673.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-4100A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868437 | |||||||
chr3:121868463 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.485-4074G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868463 | |||||||
chr3:121868537 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485-4000G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868537 | |||||||
chr3:121868555 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-3982G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868555 | |||||||
chr3:121868603 | T | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-3934T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868603 | |||||||
chr3:121868686 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.485-3851C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868686 | |||||||
chr3:121868750 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0106 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485-3787A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868750 | |||||||
chr3:121868768 | A | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG01884.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485-3769A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868768 | |||||||
chr3:121868787 | C | G | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.485-3750C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868787 | |||||||
chr3:121868890 | A | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-3647A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868890 | |||||||
chr3:121869027 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.485-3510A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869027 | |||||||
chr3:121869157 | C | T | 1 | a0001c0002t0001g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485-3380C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869157 | |||||||
chr3:121869416 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-3121A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869416 | |||||||
chr3:121869463 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-3074A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869463 | |||||||
chr3:121869494 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.485-3043C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869494 | |||||||
chr3:121869654 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2883G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869654 | |||||||
chr3:121869717 | T | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2820T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869717 | |||||||
chr3:121869718 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-2819T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869718 | |||||||
chr3:121869937 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-2600G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869937 | |||||||
chr3:121869996 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.485-2541G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869996 | |||||||
chr3:121870061 | A | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2476A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870061 | |||||||
chr3:121870065 | C | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2472C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870065 | |||||||
chr3:121870097 | A | ATTT | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2439_485-2437d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121870097 | ||||||
chr3:121870538 | A | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-1999A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870538 | |||||||
chr3:121870566 | A | C | 1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.485-1971A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870566 | |||||||
chr3:121870705 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG01074.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.485-1832A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870705 | |||||||
chr3:121870750 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1787T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870750 | |||||||
chr3:121870756 | G | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-1781G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870756 | |||||||
chr3:121870813 | T | C | 1 | a0001c0002t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.485-1724T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870813 | |||||||
chr3:121870828 | G | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1709G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870828 | |||||||
chr3:121870867 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485-1670C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870867 | |||||||
chr3:121871169 | T | TATATA | 2 | a0001c0001t0001g0019 a0001c0001t0001g0161 |
3 | HG01069.hp2 HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-1348_485-1344d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121871169 | ||||||
chr3:121871180 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.485-1357A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871180 | |||||||
chr3:121871285 | C | T | 3 | a0001c0001t0001g0198 a0001c0002t0001g0117 a0001c0002t0001g0143 |
3 | HG00673.hp2 HG03927.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.485-1252C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871285 | |||||||
chr3:121871317 | AGAATAGA others(1): Show |
A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1211_485-1204d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121871317 | ||||||
chr3:121871326 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.485-1211G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871326 | |||||||
chr3:121871523 | G | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-1014G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871523 | |||||||
chr3:121871564 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-973A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871564 | |||||||
chr3:121871706 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-831A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871706 | |||||||
chr3:121872087 | GA | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
41 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.485-447delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121872087 | ||||||
chr3:121872112 | T | C | 1 | a0001c0002t0001g0142 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.485-425T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872112 | |||||||
chr3:121872158 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.485-379T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872158 | |||||||
chr3:121872223 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-314A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872223 | |||||||
chr3:121873052 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.736+264G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873052 | |||||||
chr3:121873115 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0099 |
4 | HG02280.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+327C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873115 | |||||||
chr3:121873560 | A | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
37 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.736+772A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873560 | |||||||
chr3:121873574 | T | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0195 others(7): Show |
13 | HG00673.hp1 HG01975.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.736+786T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873574 | |||||||
chr3:121873575 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.736+787T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873575 | |||||||
chr3:121873807 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.736+1019T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873807 | |||||||
chr3:121873817 | TTTAGA | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.736+1033_736+1037d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121873817 | ||||||
chr3:121874421 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.736+1633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874421 | |||||||
chr3:121874468 | T | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.736+1680T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874468 | |||||||
chr3:121874922 | G | A | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(41): Show |
54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+2134G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874922 | |||||||
chr3:121875196 | G | T | 1 | a0001c0002t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.736+2408G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875196 | |||||||
chr3:121875414 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.736+2626T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875414 | |||||||
chr3:121875421 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.736+2633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875421 | |||||||
chr3:121875676 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.736+2888C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875676 | |||||||
chr3:121875755 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.736+2967A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875755 | |||||||
chr3:121875844 | AG | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.736+3057delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875844 | |||||||
chr3:121876646 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00140.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.736+3858G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876646 | |||||||
chr3:121876881 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.736+4093G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876881 | |||||||
chr3:121876889 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+4101G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876889 | |||||||
chr3:121877008 | GAGAT | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+4224_736+4227d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877008 | ||||||
chr3:121877010 | GAT | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+4224_736+4225d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877010 | ||||||
chr3:121877029 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.736+4241G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877029 | |||||||
chr3:121877089 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.736+4301G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877089 | |||||||
chr3:121877648 | G | GAAC | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.736+4862_736+4864d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877648 | ||||||
chr3:121877875 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.736+5087G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877875 | |||||||
chr3:121877897 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+5109T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877897 | |||||||
chr3:121877960 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.736+5172T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877960 | |||||||
chr3:121878175 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.736+5387G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878175 | |||||||
chr3:121878191 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.736+5403G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878191 | |||||||
chr3:121878447 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736+5659A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878447 | |||||||
chr3:121878475 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736+5687T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878475 | |||||||
chr3:121878596 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.736+5808C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878596 | |||||||
chr3:121878699 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+5911C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878699 | |||||||
chr3:121878802 | T | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.736+6014T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878802 | |||||||
chr3:121878833 | A | G | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.736+6045A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878833 | |||||||
chr3:121878935 | T | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(6): Show |
11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.736+6147T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878935 | |||||||
chr3:121878948 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.736+6160T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878948 | |||||||
chr3:121879030 | T | A | 1 | a0001c0002t0001g0145 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.736+6242T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879030 | |||||||
chr3:121879041 | T | C | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(41): Show |
54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+6253T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879041 | |||||||
chr3:121879051 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.736+6263A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879051 | |||||||
chr3:121879153 | T | C | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(41): Show |
54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+6365T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879153 | |||||||
chr3:121879155 | TA | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0192 |
4 | HG02015.hp1 NA18941.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+6371delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121879155 | ||||||
chr3:121879292 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.736+6504G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879292 | |||||||
chr3:121879450 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.736+6662A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879450 | |||||||
chr3:121879467 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.736+6679T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879467 | |||||||
chr3:121879620 | C | CTT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.737-6712_737-6711d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121879620 | ||||||
chr3:121880308 | AT | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.737-6020delT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880308 | ||||||
chr3:121880455 | G | GGTGTGT | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(6): Show |
11 | HG00735.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-5854_737-5849d others(8): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0001g0107 others(3): Show |
6 | HG02258.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-5856_737-5849d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0033 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.737-5858_737-5849d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | GGT | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(78): Show |
114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.737-5850_737-5849d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | GGTGT | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(44): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.737-5852_737-5849d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | GGTGTGT | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
78 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.737-5854_737-5849d others(8): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880455 | GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0157 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.737-5856_737-5849d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | ||||||
chr3:121880461 | T | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0170 |
2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.737-5881T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880461 | |||||||
chr3:121880463 | T | G | 1 | a0001c0001t0001g0006 | 4 | HG02257.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.737-5879T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880463 | |||||||
chr3:121880465 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0056 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.737-5877T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880465 | |||||||
chr3:121880501 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.737-5841A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880501 | |||||||
chr3:121880784 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.737-5558C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880784 | |||||||
chr3:121880785 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.737-5557G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880785 | |||||||
chr3:121880825 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.737-5517G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880825 | |||||||
chr3:121881074 | T | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.737-5268T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881074 | |||||||
chr3:121881129 | C | T | 37 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(34): Show |
45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.737-5213C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881129 | |||||||
chr3:121881264 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.737-5078C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881264 | |||||||
chr3:121881465 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0180 others(2): Show |
7 | HG00735.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-4877A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881465 | |||||||
chr3:121881845 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.737-4497A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881845 | |||||||
chr3:121881984 | T | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(12): Show |
19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-4358T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881984 | |||||||
chr3:121882147 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.737-4195A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882147 | |||||||
chr3:121882314 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.737-4028A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882314 | |||||||
chr3:121882348 | CAA | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.737-3980_737-3979d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121882348 | ||||||
chr3:121882529 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.737-3813T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882529 | |||||||
chr3:121882663 | A | G | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(82): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.737-3679A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882663 | |||||||
chr3:121882685 | C | A | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.737-3657C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882685 | |||||||
chr3:121882730 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(12): Show |
19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-3612C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882730 | |||||||
chr3:121882787 | G | GT | 126 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.737-3543dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121882787 | ||||||
chr3:121882947 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.737-3395C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882947 | |||||||
chr3:121883207 | C | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.737-3135C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883207 | |||||||
chr3:121883284 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.737-3058A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883284 | |||||||
chr3:121883495 | T | C | 1 | a0003c0005t0001g0034 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.737-2847T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883495 | |||||||
chr3:121883572 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.737-2770G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883572 | |||||||
chr3:121883733 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0204 a0001c0001t0001g0214 others(1): Show |
5 | HG02723.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-2609A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883733 | |||||||
chr3:121883775 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.737-2567C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883775 | |||||||
chr3:121883813 | C | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.737-2529C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883813 | |||||||
chr3:121884156 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.737-2186G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884156 | |||||||
chr3:121884179 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-2163A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884179 | |||||||
chr3:121884217 | G | A | 2 | a0001c0002t0001g0141 a0001c0002t0001g0179 |
2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.737-2125G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884217 | |||||||
chr3:121884288 | T | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(12): Show |
19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-2054T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884288 | |||||||
chr3:121884312 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0036 others(25): Show |
36 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.737-2030C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884312 | |||||||
chr3:121884340 | C | CA | 50 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(47): Show |
61 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.737-1985dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121884340 | ||||||
chr3:121884340 | CA | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(20): Show |
27 | HG00423.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.737-1985delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121884340 | ||||||
chr3:121884435 | A | T | 7 | a0001c0002t0001g0009 a0001c0002t0001g0111 a0001c0002t0001g0115 others(4): Show |
9 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-1907A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884435 | |||||||
chr3:121884439 | T | A | 1 | a0001c0008t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.737-1903T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884439 | |||||||
chr3:121884616 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.737-1726G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884616 | |||||||
chr3:121884679 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.737-1663C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884679 | |||||||
chr3:121884685 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0110 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.737-1657G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884685 | |||||||
chr3:121884715 | GC | G | 125 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.737-1626delC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884715 | |||||||
chr3:121884724 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.737-1618A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884724 | |||||||
chr3:121885209 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.737-1133A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885209 | |||||||
chr3:121885376 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.737-966C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885376 | |||||||
chr3:121885617 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.737-725C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885617 | |||||||
chr3:121885773 | C | T | 2 | a0001c0002t0001g0141 a0001c0002t0001g0179 |
2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.737-569C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885773 | |||||||
chr3:121886057 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.737-285G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886057 | |||||||
chr3:121886089 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.737-253G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886089 | |||||||
chr3:121886093 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.737-249T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886093 |